Ariga T - Search Results

1

Confirming or excluding the diagnosis of Wiskott-Aldrich syndrome in children with thrombocytopenia of an unknown etiology.

Ariga T, Nakajima M, Yoshida J, Yamato K, Nagatoshi Y, Yanai F, Caviles AP, Nelson DL, Sakiyama Y. Ariga T, et al. J Pediatr Hematol Oncol. 2004 Jul;26(7):435-40. doi: 10.1097/00043426-200407000-00007. J Pediatr Hematol Oncol. 2004. PMID: 15218418

2

Flow cytometry analysis of adenosine deaminase (ADA) expression: a simple and reliable tool for the assessment of ADA-deficient patients before and after gene therapy.

Otsu M, Hershfield MS, Tuschong LM, Muul LM, Onodera M, Ariga T, Sakiyama Y, Candotti F. Otsu M, et al. Among authors: ariga t. Hum Gene Ther. 2002 Feb 10;13(3):425-32. doi: 10.1089/10430340252792558. Hum Gene Ther. 2002. PMID: 11860709

3

[Wiskott-Aldrich syndrome; evaluation of WASP function in vitro using clinical samples].

Ariga T. Ariga T. Nihon Rinsho Meneki Gakkai Kaishi. 2002 Feb;25(1):135-9. Nihon Rinsho Meneki Gakkai Kaishi. 2002. PMID: 11963173 Review. Japanese. No abstract available.

4

Mixed chimera status of 12 patients with Wiskott-Aldrich syndrome (WAS) after hematopoietic stem cell transplantation: evaluation by flow cytometric analysis of intracellular WAS protein expression.

Yamaguchi K, Ariga T, Yamada M, Nelson DL, Kobayashi R, Kobayashi C, Noguchi Y, Ito Y, Katamura K, Nagatoshi Y, Kondo S, Katoh H, Sakiyama Y. Yamaguchi K, et al. Among authors: ariga t. Blood. 2002 Aug 15;100(4):1208-14. doi: 10.1182/blood-2002-01-0211. Blood. 2002. PMID: 12149199 Free article.

5

The role of common gamma chain in human monocytes in vivo; evaluation from the studies of X-linked severe combined immunodeficiency (X-SCID) carriers and X-SCID patients who underwent cord blood stem cell transplantation.

Ariga T, Yamaguchi K, Yoshida J, Miyanoshita A, Watanabe T, Date T, Miura J, Kumaki S, Ishii N, Sakiyama Y. Ariga T, et al. Br J Haematol. 2002 Sep;118(3):858-63. doi: 10.1046/j.1365-2141.2002.03679.x. Br J Haematol. 2002. PMID: 12181059 Free article.

6

Treacher Collins syndrome with craniosynostosis, choanal atresia, and esophageal regurgitation caused by a novel nonsense mutation in TCOF1.

Horiuchi K, Ariga T, Fujioka H, Kawashima K, Yamamoto Y, Igawa H, Sakiyama Y, Sugihara T. Horiuchi K, et al. Among authors: ariga t. Am J Med Genet A. 2004 Jul 15;128A(2):173-5. doi: 10.1002/ajmg.a.30038. Am J Med Genet A. 2004. PMID: 15214011

7

Molecular diagnosis of Wiskott-Aldrich syndrome in Taiwan.

Chien YH, Hwu WL, Ariga T, Chang KW, Yang YH, Lin KH, Chiang BL. Chien YH, et al. Among authors: ariga t. J Microbiol Immunol Infect. 2004 Oct;37(5):276-81. J Microbiol Immunol Infect. 2004. PMID: 15497008

8

Mutational analysis of the TCOF1 gene in 11 Japanese patients with Treacher Collins Syndrome and mechanism of mutagenesis.

Horiuchi K, Ariga T, Fujioka H, Kawashima K, Yamamoto Y, Igawa H, Sugihara T, Sakiyama Y. Horiuchi K, et al. Among authors: ariga t. Am J Med Genet A. 2005 May 1;134(4):363-7. doi: 10.1002/ajmg.a.30357. Am J Med Genet A. 2005. PMID: 15759264

9

[Gene therapy for adenosine deaminase deficiency].

Sakiyama Y, Ariga T, Ohtsu M. Sakiyama Y, et al. Among authors: ariga t. Nihon Rinsho. 2005 Mar;63(3):448-52. Nihon Rinsho. 2005. PMID: 15773344 Review. Japanese.

10

A case of Wiskott-Aldrich syndrome with de novo mutation at exon 4.

Doğu F, Ariga T, Ikincioğullari A, Bozdoğan G, Aytekin C, Metin A, Babacan E. Doğu F, et al. Among authors: ariga t. Turk J Pediatr. 2006 Jan-Mar;48(1):66-8. Turk J Pediatr. 2006. PMID: 16562789

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