Masatoshi Ohtake

ACTN1 Mutations Cause Congenital Macrothrombocytopenia

Shinji Kunishima, Yusuke Okuno, Kenichi Yoshida et al. · The American Journal of Human Genetics · 2013 · 202 citations · Full text

Genetic Disorder, Hematology, Pathology +4

Compound Heterozygous Mutations in the Cholesterol Side-Chain Cleavage Enzyme Gene (<i>CYP11A</i>) Cause Congenital Adrenal Insufficiency in Humans

Noriyuki Katsumata, Masatoshi Ohtake, Toru Hojo et al. · The Journal of Clinical Endocrinology & Metabolism · 2002 · 116 citations · Full text

Acute encephalopathy with a truncation mutation in the <i>SCN1A</i> gene: A case report

Masaru Takayanagi, Kazuhiro Haginoya, Naoki Umehara et al. · Epilepsia · 2010 · 35 citations · Full text

Neurological Disorder, Genetics, Clinical Neurology +18

Serum Zinc and Copper Levels in Healthy Japanese Infants

Masatoshi Ohtake · The Tohoku Journal of Experimental Medicine · 1977 · 31 citations · Full text

Nutrition, Neonatology, Infant Nutrition +12

Changes in Zinc and Copper Concentrations in Breast Milk and Blood of Japanese Women during Lactation.

Masatoshi Ohtake, Tsunenobu Tamura · Journal of Nutritional Science and Vitaminology · 1993 · 30 citations · Full text