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Results: 1-24 |
Results: 24

Authors: Ishikawa, Y Tajima, T Nakae, J Nagashima, T Satoh, K Okuhara, K Fujieda, K
Citation: Y. Ishikawa et al., Two mutations of the Gs alpha gene in two Japanese patients with sporadic pseudohypoparathyroidism type Ia, J HUM GENET, 46(7), 2001, pp. 426-430

Authors: Kawamura, M Owada, M Kimura, Y Fujiwara, T Sasaki, A Tajima, T Fujieda, K Hiramori, K
Citation: M. Kawamura et al., 46, XY pure gonadal dysgenesis: A case with Graves' disease and exceptionally tall stature, INTERN MED, 40(8), 2001, pp. 740-743

Authors: Attie, KM Bengtsson, BA Blethen, SL Blum, W Cameron, F Carel, JC Carlsson, L Chipman, JJ Christiansen, JS Clayton, P Clemmons, DR Cohen, P Drop, S Fujieda, K Ghigo, E Hintz, RL Ho, K Ilondo, MM Jasper, H Jesussek, B Kappelgaard, AM Laron, Z Lippe, BM Malozowski, S Mullis, PE de Muinck-Keizer-Schrama, S Nishi, Y Parks, JS Phelps, C Ranke, M Robinson, I Rosenfeld, RG Rose, S Saenger, P Saggese, G Savage, M Shalet, S Sizonenko, PC Strasburger, C Tachibana, K Tanaka, T Thorner, MO Wikland, KA Zadik, Z
Citation: Km. Attie et al., Consensus guidelines for the diagnosis and treatment of growth hormone (GH) deficiency in childhood and adolescence: Summary statement of the GH Research Society (Reprinted from J Clin Endocrinol Metab, vol 85, pg 3990-3993,2000), J PED END M, 14(4), 2001, pp. 377-382

Authors: Tajima, T Fujieda, K Kouda, N Nakae, J Miller, WL
Citation: T. Tajima et al., Heterozygous mutation in the cholesterol side chain cleavage enzyme (P450scc) gene in a patient with 46,XY sex reversal and adrenal insufficiency, J CLIN END, 86(8), 2001, pp. 3820-3825

Authors: Adachi, M Tachibana, K Asakura, Y Abe, S Nakae, J Tajima, T Fujieda, K
Citation: M. Adachi et al., Clinical case seminar - Compound heterozygous mutations in the gamma subunit gene of ENaC (1627delG and 1570-1G -> A) in one sporadic Japanese patient with a systemic form of pseudohypoaldosteronism type 1, J CLIN END, 86(1), 2001, pp. 9-12

Authors: Sugawara, T Abe, S Sakuragi, N Fujimoto, Y Nomura, E Fujieda, K Saito, M Fujimoto, S
Citation: T. Sugawara et al., RIP 140 modulates transcription of the steroidogenic acute regulatory protein gene through interactions with both SF-1 and DAX-1, ENDOCRINOL, 142(8), 2001, pp. 3570-3577

Authors: Okuhara, K Tajima, T Nakae, J Fujieda, K
Citation: K. Okuhara et al., A novel missense mutation in the HMG box region of the SRY gene in a Japanese patient with an XY sex reversal, J HUM GENET, 45(2), 2000, pp. 112-114

Authors: Okuhara, K Tajima, T Abe, S Satoh, K Nakae, J Shinohara, N Fujieda, K
Citation: K. Okuhara et al., Gonadotropin-releasing hormone analog therapy failed to improve predicted final height in two children with central precocious puberty and microcephalus, ENDOCR J, 47, 2000, pp. S129-S132

Authors: Yokose, S Kadokura, H Tajima, Y Fujieda, K Katayama, I Matsuoka, T Katayama, T
Citation: S. Yokose et al., Establishment and characterization of a culture system for enzymatically released rat dental pulp cells, CALCIF TIS, 66(2), 2000, pp. 139-144

Authors: Sato, K Tajima, T Nakae, J Adachi, M Asakura, Y Tachibana, K Suwa, S Katsumata, N Tanaka, T Hayashi, Y Abe, S Murashita, M Okuhara, K Shinohara, N Fujieda, K
Citation: K. Sato et al., Three novel PHEX gene mutations in Japanese patients with X-linked hypophosphatemic rickets, PEDIAT RES, 48(4), 2000, pp. 536-540

Authors: Tajima, T Kitagawa, H Yokoya, S Tachibana, K Adachi, M Nakae, J Suwa, S Katoh, S Fujieda, K
Citation: T. Tajima et al., A novel missense mutation of mineralocorticoid receptor gene in one Japanese family with a renal form of pseudohypoaldosteronism type 1, J CLIN END, 85(12), 2000, pp. 4690-4694

