Kaplan JC - Search Results

1

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. Among authors: kaplan jc. Hum Genet. 1978 Jan 19;40(2):177-84. doi: 10.1007/BF00272298. Hum Genet. 1978. PMID: 624546

2

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: kaplan jc. Hum Genet. 1994 Nov;94(5):513-7. doi: 10.1007/BF00211017. Hum Genet. 1994. PMID: 7959686

3

[Determination of erythrocyte glucose-6-phosphate dehydrogenase].

Kaplan JC, Dreyfus JC. Kaplan JC, et al. Rev Fr Etud Clin Biol. 1965 May;10(5):552-4. Rev Fr Etud Clin Biol. 1965. PMID: 5832617 French. No abstract available.

4

PK3: a new chromosome enzyme marker for gene dosage studies in chromosome 15 imbalance.

Junien C, Rubinson-Skala H, Dreyfus JC, Ravise N, Boué J, Boué A, Kaplan JC. Junien C, et al. Among authors: kaplan jc. Hum Genet. 1980;54(2):191-6. doi: 10.1007/BF00278970. Hum Genet. 1980. PMID: 6930359

5

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: kaplan jc. Hum Genet. 1981;59(2):148-55. doi: 10.1007/BF00293065. Hum Genet. 1981. PMID: 7327574

6

Advances in hereditary red cell enzyme anomalies.

Kahn A, Kaplan JC, Dreyfus JC. Kahn A, et al. Among authors: kaplan jc. Hum Genet. 1979;50(1):1-27. doi: 10.1007/BF00295584. Hum Genet. 1979. PMID: 157322 Review. No abstract available.

7

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: kaplan jc. Hum Genet. 1990 Apr;84(5):401-5. doi: 10.1007/BF00195808. Hum Genet. 1990. PMID: 1969840

8

[Immunological study of erythrocyte glucose-6-phosphate dehydrogenase in deficient mutants].

Rosa R, Alexandre Y, Kaplan JC, Dreyfus JC. Rosa R, et al. Among authors: kaplan jc. Clin Chim Acta. 1970 Aug;29(2):209-14. doi: 10.1016/0009-8981(70)90038-0. Clin Chim Acta. 1970. PMID: 5493178 French. No abstract available.

9

Glucose-6-phosphate dehydrogenase and hemoglobin variants in Kel Kummer Tuareg and related groups. Indirect evidence for alpha-thalassemia trait.

Junien C, Chaventré A, Fofana Y, Lapouméroulie C, Floury B, Duflo B, Labie D, Kaplan JC. Junien C, et al. Among authors: kaplan jc. Hum Hered. 1982;32(5):318-28. doi: 10.1159/000153318. Hum Hered. 1982. PMID: 7152536

10

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: kaplan jc. 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.

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