Hannu O. Kalimo
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Philosophy Biology
Hannu O. Kalimo's Degrees
- PhD Medical Genetics University of Helsinki
- Doctorate Medicine University of Helsinki
Why Is Hannu O. Kalimo Influential?
(Suggest an Edit or Addition)Hannu O. Kalimo's Published Works
Number of citations in a given year to any of this author's works
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
- A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD (2011) (3746)
- Muscle Injuries (2005) (508)
- Muscle strain injuries. (2000) (421)
- Interstitial chemotherapy with carmustine-loaded polymers for high-grade gliomas: a randomized double-blind study. (1997) (405)
- Brain Lactic Acidosis and Ischemic Cell Damage: 2. Histopathology (1981) (401)
- The Lumbar Multifidus Muscle Five Years After Surgery for a Lumbar Intervertebral Disc Herniation (1993) (382)
- Muscle injuries: optimising recovery. (2007) (369)
- A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1 (1998) (339)
- The Arctic Alzheimer mutation facilitates early intraneuronal Aβ aggregation and senile plaque formation in transgenic mice (2006) (251)
- CADASIL: a Common Form of Hereditary Arteriopathy Causing Brain Infarcts and Dementia (2002) (246)
- Satellite cell proliferation and the expression of myogenin and desmin in regenerating skeletal muscle: evidence for two different populations of satellite cells. (1995) (237)
- Healing of skeletal muscle injury: an ultrastructural and immunohistochemical study. (1991) (233)
- The gene disrupted in Marinesco-Sjögren syndrome encodes SIL1, an HSPA5 cochaperone (2005) (214)
- Regeneration of injured skeletal muscle after the injury. (2013) (197)
- Regulated expression of exon v6 containing isoforms of CD44 in man: downregulation during malignant transformation of tumors of squamocellular origin (1993) (186)
- Relation between myofibers and connective tissue during muscle injury repair (2000) (185)
- Activation of myogenic precursor cells after muscle injury. (1992) (184)
- The temporal evolution of hypoglycemic brain damage (2004) (181)
- Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients (2009) (178)
- Notch Signaling Regulates Platelet-Derived Growth Factor Receptor-β Expression in Vascular Smooth Muscle Cells (2008) (178)
- The Expression of Intermediate Filament Protein Nestin as Related to Vimentin and Desmin in Regenerating Skeletal Muscle (2001) (178)
- The Multifidus Muscle in Patients with Lumbar Disc Herniation: A Histochemical and Morphometric Analysis of Intraoperative Biopsies (1986) (170)
- Identification of fibroblasts responsible for increased collagen production in localized scleroderma by in situ hybridization. (1988) (170)
- Neuronal histamine deficit in Alzheimer's disease (1997) (168)
- Inflammatory brain changes in Lyme borreliosis. A report on three patients and review of literature. (1996) (161)
- Cdk5 Regulates the Organization of Nestin and Its Association with p35 (2003) (152)
- Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS‐1 mutations that lead to exceptionally high amyloid‐β concentrations (2000) (148)
- Mechanical loading regulates the expression of tenascin-C in the myotendinous junction and tendon but does not induce de novo synthesis in the skeletal muscle (2003) (143)
- Effect of Intensive Training on the Isokinetic Strength and Structure of Lumbar Muscles in Patients With Chronic Low Back Pain (1995) (139)
- Fibrosis and Stenosis of the Long Penetrating Cerebral Arteries: the Cause of the White Matter Pathology in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (2004) (138)
- Tibial muscular dystrophy. Late adult-onset distal myopathy in 66 Finnish patients. (1993) (137)
- CADASIL and CARASIL (2014) (137)
- An Altered Histaminergic Innervation of the Substantia Nigra in Parkinson's Disease (2000) (136)
- Increased brain histamine levels in Parkinson's disease but not in multiple system atrophy (2002) (135)
- Proximal myotonic dystrophy—a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes? (1997) (130)
- X‐Linked myopathy with excessive autophagy: A new hereditary muscle disease (1988) (122)
- PET amyloid ligand [11C]PIB uptake shows predominantly striatal increase in variant Alzheimer's disease. (2008) (119)
- Cellular events during partial cerebral ischemia (1977) (118)
- Effects of severe hypoglycemia on the human brain neuropathological case reports (1980) (117)
- Distal myopathy caused by homozygous missense mutations in the nebulin gene. (2007) (115)
- VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy (2013) (110)
- Review: Molecular genetics and pathology of hereditary small vessel diseases of the brain (2011) (110)
- Metabolic characterization of childhood brain tumors (2002) (110)
- Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel disease (2011) (108)
- Distribution and Modulation of Histamine H3 Receptors in Basal Ganglia and Frontal Cortex of Healthy Controls and Patients with Parkinson's Disease (2001) (105)
- Mechanical loading regulates tenascin-C expression in the osteotendinous junction. (1999) (104)
- Epidemiology of hereditary neuropathy with liability to pressure palsies (HNPP) in south western Finland (1997) (101)
- Pyroglutamate Abeta pathology in APP/PS1KI mice, sporadic and familial Alzheimer’s disease cases (2009) (99)
- Localization of type I and III collagen and fibronectin production in injured gastrocnemius muscle. (1991) (97)
- Evaluation of brain tumor metabolism with [11C]choline PET and 1H-MRS (2003) (97)
- Insidious Cognitive Decline in CADASIL (2004) (96)
