Horikawa R - Search Results

1

Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.

Sato N, Katsumata N, Kagami M, Hasegawa T, Hori N, Kawakita S, Minowada S, Shimotsuka A, Shishiba Y, Yokozawa M, Yasuda T, Nagasaki K, Hasegawa D, Hasegawa Y, Tachibana K, Naiki Y, Horikawa R, Tanaka T, Ogata T. Sato N, et al. Among authors: horikawa r. J Clin Endocrinol Metab. 2004 Mar;89(3):1079-88. doi: 10.1210/jc.2003-030476. J Clin Endocrinol Metab. 2004. PMID: 15001591

2

A novel missense mutation in the type II 3 beta-hydroxysteroid dehydrogenase gene in a family with classical salt-wasting congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency.

Katsumata N, Tanae A, Yasunaga T, Horikawa R, Tanaka T, Hibi I. Katsumata N, et al. Among authors: horikawa r. Hum Mol Genet. 1995 Apr;4(4):745-6. doi: 10.1093/hmg/4.4.745. Hum Mol Genet. 1995. PMID: 7633426 No abstract available.

3

Clinical significance of growth hormone-binding protein measurements in children.

Horikawa R, Tanaka T, Katsumata N, Satoh M, Nagashima A, Watanabe T, Kokai Y, Tanae A, Hibi I. Horikawa R, et al. Proc Soc Exp Biol Med. 1994 Jul;206(3):320-3. doi: 10.3181/00379727-206-43768. Proc Soc Exp Biol Med. 1994. PMID: 8016173

4

Growth hormone (GH) secretory dynamics in a case of acromegalic gigantism associated with hyperprolactinemia: nonpulsatile secretion of GH may induce elevated insulin-like growth factor-I (IGF-I) and IGF-binding protein-3 levels.

Yoshida T, Shimatsu A, Sakane N, Hizuka N, Horikawa R, Tanaka T. Yoshida T, et al. Among authors: horikawa r. J Clin Endocrinol Metab. 1996 Jan;81(1):310-3. doi: 10.1210/jcem.81.1.8550769. J Clin Endocrinol Metab. 1996. PMID: 8550769

5

GH and GnRH analog treatment in children who enter puberty at short stature.

Tanaka T, Satoh M, Yasunaga T, Horikawa R, Tanae A, Hibi I. Tanaka T, et al. Among authors: horikawa r. J Pediatr Endocrinol Metab. 1997 Nov-Dec;10(6):623-8. doi: 10.1515/jpem.1997.10.6.623. J Pediatr Endocrinol Metab. 1997. PMID: 9467133 Clinical Trial.

6

Nutrition related hormonal changes in obese children.

Yasunaga T, Furukawa S, Katsumata N, Horikawa R, Tanaka T, Tanae A, Hibi I. Yasunaga T, et al. Among authors: horikawa r. Endocr J. 1998 Apr;45(2):221-7. doi: 10.1507/endocrj.45.221. Endocr J. 1998. PMID: 9700475 Free article.

7

The regulatory effect of growth hormone on growth hormone-binding protein in human serum.

Horikawa R, Tanaka T, Katsumata N, Tanae A. Horikawa R, et al. Endocr J. 1998 Apr;45 Suppl:S113-5. doi: 10.1507/endocrj.45.suppl_s113. Endocr J. 1998. PMID: 9790243 Free article. Clinical Trial.

8

G370C mutation in the FGFR3 gene in a Japanese patient with thanatophoric dysplasia.

Katsumata N, Kuno T, Miyazaki S, Mikami S, Nagashima-Miyokawa A, Nimura A, Horikawa R, Tanaka T. Katsumata N, et al. Among authors: horikawa r. Endocr J. 1998 Apr;45 Suppl:S171-4. doi: 10.1507/endocrj.45.suppl_s171. Endocr J. 1998. PMID: 9790257 Free article.

9

When and how to combine growth hormone with a luteinizing hormone-releasing hormone analogue.

Tanaka T, Satoh M, Yasunaga T, Horikawa R, Tanae A, Katsumata N, Tachibana K, Nose O, Hibi I. Tanaka T, et al. Among authors: horikawa r. Acta Paediatr Suppl. 1999 Feb;88(428):85-8. doi: 10.1111/j.1651-2227.1999.tb14359.x. Acta Paediatr Suppl. 1999. PMID: 10102060 Clinical Trial.

10

A novel compound heterozygous mutation in the steroidogenic acute regulatory protein gene in a patient with congenital lipoid adrenal hyperplasia.

Katsumata N, Kawada Y, Yamamoto Y, Noda M, Nimura A, Horikawa R, Tanaka T. Katsumata N, et al. Among authors: horikawa r. J Clin Endocrinol Metab. 1999 Nov;84(11):3983-7. doi: 10.1210/jcem.84.11.6118. J Clin Endocrinol Metab. 1999. PMID: 10566637

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