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

Yoshifumi Irie, Ke-ita Tatsumi, Masamichi Ogawa, +4

Endocrine Journal

Pit1 AbnormalityDevelopmental BiologyGenetic AbnormalityPituitary GlandGenetic Disorder +12

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, +3

The Journal of Clinical Endocrinology & Metabolism

Wild-type Gh SecretionGeneticsNeuroendocrinologyMolecular GeneticsDisease Gene Identification +15

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

Toshiaki Tanaka, Yutaka Igarashi, Keiichi Ozono, +17

Clinical Pediatric Endocrinology

FertilityHuman GrowthGeneticsGynecologyPathology +16

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, +5

Human Molecular Genetics

Reproductive SciencesKb DeletionBase DeletionHuman GrowthGenetics +19

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, +4

Endocrine Journal

Mutations in intron 3 of GH‐1 gene associated with isolated GH deficiency type II in three Japanese families

Takashi Kamijo, Yoshitaka Hayashi, Akira Shimatsu, +4

Clinical Endocrinology

Detection of Growth Hormone Gene Defects by Dideoxy Fingerprinting (ddF).

Ichiro Miyata, Joy D. Cogan, Melissa Prince, +3

Endocrine Journal

A novel mutation at the donor splice site of intron 3 of the GH-I gene in a patient with isolated growth hormone deficiency

Yoshitaka Hayashi, Takashi Kamijo, Michiyo Yamamoto, +5

Growth Hormone & IGF Research

Developmental BiologyGrowth HormoneMendelian DisorderHuman GrowthGenetic Disorder +8

Clinical Evaluation of Recombinant Human Growth Hormone in Noonan Syndrome

Masamichi Ogawa, Naoki Moriya, Hiroyuki Ikeda, +11

Endocrine Journal

Treatment of pituitary dwarfism with methionyl human growth hormone in Japan.

Kazue Takano, KAZUO SHIZUME, Naomi Hizuka, +20

Endocrinologia Japonica