- Etiologic aspects of chronic urticaria (1998) (95)
- Variant Alzheimer Disease With Spastic Paraparesis: Neuropathological Phenotype (2001) (93)
- Correlation between the Clinical Symptoms and the Proportion of Mitochondrial DNA Carrying the 8993 Point Mutation in the NARP Syndrome (1995) (92)
- Hypoglycemic brain injury (2004) (91)
- Specific and innervation-regulated expression of the intermediate filament protein nestin at neuromuscular and myotendinous junctions in skeletal muscle. (1999) (91)
- Aberrant p53 expression in astrocytic neoplasms of the brain: association with proliferation. (1993) (90)
- Variant Alzheimer’s disease with spastic paraparesis (2000) (90)
- A highly insoluble state of Aβ similar to that of Alzheimer's disease brain is found in Arctic APP transgenic mice (2009) (90)
- Biology and Treatment (2009) (89)
- Dynamic changes of excitatory amino acid receptors in the rat hippocampus following transient cerebral ischemia (1989) (88)
- Tenascin‐C in the pathobiology and healing process of musculoskeletal tissue injury (2000) (88)
- Lymphocyte homing receptors and adhesion molecules in intravascular malignant lymphomatosis (1989) (88)
- Identification of low molecular weight pyroglutamate A{beta} oligomers in Alzheimer disease: a novel tool for therapy and diagnosis. (2010) (88)
- Ultrastructural changes in the hippocampal CA1 region following transient cerebral ischemia: evidence against programmed cell death (2005) (87)
- INFLUENCE OF GLUTARALDEHYDE AND/OR OSMIUM TETROXIDE ON CELL VOLUME, ION CONTENT, MECHANICAL STABILITY, AND MEMBRANE PERMEABILITY OF EHRLICH ASCITES TUMOR CELLS (1974) (87)
- The ultrastructure of "brain death". II. Electron microscopy of feline cortex after complete ischemia. (1977) (87)
- Monoclonal antibodies selective for α‐synuclein oligomers/protofibrils recognize brain pathology in Lewy body disorders and α‐synuclein transgenic mice with the disease‐causing A30P mutation (2013) (82)
- The pathogenesis of CADASIL: an update (2004) (81)
- Low TENS treatment on post-stroke paretic arm: a three-year follow-up (2000) (80)
- Phenotype of a Homozygous CADASIL Patient in Comparison to 9 Age-Matched Heterozygous Patients With the Same R133C Notch3 Mutation (2001) (80)
- Positron Emission Tomography Examination of Cerebral Blood Flow and Glucose Metabolism in Young CADASIL Patients (2004) (80)
- Low expression of p27 indicates a poor prognosis in patients with high‐grade astrocytomas (2003) (79)
- Peripheral neuromuscular manifestations in systemic sclerosis (scleroderma) (1993) (79)
- Heparan Sulfate Accumulation with Aβ Deposits in Alzheimer's Disease and Tg2576 Mice is Contributed by Glial Cells (2008) (78)
- Similar brain tau pathology in DM2/PROMM and DM1/Steinert disease (2005) (78)
- Correlation between biomechanical and structural changes during the regeneration of skeletal muscle after laceration injury (1998) (77)
- Hypoglycemic Brain Injury: Metabolic and Structural Findings in Rat Cerebellar Cortex during Profound Insulin-Induced Hypoglycemia and in the Recovery Period following Glucose Administration (1981) (74)
- Gene deletions in X-linked muscular dystrophy. (1989) (72)
- Parenchymal Changes Related to Plasma Protein Extravasation in Experimental Seizures (1990) (70)
- Effects of Nonsteroidal Antiinflammatory Medication on Satellite Cell Proliferation During Muscle Regeneration (1998) (69)
- Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene (2012) (69)
- Improvements in the method for the electron microscopic localization of arylsulphatase activity (1966) (69)
- Cellular events during partial cerebral ischemia. I. Electron microscopy of feline cerebral cortex after middle-cerebral-artery occlusion. (1977) (68)
- Structural changes in the rat brain after carotid infusions of hyperosmolar solutions. An electron microscopic study. (1988) (68)
- Hypoglycemic brain injury. I. Metabolic and light microscopic findings in rat cerebral cortex during profound insulin-induced hypoglycemia and in the recovery period following glucose administration. (1980) (66)
- Fatal encephalitis caused by concomitant infection with tick-borne encephalitis virus and Borrelia burgdorferi. (1993) (66)
- Pathology of skeletal muscle and impaired respiratory chain function in long-chain 3-hydroxyacyl-coa dehydrogenase deficiency with the G1528C mutation (1996) (65)
- Lumbar muscles: structure and function. (1989) (64)
- The N-myc proto-oncogene and IGF-II growth factor mRNAs are expressed by distinct cells in human fetal kidney and brain (1989) (64)
- Metabolic, Circulatory, and Structural Alterations in the Rat Brain Induced by Sustained Pentylenetetrazole Seizures (1984) (63)
- Arterioles of the Lenticular Nucleus in CADASIL (2006) (61)
- Alveolar soft part sarcoma: A report of two cases with some histochemical and ultrastructural observations (1979) (61)
- MR characteristics and neuropathology in adult-onset autosomal dominant leukodystrophy with autonomic symptoms. (2006) (61)
- Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2 (2010) (60)
- Prognostic Value of the Expression of Tumor Suppressor Genes p53, p21, p16 and pRb, and Ki-67 Labelling in High Grade Astrocytomas Treated with Radiotherapy (2004) (58)
- Restoration of myofiber continuity after transection injury in the rat soleus (2004) (58)
- Changes in intramuscular collagen and fibronectin in denervation atrophy (1985) (58)
- The dentate gyrus in hypoglycemia: Pathology implicating excititoxin-mediated neuronal necrosis (2004) (57)
- Cerebral microangiopathy in stroke-prone spontaneously hypertensive rats (2004) (57)
