Nafa K - Search Results

1

Factor V Leiden mutation investigated by amplification created restriction enzyme site (ACRES) in PNH patients with and without thrombosis.

Nafa K, Bessler M, Mason P, Vulliamy T, Hillmen P, Castro-Malaspina H, Luzzatto L. Nafa K, et al. Haematologica. 1996 Nov-Dec;81(6):540-2. Haematologica. 1996. PMID: 9009443

2

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.

3

At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria.

Nafa K, Reghis A, Osmani N, Baghli L, Aït-Abbes H, Benabadji M, Kaplan JC, Vulliamy T, Luzzatto L. Nafa K, et al. Hum Genet. 1994 Nov;94(5):513-7. doi: 10.1007/BF00211017. Hum Genet. 1994. PMID: 7959686

4

G6PD Aures: a new mutation (48 Ile-->Thr) causing mild G6PD deficiency is associated with favism.

Nafa K, Reghis A, Osmani N, Baghli L, Benabadji M, Kaplan JC, Vulliamy TJ, Luzzatto L. Nafa K, et al. Hum Mol Genet. 1993 Jan;2(1):81-2. doi: 10.1093/hmg/2.1.81. Hum Mol Genet. 1993. PMID: 8490627 No abstract available.

5

Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift type.

Nafa K, Mason PJ, Hillmen P, Luzzatto L, Bessler M. Nafa K, et al. Blood. 1995 Dec 15;86(12):4650-5. Blood. 1995. PMID: 8541557 Free article.

6

New somatic mutation in the PIG-A gene emerges at relapse of paroxysmal nocturnal hemoglobinuria.

Nafa K, Bessler M, Deeg HJ, Luzzatto L. Nafa K, et al. Blood. 1998 Nov 1;92(9):3422-7. Blood. 1998. PMID: 9787183 Free article.

7

The spectrum of somatic mutations in the PIG-A gene in paroxysmal nocturnal hemoglobinuria includes large deletions and small duplications.

Nafa K, Bessler M, Castro-Malaspina H, Jhanwar S, Luzzatto L. Nafa K, et al. Blood Cells Mol Dis. 1998 Sep;24(3):370-84. doi: 10.1006/bcmd.1998.0203. Blood Cells Mol Dis. 1998. PMID: 10087994

8

Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals.

Araten DJ, Nafa K, Pakdeesuwan K, Luzzatto L. Araten DJ, et al. Among authors: nafa k. Proc Natl Acad Sci U S A. 1999 Apr 27;96(9):5209-14. doi: 10.1073/pnas.96.9.5209. Proc Natl Acad Sci U S A. 1999. PMID: 10220445 Free PMC article.

9

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

10

Mendelian diseases among Roman Jews: implications for the origins of disease alleles.

Oddoux C, Guillen-Navarro E, Ditivoli C, Dicave E, Cilio MR, Clayton CM, Nelson H, Sarafoglou K, McCain N, Peretz H, Seligsohn U, Luzzatto L, Nafa K, Nardi M, Karpatkin M, Aksentijevich I, Kastner D, Axelrod F, Ostrer H. Oddoux C, et al. Among authors: nafa k. J Clin Endocrinol Metab. 1999 Dec;84(12):4405-9. doi: 10.1210/jcem.84.12.6268. J Clin Endocrinol Metab. 1999. PMID: 10599695 Review.

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