Matsuo M - Search Results

1

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.

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

[Dystrophin gene analysis on 76 families with dystrophinopathy].

Adachi K, Yagi M, Ito T, Takeshima Y, Nishio H, Wada H, Nakamura H, Matsuo M. Adachi K, et al. Among authors: matsuo m. No To Hattatsu. 2002 Sep;34(5):391-7. No To Hattatsu. 2002. PMID: 12233050 Japanese.

5

Correlation between SMN2 copy number and clinical phenotype of spinal muscular atrophy: three SMN2 copies fail to rescue some patients from the disease severity.

Harada Y, Sutomo R, Sadewa AH, Akutsu T, Takeshima Y, Wada H, Matsuo M, Nishio H. Harada Y, et al. Among authors: matsuo m. J Neurol. 2002 Sep;249(9):1211-9. doi: 10.1007/s00415-002-0811-4. J Neurol. 2002. PMID: 12242541

6

Rapid SMN1 deletion test using DHPLC to screen patients with spinal muscular atrophy.

Sutomo R, Akutsu T, Takeshima Y, Nishio H, Sadewa AH, Harada Y, Matsuo M. Sutomo R, et al. Among authors: matsuo m. Am J Med Genet. 2002 Nov 22;113(2):225-6. doi: 10.1002/ajmg.10744. Am J Med Genet. 2002. PMID: 12407717 No abstract available.

7

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.

8

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.

9

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.

10

A novel mitochondrial mutation, 1556C --> T, in a Japanese patient with streptomycin-induced tinnitus.

Tanimoto H, Nishio H, Matsuo M, Nibu K. Tanimoto H, et al. Among authors: matsuo m. Acta Otolaryngol. 2004 Apr;124(3):258-61. doi: 10.1080/00016480310015740. Acta Otolaryngol. 2004. PMID: 15141753

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