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Journal Abstract Search

403 related items for PubMed ID: 18227012

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  • 23. Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR.
    Proust A, Guillet B, Picard C, de Saint Basile G, Pondarré C, Tamary H, Dreyfus M, Tchernia G, Fischer A, Delaunay J.
    Blood Cells Mol Dis; 2007; 39(1):102-6. PubMed ID: 17400488
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  • 26. Wiskott-Aldrich syndrome.
    Notarangelo LD, Miao CH, Ochs HD.
    Curr Opin Hematol; 2008 Jan; 15(1):30-6. PubMed ID: 18043243
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  • 28. [Platelet function after allogeneic bone marrow transplantation in Wiskott-Aldrich syndrome].
    Megido M, Cesar JM, Maldonado MS, Otheo E, Muñoz A, Navarro JL.
    Sangre (Barc); 1993 Jun; 38(3):233-4. PubMed ID: 8211550
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  • 29. [Wiskott-Aldrich syndrome (literature review)].
    Shabalov NP.
    Vopr Okhr Materin Det; 1975 Feb; 20(2):50-4. PubMed ID: 1094723
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  • 30. Allogeneic peripheral blood stem cell transplantation in a Wiskott-Aldrich syndrome patient.
    Hongeng S, Pakakasama S, Hathirat P, Chaisiripoomkere W, Ungkanont A.
    Bone Marrow Transplant; 1999 Aug; 24(4):445-6. PubMed ID: 10467341
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  • 31. Wiskott-Aldrich Syndrome: Description of a New Gene Mutation With Normal Platelet Volume.
    Yoonessi L, Randhawa I, Nussbaum E, Saharti S, Do P, Chin T, Zwerdling T.
    J Pediatr Hematol Oncol; 2015 Oct; 37(7):515-8. PubMed ID: 26241726
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  • 32. 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.
    J Pediatr Hematol Oncol; 2004 Jul; 26(7):435-40. PubMed ID: 15218418
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  • 33. 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.
    Turk J Pediatr; 2006 Jul; 48(1):66-8. PubMed ID: 16562789
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  • 34. Platelet survival studies in Aldrich syndrome.
    Krivit W, Yunis E, White JG.
    Pediatrics; 1966 Feb; 37(2):339-41. PubMed ID: 5948131
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  • 35. Intermittent low platelet counts hampering diagnosis of X-linked thrombocytopenia in children: report of two unrelated cases and a novel mutation in the gene coding for the Wiskott-Aldrich syndrome protein.
    Medina SS, Siqueira LH, Colella MP, Yamaguti-Hayakawa GG, Duarte BKL, Dos Santos Vilela MM, Ozelo MC.
    BMC Pediatr; 2017 Jun 22; 17(1):151. PubMed ID: 28641574
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  • 36. Wiskott-Aldrich syndrome: molecular pieces slide into place.
    Kuska B.
    J Natl Cancer Inst; 2000 Jan 05; 92(1):9-11. PubMed ID: 10620622
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