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Results:
1-10
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Results: 10
Authors:
Nagashima, T
Murakami, M
Onigata, K
Morimura, T
Nagashima, K
Mori, M
Morikawa, A
Citation: T. Nagashima et al., Novel inactivating missense mutations in the thyrotropin receptor gene in Japanese children with resistance to thyrotropin, THYROID, 11(6), 2001, pp. 551-559
Authors:
Ogata, T
Onigata, K
Hotsubo, T
Matsuo, N
Rappold, G
Citation: T. Ogata et al., Growth hormone and gonadotropin-releasing hormone analog therapy in haploinsufficiency of SHOX, ENDOCR J, 48(3), 2001, pp. 317-322
Authors:
Miyamoto, J
Hasegawa, Y
Ohnami, N
Onigata, K
Kinoshita, E
Nishi, Y
Tachibana, K
Hasegawa, T
Citation: J. Miyamoto et al., Development of growth hormone and adrenocorticotropic hormone deficienciesin patients with prenatal or perinatal-onset hypothalamic hypopituitarism having invisible or thin pituitary stalk on magnetic resonance imaging, ENDOCR J, 48(3), 2001, pp. 355-362
Authors:
Koike, H
Motooka, M
Kanda, T
Onigata, K
Murakami, M
Suzuk, T
Kobayashi, I
Citation: H. Koike et al., Detection of point mutation for human growth hormone in patients with anti-pituitary antibody positive type 1 diabetes mellitus, J INT MED R, 29(5), 2001, pp. 397-408
Authors:
Nishigori, H
Tomura, H
Tonooka, N
Kanamori, M
Yamada, S
Sho, K
Inoue, I
Kikuchi, N
Onigata, K
Kojima, I
Kohama, T
Yamagata, K
Yang, Q
Matsuzawa, Y
Miki, T
Seino, S
Kim, MY
Choi, HS
Lee, YK
Moore, DD
Takeda, J
Citation: H. Nishigori et al., Mutations in the small heterodimer partner gene are associated with mild obesity in Japanese subjects, P NAS US, 98(2), 2001, pp. 575-580
Authors:
Muroi, J
Yorifuji, T
Uematsu, A
Shigematsu, Y
Onigata, K
Maruyama, H
Nobutoki, T
Kitamura, A
Nakahata, T
Citation: J. Muroi et al., Molecular and clinical analysis of Japanese patients with 3-hydroxy-3-methylglutaryl CoA lyase (HL) deficiency, HUM GENET, 107(4), 2000, pp. 320-326
Authors:
Hasegawa, Y
Fujii, K
Yamada, M
Igarashi, Y
Tachibana, K
Tanaka, T
Onigata, K
Nishi, Y
Kato, S
Hasegawa, T
Citation: Y. Hasegawa et al., Identification of novel human GH-1 gene polymorphisms that are associated with growth hormone secretion and height, J CLIN END, 85(3), 2000, pp. 1290-1295
Authors:
Miyake, H
Nagashima, K
Onigata, K
Nagashima, T
Takano, Y
Morikawa, A
Citation: H. Miyake et al., Allelic variations of the D2 dopamine receptor gene in children with idiopathic short stature, J HUM GENET, 44(1), 1999, pp. 26-29
Authors:
Yamada, S
Tomura, H
Nishigori, H
Sho, K
Mabe, H
Iwatani, N
Takumi, T
Kito, Y
Moriya, N
Muroya, K
Ogata, T
Onigata, K
Morikawa, A
Inoue, I
Takeda, J
Citation: S. Yamada et al., Identification of mutations in the hepatocyte nuclear factor-1 alpha gene in Japanese subjects with early-onset NIDDM and functional analysis of the mutant proteins, DIABETES, 48(3), 1999, pp. 645-648
Authors:
Harigaya, A
Onigata, K
Nako, Y
Nagashima, K
Morikawa, A
Citation: A. Harigaya et al., Role of serum leptin in the regulation of weight gain in early infancy, BIOL NEONAT, 75(4), 1999, pp. 234-238
Risultati:
1-10
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