- Denervated Segments of Injured Skeletal Muscle Fibers Are Reinnervated by Newly Formed Neuromuscular Junctions (1995) (57)
- Alzheimer disease PS-1 exon 9 deletion defined (1999) (55)
- Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASIL. (2007) (55)
- RETRACTED: VMA21 Deficiency Causes an Autophagic Myopathy by Compromising V-ATPase Activity and Lysosomal Acidification (2009) (55)
- Integrin and dystrophin associated adhesion protein complexes during regeneration of shearing-type muscle injury (2000) (55)
- Dipeptidyl carboxypeptidase 1 (DCP1) and butyrylcholinesterase (BCHE) gene interactions with the apolipoprotein E ε4 allele as risk factors in Alzheimer's disease and in Parkinson's disease with coexisting Alzheimer pathology (2000) (55)
- Alzheimer's disease and apolipoprotein E ε4 allele in older drivers who died in automobile accidents (1997) (53)
- Detection of the founder effect in Finnish CADASIL families (2004) (53)
- Tibial muscular dystrophy – from clinical description to linkage on chromosome 2q31 (1998) (53)
- New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2) (2004) (53)
- MR classification of brain gliomas: value of magnetization transfer and conventional imaging. (1995) (53)
- Neuropathologic findings of dementia with lewy bodies (DLB) in a population-based Vantaa 85+ study. (2009) (52)
- A syndrome of multiple congenital contractures: neuropathological analysis on five fetal cases. (1988) (52)
- Expression of the myc proto-oncogenes in developing human fetal brain. (1990) (52)
- Cerebrovascular lesions in stroke-prone spontaneously hypertensive rats (2004) (52)
- Quantitative Vascular Pathology and Phenotyping Familial and Sporadic Cerebral Small Vessel Diseases (2013) (50)
- STRUCTURAL CHANGES IN THE RAT BRAIN AFTER CAROTID INFUSIONS OF HYPEROSMOLAR SOLUTIONS: A LIGHT MICROSCOPIC AND IMMUNOHISTOCHEMICAL STUDY (1988) (49)
- Lumbar muscle fiber size and type distribution in normal subjects (2005) (49)
- Magnetic Resonance Imaging and Magnetization Transfer in Experimental Myonecrosis in the Rat (1995) (49)
- Lymphocyte migration into the skin: the role of lymphocyte homing receptor (CD44) and endothelial cell antigen (HECA-452). (1990) (49)
- Grading of diffusely infiltrating astrocytomas by quantitative histopathology, cell proliferation and image cytometric DNA analysis (2000) (48)
- Calf muscle atrophy and Achilles tendon healing following experimental tendon division and surgery in rats (1999) (48)
- Experimental myocarditis induced by two different coxsackievirus B3 variants: Aspects of pathogenesis and comparison of diagnostic methods (1995) (47)
- Impaired Endothelial Function of Forearm Resistance Arteries in CADASIL Patients (2007) (47)
- Adhesion in skeletal muscle during regteneration (1992) (47)
- Neurophysiological and mitochondrial abnormalities in MuSK antibody seropositive myasthenia gravis compared to other immunological subtypes (2006) (46)
- Genetically distinct astrocytic and oligodendroglial components in oligoastrocytomas (2007) (46)
- Pathogenetic differences between coxsackie A and B virus infections in newborn mice. (1993) (45)
- Brain lactic acidosis and ischemic cell damage: Quantitative ultrastructural changes in capillaries of rat cerebral cortex (2004) (45)
- Proteome Analysis of Cultivated Vascular Smooth Muscle Cells from a CADASIL Patient (2007) (43)
- High topoisomerase IIα expression associates with high proliferation rate and and poor prognosis in oligodendrogliomas (2000) (43)
- The spread of brain oedema in hypertensive brain injury. (1986) (43)
- Mice carrying a R142C Notch 3 knock–in mutation do not develop a CADASIL‐like phenotype (2005) (43)
- Mapping of tissue tropism determinants in coxsackievirus genomes. (2002) (43)
- A transient hypertensive opening of the blood-brain barrier can lead to brain damage (1988) (42)
- Cases of Alzheimer's disease due to deletion of exon 9 of the presenilin‐1 gene show an unusual but characteristic β‐amyloid pathology known as ‘cotton wool’ plaques (2001) (42)
- Differential expression of two α2-adrenergic receptor subtype mRNAs in human tissues (1992) (42)
- Intracranial aneurysms in three patients with disseminated Lyme borreliosis: cause or chance association? (1998) (41)
- Morphological lesions in the brain preceding the development of postischemic seizures (2004) (41)
- Pathogenesis of brain lesions caused by experimental epilepsy (2004) (41)
- MR Imaging Characteristics and Neuropathology of the Spinal Cord in Adult-Onset Autosomal Dominant Leukodystrophy with Autonomic Symptoms (2008) (40)
- CDKN2/p16 Predicts Survival in Oligodendrogliomas: Comparison with Astrocytomas (1999) (40)
- Expression of α7β1 Integrin Splicing Variants during Skeletal Muscle Regeneration (2002) (40)
- Prevalence and severity of cerebral amyloid angiopathy: a population‐based study on very elderly Finns (Vantaa 85+) (2012) (39)
- Tissue tropism of recombinant coxsackieviruses in an adult mouse model. (2005) (39)
- Ophthalmologic findings in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a cross-sectional study. (2006) (39)
- Normal and hypertrophic scars: quantification and localization of messenger RNAs for type I, III and VI collagens (1994) (39)
- LEBER'S HEREDITARY OPTIC NEURORETINOPATHY, A MITOCHONDRIAL DISEASE? (1984) (38)
- The temporal evolution of hypoglycemic brain damage (2004) (38)
- Molecular Genetic Analysis of p53 Intratumoral Heterogeneity in Human Astrocytic Brain Tumors (2007) (38)
