Ogawa M - Search Results

1

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: ogawa m. Endocr J. 1997 Feb;44(1):149-54. doi: 10.1507/endocrj.44.149. Endocr J. 1997. PMID: 9152628 Free article.

2

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. Among authors: ogawa m. 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.

3

Prevalence of GH-1 gene deletion in patients with isolated growth hormone deficiency in Japan. GH Gene Study Group.

Ogawa M, Kamijo T, Igarashi Y, Nishi Y, Iwatani N, Kohno H, Koga J, Byun YJ. Ogawa M, et al. Endocr J. 2000 Apr;47(2):157-62. doi: 10.1507/endocrj.47.157. Endocr J. 2000. PMID: 10943739 Free article.

4

Screening for mutations in the GH-1 gene by dideoxy fingerprinting (ddF).

Miyata I, Eto Y, Kamijo T, Ogawa M, Futrakul A, Phillips JA 3rd. Miyata I, et al. Among authors: ogawa m. Endocr J. 1999 Mar;46 Suppl:S71-4. doi: 10.1507/endocrj.46.suppl_s71. Endocr J. 1999. PMID: 12054125 Free article. No abstract available.

5

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. Among authors: ogawa m. J Pediatr. 1991 Feb;118(2):245-8. doi: 10.1016/s0022-3476(05)80492-5. J Pediatr. 1991. PMID: 1993953 No abstract available.

6

A novel E250X mutation of the PIT1 gene in a patient with combined pituitary hormone deficiency.

Irie Y, Tatsumi K, Ogawa M, Kamijo T, Preeyasombat C, Suprasongsin C, Amino N. Irie Y, et al. Among authors: ogawa m. Endocr J. 1995 Jun;42(3):351-4. doi: 10.1507/endocrj.42.351. Endocr J. 1995. PMID: 7670563 Free article.

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: ogawa m. 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 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: ogawa m. 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

9

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: ogawa m. Growth Horm IGF Res. 1999 Dec;9(6):434-7. doi: 10.1054/ghir.1999.0126. Growth Horm IGF Res. 1999. PMID: 10629163

10

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. Jpn J Clin Oncol. 1988 Sep;18(3):255-60. Jpn J Clin Oncol. 1988. PMID: 3166073

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