Valerio Carelli
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Computer Science
Valerio Carelli's Degrees
- PhD Computer Science University of Milan
- Masters Computer Science University of Milan
- Bachelors Computer Science University of Milan
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(Suggest an Edit or Addition)Valerio Carelli's Published Works
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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Mitochondrial dysfunction as a cause of optic neuropathies (2004) (721)
- Disturbed mitochondrial dynamics and neurodegenerative disorders (2015) (534)
- OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes. (2008) (479)
- Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484. (1997) (471)
- The molecular dissection of mtDNA haplogroup H confirms that the Franco-Cantabrian glacial refuge was a major source for the European gene pool. (2004) (458)
- Multi-system neurological disease is common in patients with OPA1 mutations (2010) (384)
- Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background. (2007) (344)
- Proteolytic cleavage of Opa1 stimulates mitochondrial inner membrane fusion and couples fusion to oxidative phosphorylation. (2014) (339)
- OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion. (2008) (324)
- Complex I deficiency primes Bax-dependent neuronal apoptosis through mitochondrial oxidative damage. (2005) (300)
- The clinical maze of mitochondrial neurology (2013) (298)
- Melanopsin retinal ganglion cell loss in Alzheimer disease (2015) (283)
- Optic nerve degeneration and mitochondrial dysfunction: genetic and acquired optic neuropathies (2002) (265)
- Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy (2002) (254)
- Leber's hereditary optic neuropathy (1997) (254)
- Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors (2007) (252)
- Efficient mitochondrial biogenesis drives incomplete penetrance in Leber’s hereditary optic neuropathy (2013) (233)
- Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy. (2011) (228)
- Leber's hereditary optic neuropathy differentially affects smaller axons in the optic nerve. (2000) (223)
- Retinal nerve fiber layer evaluation by optical coherence tomography in Leber's hereditary optic neuropathy. (2005) (223)
- Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III. (2006) (211)
- Idebenone treatment in Leber's hereditary optic neuropathy. (2011) (210)
- OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution. (2011) (206)
- Mouse mtDNA mutant model of Leber hereditary optic neuropathy (2012) (196)
- Correlation between retinal nerve fibre layer thickness and optic nerve head size: an optical coherence tomography study (2005) (195)
- Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians (2005) (190)
- Leber's Hereditary Optic Neuropathy (LHON) Pathogenic Mutations Induce Mitochondrial-dependent Apoptotic Death in Transmitochondrial Cells Incubated with Galactose Medium* (2003) (187)
- Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees. (2006) (187)
- Melanopsin retinal ganglion cells are resistant to neurodegeneration in mitochondrial optic neuropathies. (2010) (178)
- Severe impairment of complex I-driven adenosine triphosphate synthesis in leber hereditary optic neuropathy cybrids. (2005) (166)
- Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders. (2009) (165)
- Mitochondrial DNA signals of late glacial recolonization of Europe from near eastern refugia. (2012) (165)
- Effect of EPI-743 on the clinical course of the mitochondrial disease Leber hereditary optic neuropathy. (2012) (161)
- The glutamate/cystine xCT antiporter antagonizes glutamine metabolism and reduces nutrient flexibility (2017) (159)
- Phenotypic heterogeneity of the 8344A>G mtDNA “MERRF” mutation (2013) (158)
- New treatments for mitochondrial disease—no time to drop our standards (2013) (155)
- Extensive investigation of a large Brazilian pedigree of 11778/haplogroup J Leber hereditary optic neuropathy. (2003) (152)
- Detection and quantification of retinal nerve fiber layer thickness in optic disc edema using stratus OCT. (2006) (150)
- Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease. (2008) (148)
- Syndromic parkinsonism and dementia associated with OPA 1 missense mutations (2015) (144)
- Visual system involvement in patients with Friedreich's ataxia. (2009) (140)
- Biochemical features of mtDNA 14484 (ND6/m64V) point mutation associated with Leber's hereditary optic neuropathy (1999) (138)
- Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction. (2003) (136)
- OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions. (2017) (135)
- Cells Bearing Mutations Causing Leber's Hereditary Optic Neuropathy Are Sensitized to Fas-induced Apoptosis* (2002) (130)
- Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson’s Disease Models (2018) (129)
- International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic Neuropathy (2017) (128)
- Retinal nerve fiber layer evaluation by optical coherence tomography in unaffected carriers with Leber's hereditary optic neuropathy mutations. (2005) (127)
- Functional alterations of the mitochondrially encoded ND4 subunit associated with Leber's hereditary optic neuropathy (1994) (126)
- MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cells. (1995) (124)
- A neurodegenerative perspective on mitochondrial optic neuropathies (2016) (124)
- Caspase-independent death of Leber’s hereditary optic neuropathy cybrids is driven by energetic failure and mediated by AIF and Endonuclease G (2005) (123)
- Leber's hereditary optic neuropathy with childhood onset. (2006) (123)
- Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell lines. (2004) (121)
- Evidence for a Novel X-Linked Modifier Locus for Leber Hereditary Optic Neuropathy (2008) (117)
- Bioenergetics shapes cellular death pathways in Leber's hereditary optic neuropathy: a model of mitochondrial neurodegeneration. (2004) (116)
- Inefficient coupling between proton transport and ATP synthesis may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the T8993G mutation in mtDNA. (2006) (113)
- Mutations in the UGO1-like protein SLC25A46 cause an optic atrophy spectrum disorder (2015) (113)
- Rewiring of Glutamine Metabolism Is a Bioenergetic Adaptation of Human Cells with Mitochondrial DNA Mutations. (2018) (112)
- The effects of idebenone on mitochondrial bioenergetics (2012) (112)
- The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender? (2014) (112)
- The genetic and metabolic signature of oncocytic transformation implicates HIF1alpha destabilization. (2010) (110)
- Nuclear genes in mitochondrial disorders. (2003) (110)
- Antioxidant defences in cybrids harboring mtDNA mutations associated with Leber's hereditary optic neuropathy (2005) (110)
- Catalytic Activities of Mitochondrial ATP Synthase in Patients with Mitochondrial DNA T8993G Mutation in the ATPase 6 Gene Encoding Subunit a * (2000) (108)
- Gastrointestinal dysmotility in mitochondrial neurogastrointestinal encephalomyopathy is caused by mitochondrial DNA depletion. (2008) (108)
- Mitochondrial DNA and primary mitochondrial dysfunction in Parkinson's disease (2017) (106)
- Infant and Adult Gut Microbiome and Metabolome in Rural Bassa and Urban Settlers from Nigeria. (2018) (106)
- Mathematically modeling the involvement of axons in Leber's hereditary optic neuropathy. (2012) (105)
- Biochemical phenotypes associated with the mitochondrial ATP6 gene mutations at nt8993. (2007) (105)
- Natural history of Leber's hereditary optic neuropathy: longitudinal analysis of the retinal nerve fiber layer by optical coherence tomography. (2010) (103)
- Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways (2015) (103)
- Leber’s Hereditary Optic Neuropathy (2011) (101)
- Bioenergetics of mitochondrial diseases associated with mtDNA mutations. (2004) (100)
- Mitochondrial DNA: Impacting Central and Peripheral Nervous Systems (2014) (97)
- Mitochondrial disorders. (2003) (95)
