Matsuo M - Search Results

1

Molecular analysis of patients with type III Bartter syndrome: picking up large heterozygous deletions with semiquantitative PCR.

Nozu K, Fu XJ, Nakanishi K, Yoshikawa N, Kaito H, Kanda K, Krol RP, Miyashita R, Kamitsuji H, Kanda S, Hayashi Y, Satomura K, Shimizu N, Iijima K, Matsuo M. Nozu K, et al. Among authors: matsuo m. Pediatr Res. 2007 Sep;62(3):364-9. doi: 10.1203/PDR.0b013e318123fb90. Pediatr Res. 2007. PMID: 17622951

2

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

3

Heterogous dystrophin mRNA produced by a novel splice acceptor site mutation in intermediate dystrophinopathy.

Adachi K, Takeshima Y, Wada H, Yagi M, Nakamura H, Matsuo M. Adachi K, et al. Among authors: matsuo m. Pediatr Res. 2003 Jan;53(1):125-31. doi: 10.1203/00006450-200301000-00021. Pediatr Res. 2003. PMID: 12508091

4

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.

5

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.

6

Role of p38 MAP kinase pathway in a toxin-induced model of hemolytic uremic syndrome.

Fu XJ, Iijima K, Nozu K, Hamahira K, Tanaka R, Oda T, Yoshikawa N, Matsuo M. Fu XJ, et al. Among authors: matsuo m. Pediatr Nephrol. 2004 Aug;19(8):844-52. doi: 10.1007/s00467-004-1502-4. Epub 2004 Jun 17. Pediatr Nephrol. 2004. PMID: 15206036

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

C-terminal truncated dystrophin identified in skeletal muscle of an asymptomatic boy with a novel nonsense mutation of the dystrophin gene.

Suminaga R, Takeshima Y, Wada H, Yagi M, Matsuo M. Suminaga R, et al. Among authors: matsuo m. Pediatr Res. 2004 Nov;56(5):739-43. doi: 10.1203/01.PDR.0000142734.46609.43. Epub 2004 Sep 15. Pediatr Res. 2004. PMID: 15371569

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

Cyclosporin A absorption profiles in children with nephrotic syndrome.

Nozu K, Iijima K, Sakaeda T, Okumura K, Nakanishi K, Yoshikawa N, Honda M, Ikeda M, Matsuo M. Nozu K, et al. Among authors: matsuo m. Pediatr Nephrol. 2005 Jul;20(7):910-3. doi: 10.1007/s00467-005-1844-6. Epub 2005 Apr 23. Pediatr Nephrol. 2005. PMID: 15856324

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