Jun Shimizu

Q: What Schools Are Affiliated With Jun Shimizu

Jun Shimizu is affiliated with the following schools: University of Tokyo, Tokyo University of Technology, Nagoya University

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Jun Shimizu

Computer Science

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Machine Learning

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Artificial Intelligence

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Computer Science

Jun Shimizu's Degrees

PhD Computer Science University of Tokyo
Masters Computer Science University of Tokyo
Bachelors Computer Science University of Tokyo

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Jun Shimizu'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

Experimental sensory neuropathy induced by sensitization with ganglioside GD1b (1996) (204)
Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease (2019) (204)
Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy (2018) (193)
IFNβ-1b may severely exacerbate Japanese optic-spinal MS in neuromyelitis optica spectrum (2010) (186)
RESPONSE OF ANTI-NMDA RECEPTOR ENCEPHALITIS WITHOUT TUMOR TO IMMUNOTHERAPY INCLUDING RITUXIMAB (2008) (157)
Inflammatory myopathies associated with anti-mitochondrial antibodies. (2012) (86)
Safety and efficacy of eculizumab in Guillain-Barré syndrome: a multicentre, double-blind, randomised phase 2 trial (2018) (82)
Anti-TIF1-&ggr; antibody and cancer-associated myositis: A clinicohistopathologic study (2016) (76)
IgG4 anti-neurofascin155 antibodies in chronic inflammatory demyelinating polyradiculoneuropathy: Clinical significance and diagnostic utility of a conventional assay (2016) (71)
Pathology of the sympathetic nervous system corresponding to the decreased cardiac uptake in 123I-metaiodobenzylguanidine (MIBG) scintigraphy in a patient with Parkinson disease (2006) (71)
Distal myopathy with rimmed vacuoles: Novel mutations in the GNE gene (2002) (70)
Cancer association as a risk factor for anti-HMGCR antibody-positive myopathy (2016) (66)
Role of a streptococcal antigen in the pathogenesis of acute poststreptococcal glomerulonephritis. Characterization of the antigen and a proposed mechanism for the disease. (1992) (47)
Spontaneous regression of an asymptomatic meningioma associated with discontinuation of progesterone agonist administration. (2008) (45)
Clinical features and a mutation with late onset of limb girdle muscular dystrophy 2B (2012) (44)
Migraine with aura‐like headache associated with moyamoya disease (1999) (44)
Heterozygous UDP-GlcNAc 2-epimerase and N-acetylmannosamine kinase domain mutations in the GNE gene result in a less severe GNE myopathy phenotype compared to homozygous N-acetylmannosamine kinase domain mutations (2012) (43)
Distal myopathy with rimmed vacuoles (DMRV) (2004) (41)
Treatment consensus for management of polymyositis and dermatomyositis among rheumatologists, neurologists and dermatologists (2018) (39)
Splicing variant of WDFY4 augments MDA5 signalling and the risk of clinically amyopathic dermatomyositis (2018) (39)
Clinical features and a mutation with late onset of limb girdle muscular dystrophy 2 B (2012) (36)
Severe hypokinesis caused by paraneoplastic anti‐Ma2 encephalitis associated with bilateral intratubular germ‐cell neoplasm of the testes (2007) (33)
Cu/Zn superoxide dismutase-like immunoreactivity is present in Lewy bodies from Parkinson disease: a light and electron microscopic immunocytochemical study (2004) (33)
Upregulation of the pro-apoptotic BH3-only peptide harakiri in spinal neurons of amyotrophic lateral sclerosis patients (2001) (32)
Increased gene dosage of myelin protein zero causes Charcot‐Marie‐Tooth disease (2012) (31)
Adult-onset leukoencephalopathies with vanishing white matter with novel missense mutations in EIF2B2, EIF2B3, and EIF2B5 (2011) (29)
Apoptosis of primary sensory neurons in GD1b-induced sensory ataxic neuropathy (2008) (28)
Investigation of diamond-like carbon films as a promising dielectric material for triboelectric nanogenerator (2019) (28)
Anti-TIF1-γ antibody and cancer-associated myositis (2016) (27)
Chondroitin beta-1,4-N-acetylgalactosaminyltransferase-1 missense mutations are associated with neuropathies (2011) (27)
