Kamijo T - Search Results

1

Isolated growth hormone deficiency in two siblings because of paternal mosaicism for a mutation in the GH1 gene.

Tsubahara M, Hayashi Y, Niijima S, Yamamoto M, Kamijo T, Murata Y, Haruna H, Okumura A, Shimizu T. Tsubahara M, et al. Among authors: kamijo t. Clin Endocrinol (Oxf). 2012 Mar;76(3):420-4. doi: 10.1111/j.1365-2265.2011.04224.x. Clin Endocrinol (Oxf). 2012. PMID: 21933221

2

Growth hormone releasing hormone receptor (GHRH-r) gene mutation in Indian children with familial isolated growth hormone deficiency: a study from western India.

Desai MP, Upadhye PS, Kamijo T, Yamamoto M, Ogawa M, Hayashi Y, Seo H, Nair SR. Desai MP, et al. Among authors: kamijo t. J Pediatr Endocrinol Metab. 2005 Oct;18(10):955-73. doi: 10.1515/jpem.2005.18.10.955. J Pediatr Endocrinol Metab. 2005. PMID: 16355809

3

A case with isolated growth hormone deficiency caused by compound heterozygous mutations in GH-1: a novel missense mutation in the initiation codon and a 7.6kb deletion.

Hayashi Y, Kamijo T, Yamamoto M, Murata Y, Phillips JA 3rd, Ogawa M, Seo H. Hayashi Y, et al. Among authors: kamijo t. Growth Horm IGF Res. 2007 Jun;17(3):249-53. doi: 10.1016/j.ghir.2007.01.019. Epub 2007 Mar 13. Growth Horm IGF Res. 2007. PMID: 17360216

4

Inhibition of growth hormone (GH) secretion by a mutant GH-I gene product in neuroendocrine cells containing secretory granules: an implication for isolated GH deficiency inherited in an autosomal dominant manner.

Hayashi Y, Yamamoto M, Ohmori S, Kamijo T, Ogawa M, Seo H. Hayashi Y, et al. Among authors: kamijo t. J Clin Endocrinol Metab. 1999 Jun;84(6):2134-9. doi: 10.1210/jcem.84.6.5736. J Clin Endocrinol Metab. 1999. PMID: 10372722

5

Mutations in intron 3 of GH-1 gene associated with isolated GH deficiency type II in three Japanese families.

Kamijo T, Hayashi Y, Shimatsu A, Kinoshita E, Yoshimoto M, Ogawa M, Seo H. Kamijo T, et al. Clin Endocrinol (Oxf). 1999 Sep;51(3):355-60. doi: 10.1046/j.1365-2265.1999.00798.x. Clin Endocrinol (Oxf). 1999. PMID: 10469016

6

Hereditary isolated growth hormone deficiency caused by GH1 gene mutations in Japanese patients.

Kamijo T, Hayashi Y, Seo H, Ogawa M. Kamijo T, et al. Growth Horm IGF Res. 1999 Jun;9 Suppl B:31-4; discussion 35-6. doi: 10.1016/s1096-6374(99)80078-1. Growth Horm IGF Res. 1999. PMID: 10549303 Review.

7

A nonsense mutation (E72X) in growth hormone releasing hormone receptor (GHRHR) gene is the major cause of familial isolated growth hormone deficiency in Western region of India: founder effect suggested by analysis of dinucleotide repeat polymorphism close to GHRHR gene.

Kamijo T, Hayashi Y, Seo H, Yamamoto M, Ogawa M, Choski CS, Sawant NJ, Colaco MP, Desai MP. Kamijo T, et al. Growth Horm IGF Res. 2004 Oct;14(5):394-401. doi: 10.1016/j.ghir.2004.05.001. Growth Horm IGF Res. 2004. PMID: 15336233

8

A novel mutation at the donor splice site of intron 3 of the GH-I gene in a patient with isolated growth hormone deficiency.

Hayashi Y, Kamijo T, Yamamoto M, Ohmori S, Phillips JA 3rd, Ogawa M, Igarashi Y, Seo H. Hayashi Y, et al. Among authors: kamijo t. Growth Horm IGF Res. 1999 Dec;9(6):434-7. doi: 10.1054/ghir.1999.0126. Growth Horm IGF Res. 1999. PMID: 10629163

9

A Japanese family with autosomal dominant growth hormone deficiency.

Saitoh H, Fukushima T, Kamoda T, Tanae A, Kamijo T, Yamamoto M, Ogawa M, Hayashi Y, Ohmori S, Seo H. Saitoh H, et al. Among authors: kamijo t. Eur J Pediatr. 1999 Aug;158(8):624-7. doi: 10.1007/s004310051164. Eur J Pediatr. 1999. PMID: 10445339

10

A case of isolated growth hormone (GH) deficiency with compound heterozygous abnormality at the GH-1 gene locus.

Nishi Y, Ogawa M, Kamijo T, Igarashi Y, Iwatani N, Kohno H, Masumura T, Byun Y, Koga J. Nishi Y, et al. Among authors: kamijo t. J Pediatr Endocrinol Metab. 1997 Jan-Feb;10(1):73-6. doi: 10.1515/jpem.1997.10.1.73. J Pediatr Endocrinol Metab. 1997. PMID: 9364346

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