- Hypoglycemic brain injury. II. Electron-microscopic findings in rat cerebral cortical neurons during profound insulin-induced hypoglycemia and in the recovery period following glucose administration. (1980) (38)
- Connective Tissue Changes of the Multifidus Muscle in Patients with Lumbar Disc Herniation An Immunohistologic Study of Collagen Types I and III and Fibronectin (1989) (37)
- The histaminergic system in human thalamus: correlation of innervation to receptor expression (2002) (37)
- α-Synuclein pathology in the spinal cord autonomic nuclei associates with α-synuclein pathology in the brain: a population-based Vantaa 85+ study (2010) (37)
- The role of lactic acidosis in the ischemic nerve cell injury. (1981) (36)
- Pigmented primitive neuroectodermal tumor with multipotential differentiation in cerebellum (pigmented medullomyoblastoma). A case with light- and electron-microscopic, and immunohistochemical analysis. (1987) (36)
- Vascular changes and blood‐brain barrier damage in the pathogenesis of polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (membranous lipodystrophy) (1994) (36)
- Different Clinical Phenotypes in Monozygotic CADASIL Twins With a Novel NOTCH3 Mutation (2009) (35)
- Neurologic symptoms are common during gestation and puerperium in CADASIL (2005) (35)
- Ultrastructural studies on the hypothalamic neurosecretory neurons of the rat (2004) (35)
- Scanning Laser Doppler Flowmetry Shows Reduced Retinal Capillary Blood Flow in CADASIL (2004) (35)
- Observations on exsudation of fibronectin, fibrinogen and albumin in the brain after carotid infusion of hyperosmolar solutions (2004) (34)
- Differential expression of myc, max and RB1 genes in human gliomas and glioma cell lines. (1994) (34)
- Ultrasound, computed tomography and magnetic resonance imaging in myopathies: correlations with electromyography and histopathology (1994) (34)
- The Arctic AβPP mutation leads to Alzheimer’s disease pathology with highly variable topographic deposition of differentially truncated Aβ (2013) (34)
- Pathogenesis of brain lesions caused by experimental epilepsy (2004) (33)
- Transected myofibres may remain permanently divided in two parts (2002) (33)
- Blood-brain barrier leakage and brain edema in stroke-prone spontaneously hypertensive rats. Effect of chronic sympathectomy and low protein/high salt diet. (1987) (32)
- Familial subacute necrotizing encephalomyelopathy of the adult form (adult Leigh syndrome) (1979) (32)
- Ultrastructural studies on the hypothalamic neurosecretory neurons of the rat (1975) (32)
- Muscle paralysis and myosin loss in a patient with cancer cachexia. (2007) (32)
- Tibial muscular dystrophy (1997) (32)
- Myelocystocele with cerebellar heterotopia. Case report. (1979) (32)
- Changes in the integrity of the blood-brain barrier in suckling rats with low dose lead encephalopathy (2004) (31)
- Structural changes in brain tissue under hypoxic-ischemic conditions. (1982) (31)
- Pathogenesis of primary central nervous system lymphoma: invasion of malignant lymphoid cells into and within the brain parenchyme (2004) (30)
- Antioxidant enzymes in oligodendroglial brain tumors: association with proliferation, apoptotic activity and survival (2006) (30)
- Absence of polysialylated NCAM is an unfavorable prognostic phenotype for advanced stage neuroblastoma (2009) (30)
- The Arctic amyloid-β precursor protein (AβPP) mutation results in distinct plaques and accumulation of N- and C-truncated Aβ (2012) (30)
- Blood brain barrier leakage is not a consistent feature of white matter lesions in CADASIL (2019) (30)
- X-linked myopathy with excessive autophagy: a failure of self-eating (2015) (29)
- Cell Cycle Regulators (p21, p53, pRb) in Oligodendrocytic Tumors: a Study by Novel Tumor Microarray Technique (2001) (29)
- Endogenous serum albumin content in brain after short-lasting epileptic seizures (1989) (29)
- The temporal evolution of hypoglycemic brain damage (2004) (29)
- The Significance of Latissimus Dorsi Flap Innervation in Delayed Breast Reconstruction: A Prospective Randomized Study—Magnetic Resonance Imaging and Histologic Findings (2011) (29)
- White matter degeneration with Unverricht-Lundborg progressive myoclonus epilepsy: a translational diffusion-tensor imaging study in patients and cystatin B-deficient mice. (2013) (28)
- Mutant bacteriophage with non-catalytic endosialidase binds to both bacterial and eukaryotic polysialic acid and can be used as probe for its detection (2001) (28)
- Prolonged myalgia in Sindbis virus infection: case description and in vitro infection of myotubes and myoblasts. (2012) (28)
- Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1. (2017) (28)
- Sources of variation in the assessment of cell proliferation using proliferating cell nuclear antigen immunohistochemistry. (1994) (27)
- Reactions of vessel walls and brain parenchyma to the accumulation of Gaucher cells in the Norrbottnian type (type III) of Gaucher disease (2004) (27)
- Mild eccentric stretch injury in skeletal muscle causes transient effects on tensile load and cell proliferation (2004) (27)
- Bicuculline-induced epileptic brain injury (1983) (27)
- Blood-brain barrier leakage and brain edema in stroke-prone spontaneously hypertensive rats (2004) (26)
- Neurofibrillary tau pathology modulated by genetic variation of α‐synuclein (2008) (26)
- Nerve cell injury in the brain of stroke-prone spontaneously hypertensive rats (2004) (26)
- Regulation of α7 integrin by mechanical stress during skeletal muscle regeneration (2001) (25)
- Four new Finnish families with LGMD1D; refinement of the clinical phenotype and the linked 7q36 locus (2011) (25)
