Nishi Y - Search Results

1

Mild adrenal 3 beta-hydroxysteroid dehydrogenase deficiency in children with accelerated growth, premature pubarche and/or hirsutism.

Nishi Y, Tezuka T. Nishi Y, et al. Eur J Pediatr. 1992 Jan;151(1):19-23. doi: 10.1007/BF02073883. Eur J Pediatr. 1992. PMID: 1309452

2

Nonclassical 3 beta-hydroxysteroid dehydrogenase deficiency in young girls with hirsutism and premature pubarche.

Nishi Y. Nishi Y. Endocrinol Jpn. 1990 Oct;37(5):763-7. doi: 10.1507/endocrj1954.37.763. Endocrinol Jpn. 1990. PMID: 2150813 Free article.

3

Transient partial growth hormone deficiency due to zinc deficiency.

Nishi Y, Hatano S, Aihara K, Fujie A, Kihara M. Nishi Y, et al. J Am Coll Nutr. 1989 Apr;8(2):93-7. doi: 10.1080/07315724.1989.10720283. J Am Coll Nutr. 1989. PMID: 2708733

4

Effect of long-term calcitonin therapy by injection and nasal spray on the incidence of fractures in osteogenesis imperfecta.

Nishi Y, Hamamoto K, Kajiyama M, Ono H, Kihara M, Jinno K. Nishi Y, et al. J Pediatr. 1992 Sep;121(3):477-80. doi: 10.1016/s0022-3476(05)81809-8. J Pediatr. 1992. PMID: 1517930

5

Zinc and growth.

Nishi Y. Nishi Y. J Am Coll Nutr. 1996 Aug;15(4):340-4. doi: 10.1080/07315724.1996.10718608. J Am Coll Nutr. 1996. PMID: 8829089 Review.

6

No genetic mutation in type II 3 beta-hydroxysteroid dehydrogenase gene in patients with biochemical evidence of enzyme deficiency.

Tajima T, Nishi Y, Takase A, Nakae J, Murashita M, Fujieda K. Tajima T, et al. Among authors: nishi y. Horm Res. 1997;47(2):49-53. doi: 10.1159/000185430. Horm Res. 1997. PMID: 9030967

7

Growth hormone therapy in achondroplasia.

Nishi Y, Kajiyama M, Miyagawa S, Fujiwara M, Hamamoto K. Nishi Y, et al. Acta Endocrinol (Copenh). 1993 May;128(5):394-6. doi: 10.1530/acta.0.1280394. Acta Endocrinol (Copenh). 1993. PMID: 8317186 Clinical Trial.

8

[Copper].

Nishi Y. Nishi Y. Nihon Rinsho. 1995 Feb;53 Su Pt 1:815-8. Nihon Rinsho. 1995. PMID: 8753561 Review. Japanese. No abstract available.

9

Treatment of isolated growth hormone deficiency type IA due to GH-I gene deletion with recombinant human insulin-like growth factor I.

Nishi Y, Hamamoto K, Kajiyama M, Fujiwara M, Miyagawa S, Hasegawa Y, Hasegawa T. Nishi Y, et al. Acta Paediatr. 1993 Nov;82(11):983-6. doi: 10.1111/j.1651-2227.1993.tb12616.x. Acta Paediatr. 1993. PMID: 7509217

10

Isolated human growth hormone deficiency due to the hGH-I gene deletion with (type IA) and without (the Israeli-type) hGH antibody formation during hGH therapy.

Nishi Y, Masuda H, Nishimura S, Kihara M, Suwa S, Tachibana K, Takeda M, Okada Y, Matsuda I. Nishi Y, et al. Acta Endocrinol (Copenh). 1990 Feb;122(2):267-71. doi: 10.1530/acta.0.1220267. Acta Endocrinol (Copenh). 1990. PMID: 1969217

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