Matsuo M - Search Results

1

Ureaplasma urealyticum and Mycoplasma hominis presence in umbilical cord is associated with pathogenesis of funisitis.

Egawa T, Morioka I, Morisawa T, Yokoyama N, Nakao H, Ohashi M, Matsuo M. Egawa T, et al. Among authors: matsuo m. Kobe J Med Sci. 2007;53(5):241-9. Kobe J Med Sci. 2007. PMID: 18204300 Free article.

2

Molecular genetics of spinal muscular atrophy: contribution of the NAIP gene to clinical severity.

Akutsu T, Nishio H, Sumino K, Takeshima Y, Tsuneishi S, Wada H, Takada S, Matsuo M, Nakamura H. Akutsu T, et al. Among authors: matsuo m. Kobe J Med Sci. 2002 Apr;48(1-2):25-31. Kobe J Med Sci. 2002. PMID: 11912351 Free article.

3

Novel missense mutation of the UGT1A1 gene in Thai siblings with Gilbert's syndrome.

Sutomo R, Laosombat V, Sadewa AH, Yokoyama N, Nakamura H, Matsuo M, Nishio H. Sutomo R, et al. Among authors: matsuo m. Pediatr Int. 2002 Aug;44(4):427-32. Pediatr Int. 2002. PMID: 12139570

4

The C677T mutation in the methylenetetrahydrofolate reductase gene among the Indonesian Javanese population.

Sadewa AH, Sunarti, Sutomo R, Hayashi C, Lee MJ, Ayaki H, Sofro AS, Matsuo M, Nishio H. Sadewa AH, et al. Among authors: matsuo m. Kobe J Med Sci. 2002 Dec;48(5-6):137-44. Kobe J Med Sci. 2002. PMID: 12594357 Free article.

5

Molecular genetic analyses of five Vietnamese patients with spinal muscular atrophy.

Khanh TV, Takeshima Y, Harada Y, Nishio H, Dao NT, Hoan NT, Thao BP, Matsuo M. Khanh TV, et al. Among authors: matsuo m. Kobe J Med Sci. 2002 Dec;48(5-6):177-82. Kobe J Med Sci. 2002. PMID: 12657835 Free article.

6

Deletion of the SMN1 and NAIP genes in Vietnamese patients with spinal muscular atrophy.

Nguyen DB, Sadewa AH, Takeshima Y, Sutomo R, Tran VK, Nguyen TN, Nguyen TH, Vu CD, Dang DH, Harada Y, Nishio H, Matsuo M. Nguyen DB, et al. Among authors: matsuo m. Kobe J Med Sci. 2003;49(3-4):55-8. Kobe J Med Sci. 2003. PMID: 14676483 Free article.

7

Novel double-deletion mutations of the OFD1 gene creating multiple novel transcripts.

Morisawa T, Yagi M, Surono A, Yokoyama N, Ohmori M, Terashi H, Matsuo M. Morisawa T, et al. Among authors: matsuo m. Hum Genet. 2004 Jul;115(2):97-103. doi: 10.1007/s00439-004-1139-1. Epub 2004 Jun 2. Hum Genet. 2004. PMID: 15221448

8

PDGF-alpha receptor expression following hypoxic-ischemic injury in the neonatal rat brain.

Morioka I, Tsuneishi S, Takada S, Matsuo M. Morioka I, et al. Among authors: matsuo m. Kobe J Med Sci. 2004 Jan;50(1-2):21-30. Kobe J Med Sci. 2004. PMID: 15342968 Free article.

9

Screening for G71R mutation of the UGT1A1 gene in the Javanese-Indonesian and Malay-Malaysian populations.

Sutomo R, Talib NA, Yusoff NM, Van Rostenberghe H, Sadewa AH, Sunarti, Sofro AS, Yokoyama N, Lee MJ, Matsuo M, Nishio H. Sutomo R, et al. Among authors: matsuo m. Pediatr Int. 2004 Oct;46(5):565-9. doi: 10.1111/j.1442-200x.2004.01959.x. Pediatr Int. 2004. PMID: 15491385

10

ACE gene polymorphism in children with nephrotic syndrome in the Indonesian population.

Sasongko TH, Sadewa AH, Kusuma PA, Damanik MP, Lee MJ, Ayaki H, Nozu K, Goto A, Matsuo M, Nishio H. Sasongko TH, et al. Among authors: matsuo m. Kobe J Med Sci. 2005;51(3-4):41-7. Kobe J Med Sci. 2005. PMID: 16421456 Free article.

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