Tubular aggregate myopathy caused by a novel mutation in the cytoplasmic domain of STIM1 (2016) (26)
A positron emission tomography study on the role of nigral lesions in parkinsonism in patients with amyotrophic lateral sclerosis. (2006) (25)
Polymyositis associated with focal mesangial proliferative glomerulonephritis with depositions of immune complexes (2006) (21)
Respiratory and cardiac function in japanese patients with dysferlinopathy (2016) (21)
Clinicopathologic features of myositis patients with CD8-MHC-1 complex pathology (2017) (21)
Successful treatment of an unresectable inflammatory myofibroblastic tumor of the frontal bone using a cyclooxygenase-2 inhibitor and methotrexate. (2013) (21)
An Autopsy Case of Familial Neuronal Intranuclear Inclusion Disease with Dementia and Neuropathy (2018) (20)
Culture-negative brain abscess with Streptococcus intermedius infection with diagnosis established by direct nucleotide sequence analysis of the 16s ribosomal RNA gene. (2012) (20)
Identification and segmentation of myelinated nerve fibers in a cross-sectional optical microscopic image using a deep learning model (2017) (20)
[Chondroblastoma of the temporal bone: a case report]. (1997) (16)
Clinical features and haplotype analysis of newly identified Japanese patients with gelsolin-related familial amyloidosis of Finnish type (2012) (16)
Experimental acute glomerulonephritis induced in the rabbit with a specific streptococcal antigen (1997) (16)
Chronic Myopathy Associated With Anti–Signal Recognition Particle Antibodies Can Be Misdiagnosed As Facioscapulohumeral Muscular Dystrophy (2016) (15)
[A case of long thoracic nerve palsy, with winged scapula, as a result of prolonged exertion on practicing archery]. (1990) (15)
IFNβ-1b may severely exacerbate Japanese opticspinal MS in neuromyelitis optica spectrum: Japanese optic-spinal MS: Is it MS or neuromyelitis optica and does the answer dictate treatment? (2011) (15)
Unilaterally and rapidly progressing white matter lesion and elevated cytokines in a patient with Tay–Sachs disease (2010) (15)
Inflammatory myopathy with myasthenia gravis (2018) (14)
Molecular Dynamics Simulation of Flattening Process of a High-Temperature, High-Speed Droplet—Influence of Impact Parameters (2007) (14)
Sporadic late‐onset nemaline myopathy as a rare cause of slowly progressive muscle weakness with young adult onset (2015) (14)
Granulomatous myositis induced by anti–PD-1 monoclonal antibodies (2018) (14)
Partial duplication of DHH causes minifascicular neuropathy (2017) (14)
Surgical treatment of blepharoptosis caused by chronic progressive external ophthalmoplegia. (2006) (14)
Novel De Novo KCND3 Mutation in a Japanese Patient with Intellectual Disability, Cerebellar Ataxia, Myoclonus, and Dystonia (2018) (13)
Low back pain due to superior cluneal nerve entrapment: A clinicopathologic study (2018) (13)
Fukutin gene mutations that cause left ventricular noncompaction. (2016) (13)
[Gerstmann-Sträussler-Scheinker disease with heterozygous codon change at prion protein codon 129]. (1992) (12)
First external validation of sensitivity and specificity of the European League Against Rheumatism (EULAR)/American College of Rheumatology (ACR) classification criteria for idiopathic inflammatory myopathies with a Japanese cohort (2019) (12)
A chondroitin synthase-1 (ChSy-1) missense mutation in a patient with neuropathy impairs the elongation of chondroitin sulfate chains initiated by chondroitin N-acetylgalactosaminyltransferase-1. (2013) (11)
Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis with diffuse tubulointerstitial nephritis. (2009) (10)
Rapidly progressive polymyositis with elevated antiacetylcholine receptor antibody activity. (2000) (10)
Atypical parkinsonism caused by Pro105Leu mutation of prion protein (2016) (10)
Clinical efficacy of haematopoietic stem cell transplantation for adult adrenoleukodystrophy (2020) (10)
Successful treatment of infliximab-associated immune-mediated sensory polyradiculopathy with intravenous immunoglobulin (2013) (10)
Familial amyotrophic lateral sclerosis with novel A4D SOD1 mutation with late age at onset and rapid progressive course (2013) (9)