- Report of five rare or previously unknown amyloidogenic transthyretin mutations disclosed in Sweden (2009) (25)
- Cultivation of Borrelia burgdorferi from the blood and a subcutaneous lesion of a patient with relapsing febrile nodular nonsuppurative panniculitis. (1992) (25)
- Mutations in the V‐ATPase Assembly Factor VMA21 Cause a Congenital Disorder of Glycosylation With Autophagic Liver Disease (2020) (25)
- The tau S305S mutation causes frontotemporal dementia with parkinsonism (2007) (25)
- Chromogenic in situ hybridization-detected hotspot MYCN amplification associates with Ki-67 expression and inversely with nestin expression in neuroblastomas (2005) (24)
- Familial olivopontocerebellar atrophy with macular degeneration: a separate entity among the olivopontocerebellar atrophies (1986) (24)
- Hypoglycemic brain injury (2004) (24)
- Adult course in dynamin 2 dominant centronuclear myopathy with neonatal onset (2010) (24)
- Enrichment of the R77C α‐sarcoglycan gene mutation in finnish LGMD2D patients (2005) (23)
- Mast cells and IgE in intestinal mucosa in adult atopic dermatitis patients (1988) (23)
- Adrenaline‐induced hypertension: morphological consequences of the blood‐brain barrier disturbance (1988) (23)
- Hereditary Forms of Vascular Dementia (2005) (22)
- Cellular and subcellular alterations of human CNS: studies utilizing in situ perfusion fixation at immediate autopsy. (1974) (22)
- Minicore myopathy with dominant inheritance (1987) (22)
- Pathogenesis of coxsackievirus A9 in mice: role of the viral arginine-glycine-aspartic acid motif. (2003) (21)
- Ultrastructural studies on the hypothalamic neurosecretory neurones of the rat (2004) (21)
- CADASIL mutations and shRNA silencing of NOTCH3 affect actin organization in cultured vascular smooth muscle cells (2012) (21)
- THE EARLY ULTRASTRUCTURAL ALTERATIONS IN THE RABBIT CEREBRAL AND CEREBELLAR CORTEX AFTER COMPRESSION ISCHAEMIA (1979) (20)
- Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL (2006) (20)
- Clusterin/Apolipoprotein J immunoreactivity is associated with white matter damage in cerebral small vessel diseases (2015) (20)
- APOE and AβPP gene variation in cortical and cerebrovascular amyloid-β pathology and Alzheimer's disease: a population-based analysis. (2011) (19)
- Cyst formation and glial response in the brain lesions of stroke-prone spontaneously hypertensive rats (2004) (19)
- Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq. (1988) (19)
- Narrowing in on the causative defect of an intriguing X-linked myopathy with excessive autophagy (2002) (19)
- The efficiency of aldehyde fixation for electron microscopy: Stabilization of rat brain tissue to withstand osmotic stress (1979) (19)
- In situ detection of enterovirus genomes in mouse myocardial tissue by ribonucleic acid probes. (1990) (18)
- Alzheimer changes are common in aged drivers killed in single car crashes and at intersections. (1998) (18)
- Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutation (2009) (18)
- Developmental regulation of NF1 tumor suppressor gene in human peripheral nerve (1998) (18)
- Neuropathological examination in forensic context. (2004) (18)
- Skeletal Muscle Repair After Exercise-Induced Injury (2008) (17)
- Polymorphonuclear neutrophil infiltration into ischemic infarctions: myth or truth? (2013) (17)
- The brain in extreme respiratory acidosis (2004) (17)
- Low field T1ρ imaging of myositis (1998) (16)
- MR relaxation times and fiber type predominance of the psoas and multifidus muscle. An autopsy study. (1993) (16)
- CADASIL: the most common hereditary subcortical vascular dementia (2008) (16)
- Enrichment of the R77C alpha-sarcoglycan gene mutation in Finnish LGMD2D patients. (2005) (16)
- Clinical and muscle biopsy findings in malignant hyperthermia susceptibility (1986) (16)
- VMA21 Deficiency Causes an Autophagic Myopathy by Compromising V-ATPase Activity and Lysosomal Acidification (Retracted article. See vol. 142, pg. 984, 2010) (2009) (16)
- DNA analysis in Finnish patients with hereditary neuropathy with liability to pressure palsies (HNPP). (1994) (16)
- Cardiac autophagic vacuolation in severe X-linked myopathy with excessive autophagy (2017) (16)
- Identification of Low Molecular Weight Pyroglutamate Aβ Oligomers in Alzheimer Disease (2010) (16)
- The ultrastructure of “brain death” (1977) (16)
- Structural changes in the rat brain after carotid infusions of hyperosmolar solutions (2004) (16)
- Electromyography and morphology during regeneration of muscle injury in rats. (1991) (16)
- Peroxiredoxins and antioxidant enzymes in pilocytic astrocytomas. (2007) (15)
- Expression of alpha7beta1 integrin splicing variants during skeletal muscle regeneration. (2002) (15)
- Gene expression analyses of grade II gliomas and identification of rPTPβ/ζ as a candidate oligodendroglioma marker (2008) (15)
- Inclusion body myositis and paramyxoviruses. (1991) (15)
- Mast cells and IgE‐containing cells in gastric mucosa of Helicobacter pylori infected and non‐infected patients with chronic urticaria (2004) (15)
- Importance of storing emergency serum samples for uncovering murder with insulin. (1999) (14)
- Relationships between white matter hyperintensities, cerebral amyloid angiopathy and dementia in a population-based sample of the oldest old. (2013) (13)
- Morphology and function of the parietal cells after proximal selective vagotomy in duodenal ulcer patients. (1984) (13)
- Electrophysiological findings in X‐linked myopathy with excessive autophagy (2002) (13)