- The interaction of Q analogs, particularly hydroxydecyl benzoquinone (idebenone), with the respiratory complexes of heart mitochondria. (1996) (95)
- Bilateral visual improvement with unilateral gene therapy injection for Leber hereditary optic neuropathy (2020) (92)
- Eight human OPA1 isoforms, long and short: What are they for? (2018) (92)
- Microcystic macular degeneration from optic neuropathy: not inflammatory, not trans-synaptic degeneration. (2013) (90)
- Deficit of in vivo mitochondrial ATP production in OPA1‐related dominant optic atrophy (2004) (90)
- Ophthalmologic findings in a large pedigree of 11778/Haplogroup J Leber hereditary optic neuropathy. (2004) (89)
- Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment. (2014) (85)
- A mutation threshold distinguishes the antitumorigenic effects of the mitochondrial gene MTND1, an oncojanus function. (2011) (85)
- Retinal nerve fiber layer thickness in nonarteritic anterior ischemic optic neuropathy: OCT characterization of the acute and resolving phases (2008) (84)
- Clinical and brain bioenergetics improvement with idebenone in a patient with Leber's hereditary optic neuropathy: a clinical and 31P-MRS study (1997) (83)
- Association of optic disc size with development and prognosis of Leber's hereditary optic neuropathy. (2009) (83)
- Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy (2016) (82)
- Mitochondrial Optic Neuropathies: How Two Genomes may Kill the Same Cell Type? (2007) (81)
- Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells (2013) (80)
- The optic nerve: A “mito-window” on mitochondrial neurodegeneration (2013) (80)
- The Background of Mitochondrial DNA Haplogroup J Increases the Sensitivity of Leber's Hereditary Optic Neuropathy Cells to 2,5-Hexanedione Toxicity (2009) (79)
- Effects of Light Treatment on Sleep, Cognition, Mood, and Behavior in Alzheimer’s Disease: A Systematic Review (2018) (79)
- Testing Models for Genetic Determination in Migraine (1993) (79)
- The pupil light reflex in Leber's hereditary optic neuropathy: evidence for preservation of melanopsin-expressing retinal ganglion cells. (2013) (78)
- Retinal Ganglion Cells and Circadian Rhythms in Alzheimer’s Disease, Parkinson’s Disease, and Beyond (2017) (78)
- Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber’s Hereditary Optic Neuropathy (2012) (77)
- Patterns of Retinal Ganglion Cell Damage in Neurodegenerative Disorders: Parvocellular vs Magnocellular Degeneration in Optical Coherence Tomography Studies (2017) (76)
- Melanopsin-expressing retinal ganglion cells: implications for human diseases (2011) (75)
- Subclinical carriers and conversions in Leber hereditary optic neuropathy: a prospective psychophysical study. (2006) (75)
- Respiratory Complex I Dysfunction Due to Mitochondrial DNA Mutations Shifts the Voltage Threshold for Opening of the Permeability Transition Pore toward Resting Levels* (2009) (74)
- Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus (2008) (73)
- Idebenone treatment in patients with OPA1-mutant dominant optic atrophy. (2013) (73)
- The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy (2004) (73)
- Optic neuropathies: the tip of the neurodegeneration iceberg (2017) (72)
- Thymidine and deoxyuridine accumulate in tissues of patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) (2007) (72)
- An international classification of inherited metabolic disorders (ICIMD) (2020) (71)
- Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation. (2002) (69)
- Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophy. (2005) (69)
- Redefining phenotypes associated with mitochondrial DNA single deletion (2015) (69)
- Retinal nerve fiber layer thickness in dominant optic atrophy measurements by optical coherence tomography and correlation with age. (2011) (69)
- OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation (2015) (68)
- Macular nerve fibre and ganglion cell layer changes in acute Leber's hereditary optic neuropathy (2015) (68)
- Inhibition of mitochondrial function induces an integrated stress response in oligodendroglia (2009) (68)
- DNA methyltransferase 1 mutations and mitochondrial pathology: is mtDNA methylated? (2015) (66)
- Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy. (2015) (65)
- A Novel Null Homozygous Mutation Confirms CACNA2D2 as a Gene Mutated in Epileptic Encephalopathy (2013) (65)
- Male prevalence of acquired color vision defects in asymptomatic carriers of Leber's hereditary optic neuropathy. (2007) (63)
- Pure and syndromic optic atrophy explained by deep intronic OPA1 mutations and an intralocus modifier. (2014) (63)
- Respiratory function in cybrid cell lines carrying European mtDNA haplogroups: implications for Leber's hereditary optic neuropathy. (2002) (62)
- 'Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation. (2000) (61)
- OPA1 mutations associated with dominant optic atrophy influence optic nerve head size. (2010) (61)
- Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck (2016) (59)
- Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy (2021) (58)
- Efficacy and Safety of Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy Treated within 6 Months of Disease Onset. (2021) (58)
- Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestine. (2006) (56)
- Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy (2002) (55)
- Mitochondria: Biogenesis and mitophagy balance in segregation and clonal expansion of mitochondrial DNA mutations. (2015) (55)
- A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy. (2002) (54)
- Early macular retinal ganglion cell loss in dominant optic atrophy: genotype-phenotype correlation. (2014) (54)
- Medical Management of Hereditary Optic Neuropathies (2014) (54)
- Protection against oxidant-induced apoptosis by exogenous glutathione in Leber hereditary optic neuropathy cybrids. (2008) (53)
- Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patient (1998) (53)
- Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies. (2015) (53)
- Natural History of Conversion of Leber's Hereditary Optic Neuropathy: A Prospective Case Series. (2017) (52)
- Grand Rounds: Could Occupational Exposure to n-Hexane and Other Solvents Precipitate Visual Failure in Leber Hereditary Optic Neuropathy? (2006) (52)
- SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder. (2019) (52)
- Isolation of transcriptomal changes attributable to LHON mutations and the cybridization process. (2005) (51)
- Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy. (2005) (51)
- Mitochondrial disease activates transcripts of the unfolded protein response and cell cycle and inhibits vesicular secretion and oligodendrocyte-specific transcripts. (2006) (51)
- Apoptotic Cell Death of Cybrid Cells Bearing Leber's Hereditary Optic Neuropathy Mutations Is Caspase Independent (2003) (50)
- Parsing the differences in affected with LHON: genetic versus environmental triggers of disease conversion. (2016) (50)
- 'Behr syndrome' with OPA1 compound heterozygote mutations. (2015) (50)
- Brain diffusion‐weighted imaging in Friedreich's ataxia (2011) (50)
- Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy (2002) (49)
- Incomplete penetrance in mitochondrial optic neuropathies. (2017) (49)
- An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells (2009) (47)
- Low Brain Intracellular Free Magnesium in Mitochondrial Cytopathies (1999) (46)
- The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy. (2005) (45)
- International Workshop: Outcome measures and clinical trial readiness in primary mitochondrial myopathies in children and adults. Consensus recommendations. 16–18 November 2016, Rome, Italy (2017) (44)
- Peripapillary vessel density changes in Leber's hereditary optic neuropathy: a new biomarker (2018) (44)
- Visual Outcomes in Leber Hereditary Optic Neuropathy Patients With the m.11778G>A (MTND4) Mitochondrial DNA Mutation. (2020) (44)
- Narcolepsy is a common phenotype in HSAN IE and ADCA-DN. (2014) (44)
- Liver as a Source for Thymidine Phosphorylase Replacement in Mitochondrial Neurogastrointestinal Encephalomyopathy (2014) (44)
- Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy (2015) (43)
- Melanopsin Retinal Ganglion Cells and Pupil: Clinical Implications for Neuro-Ophthalmology (2018) (43)
- Mitochondrial optic neuropathies: our travels from bench to bedside and back again (2013) (43)
- X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinant. (1996) (43)
- Defective mitochondrial adenosine triphosphate production in skeletal muscle from patients with dominant optic atrophy due to OPA1 mutations. (2011) (43)
- Mitochondrial dysfunction in optic neuropathies: animal models and therapeutic options. (2013) (41)
- Secondary Post-Geniculate Involvement in Leber’s Hereditary Optic Neuropathy (2012) (40)
- A Novel in‐Frame 18‐bp Microdeletion in MT‐CYB Causes a Multisystem Disorder with Prominent Exercise Intolerance (2014) (39)
- Inhibition of autophagy curtails visual loss in a model of autosomal dominant optic atrophy (2020) (38)
- “Mitochondrial neuropathies”: A survey from the large cohort of the Italian Network (2016) (38)
- Lack of association between mitochondrial tRNALeu(UUR) point mutation and cluster headache (1995) (38)
- Retinal function and neural conduction along the visual pathways in affected and unaffected carriers with Leber's hereditary optic neuropathy. (2013) (36)
- Colour vision defects in asymptomatic carriers of the Leber’s hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case-control study (2006) (36)
- Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases (2012) (36)
- OPA1: How much do we know to approach therapy? (2018) (35)
- Myoclonus in mitochondrial disorders (2014) (35)
- Leber hereditary optic neuropathy possibly triggered by exposure to tire fire. (2006) (35)
- Retinal Nerve Fiber Layer Thickness Variability in Leber Hereditary Optic Neuropathy Carriers (2012) (35)
- A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. (2011) (35)
- Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber’s hereditary optic neuropathy (2018) (33)
- Expanding and validating the biomarkers for mitochondrial diseases (2020) (33)
- Visual Electrophysiologic Findings in Patients From an Extensive Brazilian Family with Leber's Hereditary Optic Neuropathy Visual electrophysiology in LHON (2004) (32)
- Therapeutic Options in Hereditary Optic Neuropathies (2020) (31)
- Pattern of care and effectiveness of treatment for glioblastoma patients in the real world: Results from a prospective population-based registry. Could survival differ in a high-volume center? (2014) (30)
- Phosphorylated neurofilament heavy chain is a marker of neurodegeneration in Leber hereditary optic neuropathy (LHON) (2008) (30)
- Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models. (2018) (29)
- Macular Microcysts in Mitochondrial Optic Neuropathies: Prevalence and Retinal Layer Thickness Measurements (2015) (29)
- First application of extremely high-resolution magnetic resonance imaging to study microscopic features of normal and LHON human optic nerve. (2002) (29)
- Changes in Choroidal Thickness follow the RNFL Changes in Leber’s Hereditary Optic Neuropathy (2016) (28)
- Revisiting mitochondrial ocular myopathies: a study from the Italian Network (2017) (28)
- SEVERE CMT TYPE 2 WITH FATAL ENCEPHALOPATHY ASSOCIATED WITH A NOVEL MFN2 SPLICING MUTATION (2010) (28)
- Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations (2016) (28)
- Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Position paper on diagnosis, prognosis, and treatment by the MNGIE International Network (2020) (28)
- Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome (2020) (28)
- ATP depletion and caspase independent death of cybrids bearing Leber's Hereditary Optic neuropathy MTDNA mutations incubated in galactose medium. A model for endonuclease G-mediated apoptosis (2004) (27)
- Detection of the mtDNA 14484 mutation on an African-specific haplotype: implications about its role in causing Leber hereditary optic neuropathy. (1996) (27)
- Diffusion Tensor Imaging Mapping of Brain White Matter Pathology in Mitochondrial Optic Neuropathies (2015) (27)
- Intravitreal Gene Therapy vs. Natural History in Patients With Leber Hereditary Optic Neuropathy Carrying the m.11778G>A ND4 Mutation: Systematic Review and Indirect Comparison (2021) (27)
- X-Inactivation patterns in females harboring mtDNA mutations that cause Leber hereditary optic neuropathy. (2007) (27)
- Association of the mtDNA m.4171C>A/MT-ND1 mutation with both optic neuropathy and bilateral brainstem lesions (2014) (27)
- Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis (2008) (26)
- Optic nerve histopathology in a case of Wolfram Syndrome: a mitochondrial pattern of axonal loss. (2013) (26)
- X‐inactivation pattern in multiple tissues from two leber's hereditary optic neuropathy (LHON) patients (2003) (25)
- Liver transplant reverses biochemical imbalance in mitochondrial neurogastrointestinal encephalomyopathy. (2017) (25)
- Natural history of patients with Leber hereditary optic neuropathy—results from the REALITY study (2021) (25)
- Respiratory Complex I Dysfunction Due to Mitochondrial DNA Mutations Shifts the Voltage Threshold for Opening of the Permeability Transition Pore toward Resting Levels (2009) (24)
- Nocturnal melatonin regulation in post-traumatic vegetative state: A possible role for melatonin supplementation? (2014) (23)
- Abnormal lactate after effort in healthy carriers of Leber's hereditary optic neuropathy. (1995) (23)
- The 13042G→A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotype (2005) (23)
- Antioxidants partially restore glutamate transport defect in leber hereditary optic neuropathy cybrids (2008) (23)
- The mitochondrial single-stranded DNA binding protein is essential for initiation of mtDNA replication (2021) (23)
- The Photopic Negative Response: An Objective Measure of Retinal Ganglion Cell Function in Patients With Leber's Hereditary Optic Neuropathy. (2017) (22)
- ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy (2020) (22)
- Keeping in Shape the Dogma of Mitochondrial DNA Maternal Inheritance (2015) (22)
- Optic neuropathy in Lhon and Leigh syndrome. (2001) (21)
- Visual evoked potentials findings in non-affected subjects from a large Brazilian pedigree of 11778 Leber’s hereditary optic neuropathy (2010) (21)
- Clinical syndromes associated with mtDNA mutations: where we stand after 30 years. (2018) (21)
- Optical coherence tomography angiography of the peripapillary retina and optic nerve head in dominant optic atrophy. (2017) (21)
- The idebenone metabolite QS10 restores electron transfer in complex I and coenzyme Q defects. (2018) (21)
- Human extraocular muscles in mitochondrial diseases: comparing chronic progressive external ophthalmoplegia with Leber’s hereditary optic neuropathy (2005) (20)
- Idebenone increases chance of stabilization/recovery of visual acuity in OPA1‐dominant optic atrophy (2020) (20)
- Psychophysical analysis of contrast processing segregated into magnocellular and parvocellular systems in asymptomatic carriers of 11778 Leber's hereditary optic neuropathy (2008) (20)
- Relative post-mortem sparing of afferent pupil fibers in a patient with 3460 Leber's hereditary optic neuropathy (2005) (20)
- Melanopsin-expressing retinal ganglion cells are resistant to cell injury, but not always. (2017) (20)
- Childhood Leber's hereditary optic neuropathy (ND1/3460) with visual recovery. (1998) (20)
- Haplogroup J mitogenomes are the most sensitive to the pesticide rotenone: Relevance for human diseases (2018) (19)
- Changes in mitochondrial complex I activity and coenzyme Q binding site in Leber's hereditary optic neuropathy (LHON). (1997) (19)
- Mitochondrial diseases in adults (2020) (19)
- Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy (2020) (18)
- Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy. (2021) (17)
- Whole‐exome sequencing in adult patients with developmental and epileptic encephalopathy: It is never too late (2020) (17)
- Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies (2012) (17)
- Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells (2018) (17)
- Axonal Degeneration in Peripheral Nerves in a Case of Leber Hereditary Optic Neuropathy (2011) (17)
- Oncocytic glioblastoma: a glioblastoma showing oncocytic changes and increased mitochondrial DNA copy number. (2013) (16)
- Multifocal VEP provide electrophysiological evidence of predominant dysfunction of the optic nerve fibers derived from the central retina in Leber’s hereditary optic neuropathy (2015) (16)
- Familial Unverricht‐Lundborg Disease: A Clinical, Neurophysiologic, and Genetic Study (1997) (16)
- The role of mitochondria in health, ageing, and diseases affecting vision (2006) (15)
- Genetic Basis of Mitochondrial Optic Neuropathies. (2014) (15)
- Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions (2013) (14)
- Metabolomics hallmarks OPA1 variants correlating with their in vitro phenotype and predicting clinical severity (2020) (14)
- Ocular findings in mitochondrial neurogastrointestinal encephalomyopathy: a case report (2004) (14)
- Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy (2018) (14)
- Exploring Metabolic Adaptations to the Acidic Microenvironment of Osteosarcoma Cells Unveils Sphingosine 1-Phosphate as a Valuable Therapeutic Target (2021) (14)
- Long-Term Follow-Up After Unilateral Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy: The RESTORE Study (2020) (14)
- Assessing heteroplasmic load in Leber's hereditary optic neuropathy mutation 3460G->A/MT-ND1 with a real-time PCR quantitative approach. (2007) (13)
- Neuron-specific enolase is elevated in asymptomatic carriers of Leber's hereditary optic neuropathy. (2012) (13)
- DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions (2018) (13)
- Fine-tuning of the respiratory complexes stability and supercomplexes assembly in cells defective of complex III. (2019) (13)
- High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families (2010) (13)
- Functional Changes of Retinal Ganglion Cells and Visual Pathways in Patients with Chronic Leber's Hereditary Optic Neuropathy during One Year of Follow-up. (2019) (12)
- Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations (2020) (12)
- Myelin, mitochondria, and autoimmunity (2008) (12)
- Mitochondrial epilepsy: a cross-sectional nationwide Italian survey (2020) (12)
- Mitochondrial Retinopathies (2021) (11)
- DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism (2020) (11)
- Optical coherence tomography for optic disc edema. (2011) (11)
- Brain and skeletal muscle bioenergetic failure in familial hypobetalipoproteinaemia. (1997) (11)
- Mitochondrial complex I and cell death: a semi-automatic shotgun model (2011) (11)
- ITA-MNGIE: an Italian regional and national survey for mitochondrial neuro-gastro-intestinal encephalomyopathy (2016) (11)
- First TMEM126A missense mutation in an Italian proband with optic atrophy and deafness (2019) (11)
- Novel mutations in DNA2 associated with myopathy and mtDNA instability (2019) (11)
- Mitochondrial disorders (2007) (11)
- Muscle pain in mitochondrial diseases: a picture from the Italian network (2019) (10)
- Chromatic Pupillometry Findings in Alzheimer’s Disease (2020) (10)
- Retinal dysfunction characterizes subtypes of dominant optic atrophy (2018) (10)
- Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1. (2014) (10)
- Variation in OPA1 does not explain the incomplete penetrance of Leber hereditary optic neuropathy (2010) (10)
- Combined Cerebellar Proton MR Spectroscopy and DWI Study of Patients with Friedreich’s Ataxia (2017) (10)
- Biodistribution of intravitreal lenadogene nolparvovec gene therapy in nonhuman primates (2021) (10)
- A Wide Range of 3243A>G/tRNALeu(UUR) (MELAS) Mutation Loads May Segregate in Offspring through the Female Germline Bottleneck (2014) (10)
- HPLC-UV analysis of thymidine and deoxyuridine in plasma of patients with thymidine phosphorylase deficiency. (2014) (9)
- Liver transplantation in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical long-term follow-up and pathogenic implications (2020) (9)
- Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON). (2020) (9)
- Gene Therapies for the Treatment of Leber Hereditary Optic Neuropathy (2021) (9)
- Chapter 4 Leber's Hereditary Optic Neuropathy (2002) (8)
- TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective Study (2022) (8)
- Dominant ACO2 mutations are a frequent cause of isolated optic atrophy (2021) (8)
- Pathological mitophagy disrupts mitochondrial homeostasis in Leber’s hereditary optic neuropathy (2022) (8)
- Dominant Optic Atrophy (DOA) and Sensorineural Hearing Loss: Clinical, Biochemical, Spectroscopic and Molecular Genetic Study of a Large Italian Pedigree Linked to a New Locus on Chromosome 16 (2007) (7)
- Epilepsy in MT‐ATP6 ‐ related mils/NARP: correlation of elettroclinical features with heteroplasmy (2021) (7)
- Understanding the molecular basis and pathogenesis of hereditary optic neuropathies: towards improved diagnosis and management (2022) (7)
- Melanopsin retinal ganglion cells and circadian dysfunction in Alzheimer´s disease (2013) (7)
- The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs (2021) (7)
- The self-inhibited leaky integrator: Transfer functions and steady state relations (1975) (7)
- Reply: Mitochondrial DNA copy number differentiates the Leber's hereditary optic neuropathy affected individuals from the unaffected mutation carriers. (2016) (6)
- Dominant Optic Atrophy (DOA): Modeling the Kaleidoscopic Roles of OPA1 in Mitochondrial Homeostasis (2021) (6)
- Complex II phosphorylation is triggered by unbalanced redox homeostasis in cells lacking complex III. (2018) (6)
- Mitochondrial optic neuropathies: additional facts and concepts – response (2014) (6)
- Impaired Ganglion Cell Function Objectively Assessed by the Photopic Negative Response in Affected and Asymptomatic Members From Brazilian Families With Leber's Hereditary Optic Neuropathy (2021) (5)
- Molecular Mechanisms behind Inherited Neurodegeneration of the Optic Nerve (2021) (5)
- Leber’s hereditary optic neuropathy: new quinone therapies change the paradigm (2012) (5)
- Mitochondrial disorders. (2007) (5)
- Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives (2021) (5)
- Variation in MAPT is not a contributing factor to the incomplete penetrance in LHON (2011) (5)
- Capturing the pattern of transition from carrier to affected in Leber's hereditary optic neuropathy. (2022) (5)
- Chromatic Pupillometry in Isolated Rapid Eye Movement Sleep Behavior Disorder (2021) (5)
- 197th ENMC international workshop: Neuromuscular disorders of mitochondrial fusion and fission – OPA1 and MFN2 molecular mechanisms and therapeutic strategies 26–28 April 2013, Naarden, The Netherlands (2014) (5)
- Reply: Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction. (2016) (5)
- Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS‐associated mtDNA mutations (2021) (5)
- Combined Optic Atrophy and Rod-Cone Dystrophy Expands the RTN4IP1 (Optic Atrophy 10) Phenotype. (2020) (5)
- Cross-Sectional Analysis of Baseline Visual Parameters in Subjects Recruited Into the RESCUE and REVERSE ND4-LHON Gene Therapy Studies (2021) (5)
- Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East (2020) (5)
- Optic nerve structure in healthy subjects. (2006) (4)
- Exploring metabolic reprogramming in melanoma via acquired resistance to the oxidative phosphorylation inhibitor phenformin (2020) (4)
- Erratum: A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck (PLoS ONE (2014) 9:5 (e96663) DOI: 10.1371/journal.pone.0096663) (2014) (4)
- The relevance of migraine in the clinical spectrum of mitochondrial disorders (2022) (4)
- TYMP Variants Result in Late-Onset Mitochondrial Myopathy With Altered Muscle Mitochondrial DNA Homeostasis (2020) (4)
- Colpocephaly in two siblings: further evidence of a genetic transmission. (2000) (4)
- Colpocephaly in two siblings: further evidence of a genetic transmission (2000) (4)
- Retina and melanopsin neurons. (2021) (4)
