Kamijo T - Search Results

1

The occurrence of acute lymphoblastic leukemia shortly after the cessation of human growth hormone therapy.

Ogawa M, Mori O, Kamijo T, Tomita H, Yazawa T, Miwa K, Tsukidate K, Ogura M, Ohno R. Ogawa M, et al. Among authors: kamijo t. Jpn J Clin Oncol. 1988 Sep;18(3):255-60. Jpn J Clin Oncol. 1988. PMID: 3166073

2

A highly sensitive sandwich enzyme immunoassay of urinary growth hormone in children with short stature, Turner's syndrome, and simple obesity.

Tomita H, Ogawa M, Kamijo T, Mori O, Ishikawa E, Mohri Z, Murakami Y. Tomita H, et al. Among authors: kamijo t. Acta Endocrinol (Copenh). 1989 Oct;121(4):513-9. doi: 10.1530/acta.0.1210513. Acta Endocrinol (Copenh). 1989. PMID: 2678871

3

Familial isolated growth hormone deficiency: genetics and pathophysiology.

Hayashi Y, Kamijo T, Ogawa M, Seo H. Hayashi Y, et al. Among authors: kamijo t. Endocr J. 2002 Jun;49(3):265-72. doi: 10.1507/endocrj.49.265. Endocr J. 2002. PMID: 12201208 Free article. Review. No abstract available.

4

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

5

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.

6

Screening for growth hormone gene deletions in patients with isolated growth hormone deficiency.

Kamijo T, Phillips JA 3rd, Ogawa M, Yuan L, Shi Y, Bao XL. Kamijo T, et al. J Pediatr. 1991 Feb;118(2):245-8. doi: 10.1016/s0022-3476(05)80492-5. J Pediatr. 1991. PMID: 1993953 No abstract available.

7

A new mutation causing inherited growth hormone deficiency: a compound heterozygote of a 6.7 kb deletion and a two base deletion in the third exon of the GH-1 gene.

Igarashi Y, Ogawa M, Kamijo T, Iwatani N, Nishi Y, Kohno H, Masumura T, Koga J. Igarashi Y, et al. Among authors: kamijo t. Hum Mol Genet. 1993 Jul;2(7):1073-4. doi: 10.1093/hmg/2.7.1073. Hum Mol Genet. 1993. PMID: 8364549 No abstract available.

8

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

9

Detection of growth hormone gene defects by dideoxy fingerprinting (ddF).

Miyata I, Cogan JD, Prince MA, Kamijo T, Ogawa M, Phillips JA 3rd. Miyata I, et al. Among authors: kamijo t. Endocr J. 1997 Feb;44(1):149-54. doi: 10.1507/endocrj.44.149. Endocr J. 1997. PMID: 9152628 Free article.

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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