Masamichi Ogawa

A Novel E250X Mutation of the PIT1 Gene in a Patient with Combined Pituitary Hormone Deficiency.

Yoshifumi Irie, Ke-ita Tatsumi, Masamichi Ogawa et al. · Endocrine Journal · 1995 · 70 citations · Full text

Pit1 Abnormality, Developmental Biology, Genetic Abnormality +14

Inhibition of Growth Hormone (GH) Secretion by a Mutant<i>GH-I</i>Gene Product in Neuroendocrine Cells Containing Secretory Granules: An Implication for Isolated GH Deficiency Inherited in an Autosomal Dominant Manner¹

Yoshitaka Hayashi, Michiyo Yamamoto, Sachiko Ohmori et al. · The Journal of Clinical Endocrinology & Metabolism · 1999 · 62 citations · Full text

Wild-type Gh Secretion, Genetics, Neuroendocrinology +17

Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan

Toshiaki Tanaka, Yutaka Igarashi, Keiichi Ozono et al. · Clinical Pediatric Endocrinology · 2015 · 50 citations · Full text

Fertility, Human Growth, Genetics +18

A new mutation causing inherited growth hormone deficiency: a compound heterozygote of a 6.7 kb deletion and a two base deletion in the third exon of the GH-1 gene

Yutaka Igarashi, Masamichi Ogawa, Takashi Kamijo et al. · Human Molecular Genetics · 1993 · 42 citations

Reproductive Sciences, Kb Deletion, Base Deletion +21

Bone Mineral Density in Adult Patients with Turner's Syndrome: Analyses of the Effectiveness of GH and Ovarian Steroid Hormone Replacement Therapies

Nobuhiko Suganuma, Madoka Furuhashi, Takashi Hirooka et al. · Endocrine Journal · 2003 · 36 citations · Full text