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2002 4
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Page 1
Eponym: Barth syndrome.
Takeda A, Sudo A, Yamada M, Yamazawa H, Izumi G, Nishino I, Ariga T. Takeda A, et al. Among authors: ariga t. Eur J Pediatr. 2011 Nov;170(11):1365-7. doi: 10.1007/s00431-011-1575-6. Epub 2011 Sep 23. Eur J Pediatr. 2011. PMID: 21947198 Review.
Hematologically important mutations: X-linked chronic granulomatous disease (third update).
Roos D, Kuhns DB, Maddalena A, Roesler J, Lopez JA, Ariga T, Avcin T, de Boer M, Bustamante J, Condino-Neto A, Di Matteo G, He J, Hill HR, Holland SM, Kannengiesser C, Köker MY, Kondratenko I, van Leeuwen K, Malech HL, Marodi L, Nunoi H, Stasia MJ, Ventura AM, Witwer CT, Wolach B, Gallin JI. Roos D, et al. Among authors: ariga t. Blood Cells Mol Dis. 2010 Oct 15;45(3):246-65. doi: 10.1016/j.bcmd.2010.07.012. Epub 2010 Aug 21. Blood Cells Mol Dis. 2010. PMID: 20729109 Free PMC article. Review.
Clinical characteristics and genotype-phenotype correlations in C3 deficiency.
Okura Y, Kobayashi I, Yamada M, Sasaki S, Yamada Y, Kamioka I, Kanai R, Takahashi Y, Ariga T. Okura Y, et al. Among authors: ariga t. J Allergy Clin Immunol. 2016 Feb;137(2):640-644.e1. doi: 10.1016/j.jaci.2015.08.017. Epub 2015 Oct 4. J Allergy Clin Immunol. 2016. PMID: 26435005 No abstract available.
137 results