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Publications by Ikuya Nonaka

Biallelic Mutations in MYPN , Encoding Myopalladin, Are Associated With Childhood-Onset, Slowly Progressive Nemaline Myopathy

American Journal of Human Genetics

English

MKBP, a Novel Member of the Small Heat Shock Protein Family, Binds and Activates the Myotonic Dystrophy Protein Kinase

Journal of Cell Biology

English

Cardiac-Restricted Ankyrin-Repeated Protein Is Differentially Induced in Duchenne and Congenital Muscular Dystrophy

Laboratory Investigation

Forensic Medicine

Molecular Biology

English

Genotype and Phenotype Analyses in 136 Patients With Single Large-Scale Mitochondrial DNA Deletions

Journal of Human Genetics

English

A Novel POMT2 Mutation Causes Mild Congenital Muscular Dystrophy With Normal Brain MRI

Brain and Development

Developmental Neuroscience

English

Limb-Girdle Muscular Dystrophy Due to Emerin Gene Mutations

Archives of Neurology

English

Successful Treatment of Recurrent Hypoglycemia by Pioglitazone in a Patient With Myotonic Dystrophy

Clinical Neurology

English