Mrad A - Search Results

1

Elliptocytogenic alpha I/36 spectrin Sfax lacks nine amino acids in helix 3 of repeat 4. Evidence for the activation of a cryptic 5'-splice site in exon 8 of spectrin alpha-gene.

Baklouti F, Maréchal J, Wilmotte R, Alloisio N, Morlé L, Ducluzeau MT, Denoroy L, Mrad A, Ben Aribia MH, Kastally R, et al. Baklouti F, et al. Among authors: mrad a. Blood. 1992 May 1;79(9):2464-70. Blood. 1992. PMID: 1571558 Free article.

2

Compound heterozygosity of novel missense mutations in the gamma-glutamyl-carboxylase gene causes hereditary combined vitamin K-dependent coagulation factor deficiency.

Darghouth D, Hallgren KW, Shtofman RL, Mrad A, Gharbi Y, Maherzi A, Kastally R, LeRicousse S, Berkner KL, Rosa JP. Darghouth D, et al. Among authors: mrad a. Blood. 2006 Sep 15;108(6):1925-31. doi: 10.1182/blood-2005-12-010660. Epub 2006 May 23. Blood. 2006. PMID: 16720838 Free PMC article.

3

First observation of Hb Montgomery [alpha 48(CD6)Leu----Arg] in Tunisia.

Mrad A, Arous N, Kastally R, Blibech R, Rosa J, Galacteros F. Mrad A, et al. Hemoglobin. 1988;12(1):67-70. doi: 10.3109/03630268808996884. Hemoglobin. 1988. PMID: 3384700 No abstract available.

4

[Association of heterozygote drepanocytosis and G6PD deficiency: apropos of a case].

Znaidi R, Hafsia R, M'Rad A, Kastally R, Hafsia A. Znaidi R, et al. Tunis Med. 1995 Oct;73(10):415-7. Tunis Med. 1995. PMID: 9506167 French. No abstract available.

5

[Prevalence of hemoglobinopathies in Nefza: study of 1303 patients].

Znaidi R, Hafsia R, M'Rad A, Belhadj A, Kastally R, Hafsia A. Znaidi R, et al. Tunis Med. 1992 Aug-Sep;70(8-9):400-4. Tunis Med. 1992. PMID: 1485391 French. No abstract available.

6

Hemoglobin Athens-Georgia [alpha 2 beta 2 40(C6)Arg----Lys] in association with beta 0-thalassemia in Tunisia.

Mrad A, Kister J, Feo C, Poyart C, Kastally R, Blibech R, Galacteros F, Wajcman H. Mrad A, et al. Am J Hematol. 1989 Oct;32(2):117-22. doi: 10.1002/ajh.2830320208. Am J Hematol. 1989. PMID: 2757008

7

Hb Tunis [alpha 2 beta 2 124 (H2)Pro----Ser], a new beta chain variant identified by HPLC.

Mrad A, Blouquit Y, Lacombe C, Blibech R, Arous N, Bardakdjian J, Kastally R, Rosa J, Galacteros F. Mrad A, et al. Hemoglobin. 1988;12(1):23-30. doi: 10.3109/03630268808996879. Hemoglobin. 1988. PMID: 3384695

8

[Hemoglobinopathies in Nefza: a model of health intervention].

Znaidi R, Hafsia R, Megid M, M'Rad A, Kastally R, Hafsia A. Znaidi R, et al. Tunis Med. 1996 Jan;74(1):33-8. Tunis Med. 1996. PMID: 9507311 French. No abstract available.

9

[Abnormal hemoglobins screened in Tunisia].

Blibech A, Mrad A, Belhas A, M'Henni A, Kastally R, Galacteros F, Riou J, Rosa J. Blibech A, et al. Among authors: mrad a. Nouv Rev Fr Hematol (1978). 1986;28(4):223-5. Nouv Rev Fr Hematol (1978). 1986. PMID: 3774530 French.

10

Incidence of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Tunisian populations.

Blibech R, Gharbi Y, Mrad A, Zahra H, Mahjoub T, Belhaj A, Laatiri Z, Kastally R, Rosa R. Blibech R, et al. Among authors: mrad a. Nouv Rev Fr Hematol (1978). 1989;31(3):189-91. Nouv Rev Fr Hematol (1978). 1989. PMID: 2616266

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