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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
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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
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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
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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
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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
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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
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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
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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
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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
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Tachibana, K
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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
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Israel, E
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Bengtsson, BA
Blethen, SL
Blum, W
Cameron, F
Carel, JC
Carlsson, L
Chipman, JJ
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Clayton, P
Clemmons, DR
Cohen, P
Drop, S
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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
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
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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
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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
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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
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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
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Citation: S. Yokoya et al., High-dose growth hormone (GH) treatment in prepubertal GH-deficient children, ACT PAEDIAT, 88, 1999, pp. 76-79
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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
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Abe, S
Nakae, J
Yasoshima, K
Tajima, T
Shinohara, N
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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
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
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Tanaka, T
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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
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Tonoki, H
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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