Ogawa E - Search Results

1

Peripheral blood stem cell transplantation for hepatoblastoma with microscopical residue: a therapeutic approach for incompletely resected tumor.

Yoshinari M, Imaizumi M, Hayashi Y, Sato A, Saito T, Suzuki H, Saisho T, Abukawa D, Ogawa E, Aikawa J, Goto K, Satoh T, Ohi R, Iinuma K. Yoshinari M, et al. Among authors: ogawa e. Tohoku J Exp Med. 1998 Mar;184(3):247-54. doi: 10.1620/tjem.184.247. Tohoku J Exp Med. 1998. PMID: 9591340 Free article.

2

Refractory autoimmune hemolytic anemia in a patient with chromosome 22q11.2 deletion syndrome.

Sakamoto O, Imaizumi M, Suzuki A, Sato A, Tanaka T, Ogawa E, Kumaki S, Iinuma K. Sakamoto O, et al. Among authors: ogawa e. Pediatr Int. 2004 Oct;46(5):612-4. doi: 10.1111/j.1442-200x.2004.01940.x. Pediatr Int. 2004. PMID: 15491395 No abstract available.

3

Gonadal suppression by a GnRH analogue does not alter somatic growth in rats with complete GH deficiency.

Ogawa E, Breier BH, Fujiwara I, Iinuma K. Ogawa E, et al. J Endocrinol. 2000 Aug;166(2):355-61. doi: 10.1677/joe.0.1660355. J Endocrinol. 2000. PMID: 10927624

4

Growth of two children after six months interruption of GH therapy.

Katsushima Y, Ogawa E, Fujiwara I, Asanuma A, Iinuma K. Katsushima Y, et al. Among authors: ogawa e. Endocr J. 1999 Mar;46 Suppl:S43-5. doi: 10.1507/endocrj.46.suppl_s43. Endocr J. 1999. PMID: 12054117 Free article.

5

Subacute thyroiditis in children: patient report and review of the literature.

Ogawa E, Katsushima Y, Fujiwara I, Iinuma K. Ogawa E, et al. J Pediatr Endocrinol Metab. 2003 Jul-Aug;16(6):897-900. doi: 10.1515/jpem.2003.16.6.897. J Pediatr Endocrinol Metab. 2003. PMID: 12948304

6

Molecular analysis of Japanese patients with steroid 21-hydroxylase deficiency.

Asanuma A, Ohura T, Ogawa E, Sato S, Igarashi Y, Matsubara Y, Iinuma K. Asanuma A, et al. Among authors: ogawa e. J Hum Genet. 1999;44(5):312-7. doi: 10.1007/s100380050167. J Hum Genet. 1999. PMID: 10496074

7

Mutation analysis of the GLUT2 gene in patients with Fanconi-Bickel syndrome.

Sakamoto O, Ogawa E, Ohura T, Igarashi Y, Matsubara Y, Narisawa K, Iinuma K. Sakamoto O, et al. Among authors: ogawa e. Pediatr Res. 2000 Nov;48(5):586-9. doi: 10.1203/00006450-200011000-00005. Pediatr Res. 2000. PMID: 11044475

8

A novel intronic mutation of the TAZ ( G4.5) gene in a patient with Barth syndrome: creation of a 5' splice donor site with variant GC consensus and elongation of the upstream exon.

Sakamoto O, Ohura T, Katsushima Y, Fujiwara I, Ogawa E, Miyabayashi S, Iinuma K. Sakamoto O, et al. Among authors: ogawa e. Hum Genet. 2001 Nov;109(5):559-63. doi: 10.1007/s00439-001-0612-3. Epub 2001 Oct 13. Hum Genet. 2001. PMID: 11735032

9

Hypophosphatemia in juvenile patients with systemic lupus erythematosus.

Fujiwara I, Ogawa E, Kondo Y, Ohura T, Iinuma K. Fujiwara I, et al. Among authors: ogawa e. Pediatr Int. 2003 Feb;45(1):23-30. doi: 10.1046/j.1442-200x.2003.01665.x. Pediatr Int. 2003. PMID: 12654064

10

Glycogen storage disease type Ia: molecular diagnosis of 51 Japanese patients and characterization of splicing mutations by analysis of ectopically transcribed mRNA from lymphoblastoid cells.

Akanuma J, Nishigaki T, Fujii K, Matsubara Y, Inui K, Takahashi K, Kure S, Suzuki Y, Ohura T, Miyabayashi S, Ogawa E, Iinuma K, Okada S, Narisawa K. Akanuma J, et al. Among authors: ogawa e. Am J Med Genet. 2000 Mar 13;91(2):107-12. Am J Med Genet. 2000. PMID: 10748407

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