Authors: Israel, E Attie, KM Bengtsson, BA Blethen, SL Blum, W Cameron, F Carel, JC Carlsson, L Chipman, JJ Christiansen, JS Clayton, P Clemmons, DR Cohen, P Drop, S Fujieda, K Ghigo, E Hintz, RL Ho, K Ilondo, MM Jasper, H Jesussek, B Kappelgaard, AM Laron, Z Lippe, BM Malozowski, S Mullis, PE de Munick-Keizer-Schrama, S Nishi, Y Parks, JS Phelps, C Ranke, M Robinson, I Rosenfeld, RG Rose, S Saenger, P Saggese, G Savage, M Shalet, S Sizonenko, PC Strasburger, C Tachibana, K Tanaka, T Thorner, MO Wikland, KA Zadik, Z
Citation: E. Israel et al., Consensus guidelines for the diagnosis and treatment of growth hormone (GH) deficiency in childhood and adolescence: Summary statement of the GH Research Society, J CLIN END, 85(11), 2000, pp. 3990-3993

Authors: Isshiki, S Okubo, H Fujieda, K
Citation: S. Isshiki et al., Segregation of isozymes in selfed progenies of a synthetic amphidiploid between Solanum integrifolium and S-melongena, EUPHYTICA, 112(1), 2000, pp. 9-14

Authors: Abo, K Sumino, K Nishio, H Hozumi, T Ishida, Y Fujieda, K Tajima, T Kazumi, T
Citation: K. Abo et al., 21-hydroxylase deficiency presenting as massive bilateral adrenal masses in the seventh decade of life, ENDOCR J, 46(6), 1999, pp. 817-823

Authors: Okuhara, K Tajima, T Nakae, J Sasaki, S Tochimaru, H Abe, S Fujieda, K
Citation: K. Okuhara et al., A Japanese case with Frasier syndrome caused by the splice junction mutation of WT1 gene, ENDOCR J, 46(5), 1999, pp. 639-642

Authors: Tanaka, T Seino, Y Fujieda, K Igarashi, Y Yokoya, S Tachibana, K Ogawa, Y
Citation: T. Tanaka et al., Pharmacokinetics and metabolic effects of high-dose growth hormone administration in healthy adult men, ENDOCR J, 46(4), 1999, pp. 605-612

Authors: Mori, Y Jing, P Kayama, M Fujieda, K Hasegawa, T Nogimori, T Hirooka, Y Mitsuma, T
Citation: Y. Mori et al., Gene amplification as a common cause of inherited thyroxine-binding globulin excess: Analysis of one familial and two sporadic cases, ENDOCR J, 46(4), 1999, pp. 613-619

Authors: Yokoya, S Araki, K Igarashi, Y Kohno, H Nishi, Y Hasegawa, Y Fujita, K Iwatani, N Tachibana, K Ohyama, Y Seino, Y Satoh, M Fujieda, K Tanaka, T
Citation: S. Yokoya et al., High-dose growth hormone (GH) treatment in prepubertal GH-deficient children, ACT PAEDIAT, 88, 1999, pp. 76-79

Authors: Murashita, M Tajima, T Nakae, J Shinohara, N Geffner, ME Fujieda, K
Citation: M. Murashita et al., Near-normal linear growth in the setting of markedly reduced growth hormone and IGF-1 - A case report, HORMONE RES, 51(4), 1999, pp. 184-188

Authors: Abe, S Nakae, J Yasoshima, K Tajima, T Shinohara, N Murashita, M Satoh, K Koike, A Takahashi, Y Fujieda, K
Citation: S. Abe et al., Novel missense mutation (Leu466Arg) of the DAX1 gene in a patient with X-linked congenital adrenal hypoplasia, AM J MED G, 84(2), 1999, pp. 87-89

Authors: Sugawara, A Fujieda, K Otsuka, N
Citation: A. Sugawara et al., Phase transition between charge-induced long-period and (2 x 4) reconstructions of GaAs(001) surface, SURF SCI, 438(1-3), 1999, pp. 142-147

Authors: Nishi, Y Tanaka, T Takano, K Fujieda, K Igarashi, Y Hanew, K Hirano, T Yokoya, S
Citation: Y. Nishi et al., Recent status in the occurrence of leukemia in growth hormone-treated patients in Japan, J CLIN END, 84(6), 1999, pp. 1961-1965

Authors: Hoshi, N Tonoki, H Handa, Y Fujino, T Okuyama, K Koga, Y Matsumoto, Y Yamada, T Yamada, H Kishida, T Sagawa, T Fujieda, K Nakahori, Y Kant, JA Fujimoto, S
Citation: N. Hoshi et al., Prenatal identification of mos45,X/46,X,+mar in a normal male baby by cytogenetic and molecular analysis, PRENAT DIAG, 18(12), 1998, pp. 1316-1322

Authors: Fujieda, K
Citation: K. Fujieda, Endocrinological manifestations, INTRACRANIAL GERM CELL TUMORS, 1998, pp. 128-136
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