Get started
Author

Masamichi Ogawa

A Novel E250X Mutation of the PIT1 Gene in a Patient with Combined Pituitary Hormone Deficiency.
1995 · YOSHIFUMI IRIE, KE-ITA TATSUMI, et al. · Endocrine Journal · 69
PDF
Inhibition of Growth Hormone (GH) Secretion by a Mutant GH-I Gene Product in Neuroendocrine Cells Containing Secretory Granules: An Implication for Isolated GH Deficiency Inherited in an Autosomal Dominant Manner
1999 · Yoshitaka Hayashi, Michiyo Yamamoto, et al. · The Journal of Clinical Endocrinology & Metabolism · 65
Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan
2015 · Toshiaki Tanaka, Yutaka Igarashi, et al. · Clinical Pediatric Endocrinology · 51
PDF
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
1993 · Yutaka Igarashi, Masamichi Ogawa, et al. · Human Molecular Genetics · 42
Bone Mineral Density in Adult Patients with Turner's Syndrome: Analyses of the Effectiveness of GH and Ovarian Steroid Hormone Replacement Therapies
2003 · NOBUHIKO SUGANUMA, MADOKA FURUHASHI, et al. · Endocrine Journal · 35
PDF
Mutations in intron 3 of GH‐1 gene associated with isolated GH deficiency type II in three Japanese families
1999 · Takashi Kamijo, Yoshitaka Hayashi, et al. · Clinical Endocrinology · 29
Detection of Growth Hormone Gene Defects by Dideoxy Fingerprinting (ddF).
1997 · ICHIRO MIYATA, JOY D. COGAN, et al. · Endocrine Journal · 29
PDF
A novel mutation at the donor splice site of intron 3 of the GH-I gene in a patient with isolated growth hormone deficiency
1999 · Yoshitaka Hayashi, Takashi Kamijo, et al. · Growth Hormone & IGF Research · 25
Clinical Evaluation of Recombinant Human Growth Hormone in Noonan Syndrome
2004 · Masamichi OGAWA, Naoki MORIYA, et al. · Endocrine Journal · 22
PDF
Screening for growth hormone gene deletions in patients with isolated growth hormone deficiency
1991 · Takashi Kamijo, John A. Phillips, et al. · The Journal of Pediatrics · 19
Treatment of pituitary dwarfism with methionyl human growth hormone in Japan.
1986 · KAZUE TAKANO, KAZUO SHIZUME, et al. · Endocrinologia Japonica · 19
PDF
Growth Hormone Releasing Hormone Receptor (GHRH-R) Gene Mutation in Indian Children with Familial Isolated Growth Hormone Deficiency: A Study from Western India
2005 · M P. Desai, P.S. Upadhye, et al. · Journal of Pediatric Endocrinology and Metabolism · 18
Induction of Ovulation and Spermatogenesis by hMG/hCG in Hypogonadotropic GH-Deficient Patients.
1992 · YOSHIAKI OKADA, TAKUMA KONDO, et al. · Endocrinologia Japonica · 18
PDF
Hereditary isolated growth hormone deficiency caused by GH1 gene mutations in Japanese patients
1999 · Takashi Kamijo, Yoshitaka Hayashi, et al. · Growth Hormone & IGF Research · 17
A highly sensitive sandwich enzyme immunoassay of urinary growth hormone in children with short stature, Turner's syndrome, and simple obesity
1989 · Hiroshi Tomita, Masamichi Ogawa, et al. · European Journal of Endocrinology · 17
Treatment of idiopathic pituitary dwarfism with methionyl human growth hormone.
1983 · KAZUE TAKANO, KAZUO SHIZUME, et al. · Endocrinologia Japonica · 17
PDF
Placental hypoplasia in maternal uniparental disomy for chromosome 7
2008 · Kazuki Yamazawa, Masayo Kagami, et al. · American Journal of Medical Genetics Part A · 13
A nonsense mutation (E72X) in growth hormone releasing hormone receptor (GHRHR) gene is the major cause of familial isolated growth hormone deficiency in Western region of India: founder effect suggested by analysis of dinucleotide repeat polymorphism close to GHRHR gene
2004 · Takashi Kamijo, Yoshitaka Hayashi, et al. · Growth Hormone & IGF Research · 12
Prevalence of GH-1 Gene Deletion in Patients with Isolated Growth Hormone Deficiency in Japan.
2000 · MASAMICHI OGAWA, TAKASHI KAMIJO, et al. · Endocrine Journal · 9
PDF
Favorable Impact of Growth Hormone Treatment on Cholesterol Levels in Turner Syndrome
2012 · Hitoshi Kohno, Yutaka Igarashi, et al. · Clinical Pediatric Endocrinology · 7
PDF
A case with isolated growth hormone deficiency caused by compound heterozygous mutations in GH-1: A novel missense mutation in the initiation codon and a 7.6 kb deletion
2007 · Yoshitaka Hayashi, Takashi Kamijo, et al. · Growth Hormone & IGF Research · 7
Experience in Growth Hormone Therapy in Noonan Syndrome in Japan
1995 · Yoshikazu Nishi, Kazuo Shizume, et al. · Clinical Pediatric Endocrinology · 5
PDF
Screening for Mutations in the GH-1 Gene by Dideoxy Fingerprinting (ddF)
1999 · ICHIRO MIYATA, YOSHIKATSU ETO, et al. · Endocrine Journal · 3
PDF
Growth Hormone (GH) Treatment in Achondroplasia*
1994 · Masamichi OGAWA, Osamu MORI, et al. · Congenital Anomalies · 3
Successful Treatment of Dwarfism and Hypogonadism after Total Removal of Craniopharyngioma
1985 · Tatsuya KOBAYASHI, Jun YOSHIDA, et al. · Neurologia medico-chirurgica · 3
PDF
Works count: 40
Citation count: 564
H-index: 16
I10-index: 18
Year
Topic
Type