Harumasa Nakamura Clinical Research Support Office, Translational Medical Center National Center of Neurology and Psychiatry Biography Publications Institution JoVE Articles Harumasa Nakamura has not added a biography. If you are Harumasa Nakamura and would like to personalize this page please email our Author Liaison for assistance. Publications Pregnancy in GNE Myopathy Patients: a Nationwide Repository Survey in Japan Orphanet Journal of Rare Diseases. Sep, 2020 | Pubmed ID: 32917266 Clinical Practice with Steroid Therapy for Duchenne Muscular Dystrophy: An Expert Survey in Asia and Oceania Brain & Development. Mar, 2020 | Pubmed ID: 31980267 Exon Skipping Induced by Nonsense/frameshift Mutations in DMD Gene Results in Becker Muscular Dystrophy Human Genetics. Feb, 2020 | Pubmed ID: 31919629 National Registry of Patients with Fukuyama Congenital Muscular Dystrophy in Japan Neuromuscular Disorders : NMD. 10, 2018 | Pubmed ID: 30220444 Systemic Administration of the Antisense Oligonucleotide NS-065/NCNP-01 for Skipping of Exon 53 in Patients with Duchenne Muscular Dystrophy Science Translational Medicine. 04, 2018 | Pubmed ID: 29669851 Characteristics of Japanese Patients with Becker Muscular Dystrophy and Intermediate Muscular Dystrophy in a Japanese National Registry of Muscular Dystrophy (Remudy): Heterogeneity and Clinical Variation Journal of Neuromuscular Diseases. 2018 | Pubmed ID: 29614690 [Medical Needs Survey on Neurological Disorders] Brain and Nerve = Shinkei Kenkyu No Shinpo. Mar, 2018 | Pubmed ID: 29519967 Comprehensive Analysis for Genetic Diagnosis of Dystrophinopathies in Japan Orphanet Journal of Rare Diseases. 08, 2017 | Pubmed ID: 28859693 A Comparative Study of Care Practices for Young Boys with Duchenne Muscular Dystrophy Between Japan and European Countries: Implications of Early Diagnosis Neuromuscular Disorders : NMD. Oct, 2017 | Pubmed ID: 28807665 Clinical Trial Network for the Promotion of Clinical Research for Rare Diseases in Japan: Muscular Dystrophy Clinical Trial Network BMC Health Services Research. 07, 2016 | Pubmed ID: 27401940 Chronic Myopathy Associated With Anti-Signal Recognition Particle Antibodies Can Be Misdiagnosed As Facioscapulohumeral Muscular Dystrophy Journal of Clinical Neuromuscular Disease. Jun, 2016 | Pubmed ID: 27224434 Trends in Steroid Therapy for Duchenne Muscular Dystrophy in Japan Muscle & Nerve. Feb, 2016 | Pubmed ID: 26910583 [Drug Development for Overcoming Dementia in Japan] Rinsho Shinkeigaku = Clinical Neurology. 2014 | Pubmed ID: 25672739 [Infrastructure for the Clinical Research of Muscular Dystrophies: Remudy and MDCTN] Rinshō Shinkeigaku = Clinical Neurology. 2014 | Pubmed ID: 25519964 [Remudy] Brain and Nerve = Shinkei Kenkyu No Shinpo. Nov, 2014 | Pubmed ID: 25407075 Nationwide Patient Registry for GNE Myopathy in Japan Orphanet Journal of Rare Diseases. 2014 | Pubmed ID: 25303967 Clinical and Genetic Analysis of the First Known Asian Family with Myotonic Dystrophy Type 2 Journal of Human Genetics. Mar, 2014 | Pubmed ID: 24430576 Characteristics of Japanese Duchenne and Becker Muscular Dystrophy Patients in a Novel Japanese National Registry of Muscular Dystrophy (Remudy) Orphanet Journal of Rare Diseases. 2013 | Pubmed ID: 23601510 Long-term Effect of Repeated Lidocaine Injections into the External Oblique for Upper Camptocormia in Parkinson's Disease Parkinsonism & Related Disorders. Mar, 2013 | Pubmed ID: 23043967 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 Journal of the Neurological Sciences. Jul, 2012 | Pubmed ID: 22507750 Caractérisation de l’efficacité de saut d’Exon dans les échantillons de patients de DMD dans les essais cliniques d’oligonucléotides d’Antisense Joel Z. Nordin*1, Yoshitaka Mizobe*1, Harumasa Nakamura2, Hirofumi Komaki3, Shin'ichi Takeda1, Yoshitsugu Aoki1 1Department of Molecular Therapy, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 2Clinical Research Support Office, Translational Medical Center, National Center of Neurology and Psychiatry, 3Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry JoVE 60672 Medicine
Caractérisation de l’efficacité de saut d’Exon dans les échantillons de patients de DMD dans les essais cliniques d’oligonucléotides d’Antisense Joel Z. Nordin*1, Yoshitaka Mizobe*1, Harumasa Nakamura2, Hirofumi Komaki3, Shin'ichi Takeda1, Yoshitsugu Aoki1 1Department of Molecular Therapy, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 2Clinical Research Support Office, Translational Medical Center, National Center of Neurology and Psychiatry, 3Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry JoVE 60672 Medicine