Bejaoui M - Search Results

1

High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis.

Amouri A, Talmoudi F, Messaoud O, d'Enghien CD, Rekaya MB, Allegui I, Azaiez H, Kefi R, Abdelhak A, Meseddi SH, Torjemane L, Ouederni M, Mellouli F, Abid HB, Aissaoui L, Bejaoui M, Othmen TB, Lyonnet DS, Soulier J, Hachicha M, Dellagi K, Abdelhak S, Fanconi T. Amouri A, et al. Among authors: bejaoui m. Mol Genet Genomic Med. 2014 Mar;2(2):160-5. doi: 10.1002/mgg3.55. Epub 2014 Feb 5. Mol Genet Genomic Med. 2014. PMID: 24689079 Free PMC article.

2

[Leukocyte adhesion molecules].

Bejaoui M, Dellagi K. Bejaoui M, et al. Arch Inst Pasteur Tunis. 1992 Jan-Apr;69(1-2):5-12. Arch Inst Pasteur Tunis. 1992. PMID: 1489246 Review. French. No abstract available.

3

[NADPH oxidase complex of phagocytic cells and molecular basis of genetic deficiency in their bactericidal activity].

Bejaoui M, Dellagi K. Bejaoui M, et al. Arch Inst Pasteur Tunis. 1991 Jul-Oct;68(3-4):237-42. Arch Inst Pasteur Tunis. 1991. PMID: 1824504 Review. French. No abstract available.

4

A unique mutation underlying carbonic anhydrase II deficiency syndrome in patients of Arab descent.

Fathallah DM, Bejaoui M, Sly WS, Lakhoua R, Dellagi K. Fathallah DM, et al. Among authors: bejaoui m. Hum Genet. 1994 Nov;94(5):581-2. doi: 10.1007/BF00211035. Hum Genet. 1994. PMID: 7959703

5

Carbonic anhydrase II (CA II) deficiency in Maghrebian patients: evidence for founder effect and genomic recombination at the CA II locus.

Fathallah DM, Bejaoui M, Lepaslier D, Chater K, Sly WS, Dellagi K. Fathallah DM, et al. Among authors: bejaoui m. Hum Genet. 1997 May;99(5):634-7. doi: 10.1007/s004390050419. Hum Genet. 1997. PMID: 9150731

6

[Agammaglobulinemia with the absence of circulating B-lymphocytes. 9 cases].

Bejaoui M, Barbouche MR, Mellouli F, Tirellil N, Dellagi K. Bejaoui M, et al. Presse Med. 1998 Mar 28;27(12):562-6. Presse Med. 1998. PMID: 9767948 French.

7

[Primary immunologic deficiency by deficiency of HLA class II antigens: nine new Tunisian cases].

Bejaoui M, Barbouche MR, Mellouli F, Largueche B, Dellagi K. Bejaoui M, et al. Arch Pediatr. 1998 Oct;5(10):1089-93. doi: 10.1016/s0929-693x(99)80005-0. Arch Pediatr. 1998. PMID: 9809151 French.

8

[Chronic septic granulomatous disease. 14 cases].

Barbouche MR, Sghiri R, Mellouli F, Boukhdir Y, Dellagi K, Béjaoui M. Barbouche MR, et al. Among authors: bejaoui m. Presse Med. 1999 Nov 27;28(37):2034-6. Presse Med. 1999. PMID: 10605470 French.

9

Clinical and genetic heterogeneity of inherited autosomal recessive susceptibility to disseminated Mycobacterium bovis bacille calmette-guérin infection.

Elloumi-Zghal H, Barbouche MR, Chemli J, Béjaoui M, Harbi A, Snoussi N, Abdelhak S, Dellagi K. Elloumi-Zghal H, et al. Among authors: bejaoui m. J Infect Dis. 2002 May 15;185(10):1468-75. doi: 10.1086/340510. Epub 2002 Apr 30. J Infect Dis. 2002. PMID: 11992283

10

Community-acquired poliovirus infection in children with primary immunodeficiencies in Tunisia.

Triki H, Barbouche MR, Bahri O, Bejaoui M, Dellagi K. Triki H, et al. Among authors: bejaoui m. J Clin Microbiol. 2003 Mar;41(3):1203-11. doi: 10.1128/JCM.41.3.1203-1211.2003. J Clin Microbiol. 2003. PMID: 12624052 Free PMC article.

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