Slowly progressive d-bifunctional protein deficiency with survival to adulthood diagnosed by whole-exome sequencing (2017) (9)
Inflammatory myopathy with myasthenia gravis: thymoma association and polymyositis pathology (2018) (9)
A Novel de novo KIF1A Mutation in a Patient with Autism, Hyperactivity, Epilepsy, Sensory Disturbance, and Spastic Paraplegia (2019) (9)
[Wallenberg's syndrome due to vertebral artery dissection following minimal neck injury--report of two cases]. (1992) (9)
Neuronal intranuclear inclusion disease presenting with recurrent cerebral infarct‐like lesions (2015) (8)
[Malignancy-associated myositis]. (2010) (8)
A case of atypical amyloid polyneuropathy with predominant upper-limb involvement with the diagnosis unexpectedly found at lung operation. (2010) (8)
Antineutrophil cytoplasmic antibody (ANCA)-associated glomerulonephritis with intrarenal aneurysms and renal arteriovenous fistulaes. (2002) (7)
Late‐onset Pompe disease after 4 years of enzyme replacement therapy: An autopsy case (2014) (7)
[A case with myositis as a manifestation of chronic graft-versus-host-disease (GVHD) with severe muscle swelling developed after aggressive muscular exercise]. (2003) (7)
[Skeletal muscle pathology of chronic graft versus host disease accompanied with myositis, affecting predominantly respiratory and distal muscles, and hemosiderosis]. (2001) (7)
[Clinical and histopathological features of myositis associated with anti-mitochondrial antibodies]. (2013) (6)
Hemolytic uremic syndrome without hemolytic anemia: a case report. (1994) (6)
A case of systemic sclerosis with sarcoidosis. (2011) (6)
Hyperkalemia in familial mitochondrial cytopathy. (2008) (6)
A Numerical Study for the Role of Natural Convection in the Melting of a GaSb/InSb/GaSb Sandwich System (2003) (6)
Linear scleroderma with prominent multiple lymphadenopathy followed by the development of polymyositis: A case report and review of published work (2016) (6)
A Homozygous LAMA2 Mutation of c.818G＞A Caused Partial Merosin Deficiency in a Japanese Patient (2017) (6)
Cell-mediated immune response in acute poststreptococcal glomerulonephritis. (1994) (6)
A case report of mixed P- and C-ANCA positive patients with pauci-immune crescentic glomerulonephritis. (1995) (6)
An aneurysm rupturing into a middle cranial fossa arachnoid cyst presenting as an intracystic hemorrhage. (2012) (5)
[X-ray CT of Duchenne muscular dystrophy skeletal muscles--chronological study for five years]. (1991) (5)
Laminarization in Low Reynolds Number Turbulent Duct Flows (1977) (5)
[Meningioma associated with acute subdural hematoma: a case report]. (1998) (5)
Treatment consensus for management of polymyositis and dermatomyositis among rheumatologists, neurologists and dermatologists (2018) (5)
Short communication Pathology of the sympathetic nervous system corresponding to the decreased cardiac uptake in 123 I-metaiodobenzylguanidine (MIBG) scintigraphy in a patient with Parkinson disease (2006) (5)
Transient analysis of LE‐VGF growth of compound semiconductors (1998) (4)
Syndrome of Inappropriate Antidiuretic Hormone Associated with Eosinophilic Granulomatosis with Polyangiitis. (2016) (4)
Unique angiopathy after herpes virus infection. (2004) (4)
Muscle Transcriptomics Shows Overexpression of Cadherin 1 in Inclusion Body Myositis (2022) (4)
[Alien hand sign observed at the initial stage of a case of Creutzfeldt-Jakob disease]. (2009) (3)
[A case of Crow-Fukase syndrome with increased serum interleukin-6]. (1991) (3)
[A case of acid maltase deficiency (juvenile type)--immunohistochemical and biochemical study]. (1992) (3)
Pembrolizumab on pre-existing inclusion body myositis: a case report (2020) (3)
短期記憶障害を呈し抗Ma2抗体，抗NMDAR抗体，抗GluRε2抗体陽性で，後に精巣腫瘍をみとめた傍腫瘍性辺縁系脳炎の1例 (2012) (3)
Repeated treatments with rituximab in a patient with amyloid-like IgM deposition neuropathy (2016) (3)
[A case of fibromuscular dysplasia presenting with Wallenberg syndrome, and developing a giant aneurysm of the internal carotid artery in the cavernous sinus]. (1992) (3)
[Anti-Ma2, anti-NMDA-receptor and anti-GluRε2 limbic encephalitis with testicular seminoma: short-term memory disturbance]. (2012) (2)