- Involvement of autonomic nervous system in experimental allergic neuritis A light- and electron-microscopic study (1982) (13)
- Gelsolin co-occurs with Lewy bodies in vivo and accelerates α-synuclein aggregation in vitro. (2011) (13)
- Muscle pathology in idiopathic cricopharyngeal dysphagia (2004) (13)
- Inhaled nitric oxide treatment inhibits neuronal injury after meconium aspiration in piglets. (2007) (13)
- CD44‐Hyaluronate Interaction Mediates In Vitro Lymphocyte Binding to the White Matter of the Central Nervous System (1994) (13)
- Early ultrasound diagnosis of fetal intracranial tumors (1994) (13)
- Cerebral arteriolar pathology in a 32-year-old patient with CADASIL. (2006) (13)
- Muscle membrane–skeleton protein changes and histopathological characterization of muscle-eye-brain disease (2000) (12)
- Binding of Malignant Lymphoid Cells to the White Matter of the Human Central Nervous System: Role of Different CD44 Isoforms, β1,β2 and β7 Integrins, and L‐selectin (1997) (12)
- Characterization of the perivascular reticulin network in a case of primary brain lymphoma (1985) (12)
- Spread of malignant lymphoid cells into rat central nervous system with intact and disrupted blood–brain barrier (1994) (12)
- Alzheimer's disease and apolipoprotein E epsilon 4 allele in older drivers who died in automobile accidents. (1997) (12)
- The firing rate of motor units in neuromuscular disorders (2004) (12)
- LEBER'S HEREDITARY OPTIC NEURORETINOPATHY: A MITOCHONDRIAL DISEASE? (1984) (11)
- Retraction Notice to: VMA21 Deficiency Causes an Autophagic Myopathy by Compromising V-ATPase Activity and Lysosomal Acidification (2010) (11)
- Regulation of alpha7 integrin by mechanical stress during skeletal muscle regeneration. (2001) (11)
- No cardiomyopathy in X-linked myopathy with excessive autophagy (2015) (11)
- Human adenohypophysis in Nelson syndrome. Ultrastructural and clinical study. (1976) (11)
- Histopathological changes in the rat brain during bicuculline-induced status epilepticus. (1983) (11)
- Wound Healing in Denervated Rat Groin Skin Flap (2000) (11)
- Proliferative Activity and DNA Index Do Not Significantly Predict Survival in Primary Central Nervous System Lymphoma (1995) (10)
- Can the site of brain lesion predict improved motor function after Low-TENS treatment on the post-stroke paretic arm? (2001) (10)
- Protective effect of lesion to the glutamatergic cortico-striatal projections on the hypoglycemic nerve cell injury in rat striatum (2004) (10)
- Gene expression analyses of grade II gliomas and identification of rPTPbeta/zeta as a candidate oligodendroglioma marker. (2008) (10)
- Pathology a Genetics : Cerebrovascular diseases (2005) (10)
- Microanalysis of perineural calcification in diabetic nephropathy (1981) (10)
- The role of the blood-brain barrier in perfusion fixation of the brain for electron microscopy (2005) (10)
- Bedside diagnosis of rippling muscle disease in CAV3 p.A46T mutation carriers (2010) (9)
- Differential expression of two alpha 2-adrenergic receptor subtype mRNAs in human tissues. (1992) (9)
- ACETYLCHOLINESTERASE ACTIVITY AND ITS FAST AXONAL TRANSPORT IN RABBIT SCIATIC NERVES DURING THE RECOVERY PHASE OF EXPERIMENTAL ALLERGIC NEURITIS (1984) (9)
- Influence of systemic factors on experimental epileptic brain injury (1983) (9)
- Intraspinal pigmented schwannoma with malignant progression (2005) (9)
- Reappraisal of a consecutive autopsy series of patients with primary degenerative dementia: Lewy‐related pathology (2007) (9)
- Meconium aspiration induces neuronal injury in piglets (2005) (8)
- PRIMARY MALIGNANT LYMPHOMAS OF THE BRAIN: (1982) (8)
- Cholinesterase activities in the somatic nervous system of rabbits with experimental allergic neuritis (1983) (8)
- Binding of malignant lymphoid cells to the white matter of the human central nervous system: role of different CD44 isoforms, beta 1, beta 2 and beta 7 integrins, and L-selectin. (1997) (8)
- Skeletal muscle HSP expression in response to immobilization and remobilization. (2007) (8)
- Recovery from immobilisation: responses of fast-twitch muscle fibres to spontaneous and intensive exercise in rat calf muscles. (2004) (8)
- Skeletal muscle of patients with gyrate atrophy of the choroid and retina and hyperornithinaemia in ultralow-field magnetic resonance imaging and computed tomography (1996) (8)
- Reply to the remarks by J. B. Brierley and A. W. Brown (2004) (8)
- Introduction: Non‐atherosclerotic Cerebrovascular Disorders (2002) (8)
- Gelsolin amyloid angiopathy causes severe disruption of the arterial wall (2016) (7)
- Late-onset malignant astrocytoma in a case of multiple sclerosis (1979) (7)
- Altered muscle saccharide pattern in X-linked muscular dystrophy. (1984) (7)
- Structural Aspects of Energy Failure States in the Brain (1983) (7)
- Structural aspects of ischemic brain damage. (1986) (7)
- Decreased expression of antioxidant enzymes is associated with aggressive features in ependymomas (2008) (6)
- Non-traumatic forensic neuropathology. (2004) (6)
- Mr Relaxation Times and Fiber Type Predominance of the Psoas and Multifidus Muscle (1993) (6)
- Skeletal Muscle: Physiology, Training and Repair After Injury (2008) (6)
- NATURAL HISTORY OF JUVENILE RHEUMATOID ARTHRITIS A Follow‐up Study of a Case with Special Reference to Clinical, Electroencephalographic and Neuropathological Findings (1978) (6)
- The effects of the method of death and lapsed time on proton relaxation time T1 in autopsied muscle samples. (1993) (6)
- Does chronic brain edema explain the consequences of cerebral small-vessel disease? (2003) (6)
