Matsuo M - Search Results

1

Early detection of tumor relapse/regrowth by consecutive minimal residual disease monitoring in high-risk neuroblastoma patients.

Hirase S, Saitoh A, Hartomo TB, Kozaki A, Yanai T, Hasegawa D, Kawasaki K, Kosaka Y, Matsuo M, Yamamoto N, Mori T, Hayakawa A, Iijima K, Nishio H, Nishimura N. Hirase S, et al. Among authors: matsuo m. Oncol Lett. 2016 Aug;12(2):1119-1123. doi: 10.3892/ol.2016.4682. Epub 2016 Jun 7. Oncol Lett. 2016. PMID: 27446404 Free PMC 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

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.

7

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.

8

Blockade of TGF-beta action ameliorates renal dysfunction and histologic progression in anti-GBM nephritis.

Zhou A, Ueno H, Shimomura M, Tanaka R, Shirakawa T, Nakamura H, Matsuo M, Iijima K. Zhou A, et al. Among authors: matsuo m. Kidney Int. 2003 Jul;64(1):92-101. doi: 10.1046/j.1523-1755.2003.00045.x. Kidney Int. 2003. PMID: 12787399 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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