Expanded clinical spectrum of oculopharyngodistal myopathy type 1 (2022) (2)
A case of late‐onset Krabbe disease which showed subacute progression of spastic paresis with bilateral spinal cord lesions (2018) (2)
DMD exon 2 duplication due to a complex genomic rearrangement is associated with a somatic mosaicism (2021) (2)
[Identification and analysis of immune cells infiltrating into the glomerulus and interstitium in lupus nephritis]. (1995) (2)
Sarcolemmal Coexpression of Intercellular Adhesion Molecule‐1 (ICAM‐1) and HLA‐DR in Inflammatory Myopathy (1994) (2)
The pro-apoptotic human BH3-only peptide harakiri is expressed in cryptococcus-infected perivascular macrophages in HIV-1 encephalitis patients (2006) (2)
Optic neuropathy and decorticate-like posture as presenting symptoms of Bickerstaff’s brainstem encephalitis: A case report and literature review (2018) (2)
A case of granulomatous myositis in a patient with rheumatoid arthritis receiving anti-TNF-α treatment (2020) (2)
[A case of chronic inflammatory demyelinating polyneuropathy presenting with acute pain and SIADH followed by weakness of all four limbs 2 month after the first symptoms]. (2004) (2)
Tumefactive multiple sclerosis which initially presented with brainstem encephalitis with a long-term follow-up. (2019) (2)
[Two cases of an intracranial large hemangiopericytoma associated with brain swelling in the early operative stage]. (1999) (2)
Effects of Contact Line Condition on Excitation of Internal Waves Confined by a Cylindrical Wall (2004) (1)
A 52‐year‐old man with hypohidrosis (2006) (1)
Evaluation for the clinical significance of cancer-association in anti-SRP antibody-positive myopathy (2017) (1)
Diagnostic Values of Venous Peak Lactate, Lactate-to-pyruvate Ratio, and Fold Increase in Lactate from Baseline in Aerobic Exercise Tests in Patients with Mitochondrial Diseases (2021) (1)
Novel COL6A2 mutation in a case of limb girdle muscular dystrophy phenotype with autosomal recessive inheritance (2016) (1)
[Remarkable effect of class Ib Na channel blocker on painful alcoholic neuropathy]. (1990) (1)
Alanine transaminase is predominantly increased in the active phase of anti-HMGCR myopathy (2021) (1)
[A case of severe infantile form of congenital nemaline myopathy with extensive fatty replacement of the skeletal muscles]. (1990) (1)
Cerebral microbleeding in varicella-zoster viral meningitis: An early sign of vasculopathy? (2014) (1)
[A case of unilateral recurrent calf myalgia with muscle edema due to venous congestion]. (2000) (1)
A case of inclusion body myositis complicated by microscopic polyangiitis (2018) (1)
Laryngeal Cancer in a Patient with Amyotrophic Lateral Sclerosis (2014) (1)
[The painful multiple mononeuropathy of acute onset in the left arm which was diagnosed as leprous neuropathy]. (2003) (1)
[A case report of light and heavy chain deposition disease (IgG2 lambda)]. (1994) (1)
Pathological Changes of Necrotizing Autoimmune Myopathy Associated with Anti-Signal Recognition Particle Antibody (P07.044) (2013) (1)
A new familial disorder presenting with amyotrophic lateral sclerosis-like manifestation: a clinicopathological study (1995) (1)
Reduced impact of viral load of HHV-6 in liquor on severity of AESD due to exanthema subitum: A case report and literature review (2021) (1)
A case of late‐onset Leber's hereditary optic neuropathy with elevated serum lactic acid and pyruvic acid levels by cycle ergometer exercise (2018) (1)
DNMT1 p.Y495H mutation is frequently associated with cerebellar ataxia compared with p.Y495C mutation (2017) (0)
Clinical features of ocular myasthenia gravis in japan (2017) (0)
Single institutional study on the clinical features of anti-MOG antibody-associated brain lesions (2017) (0)
Idiopathic inflammatory myopathy with delayed finger opening resembling grip myotonia: A case report. (2023) (0)
Clinicopathological features of patients with inflammatory myopathy associated with myasthenia gravis (2017) (0)
Motin of Air-Bubbles Rising in a Cylindrical Vessel at Low Reynolds Numbers (2000) (0)
Rippling Muscle Disease with Irregular Toe Jerks and Anti-acetylcholine Receptor Antibodies: Remission after Extended Thymectomy (2021) (0)