- Pulmonary Reactions Induced By Gold Therapy (1979) (6)
- Chronic urticaria and Helicobacter pylori infection (1998) (5)
- The Modernization of the Autopsy: Application of Ultrastructural and Biochemical Methods to Human Disease (1973) (5)
- Extracellular edema and glial response to it in the cerebellum of suckling rats with low-dose lead encephalopathy (1987) (5)
- Comparison Between Regional Cerebral Ischemia and Total Cerebral Ischemia. an Ultrastructural Study in the Cat (1973) (5)
- Alzheimer changes are common in aged drivers killed in single car crashes and at intersections (1999) (5)
- Accumulation of plasma proteins in Purkinje cells as an indicator of blood-brain barrier breakdown. (2004) (5)
- Neuropsychological functions in variant Alzheimer's disease with spastic paraparesis (2004) (5)
- [Extracranial metastasis of glioblastoma multiforme in a child]. (1974) (4)
- Low field T1rho imaging of myositis. (1998) (4)
- SIGNIFICANCE OF FLUID FLOW FOR MORPHOLOGY OF ACUTE HYPOXIC‐ISCHAEMIC BRAIN CELL INJURY (1984) (4)
- Benzodiazepine sensitivity in Leber's hereditary optic neuroretinopathy (1992) (4)
- The loss of enzyme reaction products from ultrathin sections during the staining for electron microscopy (2004) (3)
- Pitfalls in the preparation of buffers for electron microscopy (1977) (3)
- NEUROPATHOLOGICAL ALTERATIONS FOUND AT FORENSIC AUTOPSY OF DEAD OLD DRIVERS (1994) (3)
- Two cases of Dandy-Walker syndrome and chronic polyneuropathy. (1989) (3)
- [Pompe's disease or glycogen storage disease]. (1982) (3)
- Infantile SPASMS as presenting symptom of mitochondrial DNA 8993 T → G point mutation (1994) (3)
- Mitochondrial encephalomyopathy (2004) (3)
- 5-33-06 Proximal myotonic dystrophy — a family with autosomal dominant muscular dystrophy, cataracts, hearing loss, male hypogonadism and insulin resistance (1997) (3)
- [The regenerative capacity of skeletal muscle]. (1993) (3)
- Vascular changes in rat cerebral cortex during severe incomplete ischemia (1981) (3)
- CADASIL in monozygotic twins (2002) (3)
- Severe elastolysis in hereditary gelsolin (AGel) amyloidosis (2019) (3)
- The Neuropathology of Dementia: Vascular dementias (2004) (3)
- Duchenne muscular dystrophy and idiopathic hyperCKemia in the same family. (2007) (3)
- UvA-DARE ( Digital Academic Repository ) Pyroglutamate Abeta pathology in APP / PS 1 KI mice , sporadic and familial Alzheimer ’ s disease cases (2009) (2)
- Autophagy in neuropathology (2015) (2)
- Details of neuropathology in Arctic Alzheimer's disease (2010) (2)
- [Hypertrophic scar and keloid]. (1995) (2)
- Stable expression of mutated and non-mutated mouse NOTCH3 in C2C12 mouse myoblast (2009) (2)
- Nebulin: Nemaline Myopathies and Associated Disorders (2013) (2)
- LECTIN HISTOCHEMISTRY OF NORMAL AND DISEASED HUMAN MUSCLE: (1982) (1)
- Nerves and muscles of patients after multipolar sequential phrenic nerve stimulation (1996) (1)
- POLG MUTATIONS CAUSE SEVERE EARLY ONSET EPILEPSY WITH LIVER FAILURE (2009) (1)
- The Arctic AβPP mutation leads to Alzheimer’s disease pathology with highly variable topographic deposition of differentially truncated Aβ (2013) (1)
- Scanning electron microscopic appearance of viral-antigen-coated polystyrene balls. (1978) (1)
- Immunohistochemistry and ultrastructure of rimmed vacuolar fibers in tibial muscular dystrophy (1997) (1)
- Diagnostic utility of MUP parameters in chronic neuropathy (1993) (1)
- Diagnosing Vascular Dementia by Skin Biopsy - Uniqueness of CADASIL (2011) (1)
- 485 Neuropsychology and imaging at the preclinical state of cadasil (1998) (1)
- NEURODEGENERATIVE ALTERATIONS OF BRAIN TISSUE AND OTHER CONDITIONS INDICATING POSSIBLE COGNITIVE IMPAIRMENT AMONG ELDERLY DRIVERS, DEAD IN CONNECTION WITH CAR CRASHES (1996) (1)
- Genetic factors modify the clinical course of CADASIL (2009) (1)
- Cerebrovascular Diseases. Pathology and Genetics (2005) (1)
- Catechol-O-methyltransferase in human brain (1994) (1)
- HEREDITARY MYOPATHY WITH ENHANCED AUTOPHAGY (1984) (1)
- [Primary benign lymphoma--tumor biology, pathology and clinical aspects]. (1988) (1)
- Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH 3 causing (2007) (1)
- [Skeletal muscle weakness in a young woman]. (1994) (1)
- Scientific correspondence (2006) (0)
- [Rare extrapyramidal disorders: progressive supranuclear paralysis and striato-nigral degeneration]. (1982) (0)
- [Prions today]. (1993) (0)
- [Skin eruptions and paraparesis resembling pedal signs in a pre- viously healthy male subject]. (1988) (0)
- [Primary brain lymphoma--an insidious tumor of the central nervous system]. (1984) (0)
- Blood brain barrier leakage is not a consistent feature of white matter lesions in CADASIL (2019) (0)
- IN VITRO EVALUATION OF [18F]AH110690 (GE-067) FOR BETA-AMYLOID PLAQUE IMAGING OF ALZHEIMER'S DISEASE (2009) (0)
- Decreased CDKN2 expression in astrocytomas and oligodendrogliomas is associated with poor prognosis (1999) (0)
- [Carnitine deficiency and severe nausea-induced thiamine deficiency causing a metabolic crisis]. (1992) (0)
- Reply (2003) (0)
- Lyme borreliosis andintracranial aneurysm (1999) (0)
- Cerebrovascular Diseases : PathologyaGenetics (2005) (0)
- LYME BORRELIOSIS AND INTRACRANIAL ANEURYSM. AUTHORS' REPLY (1999) (0)
- [In which brain cells does ischemia occur?]. (1989) (0)
- FC032 Chronic urticaria and helicobacter pylori infection (1997) (0)
- Expression of tumor suppressor gene p27 in high grade astrocytomas correlates with survival (1999) (0)
- [Hypothyroidism-associated alveolar hypoventilation and myopathy]. (1993) (0)
