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Page 1
Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuria.
Araten DJ, Swirsky D, Karadimitris A, Notaro R, Nafa K, Bessler M, Thaler HT, Castro-Malaspina H, Childs BH, Boulad F, Weiss M, Anagnostopoulos N, Kutlar A, Savage DG, Maziarz RT, Jhanwar S, Luzzatto L. Araten DJ, et al. Among authors: nafa k. Br J Haematol. 2001 Nov;115(2):360-8. doi: 10.1046/j.1365-2141.2001.03113.x. Br J Haematol. 2001. PMID: 11703336 Free article. Review.
CpG methylation analysis--current status of clinical assays and potential applications in molecular diagnostics: a report of the Association for Molecular Pathology.
Sepulveda AR, Jones D, Ogino S, Samowitz W, Gulley ML, Edwards R, Levenson V, Pratt VM, Yang B, Nafa K, Yan L, Vitazka P. Sepulveda AR, et al. Among authors: nafa k. J Mol Diagn. 2009 Jul;11(4):266-78. doi: 10.2353/jmoldx.2009.080125. Epub 2009 Jun 18. J Mol Diagn. 2009. PMID: 19541921 Free PMC article.
TbetaR-I(6A) is a candidate tumor susceptibility allele.
Pasche B, Kolachana P, Nafa K, Satagopan J, Chen YG, Lo RS, Brener D, Yang D, Kirstein L, Oddoux C, Ostrer H, Vineis P, Varesco L, Jhanwar S, Luzzatto L, Massagué J, Offit K. Pasche B, et al. Among authors: nafa k. Cancer Res. 1999 Nov 15;59(22):5678-82. Cancer Res. 1999. PMID: 10582683
Association of clonal T-cell large granular lymphocyte disease and paroxysmal nocturnal haemoglobinuria (PNH): further evidence for a pathogenetic link between T cells, aplastic anaemia and PNH.
Karadimitris A, Li K, Notaro R, Araten DJ, Nafa K, Thertulien R, Ladanyi M, Stevens AE, Rosenfeld CS, Roberts IA, Luzzatto L. Karadimitris A, et al. Among authors: nafa k. Br J Haematol. 2001 Dec;115(4):1010-4. doi: 10.1046/j.1365-2141.2001.03172.x. Br J Haematol. 2001. PMID: 11843843 Free article.
115 results