Macroscopic Streaming Associated With Vertical, Cyclic Motion of Interface Confined in a Cylindrical Enclosure (2002) (0)
Wave-Induced Streaming in Vertically-Excited, Stratified Fluids (2004) (0)
PIV and LIF Measurements of Flow in the Vicinity of Moving Interface (2002) (0)
Large-Scale Streaming Caused by Forced Vertical, Cyclic Motion of Fluid-Fluid Interface: Interface Wave Profile and Overall Flow Behavior (2004) (0)
ICONE11-36525 Macroscopic Streaming Associated with Standing Internal Wave (2003) (0)
78. The correlation between electrophysiological subgroups and antibodies in Guillain–Barré syndrome (2009) (0)
ICONE11-36609 Steady Streaming Associated with Forced Oscillation of Overlaid Immiscible Fluids (2003) (0)
A rare clinical presentation of neurogenic muscle weakness, ataxia, and retinitis pigmentosa (NARP) accompanied with spinal cord atrophy: A case report (2017) (0)
Late-onset familial neuronal intranuclear inclusion disease presenting with dementia and unique MRI findings (2013) (0)
Dermatomyositis‐like eruptions and fasciitis with novel compound heterozygous MEFV mutations: Newly recognized features of a variant of familial Mediterranean fever (2021) (0)
Cardiac Involvements in Anti-Mitochondrial Antibody-Positive Myositis (P07.046) (2013) (0)
CT Findings of Gynecomastia Led to a Diagnosis of POEMS Syndrome (2018) (0)
P2.04 DMRV and GNE mutations: genotype–phenotype correlation in 100 Japanese patients (2010) (0)
Anti‐3‐hydroxy‐3‐methylglutaryl‐coenzyme A reductase antibody‐positive myopathy associated with advanced stage of cutaneous squamous cell carcinoma (2021) (0)
The effect of immunosuppressive therapy on cardiac involvements in anti‐mitochondrial antibody‐positive myositis (2022) (0)
Malignant HPB Diseases APHPB-0552 THE POTASSIUM CHANNEL BETA-SUBUNIT , KCNE 3 , IS A NOVEL PROGNOSTIC MARKER FOR HEPATOCELLULAR CARCINOMA (2010) (0)
G.P.16.05 Clinical and pathological features of myopathy associated with anti-signal recognition particle antibodies (2009) (0)
Novel De Novo KCND3 Mutation in a Japanese Patient with Intellectual Disability, Cerebellar Ataxia, Myoclonus, and Dystonia (2017) (0)
Comprehensive genetic testing for mitochondrial disorders using sanger sequencing, southern blotting, whole exome sequencing, and whole mitochondrial genome sequencing (2017) (0)
Immunotherapy for ocular myasthenia gravis: an observational study in Japan (2023) (0)
[Case report: a case of chronic inflammatory demyelinating polyneuropathy (CIDP) exacerbated by influenza vaccination]. (2013) (0)
A novel missense mutation in valosin-containing protein gene identified in a Japanese family with a pure form of hereditary spastic paraplegia (2017) (0)
Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease (2019) (0)
Familial Creutzfeldt-Jakob disease with five octapeptide repeat insert (2005) (0)
The cut-off levels of serum creatine kinase as a diagnostic marker for myopathy with anti-hmg-cr or anti-srp autoantibodies positive (2017) (0)
Prominent Spasticity and Hyperreflexia of the Legs in a Nepalese Patient with Friedreich Ataxia (2019) (0)
A Case of Occlusal and Masticatory Function Recovery by Implant Treatment for Missing Unilateral Lower Molar Free-end (2013) (0)
Aberrant expression of myogenin in inclusion body myositis: Immunohistochemical studies of transcription factors regulating myogenesis in inflammatory myopathies (2012) (0)
Myasthenia gravis with inflammatory myopathy without elevation of creatine kinase (2021) (0)
Clinical features and haplotype analysis of newly identified Japanese patients with gelsolin-related familial amyloidosis of Finnish type (2012) (0)
Fascia in inflammatory myopathies: Histopathological findings (2017) (0)
Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy (2018) (0)
Clinical features of GM1 gangliosidosis type 3 (2013) (0)
Successful management of chronic myeloid leukemia with a complication of anti-SRP antibody-associated myopathy (2017) (0)
Clinicopathological Features of Anti-NT5c1A Positive Patients in the Group of Myositis Patients with CD8-MHC-1 Complex Pathology (P5.030) (2016) (0)
P2.48 Evaluation of the ELISA method for anti-SRP antibody detection (2010) (0)
Visualization and Measurement of Steady Streaming Induced in Oscillating Flow (2004) (0)