- Chromogenic in situ hybridization (CISH) on muscle sections - a new, direct method for molecular diagnosis of myotonic dystrophy type 2 (DM2) (2003) (0)
- [Hereditary neuropathy with liability to pressure palsies--a more common neuropathy than generally thought]. (1998) (0)
- P3-150 Frontotemporal dementia and parkinsonism: A new phenotype of the tau S305S mutation (2006) (0)
- G.P.7.03 Mutations in TPM2 and TPM3 causing nemaline myopathy or arthrogryposis (2009) (0)
- [Peripheral myopathies in Finland--a new kind of muscular dystrophy in the leg]. (1992) (0)
- Molecular genetic and clinical findings in identical twins with CADASIL (2009) (0)
- CELLULAR AND HUMORAL EVENTS IN PERIPHERAL BLOOD AND THEIR CORRELATION TO MORPHOLOGICAL AND BIOCHEMICAL CHANGES IN PERIPHERAL NERVES DURING EAN (1978) (0)
- FC17.2 Symptoms and peripheral nerve function tests in Fabry’s disease (2006) (0)
- Amino acid and protein metabolism in dorsal root ganglia of rabbits with experimental allergic neuritis. (1985) (0)
- 7th European Congress of Neuropathology `Neuropathology 2002' (2002) (0)
- [CADASIL disease: a hereditary arterial disease leading to brain infarctions and dementia]. (1998) (0)
- P3-416: Aβ stimulation leads to elevated levels of heparan sulfate proteoglycans in glial cells (2008) (0)
- [Genetics of Alzheimer disease]. (2005) (0)
- Proceedings: Glioblastoma multiforme with extracranial metastasis in children. (1975) (0)
- [Normal structure and histochemistry of muscle]. (1979) (0)
- Expression of the N- myc protooncogene in human foetal brain, retina and kidney (1987) (0)
- Biochemical and morphological analyses of Aβ deposits in postmortem brain of Arctic APP mutation carriers (2010) (0)
- P2-273 PET-imaging of amyloid depositions and astrocytosis in severe ad and histopathological correlations in one patient (2006) (0)
- Structural Changes in the Brain During the Critical Reduction of Blood Flow or Oxygen Tension (1985) (0)
- [Clinico-pathological conference XXXVII. Progressive ataxia, tetraparesis and mental deterioration in a school aged girl]. (1976) (0)
- LESIONS OF THE GLUTAMATERGIC CORTICO‐SIRIATAL PATHWAY AMELIORATE THE HYPOGLYCEMIC NERVE CELL INJURY IN THE RAT SIRIATUM: 43 (1987) (0)
- [Risk of central pontine myelinolysis in the treatment of severe hyponatremia]. (1989) (0)
- Erratum (2002) (0)
- [Exercise-induced muscular disintegration and fatal kidney failure]. (1984) (0)
- Regeneration of muscle fibres after contusion injury (1990) (0)
- Thrombocytopathy and leukocytopathy in X-linked Myopathy with Excessive Autophagy (XMEA) (2008) (0)
- [Nuclear lamins and their diseases]. (2004) (0)
- P1-038 Immunohistochemical and biochemical analyses of Aβ deposits in Tg-APP-ArcSwe and Tg-APP-Swe transgenic mouse brain (2006) (0)
- Pathogenetic aspects of experimental central pontine myelinolysis (1987) (0)
- NEURONS IN ALLERGIC DEMYELINATION. AN AUTORADIOGRAPHIC STUDY ON DORSAL ROOT GANGLIA IN EXPERIMENTAL ALLERGIC NEURITIS: (1982) (0)
- Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL (2006) (0)
- PATHOGENESIS OF GalC‐EAN. A MORPHOLOGICAL AND IMMUNOLOGICAL STUDY (1984) (0)
- The histaminergic innervation and histamine H3 receptors in basal ganglia of parkinsonian brains (2000) (0)
- Molecular genetics of recessive limb girdle muscular dystrophies in Finland (2004) (0)
- The need for electron microscopy in the diagnosis of inflammatory myopathies (1990) (0)
- MULTI-INFARCT DEMENTIA OF SWEDISH TYPE IS CAUSED BY 3’UTR COL4A1 MUTATION (2017) (0)
- [The use of video conference equipment in education and telepathology]. (1999) (0)
- P1-097: The arctic Alzheimer mutation alters structure and composition of Aβ deposits (2008) (0)
- [Progressive paraparesis]. (1995) (0)
- [Meningeal carcinosis]. (1976) (0)
- Chapter 5 Pathology and pathogenesis of muscle diseases (2003) (0)
- Cerebral amyloid angiopathy, neurodegeneration, and dementia in a population-based study on the very elderly Finns (Vantaa 85+) (2010) (0)
- COX-DEFICIENT MUSCLE FIBERS IN HUMAN CREATINE DEPLETION - A NOVEL FINDING (2003) (0)
- Clinical characterization of variant Alzheimer's disease with spastic paraparesis (2000) (0)
- Correspondence between the molecular genetic analysis and electron microscopic detection of granular osmiophilic material in CADASIL (2009) (0)
- Dipeptidyl carboxypeptidase 1 gene interactions with the apolipoprotein E epsilon4 allele as risk factors in Alzheimer's disease and in Parkinson's disease with co-existing Alzheimer pathology (2000) (0)
- [Electrolyte imbalance and central pontine myelinolysis]. (1985) (0)
- [Carnitine palmitoyltransferase deficiency: fatty acid utilization defect causing myopathy]. (1983) (0)
- Secretory Organelles of the Rat Pineal Gland: Electron Microscopic and Histochemical Studies in vivo and in vitro (2008) (0)
- The relation of migraine, depression and cognition in cadasil (2000) (0)
- [Subacute necrotizing encephalomyelopathy (Leigh's disease)]. (1980) (0)
- P2-033: Pet amyloid ligand [11C]PIB uptake shows predominantly striatal increase in variant Alzheimer's disease (2008) (0)
- Hypomorphic Alleles of the VMA21 Gene Downregulate the V-ATPase and Cause X-Linked Myopathy with Excessive Autophagy (2009) (0)
- [Electron microscopy in the diagnosis of muscle diseases]. (1979) (0)
- Neuropathological changes in rat cerebral cortex during bicuculline‐induced status epilepticus (1981) (0)
- [Inflammatory muscle diseases]. (1993) (0)
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What Schools Are Affiliated With Hannu O. Kalimo?
Hannu O. Kalimo is affiliated with the following schools:
