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Publications by Ichizo Nishino
Biallelic Mutations in MYPN , Encoding Myopalladin, Are Associated With Childhood-Onset, Slowly Progressive Nemaline Myopathy
American Journal of Human Genetics
Genetics
Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy
American Journal of Human Genetics
Genetics
Identification of Variants in the 4q35 GeneFAT1in Patients With a Facioscapulohumeral Dystrophy-Like Phenotype
Human Mutation
Genetics
The Updated Retrospective Questionnaire Study of Sporadic Inclusion Body Myositis in Japan
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
224 Th ENMC International Workshop: Clinicopathological Classification of Immune-Mediated Necrotizing Myopathies, Naarden, the Netherlands, 14-16 October 2016
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
Immune-Mediated Necrotizing Myopathy (IMNM) and HLA Polymorphisms
Major Histocompatibility Complex
Two Cases of Sporadic Late Onset Nemaline Myopathy Effectively Treated With Immunotherapy
Clinical Neurology
Neurology
Pathomechanism and Prevalence of Sporadic Inclusion Body Myositis (sIBM)
Clinical Neurology
Neurology
Disorders of Lipid Metabolism
Establishment of an Improved Mouse Model for Infantile Neuroaxonal Dystrophy That Shows Early Disease Onset and Bears a Point Mutation in Pla2g6
American Journal of Pathology
Forensic Medicine
Pathology
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