Masanori Kouwaki

Dihydropyrimidinase Deficiency: Structural Organization, Chromosomal Localization, and Mutation Analysis of the Human Dihydropyrimidinase Gene

Naoki Hamajima, Masanori Kouwaki, P. Vreken et al. · The American Journal of Human Genetics · 1998 · 77 citations · Full text

Chromatin, Mendelian Disorder, Genetic Disorder +10

Identification of novel mutations in the dihydropyrimidine dehydrogenase gene in a Japanese patient with 5-fluorouracil toxicity.

Masanori Kouwaki, Naoki Hamajima, Satoshi Sumi et al. · PubMed · 1998 · 75 citations

Genetics, Molecular Biology, Pathology +16

Therapeutic hypothermia for neonatal encephalopathy: a report from the first 3 years of the Baby Cooling Registry of Japan

Kennosuke Tsuda, Takeo Mukai, Sachiko Iwata et al. · Scientific Reports · 2017 · 36 citations · Full text

Electrolyte Disorder, Neonatology, Pediatric Hydrocephalus +19

Neurodevelopmental Outcomes at 18 Months’ Corrected Age of Infants Born at 22 Weeks of Gestation

Tokio Sugiura, Masanori Kouwaki, Yasuko Togawa et al. · Neonatology · 2011 · 18 citations

Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state

Koya Kawase, Ichizo Nishino, Mari Sugimoto et al. · Brain and Development · 2015 · 16 citations

Mendelian Disorder, Genetic Disorder, Pathology +3