Benabadji M - Search Results

1

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. Among authors: benabadji m. 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.

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. Among authors: benabadji m. 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. Among authors: benabadji m. Hum Genet. 1994 Nov;94(5):513-7. doi: 10.1007/BF00211017. Hum Genet. 1994. PMID: 7959686

4

A new TaqI allele at DXS52 frequent in Algeria.

Nafa K, Reghis A, Benabadji M, Delpech M, Kaplan JC. Nafa K, et al. Among authors: benabadji m. 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.

5

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. Among authors: benabadji m. Hum Mutat. 1995;5(4):357-9. doi: 10.1002/humu.1380050418. Hum Mutat. 1995. PMID: 7627196 No abstract available.

6

Heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Algeria. Study in Northern Algeria with description of five new variants.

Benabadji M, Merad F, Benmoussa M, Trabuchet G, Junien C, Dreyfus JC, Kaplan JC. Benabadji M, et al. Hum Genet. 1978 Jan 19;40(2):177-84. doi: 10.1007/BF00272298. Hum Genet. 1978. PMID: 624546

7

Quantitative variations of red-cell cytochrome b5 reductase (NADH-methemoglobin-reductase) in the Algerian population: evidence for defective alleles.

Reghis A, Benabadji M, Tchen P, Kaplan JC. Reghis A, et al. Among authors: benabadji m. Hum Genet. 1981;59(2):148-55. doi: 10.1007/BF00293065. Hum Genet. 1981. PMID: 7327574

8

[The enzyme defect in recessive congenital methemoglobinemia with encephalopathy. A new defective variant of NADH-diaphorase (Beni-Messous variant)].

Kaplan JC, Leroux A, Bakouri S, Grangaud JP, Benabadji M. Kaplan JC, et al. Among authors: benabadji m. Nouv Rev Fr Hematol. 1974 Nov-Dec;14(6):755-70. Nouv Rev Fr Hematol. 1974. PMID: 4282504 French. No abstract available.

9

Anthropological approach to the heterogeneity of beta-thalassemia mutations in northern Africa.

Bennani C, Bouhass R, Perrin-Pecontal P, Tamouza R, Malou M, Elion J, Trabuchet G, Beldjord C, Benabadji M, Labie D. Bennani C, et al. Among authors: benabadji m. Hum Biol. 1994 Jun;66(3):369-82. Hum Biol. 1994. PMID: 7913077

10

A new case of 'type II' inherited protein S deficiency.

Chafa O, Fischer AM, Meriane F, Chellali F, Rahal S, Sternberg C, Benabadji M. Chafa O, et al. Among authors: benabadji m. Br J Haematol. 1989 Dec;73(4):501-5. doi: 10.1111/j.1365-2141.1989.tb00288.x. Br J Haematol. 1989. PMID: 2532929

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