- Sleep-related periodic respiration with central sleep apnea in Leber Hereditary Optic Neuropathy (LHON). (2010) (4)
- Age-related Temporal Loss Of Retinal Nerve Fibers In Parkinson Disease: A Mitochondrial Pattern? (2011) (4)
- Leber's Hereditary Optic Neuropathy: A Report on Novel mtDNA Pathogenic Variants (2021) (4)
- Dominance in mitochondrial disorders (2005) (4)
- Bilateral Visual Improvement with Unilateral Gene Therapy for Leber Hereditary Optic Neuropathy (LHON) (2020) (4)
- Congenital encephalomyopathy with epilepsy, chorioretinitis, basal ganglia involvement, and muscle minicores (2000) (4)
- Missense PDSS1 mutations in CoenzymeQ10 synthesis cause optic atrophy and sensorineural deafness (2020) (4)
- Brain functional MRI responses to blue light stimulation in Leber's Hereditary Optic Neuropathy. (2021) (4)
- Association of rs3027178 polymorphism in the circadian clock gene PER1 with susceptibility to Alzheimer’s disease and longevity in an Italian population (2021) (3)
- Linkage Analysis of the X Chromosome in a Brazilian Family With Leber Hereditary Optic Neuropathy (LHON) (2005) (3)
- Estrogens Ameliorate Mitochondrial Dysfunction in Leber Hereditary Optic Neuropathy (2010) (3)
- Pathogenesis of retinal ganglion cell death in Leber hereditary optic neuropathy (LHON): possible involvement of mitochondria, light and glutamate. (2006) (3)
- Mitochondrial function and dysfunction within the optic nerve. (2003) (3)
- New Insights on Rotenone Resistance of Complex I Induced by the m.11778G>A/MT-ND4 Mutation Associated with Leber’s Hereditary Optic Neuropathy (2022) (3)
- The m.3890G>A/MT-ND1 mtDNA rare pathogenic variant: expanding clinical and MRI phenotypes. (2021) (3)
- Management of ophthalmologic manifestations of mitochondrial diseases (2017) (3)
- Randomized trial of bilateral gene therapy injection for m.11778G>A MT-ND4 Leber optic neuropathy (2022) (3)
- A novel ALG14 missense variant in an alive child with myopathy, epilepsy, and progressive cerebral atrophy (2021) (3)
- Case Report: A Novel Mutation in the Mitochondrial MT-ND5 Gene Is Associated With Leber Hereditary Optic Neuropathy (LHON) (2021) (3)
- Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 (2023) (3)
- Acute rhabdomyolysis induced by tonic–clonic epileptic seizures in a patient with glucose-6-phosphate dehydrogenase deficiency (2013) (3)
- Preliminary Baseline Characteristics of Patients with Leber Hereditary Optic Neuropathy (LHON) Enrolled in the RESCUE and REVERSE Clinical Gene Therapy Trials (2017) (3)
- An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder (2021) (3)
- Case Report: Optic Atrophy and Nephropathy With m.13513G>A/MT-ND5 mtDNA Pathogenic Variant (2022) (3)
- The pattern of retinal ganglion cell loss in Wolfram syndrome is distinct from mitochondrial optic neuropathies. (2022) (3)
- The role of mtDNA haplogroups on metabolic features in narcolepsy type 1 (2022) (3)
- SARS-CoV-2 infection in patients with primary mitochondrial diseases: Features and outcomes in Italy (2021) (3)
- Hearing Dysfunction in a Large Family Affected by Dominant Optic Atrophy (OPA8-Related DOA): A Human Model of Hidden Auditory Neuropathy (2019) (3)
- EPI-743: Preliminary report on Italian experience in open label study of three patients with acute Leber's hereditary optic neuropathy (2012) (3)
- Consensus on guidelines for idebenone administration in Leber's hereditary optic neuropathy (LHON) (2016) (3)
- Erratum: Proteolytic cleavage of Opa1 stimulates mitochondrial inner membrane fusion and couples fusion to oxidative phosphorylation (Cell Metabolism (2014) 19 (630-641)) (2014) (3)
- Recovery Of Visual Acuity In Dominant Optic Atrophy After Idebenone Treatment (2011) (2)
- Differences in onset between eyes in patients with Leber's hereditary optic neuropathy (LHON) (2017) (2)
- OPAI mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes. Commentary (2008) (2)
- Severe Defect of Complex I–Dependent ATP Synthesis Shapes the Mitochondria–Driven Path of Apoptotic Cell Death in Leber's Hereditary Optic Neuropathy (LHON). (2004) (2)
- Segregation Analysis of a Large Lhon Pedigree Is Consistent With the Existence of a Nuclear Modifying Gene (2003) (2)
- Absence of lenadogene nolparvovec DNA in a brain tumor biopsy from a patient in the REVERSE clinical study, a case report (2022) (2)
- Corrigendum to “Response to: Mitochondrial neuropathy affects peripheral and cranial nerves and is primary or secondary or both” [Neuromuscular Disorders 26/8 (2016) 549] (2017) (2)
- Movement Disorders in Children with a Mitochondrial Disease: A Cross-Sectional Survey from the Nationwide Italian Collaborative Network of Mitochondrial Diseases (2021) (2)
- Optic Nerve Histopathology in a Case of Wolfram Syndrome Demonstrates a Mitochondrial Pattern of Axonal Loss (2012) (2)
- Visual evoked potentials (VEP) and brainstem evoked potentials (BAEP) as diagnostic procedures in Leber’s hereditary optic neuropathy (2007) (2)
- Reactive Oxygen Species in Mitochondrial Optic Neuropathies: Comment. (2015) (2)
- Correction: A Wide Range of 3243A>G/tRNALeu(UUR) (MELAS) Mutation Loads May Segregate in Offspring through the Female Germline Bottleneck (2014) (2)
- Cataplexy and ataxia: red flags for the diagnosis of DNA methyltransferase 1 mutation. (2020) (2)
- Evidence of enteric angiopathy and neuromuscular hypoxia in patients with mitochondrial neurogastrointestinal encephalomyopathy. (2021) (2)
- OPA3, a new regulator of mitochondrial fission? (2012) (1)
- Papillary thyroid carcinoma tall cell variant shares accumulation of mitochondria, mitochondrial DNA mutations, and loss of oxidative phosphorylation complex I integrity with oncocytic tumors (2021) (1)
- Primary mitochondrial myopathy: 12-month follow-up results of an Italian cohort (2022) (1)
- Childhood-Onset Leber Hereditary Optic Neuropathy - Clinical and Prognostic Insights. (2022) (1)
- Implications of mitochondrial DNA mutations in human induced pluripotent stem cells (2021) (1)
- Interaction between Mitochondrial DNA Variants and Mitochondria/Endoplasmic Reticulum Contact Sites: A Perspective Review. (2020) (1)
- rAAV2/2-ND4 for the Treatment of LHON: 72-week Data from the REVERSE Phase III Clinical Trial (Plen02.002) (2019) (1)
- Serial Retinal Nerve Fiber Layer Loss Measured with the GDx VCC in a Large Brazilian Pedigree with 11778 mtDNA Leber's Hereditary Optic Neuropathy (2004) (1)
- Molecular biomarkers correlate with brain grey and white matter changes in patients with mitochondrial m.3243A > G mutation. (2021) (1)
- Case Report: Rare Homozygous RNASEH1 Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions (2022) (1)
- Editorial: Hereditary Optic Neuropathies: A New Perspective (2021) (1)
- A Histopathologic and Morphometric Analysis of Degenerating Melanopsin Retinal Ganglion Cells in Alzheimer’s Disease (2013) (1)
- Functional alteration of mitochondrial complex I in affected and nonaffected individuals with 11778/ND4 Leber's hereditary optic neuropathy (LHON) (1995) (1)
- Safety of lenadogene nolparvovec gene therapy over 5 years in 189 patients with Leber hereditary optic neuropathy. (2022) (1)
- Primary mitochondrial myopathy (2020) (1)
- S12.40 Response to metabolic stress in cybrids obtained from patients with Leber's hereditary optic neuropathy (2008) (1)
- Optic Neuropathy in a Case of Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Ultrastructural Features and Mitochondrial DNA analysis (2011) (1)
- Melanopsin-Containing Retinal Ganglion Cells are Partially Spared by Neurodegeneration in Leber’s Hereditary Optic Neuropathy (2009) (1)
- Erratum: Recessive mutations in RTN4IP1 cause isolated and syndromic optic neuropathies (The American Journal of Human Genetics (2015) 97 (754-6760)) (2015) (1)
- Cataplexy and ataxia: red flags for the diagnosis of DNA methyltransferase 1 mutation. (2019) (1)
- Contrast Sensitivity Mediated by ON- and OFF-Subsystems of the Magno- and Parvocellular Pathways of Asymptomatic Carries of 11778 LHON (2007) (1)
- Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells (2013) (1)
- DNAJC30 defect: a frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndrome (2022) (1)
- Electrocochleography in Auditory Neuropathy Related to Mutations in the OTOF or OPA1 Gene (2021) (1)
- Long term follow-up of recurrent Status Epilepticus and Stroke-Like Episodes in a MELAS family (2019) (1)
- Author Correction: Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome (2020) (1)
- The landscape of mitogenomes from LHON patients carrying the m.14484T>C/MT-ND6 mutation (2019) (1)
- Not all Inherited Mitochondrial Diseases Produce an Optic Neuropathy (2012) (1)
- Reply to: No Association between Rare TWNK Variants and Parkinson's Disease in European Cohorts (2022) (1)
- Pattern-Reversal Visually Evoked Potential (VEP) in Asymptomatic Carriers From an Extensive Brazilian Pedigree With 11778 Leber’s Hereditary Optic Neuropathy (LHON) (2003) (1)
- Longitudinal Study of Optic Disk Perfusion and Retinal Structure in Leber's Hereditary Optic Neuropathy (2022) (1)
- Genetic Analysis of Color Vision Defects in Duchenne Muscular Dystrophy and Leber's Hereditary Optic Neuropathy (2009) (1)
- Re: Pilat et al.: High-resolution imaging of the optic nerve and retina in optic nerve hypoplasia (Ophthalmology 2015;122:1330-9). (2016) (1)
- Mammalian RNase H1 directs RNA primer formation for mtDNA replication initiation and is also necessary for mtDNA replication completion (2022) (1)
- Visual Field Analysis of Leber's Hereditary Optic Neuropathy (LHON) Asymptomatic Nonaffected Carriers (2006) (1)
- Study design and baseline characteristics for the reflect gene therapy trial ofm.11778g>A/ND4-LHON (2022) (1)
- Chloramphenicol-Induced Retinal Degeneration Mimics Kearns-Sayre and NARP Syndromes in Mice: A Model for Mitochondrial Retinal Disease (2002) (1)
- The phase 3 REFLECT trial: Efficacy and safety of bilateral gene therapy for Leber hereditary optic neuropathy ( LHON ) (2022) (1)
- The Mitogenome Relationships and Phylogeography of Barn Swallows (Hirundo rustica) (2022) (1)
- Adult-onset mitochondrial movement disorders: a national picture from the Italian Network (2021) (1)
- Identification and analysis of deletion breakpoints in four Mohr-Tranebjærg syndrome (MTS) patients (2022) (1)
- An Ugo1-like protein is associated with optic atrophy ‘plus’ disorders (2015) (0)
- Optic Nerve Head Morphology Can Differentiate Dominant Optic Atrophy From Leber’s Hereditary Optic Neuropathy (2008) (0)
- Optic Nerve Head Morphology in Patients With Leber's Hereditary Optic Neuropathy Suggests That Optic Disc Size is Relevant for the Visual Outcome (2006) (0)
- Multimodal evaluation of the melanopsin retinal ganglion cells system in relation to circadian rhythms in Alzheimer's disease and aging (2021) (0)
- The Italian reappraisal on the most frequent genetic defects in hereditary optic neuropathies and the global top 10. (2023) (0)
- Assessing the impact of long‐term idebenone treatment on various visual acuity outcomes in Leber's hereditary optic neuropathy ( LHON ): Results, according to disease stage, from the prospective, natural history‐controlled LEROS study (2022) (0)
- Assessing the impact of long‐term idebenone treatment on various visual acuity outcomes in Leber's hereditary optic neuropathy ( LHON ): Results, according to primary mitochondrial DNA mutation, from the prospective, natural history‐controlled LEROS study (2022) (0)
- Neuro-ophthalmological characterization of dominant optic atrophy not due to OPA1 mutations (2021) (0)
- Analysis of Contrast Processing Segregated Into Magnocellular and Parvocellular Systems in Asymptomatic Carriers of 11778 LHON (2006) (0)
- Prospective Evaluation Of Unaffected Carriers Belonging To A Large Lhon Family From Brazil: Results From Five Years Of Follow Up (2006) (0)
- Linkage analysis in Leber’s hereditary optic neuropathy (LHON): failure to locate significant loci in a very large family indicates a polygenic/environmental complex contribution to penetrance (2013) (0)
- 6593 CEREBELLAR 1 HMR SPECTROSCOPY AND DWI STUDY IN PATIENTS WITH FRIEDREICH ’ S ATAXIA (2013) (0)
- Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations (2015) (0)
- Erratum to: Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations (2016) (0)
- Searching for genetic modifiers of Leber's hereditary optic neuropathy penetrance (2012) (0)
- P-9 Construction of a database for a nation-wide Italian collaborative network of mitochondrial diseases (2011) (0)
- Long‐term efficacy and safety of idebenone in patients with Leber's hereditary optic neuropathy ( LHON ) in the subacute/dynamic phase: Results from the prospective, natural history‐controlled LEROS study (2022) (0)
- Relationship between supercomplexes organization and electron flux in cells with complex III dysfunctions (2016) (0)
- Chloramphenicol-Induced Optic Neuropathy in a Mouse Model: An Ultrastructural Study (2008) (0)
- Distribution of Melanopsin Containing Retinal Ganglion Cells in Control and Mitochondrial Optic Neuropathy Subjects (2010) (0)
- Increased Penetrance in Siblings of Affected Females in a Large Leber’s Hereditary Optic Neuropathy Pedigree From Brazil Is Not Reflected by the Frequency of Subclinical Abnormalities (2005) (0)
- OP-BRAI140070 1..13 (2014) (0)
- Measurement of Reactive Oxygen Species Byproduct in Leber’s Hereditary Optic Neuropathy Affected and Carrier Patients (2007) (0)
- Brain & Skeletal Muscle MRS Study in Patients with Myotonic Dystrophy Type 1 (2011) (0)
- Validation of Rare Mitochondrial DNA Point Mutations Pathogenic for Leber’s Hereditary Optic Neuropathy (LHON) (2008) (0)
- Mitochondrial European Educational Training (MEET) (2015) (0)
- Contrast Sensitivity to Achromatic Spatial Drifting Gratings in Asymptomatic Carriers of the MtDNA 11778 Mutation Leber's Hereditary Optic Neuropathy (LHON) (2010) (0)
- Impairment of mitochondrial fusion in dominant optic atrophy, a model for selective neurodegeneration (2006) (0)
- Pathogenic role and biochemical dysfunctions associated with mtDNA ATP6 gene mutations. (2005) (0)
- Subclinical Visual Abnormalities Are Common In Carriers With 11778 LHON From A 300 Member Brazilian Pedigree (2004) (0)
- Results A family with severe early-onset ‘ optic atrophy plus ’ syndrome and asymptomatic parents (2014) (0)
- Mitochondrial DNA Haplogroups May Influence the Clinical Expression of Autosomal Dominant Optic Atrophy (2008) (0)
- RETINAL NERVE FIBER LAYER FEATURES IN PATIENTS AFFECTED WITH LEBER’S HEREDITARY OPTIC NEUROPATHY (2004) (0)
- Erratum to: Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations (2016) (0)
- Mild neurological phenotype in a family carrying a novel N-terminal null GRIN2A variant. (2022) (0)
- Optic Nerve Histopathology in Two Affected Brazilian Cases of 11778 Leber's Hereditary Optic Neuropathy Reveals a Specific Pattern of Axonal Loss (2006) (0)
- Melanopsin Retinal Ganglion Cells are Spared in Wolfram Syndrome (2014) (0)
- Retinal Nerve Fiber Layer Analysis in Unnaffected Carriers From a Leber's Hereditary Optic Neuropathy Brazilian Pedigree Reveals Subclinical Damage in Males (2006) (0)
- OC.08.5 NEUROLOGICAL ABNORMALITIES IN PATIENTS WITH CHRONIC INTESTINAL PSEUDO-OBSTRUCTION (2010) (0)
- Extraocular Clinical Features in Leber's Hereditary Optic Neuropathy (LHON) Italian Families. (2006) (0)
- OP-BRAI140070 1643..1655 (2014) (0)
- Indications of mitochondrial dysfunction in Wolfram syndrome. (2017) (0)
- P-9Construction of a database for a nation-wideItalian collaborative network of mitochondrialdiseases (2011) (0)
- Proceedings of the inaugural European LHON Forum Meeting , held in Frankfurt , Germany (2019) (0)
- Cigarette smoking sharpens mitochondrial dysfunction in LHON fibroblasts promoting disease penetrance (2014) (0)
- Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells (2018) (0)
- M2014 Evidence of Neurological Impairment in Patients With Severe Gut Dysmotility (2010) (0)
- SYMPOSIUM: Mitochondria in Human Disease (2020) (0)
- Melanopsin retinal ganglion cells in LHON patients: an fMRI study of brain activations under monochromatic light stimulation (2018) (0)
