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Results: 1-13 |
Results: 13
Turner syndrome and Xp deletions: Clinical and molecular studies in 47 patients
Authors: Ogata, T Muroya, K Matsuo, N Shinohara, O Yorifuji, T Nishi, Y Hasegawa, Y Horikawa, R Tachibana, K
Citation: T. Ogata et al., Turner syndrome and Xp deletions: Clinical and molecular studies in 47 patients, J CLIN END, 86(11), 2001, pp. 5498-5508
Molecular cloning of ovine and bovine growth hormone-releasing hormone receptors: The ovine receptor is C-terminally truncated
Authors: Horikawa, R Gaylinn, BD Lyons, CE Thorner, MO
Citation: R. Horikawa et al., Molecular cloning of ovine and bovine growth hormone-releasing hormone receptors: The ovine receptor is C-terminally truncated, ENDOCRINOL, 142(6), 2001, pp. 2660-2668
Comparison of the somatogenic action of 20 kDa- and 22 kDa human growth hormones in spontaneous dwarf rats
Authors: Ishikawa, M Tachibana, T Kamioka, T Horikawa, R Katsumata, N Tanaka, T
Citation: M. Ishikawa et al., Comparison of the somatogenic action of 20 kDa- and 22 kDa human growth hormones in spontaneous dwarf rats, GROWTH H I, 10(4), 2000, pp. 199-206
Regulation of pituitary growth hormone-secretagogue and growth hormone-releasing hormone receptor RNA expression in young dwarf rats
Authors: Horikawa, R Tachibana, T Katsumata, N Ishikawa, H Tanaka, T
Citation: R. Horikawa et al., Regulation of pituitary growth hormone-secretagogue and growth hormone-releasing hormone receptor RNA expression in young dwarf rats, ENDOCR J, 47, 2000, pp. S53-S56
Acid-labile subunit (ALS) measurements in children
Authors: Nimura, A Katsumata, N Horikawa, R Tanae, A Tanaka, T
Citation: A. Nimura et al., Acid-labile subunit (ALS) measurements in children, ENDOCR J, 47, 2000, pp. S111-S114
Bone mineral density in Turner syndrome: Relation to GH treatment and estrogen treatment
Authors: Sato, N Nimura, A Horikawa, R Katumata, N Tanae, A Tanaka, T
Citation: N. Sato et al., Bone mineral density in Turner syndrome: Relation to GH treatment and estrogen treatment, ENDOCR J, 47, 2000, pp. S115-S119
Analysis of the FGFR3 gene in Japanese patients with achondroplasia and hypochondroplasia
Authors: Katsumata, N Mikami, S Nagashima-Miyokawa, A Nimura, A Sato, N Horikawa, R Tanae, A Tanaka, T
Citation: N. Katsumata et al., Analysis of the FGFR3 gene in Japanese patients with achondroplasia and hypochondroplasia, ENDOCR J, 47, 2000, pp. S121-S124
Growth and metabolic disturbances in a patient with total parenteral nutrition: A case of hypercalciuric hypercalcemia
Authors: Ikema, S Horikawa, R Nakano, M Yokouchi, K Yamazaki, H Tanaka, T Tanae, A
Citation: S. Ikema et al., Growth and metabolic disturbances in a patient with total parenteral nutrition: A case of hypercalciuric hypercalcemia, ENDOCR J, 47, 2000, pp. S137-S140
Japanese familiar patients with male-limited precocious puberty
Authors: Shinagawa, T Katsumata, N Sato, N Horikawa, R Tanae, A Tanaka, T
Citation: T. Shinagawa et al., Japanese familiar patients with male-limited precocious puberty, ENDOCR J, 47(6), 2000, pp. 777-782
Genetic and endocrinological evaluations of three 46,XX patients with congenital lipoid adrenal hyperplasia previously reported as having presented spontaneous puberty
Authors: Tanae, A Katsumata, N Sato, N Horikawa, R Tanaka, T
Citation: A. Tanae et al., Genetic and endocrinological evaluations of three 46,XX patients with congenital lipoid adrenal hyperplasia previously reported as having presented spontaneous puberty, ENDOCR J, 47(5), 2000, pp. 629-634
A novel specific bioassay for serum human growth hormone
Authors: Ishikawa, M Nimura, A Horikawa, R Katsumata, N Arisaka, O Wada, M Honjo, M Tanaka, T
Citation: M. Ishikawa et al., A novel specific bioassay for serum human growth hormone, J CLIN END, 85(11), 2000, pp. 4274-4279
When and how to combine growth hormone with a luteinizing hormone-releasing hormone analogue
Authors: Tanaka, T Satoh, M Yasunaga, T Horikawa, R Tanae, A Katsumata, N Tachibana, K Nose, O Hibi, I
Citation: T. Tanaka et al., When and how to combine growth hormone with a luteinizing hormone-releasing hormone analogue, ACT PAEDIAT, 88, 1999, pp. 85-88
A novel compound heterozygous mutation in the steroidogenic acute regulatory protein gene in a patient with congenital lipoid adrenal hyperplasia
Authors: Katsumata, N Kawada, Y Yamamoto, Y Noda, M Nimura, A Horikawa, R Tanaka, T
Citation: N. Katsumata et al., A novel compound heterozygous mutation in the steroidogenic acute regulatory protein gene in a patient with congenital lipoid adrenal hyperplasia, J CLIN END, 84(11), 1999, pp. 3983-3987
Risultati: 1-13 |