Hiroyoshi Koide

Novel Mutations and Genotype-Phenotype Relationships in 107 Families With Fukuyama-Type Congenital Muscular Dystrophy (FCMD)

Eri Kondo-Iida, Kazuhiro Kobayashi, Masao Watanabe et al. · Human Molecular Genetics · 1999 · 167 citations

Neurofilament light chain polypeptide gene mutations in Charcot–Marie–Tooth disease: nonsense mutation probably causes a recessive phenotype

Akiko Abe, Chikahiko Numakura, Kayoko Saito et al. · Journal of Human Genetics · 2009 · 95 citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Mendelian Disorder +11

Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions

Shinji Ono, Koh-ichiro Yoshiura, Akira Kinoshita et al. · Journal of Human Genetics · 2012 · 93 citations · Full text

Developmental Anomaly, Developmental Biology, Genetic Disorder +6

Assessment of inhalation flow patterns of soft mist inhaler co-prescribed with dry powder inhaler using inspiratory flow meter for multi inhalation devices

Daiki Hira, Hiroyoshi Koide, Shigemi Nakamura et al. · PLoS ONE · 2018 · 40 citations · Full text

Asthma, Pulmonary Care, Inhalation Flow Pattern +17

Cooperative inhibitory effects of uremic toxins and other serum components on OATP1B1-mediated transport of SN-38

Yurie Katsube, Masayuki Tsujimoto, Hiroyoshi Koide et al. · Cancer Chemotherapy and Pharmacology · 2017 · 20 citations

Signal Transduction, Allergy, Cooperative Inhibitory Effects +8