Accumulation of transportin 1 in the fused in sarcoma‐positive neuronal inclusions in sporadic amyotrophic lateral sclerosis without FUS mutation (2015) (0)
[Idiopathic inflammatory myopathies from the viewpoint of a neurologist]. (2013) (0)
P2.49 Sensitivity and specificity of major histocompatibility complex expression on sarcoplasmic membrane for diagnosis of idiopathic inflammatory myopathies (2010) (0)
P.193 Usefulness of cytoplasmic 5'- nucleotidase 1A autoantibodies for diagnosing patients with inclusion body myositis (2017) (0)
[Immunotherapy of myositis: future prospects]. (2011) (0)
[Pathological features of myositis with myositis -specific autoantibodies]. (2014) (0)
Diagnostic Utility Of p62 Immunohistochemistry For Differentiating s-IBM from PM (S26.006) (2014) (0)
Edema localized to the lips as a novel manifestation of myositis (2022) (0)
Abstracts of the Fifth Biennial Congress of the Asian-Pacific Hepato-Pancreato-Biliary Association, 18-21 March, 2015, Singapore. (2015) (0)
Clinicopathological features of patients with neuromuscular disease showing CD8-MHC-1 complex pathology (P5.065) (2015) (0)
[XYY syndrome associated with motor neuropathy]. (1992) (0)
Anti‐mitochondrial antibody: Potential marker of myositis with chronic clinical course, muscle atrophy, cardiac involvement and granulomatous inflammation in muscle biopsy (2013) (0)
Long-term outcomes in motor and cognitive impairment with acute encephalopathy (2018) (0)
Clinical, serological, and pathological features of inflammatory myopathies with systemic sclerosis (2017) (0)
Systemic Inflammation Exacerbates Stroke in Patients with Left Ventricular Assist Device (P4.235) (2014) (0)
Recurrent HyperCKemia with Immunological Involvement of the Endomysial Capillaries in Neuromyelitis Optica (2020) (0)
Interpretation of sequence variants called by whole exome sequencing in the clinical sequence of muscular diseases (2017) (0)
G.P.65 Epidemiological study of malignancy-associated myositis in Japan (2012) (0)
RNA-sequencing analysis of muscle biopsy samples from patients with inclusion body myositis and those with polymyositis (P3.449) (2018) (0)
Cerebellar Ataxia as a Common Clinical Presentation Associated with DNMT1 p.Y511H and a Review of the Literature (2021) (0)
[A case of progressive hemiatrophy with type 2 muscle atrophy in muscle biopsy]. (1992) (0)
Analysis of the risk of cancer among myositis patients without anti-TIF1-γ OR –HMGCR antibodies (2017) (0)
Double immunofluorescence study is sensitive for detection of protein mislocalization in biopsied muscle specimen, and useful for diagnosis of muscular dystrophy (2017) (0)
Needle electromyography, muscle MRI, and muscle pathology: Correlations in idiopathic inflammatory myopathies (2020) (0)
C.P.14 A four-generation Japanese family with autosomal dominant nemaline myopathy associated with dilated cardiomyopathy (2012) (0)
Development of Polyneuropathy, Organomegaly, Endocrinopathy, M Protein, and Skin Changes Syndrome after Conversion from Plasmacytoma of Bone to Multiple Myeloma (2022) (0)
“Localized” chronic invasive fungal rhinosinusitis without serological abnormalities (2018) (0)
Useful scales for recognition of severe disease status in patients with multiple sclerosis in Japan (2017) (0)
Usefulness of cytoplasmic 5’ - nucleotidase 1A autoantibodies for the diagnosis of inclusion body myositis (2017) (0)
Familial amyloid polyneuropathy diagnosed by minor salivary gland biopsy (2018) (0)
The Myocardial Accumulation of Aggregated Desmin Protein in a Case of Desminopathy with a de novo DES p.R406W Mutation. (2023) (0)
Severe dilated cardiomyopathy and ventricular arrhythmia in a patient with Emery‐Dreifuss muscular dystrophy harboring a novel frameshift mutation in EMD (2021) (0)

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What Schools Are Affiliated With Jun Shimizu?

Jun Shimizu is affiliated with the following schools:

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Jun Shimizu's Degrees

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Why Is Jun Shimizu Influential?

Jun Shimizu's Published Works

Published Works

What Schools Are Affiliated With Jun Shimizu?

Jun Shimizu's AcademicInfluence.com Rankings