- Follow-Up of Pattern-Reversal Visually Evoked Potential in Non-Affected Carriers From an Extensive Brazilian Leber Hereditary Optic Neuropathy (LHON) Pedigree (2009) (0)
- Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome (2020) (0)
- Neurological involvement in mitochondrial eye diseases (2017) (0)
- Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys (2022) (0)
- Indirect Comparison of Lenadogene Nolparvovec Gene Therapy Versus Natural History in Patients with Leber Hereditary Optic Neuropathy Carrying the m.11778G>A MT-ND4 Mutation (2022) (0)
- Indirect Comparison of Lenadogene Nolparvovec Gene Therapy Versus Natural History in Patients with Leber Hereditary Optic Neuropathy Carrying the m.11778G>A MT-ND4 Mutation (2022) (0)
- Optic Disc Size Does Not Influence Occurance of Fundoscopic Abnormalities in Asymptomatic LHON Carriers (2007) (0)
- LHON: A look into nuclear and environmental factors; What is “sufficient”? (2017) (0)
- Opa1/twinkle Double Trouble Underlying ‘Doa Plus’ Phenotype (2012) (0)
- Neuron Specific Enolase: A Potential Serological Marker for Predicting Phenotypic Expression in Carriers and Affected Patients With Leber's Hereditary Optic Neuropathy (2007) (0)
- Hrt Findings In The Affected Members Of A Large 11778 Lhon Pedigree in Brazil (2004) (0)
- Increase of mtDNA Copy Number Is a Successful Compensatory Strategy in Leber’s Hereditary Optic Neuropathy (LHON) (2007) (0)
- DNA Mutations Affecting Complexes I and III Carcinoma Is Associated with Pathogenic Mitochondrial Defective Oxidative Phosphorylation in Thyroid Oncocytic (2006) (0)
- Mitochondrial DNA and OXPHOS Disorders (2004) (0)
- Mitochondrial DNA Haplotype Analysis as a Tool for Reconstruction of Large Leber’s Hereditary Optic Neuropathy Pedigrees (2005) (0)
- Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys (2022) (0)
- Stimulation of complex II activity, Nrf2 activation and metabolic perturbation in cells lacking complex III (2016) (0)
- Genotype–phenotype correlations in mitochondrial optic neuropathies (2009) (0)
- Conversion From Asymptomatic Carrier to Affected Status of Leber's Hereditary Optic Neuropathy (LHON) (2005) (0)
- A mouse model with a missense mutation in ND6 for pre-Leber's hereditary optic neuropathy (2012) (0)
- Erratum to: Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations (2016) (0)
- Anatomical Laser Microdissection of the Ileum Reveals mtDNA Depletion Recovery in A Mitochondrial Neuro-Gastrointestinal Encephalomyopathy (MNGIE) Patient Receiving Liver Transplant (2022) (0)
- OPA1 Mutations Result in a Deficit of In Vivo Mitochondrial ATP Production in Patients with Autosomal Dominant Optic Atrophy (2006) (0)
- Color Vision Defects in Asymptomatic Carriers of the Lebers Hereditary Optic Neuropathy (LHON) MtDNA 11778 Mutation from a Giant Brazilian LHON Pedigree: A Case Control Study (2003) (0)
- Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East (2020) (0)
- Axonal mtDNA Copy Number Correlates With the Neurodegenerative Pattern in Optic Nerve Cross-Sections of Leber’s Hereditary Optic Neuropathy Patients (2009) (0)
- Reading Performance in Asymptomatic Carriers From a Very Large Brazilian Pedigree With 11778 Leber’s Hereditary Optic Neuropathy (LHON) (2005) (0)
- Penetrance And Features In An 8 Generation 300 Member Pedigree Of 11778 Lhon In Brazil (2002) (0)
- A Second Case With the V374A KCND3 Pathogenic Variant in an Italian Patient With Early-Onset Spinocerebellar Ataxia (2022) (0)
- Cracking the nuclear-mitochondrial code in Leber hereditary optic neuropathy (2017) (0)
- Different Patterns of Optic Disc Excavation in Leber’s Hereditary Optic Neuropathy, Dominant Optic Atrophy and High Tension Glaucoma (2007) (0)
- Optic nerve involvement in relation to rest-activity circadian rhythm in Alzheimer's disease (2013) (0)
- Oral Sessions (2019) (0)
- Light-Induced Melatonin Suppression in Mitochondrial Optic Neuropathies (2009) (0)
- Electron microscopy of human melanopsin retinal ganglion cells (2015) (0)
- Demonstration of Efferent Fibers in the Human Optic Nerve (2007) (0)
- 126 Melanopsin-containing retinal ganglion cells resist degeneration in mitochondrial optic neuropathies (2010) (0)
- Cell death of fibroblasts derived from patients with Leber’s hereditary optic neuropathy mtDNA mutations (2004) (0)
- Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder (2022) (0)
- The mt11778/ND4 mutation, in Leber’s hereditary optic neuropathy, is associated with less degeneration in the peripheral nerve compared to the mt3460/ND1 mutation (2014) (0)
- Combined Cerebellar Proton MR Spectroscopy and DWI Study of Patients with Friedreich’s Ataxia (2016) (0)
- Subclinical Injury in an Asymptomatic Carrier of 11778 Leber's Hereditary Optic Neuropathy: Histopathological Evidence for Fascicular Patterns of Axonal Loss in the Optic Nerve (2006) (0)
- A New Scoring System for Scaling Patients With LHON: Getting Away From the Carrier/Affected Paradigm (2007) (0)
- Reply to: “Lack of Association between TWNK Rare Variants and Parkinson's Disease in a Chinese Cohort” (2023) (0)
- Correlations of brain 1 H-MRS , DTI , and post-mortem findings in patients with mitochondrial neurogastrointestinal encephalomyopathy ( MNGIE ) (2009) (0)
- Automatic segmentation of deep grey matter structures for the assessment of DTI images (2008) (0)
- Multimodal investigation of melanopsin retinal ganglion cells in Alzheimer's disease. (2023) (0)
- mtDNA T>G mutation at the nt8993 of the ATP6 gene impairs the coupling mechanism of the F1F0-ATPase. (2005) (0)
- RETINAL NERVE FIBER LAYER CHANGES IN UNAFFECTED MATERNAL RELATIVES OF PATIENTS WITH LEBER’S HEREDITARY OPTIC NEUROPATHY (2004) (0)
- Visual function changes in patients with Leber’s hereditary optic neuropathy during one year of follow-up. (2017) (0)
- Psychophysical analysis of contrast processing segregated into magnocellular and parvocellular systems in asymptomatic carriers of 11778 Leber's hereditary optic neuropathy (2008) (0)
- Comparison of Optic Nerve Head Analysis by CirrusTm Hd-OCT in Dominant Optic Atrophy, Normal Tension Glaucoma and Healthy Subjects (2010) (0)
- Su1722 GASTROINTESTINAL VASCULAR CHANGES IN GENETIC AND IDIOPATIC FORMS OF CRONIC INTESTINAL-PSEUDO OBSTRUCTION (2020) (0)
- The unsolved genetics of LHON: Beyond mtDNA primary mutations what else? (2013) (0)
- Sleep and circadian rhythms in neurodegenerative disorders: Role of melanopsin expressing retinal ganglion cells (2012) (0)
- Screening for Candidate Nuclear Modifying Genes in a Large Brazilian Pedigree with Leber’s Hereditary Optic Neuropathy (2006) (0)
- Contrast sensitivity, but not contrast gain, is affected in asymptomatic carriers of 11778 Leber’s Hereditary Optic Neuropathy (LHON) as assessed with the pedestal--pedestal protocol (2012) (0)
- Optic Nerve Head Morphology in Patients With OPA1-Related Dominant Optic Atrophy Suggests That OPA1 Influences Its Anatomical Conformation (2007) (0)
- Electrophysiologic Findings in Patients With 11778 Leber´s Hereditary Optic Neuropathy (LHON) (2002) (0)
- Perturbed mitochondrial homeostasis in LHON: a new target for rescue strategy (2016) (0)
- Bioenergetic changes associated with the T8993G mutation of the mtDNA ATP6 gene. (2004) (0)
- Clinically-Significant Cardiac Pathology in Leber’s Hereditary Optic Neuropathy (2015) (0)
- Longitudinal Analysis of the Retinal Nerve Fiber Layer Thickness Reduction in Patients With Leber's Hereditary Optic Neuropathy: A Two–Year Follow–Up By OCT (2006) (0)
- Impaired mitochondrial energetic function and altered supramolecular interactions of respiratory chain complexes in cells bearing a novel pathogenic cytochrome b microdeletion (2014) (0)
- Genetic landscape of Leber's hereditary optic neuropathy: reflection on pathogenic mechanisms (2015) (0)
- Mitochondrial Fusion and Leber’s Hereditary Optic Neuropathy mtDNA Point Mutations Cause Altered Nuclear Gene Expression (2003) (0)
- ARYLSULFATASE A PSEUDODEFICIENCY (ASAPD) IN NEUROLEPTIC MALIGNANT SYNDROME (NMS) (1994) (0)
- Evaluation of Potential Treatment Strategies for Leber Hereditary Optic Neuropathy (2003) (0)
- S12.20 Delayed assembly kinetics of respiratory chain complex i in cybrids harbouring primary LHON mutations (2008) (0)
- Comparing Reading Performance of Unaffected Carriers Leber’s Hereditary Optic Neuropathy (LHON) to Two Different Control Groups (2006) (0)
- Degeneration of Peripheral Nerves in Leber's Hereditary Optic Neuropathy (LHON) (2005) (0)
- Brain Diffusion Weighted Imaging Study of Friedreich Ataxia Patients (2007) (0)
- Author response for "Whole‐exome sequencing in adult patients with developmental and epileptic encephalopathy: it is never too late" (2020) (0)
- Understanding the onset of Leber's Hereditary Optic Neuropathy (2018) (0)
- Dominant optic neuropathy: analysis of the energetic efficiency and mitochondrial dynamics (2005) (0)
- Short communication Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis (2008) (0)
- Optic Nerve Head Size Correlates With Penetrance in Maternal Lineages Belonging to the Same Large Brazilian SOA-BR Family With Leber’s Hereditary Optic Neuropathy (2007) (0)
- Circulating Antioxidants, Lipid Peroxidation Products, Cytokines and Neuron-specific Enolase in Leber’s Hereditary Optic Neuropathy (LHON) Patients (2003) (0)
- OPAopathies: Widening the spectrum of human diseases associated with mutations in the OPA1 gene (2011) (0)
- Eye Movements , Strabismus , Amblyopia , and Neuro-Ophthalmology Retinal Function and Neural Conduction Along the Visual Pathways in Affected and Unaffected Carriers With Leber ’ s Hereditary Optic Neuropathy (2013) (0)
- 1 Screening of candidate nuclear genes for modifying role in Leber’s hereditary optic neuropathy penetrance: A signal from manganese superoxide dismutase (2010) (0)
- Tu1251 Mitochondrial Neurogastrointestinal Encephalomyopathy: The Liver As a Tissue Source to Restore Thymidine Phosphorylase Activity (2014) (0)
- Cardiovascular comorbidity in Leber’s hereditary optic neuropathy mtDNA 11778 (2018) (0)
- Retinal Nerve Fiber Layer Thickness in Patients Showing Visual Recovery in Leber’s Hereditary Optic Neuropathy (2005) (0)
- Contrasting the HRT II and the HRT III in Leber's Hereditary Optic Neuropathy (2007) (0)
- Multishell Diffusion MR Tractography Yields Morphological and Microstructural Information of the Anterior Optic Pathway: A Proof-of-Concept Study in Patients with Leber’s Hereditary Optic Neuropathy (2022) (0)
- Evaluation of the energetic efficiency of cells derivedfrom patients with dominant optic neuropathy (DOA). (2005) (0)
- Cardiac sympathetic innervation is an unrecognized disease target in autosomal dominant optic atrophy (2022) (0)
- Inner retina and melanopsin retinal ganglion cells in Parkinson's disease (2022) (0)
- Leber's Hereditary Optic Neuropathy (LHON) as a Chronic Disease: Evidence in Carriers and Affected in a Giant Brazilian Pedigree (2003) (0)
- Asymptomatic Carriers With Leber’s Hereditary Optic Neuropathy Often Demonstrate Visual Field Defects (2010) (0)
- Erratum to: Redefining phenotypes associated with mitochondrial DNA single deletion (2015) (0)
- New Genotype-Phenotype Correlations in OPA1 Patients With Inherited Optic Neuropathies (2008) (0)
- Asymptomatic Carriers of Leber's Hereditary Optic Neuropathy Have Elevated Serum Neuron Specific Enolase (2010) (0)
- Mitochondrial epilepsy: a cross-sectional nationwide Italian survey (2020) (0)
- Indirect Comparison of Lenadogene Nolparvovec Gene Therapy versus Natural History in m.11778G>A MT-ND4 Leber Hereditary Optic Neuropathy Patients (S12.005) (2023) (0)
- Optic Nerve Head Morphology in Unaffected Carriers of Leber’s Hereditary Optic Neuropathy Suggests that Optic Disc Size Influences Disease Expression (2006) (0)
- Natural History of Pre-Sympthomatic to Acute Stage Transition in Leber's Hereditary Optic Neuropathy (2008) (0)
- BRAIN Efficient mitochondrial biogenesis drives incomplete penetrance in Leber’s hereditary optic neuropathy (2014) (0)
- Longitudinal Evaluation of Retinal Nerve Fiber Layer Thickness in Leber’s Hereditary Optic Neuropathy Carriers Shows Relevant Variability Over Time (2009) (0)
- Although smoking and alcohol are known to increase incidence of Leber's Hereditary Optic Neuropathy (LHON) only smoking increases severity of LHON. (2014) (0)
- Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines. (2005) (0)
- A Morphological Study of the Optic Nerve in a Mito-Mouse Model Carrying an ND6 Point Mutation (2011) (0)
- A specific combination of phytoestrogens ameliorates the mitochondrial dysfunction in Leber's hereditary optic neuropathy (2013) (0)
- Long-term Follow-up of m.11778G>A MT-ND4-LHON Patients Treated with Lenadogene Nolparvovec Ocular Gene Therapy: the RESTORE Study (S12.004) (2023) (0)
- Choroidal vascularity index in hereditary optic neuropathies. (2023) (0)
- Mitochondrial optic neuropathies. (2023) (0)
- Erratum to: Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations (2016) (0)
- Co-occurrence of amyotrophic lateral sclerosis and Leber’s hereditary optic neuropathy: is mitochondrial dysfunction a modifier? (2022) (0)
- Multifocal bioelectrical cortical responses in Leber Hereditary Optic Neuropathy (2014) (0)
- Corrigendum to: "Complex II phosphorylation is triggered by unbalanced redox homeostasis in cells lacking complex III." [Biochim. Biophys. Acta 2018;1859(3):182-190.]. (2018) (0)
- Characterization of a Novel OPA1 Mouse Model by Light and Transmission Electron Microscopy (2014) (0)
- ADULT BRAIN Diffusion Tensor ImagingMapping of BrainWhiteMatter Pathology inMitochondrial Optic Neuropathies (2015) (0)
- Optic Nerve Size May Reflect Pattern of Axonal Degeneration in Leber’s Hereditary Optic Neuropathy (2009) (0)
- Optic Nerve Histopathology in a Case of Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE) with Visual System Disturbances. (2004) (0)
- Response to: Mitochondrial neuropathy affects peripheral and cranial nerves and is primary or secondary or both (2016) (0)
- Leber’s hereditary optic neuropathy prevalent phenotype in a family segregating the G13042A/ND5 mtDNA point mutation. (2005) (0)
- Multimodal evaluation of the melanopsin retinal ganglion cells system in relation to circadian rhythms in Alzheimer’s disease and aging (2021) (0)
- Author Correction: Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome (2020) (0)
- Melanopsin retinal ganglion cell-driven contribution to visual and cognitive brain responses in LHON (2020) (0)
- Dominant Optic Atrophy (DOA), Deafness and Nephropathy With Mitochondrial Myopathy Negative for OPA1 Mutations: A New Syndromic Form of DOA? (2008) (0)
- OPA3 IS AN INNER MITOCHONDRIAL MEMBRANE PROTEIN INVOLVED IN MITOCHONDRIAL DYNAMICS REGULATION (2013) (0)
- Retinal Nerve Fiber Layer (RNFL) Assessment and Patterns of RNFL Loss in 200 Members of a LHON Brazilian Pedigree (2003) (0)
- A localized autophagic filter prevents entry of mitochondria carrying pathogenic Opa1 mutations in retinal ganglion cell axons (2016) (0)
- Morphometric Analysis of Optic Nerves In Leber's Hereditary Optic Neuropathy Reveals Preferential Loss Of Small Axons and Myelin Remodeling (2002) (0)
- Search for drpla expansion in cases of mvoclonus epilepsy (1997) (0)
- 57 Modelling ND subunits of complex I: Leber’s hereditary optic neuropathy (LHON) pathogenic mutations and non-synonymous population variants in genotype–phenotype correlation (2010) (0)
- Melanopsin Driven Pupillary Light Response in Leber’s Hereditary Optic Neuropathy (LHON) (2011) (0)
- Leber's hereditary optic neuropathy: the neurologist point of view (2017) (0)
- C URRENT OPINION Mitochondrial dysfunction in optic neuropathies: animal models and therapeutic options (2013) (0)
- Long‐term efficacy and safety of idebenone in patients with Leber's hereditary optic neuropathy ( LHON ) in the chronic phase: Results from the prospective, natural history‐controlled LEROS study (2022) (0)
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What Schools Are Affiliated With Valerio Carelli?
Valerio Carelli is affiliated with the following schools:
