Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan
Tanaka, Toshiaki, Igarashi, Yutaka, Ozono, Keiichi, Ohyama, Kenji, Ogawa, Masamichi, Osada, Hisao, Onigata, Kazumichi, Kanzaki, Susumu, Kohno, Hitoshi, Seino, Yoshiki, Takahashi, Hiroaki, Tajima, Toshihiro, Tachibana, Katsuhiko, Tanaka, Hiroyuki, Nishi, Yoshikazu, Hasegawa, Tomonobu, Fujita, Keinosuke, Yorifuji, Tohru, Horikawa, Reiko, Yokoya, Susumu
Published in Clinical Pediatric Endocrinology (01.10.2015)
Published in Clinical Pediatric Endocrinology (01.10.2015)
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Placental hypoplasia in maternal uniparental disomy for chromosome 7
Yamazawa, Kazuki, Kagami, Masayo, Ogawa, Masamichi, Horikawa, Reiko, Ogata, Tsutomu
Published in American journal of medical genetics. Part A (15.02.2008)
Published in American journal of medical genetics. Part A (15.02.2008)
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Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan
Toshiaki Tanaka, Yutaka Igarashi, Keiichi Ozono, Kenji Ohyama, Masamichi Ogawa, Hisao Osada, Kazumichi Onigata, Susumu Kanzaki, Hitoshi Kohno, #, Yoshiki Seino, Hiroaki Takahashi, Toshihiro Tajima, Katsuhiko Tachibana, Hiroyuki Tanaka, Yoshikazu Nishi, Tomonobu Hasegawa, Keinosuke Fujita, Tohru Yorifuji, Reiko Horikawa, Susumu Yokoya
Published in Clinical Pediatric Endocrinology (01.10.2015)
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Published in Clinical Pediatric Endocrinology (01.10.2015)
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Bone Mineral Density in Adult Patients with Turner’s Syndrome: Analyses of the Effectiveness of GH and Ovarian Steroid Hormone Replacement Therapies
SUGANUMA, NOBUHIKO, FURUHASHI, MADOKA, HIROOKA, TAKASHI, MORIWAKI, TAKAYUKI, HASEGAWA, YUKIHARU, MORI, OSAMU, OGAWA, MASAMICHI
Published in Endocrine Journal (01.06.2003)
Published in Endocrine Journal (01.06.2003)
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Clinical Evaluation of Recombinant Human Growth Hormone in Noonan Syndrome
OGAWA, Masamichi, MORIYA, Naoki, IKEDA, Hiroyuki, TANAE, Ayako, TANAKA, Toshiaki, OHYAMA, Kenji, MORI, Osamu, YAZAWA, Takeshi, FUJITA, Keinosuke, SEINO, Yoshiki, KUBO, Toshihide, TANAKA, Hiroyuki, NISHI, Yoshikazu, YOSHIMOTO, Masaaki
Published in ENDOCRINE JOURNAL (2004)
Published in ENDOCRINE JOURNAL (2004)
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Favorable Impact of Growth Hormone Treatment on Cholesterol Levels in Turner Syndrome
Kohno, Hitoshi, Igarashi, Yutaka, Ozono, Keiichi, Ohyama, Kenji, Ogawa, Masamichi, Osada, Hisao, Onigata, Kazumichi, Kanzaki, Susumu, Seino, Yoshiki, Takahashi, Hiroaki, Tajima, Toshihiro, Tachibana, Katsuhiko, Tanaka, Hiroyuki, Nishi, Yoshikazu, Hasegawa, Tomonobu, Fujieda, Kenji, Fujita, Keinosuke, Horikawa, Reiko, Yokoya, Susumu, Yorifuji, Toru, Tanaka, Toshiaki
Published in Clinical Pediatric Endocrinology (2012)
Published in Clinical Pediatric Endocrinology (2012)
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Familial Isolated Growth Hormone Deficiency: Genetics and Pathophysiology
HAYASHI, YOSHSITAKA, KAMIJO, TAKASHI, OGAWA, MASAMICHI, SEO, HISAO
Published in ENDOCRINE JOURNAL (2002)
Published in ENDOCRINE JOURNAL (2002)
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Thermal and photo induced phase transition between smectic and cubic liquid crystalline phases in binary systems using azobenzene derivative with a methyl side group
Kondo, Tomonori, Ogawa, Masamichi, Kondo, Hideaki, Miwa, Yohei, Kutsumizu, Shoichi
Published in Proceedings of Japanese Liquid Crystal Society Annual meeting (2019)
Published in Proceedings of Japanese Liquid Crystal Society Annual meeting (2019)
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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
Kamijo, Takashi, Hayashi, Yoshitaka, Seo, Hisao, Yamamoto, Michiyo, Ogawa, Masamichi, Choski, Chandra S., Sawant, Nitin J., Colaco, Marie P., Desai, Meena P.
Published in Growth hormone & IGF research (01.10.2004)
Published in Growth hormone & IGF research (01.10.2004)
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Influence of methyl group introduced into molecular core of azobenzene on photo-induced smectic-cubic liquid crystalline phase transition
Kondo, Tomonori, Kondo, Hideaki, Ogawa, Masamichi, Miwa, Yohei, Kutsumizu, Shoichi
Published in Proceedings of Japanese Liquid Crystal Society Annual meeting (2018)
Published in Proceedings of Japanese Liquid Crystal Society Annual meeting (2018)
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Transmission of Del(X)(p11.2) from Mother to Daughter
Ogawa, Masamichi, Kamijo, Takashi, Asai, Toshi, Ohno, Yasuhiro, Aoyama, Mari, Kajii, Tadashi
Published in Clinical Pediatric Endocrinology (2002)
Published in Clinical Pediatric Endocrinology (2002)
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Hereditary isolated growth hormone deficiency caused by GH1 gene mutations in Japanese patients
Kamijo, Takashi, Hayashi, Yoshitaka, Seo, Hisao, Ogawa, Masamichi
Published in Growth hormone & IGF research (01.06.1999)
Published in Growth hormone & IGF research (01.06.1999)
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A Novel E250X Mutation of the PIT1 Gene in a Patient with Combined Pituitary Hormone Deficiency
IRIE, YOSHIFUMI, TATSUMI, KE-ITA, OGAWA, MASAMICHI, KAMIJO, TAKASHI, PREEYASOMBAT, CHAWALIT, SUPRASONGSIN, CHITTIWAT, AMINO, NOBUYUKI
Published in Endocrine Journal (01.01.1995)
Published in Endocrine Journal (01.01.1995)
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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
Igarashi, Y, Ogawa, M, Kamijo, T, Iwatani, N, Nishi, Y, Kohno, H, Masumura, T, Koga, J
Published in Human molecular genetics (01.07.1993)
Published in Human molecular genetics (01.07.1993)
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Prevalence of GH-1 Gene Deletion in Patients with Isolated Growth Hormone Deficiency in Japan
OGAWA, MASAMICHI, KAMIJO, TAKASHI, IGARASHI, YUTAKA, NISHI, YOSHIKAZU, IWATANI, NORITAKA, KOHNO, HITOSHI, KOGA, JUNICHI, BYUN, Young Jin, OTHER MEMBERS OF THE GH GENE STUDY GROUP
Published in Endocrine Journal (2000)
Published in Endocrine Journal (2000)
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