Nafa K - Search Results

1

A new TaqI allele at DXS52 frequent in Algeria.

Nafa K, Reghis A, Benabadji M, Delpech M, Kaplan JC. Nafa K, et al. Nucleic Acids Res. 1989 Feb 11;17(3):1276. doi: 10.1093/nar/17.3.1276. Nucleic Acids Res. 1989. PMID: 2564185 Free PMC article. No abstract available.

2

Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in Algeria.

Nafa K, Meriane F, Reghis A, Benabadji M, Demenais F, Guilloud-Bataille M, Sultan Y, Kaplan JC, Delpech M. Nafa K, et al. Hum Genet. 1990 Apr;84(5):401-5. doi: 10.1007/BF00195808. Hum Genet. 1990. PMID: 1969840

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

Screening for mutations in factor VIII gene using the single-strand conformation polymorphism.

Nafa K, Meriane F, Chellali T, Benabadji M, Reghis A, Viemont M, Kaplan JC, Delpech M. Nafa K, et al. Hum Mutat. 1995;5(4):357-9. doi: 10.1002/humu.1380050418. Hum Mutat. 1995. PMID: 7627196 No abstract available.

5

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.

6

A novel mutation (Arg-->Leu in exon 18) in factor VIII gene responsible for moderate hemophilia A.

Nafa K, Baudis M, Deburgrave N, Bardin JM, Sultan Y, Kaplan JC, Delpech M. Nafa K, et al. Hum Mutat. 1992;1(1):77-8. doi: 10.1002/humu.1380010114. Hum Mutat. 1992. PMID: 1301194 No abstract available.

7

Prevalence, male germ-line origin and new patterns of inversions in haemophilia A.

Valleix S, Nafa K, Stieltjes N, Viemont M, Sultan Y, Kaplan JC, Delpech M. Valleix S, et al. Among authors: nafa k. Ann Genet. 1997;40(1):35-40. Ann Genet. 1997. PMID: 9150848

8

Factor VIII gene inversions in severe hemophilia A: results of an international consortium study.

Antonarakis SE, Rossiter JP, Young M, Horst J, de Moerloose P, Sommer SS, Ketterling RP, Kazazian HH Jr, Négrier C, Vinciguerra C, Gitschier J, Goossens M, Girodon E, Ghanem N, Plassa F, Lavergne JM, Vidaud M, Costa JM, Laurian Y, Lin SW, Lin SR, Shen MC, Lillicrap D, Taylor SA, Windsor S, Valleix SV, Nafa K, Sultan Y, Delpech M, Vnencak-Jones CL, Phillips JA 3rd, Ljung RC, Koumbarelis E, Gialeraki A, Mandalaki T, Jenkins PV, Collins PW, Pasi KJ, Goodeve A, Peake I, Preston FE, Schwartz M, Scheibel E, Ingerslev J, Cooper DN, Millar DS, Kakkar VV, Giannelli F, Naylor JA, Tizzano EF, Baiget M, Domenech M, Altisent C, Tusell J, Beneyto M, Lorenzo JI, Gaucher C, Mazurier C, Peerlinck K, Matthijs G, Cassiman JJ, Vermylen J, Mori PG, Acquila M, Caprino D, Inaba H. Antonarakis SE, et al. Among authors: nafa k. Blood. 1995 Sep 15;86(6):2206-12. Blood. 1995. PMID: 7662970 Free article.

9

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.

10

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

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