Hassar M - Search Results

1

GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.

Abidi O, Boulouiz R, Nahili H, Ridal M, Alami MN, Tlili A, Rouba H, Masmoudi S, Chafik A, Hassar M, Barakat A. Abidi O, et al. Among authors: hassar m. Int J Pediatr Otorhinolaryngol. 2007 Aug;71(8):1239-45. doi: 10.1016/j.ijporl.2007.04.019. Epub 2007 Jun 5. Int J Pediatr Otorhinolaryngol. 2007. PMID: 17553572

2

Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness.

Nahili H, Ridal M, Boulouiz R, Abidi O, Imken L, Rouba H, Alami MN, Chafik A, Hassar M, Barakat A. Nahili H, et al. Among authors: hassar m. Int J Pediatr Otorhinolaryngol. 2008 Nov;72(11):1633-6. doi: 10.1016/j.ijporl.2008.07.015. Epub 2008 Sep 21. Int J Pediatr Otorhinolaryngol. 2008. PMID: 18809214

3

Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population.

Abidi O, Boulouiz R, Nahili H, Bakhouch K, Wakrim L, Rouba H, Chafik A, Hassar M, Barakat A. Abidi O, et al. Among authors: hassar m. Genet Test. 2008 Dec;12(4):569-74. doi: 10.1089/gte.2008.0063. Genet Test. 2008. PMID: 19072567

4

AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men.

Imken L, El Houate B, Chafik A, Nahili H, Boulouiz R, Abidi O, Chadli E, Louanjli N, Elfath A, Hassar M, McElreavey K, Barakat A, Rouba H. Imken L, et al. Among authors: hassar m. Asian J Androl. 2007 Sep;9(5):674-8. doi: 10.1111/j.1745-7262.2007.00290.x. Asian J Androl. 2007. PMID: 17712485 Free article.

5

Genetic polymorphism in the manganese superoxide dismutase gene is associated with an increased risk for hepatocellular carcinoma in HCV-infected Moroccan patients.

Ezzikouri S, El Feydi AE, Chafik A, Afifi R, El Kihal L, Benazzouz M, Hassar M, Pineau P, Benjelloun S. Ezzikouri S, et al. Among authors: hassar m. Mutat Res. 2008 Jan 8;649(1-2):1-6. doi: 10.1016/j.mrgentox.2007.05.019. Epub 2007 Oct 11. Mutat Res. 2008. PMID: 18023606

6

Prevalence of common HFE and SERPINA1 mutations in patients with hepatocellular carcinoma in a Moroccan population.

Ezzikouri S, El Feydi AE, El Kihal L, Afifi R, Benazzouz M, Hassar M, Chafik A, Pineau P, Benjelloun S. Ezzikouri S, et al. Among authors: hassar m. Arch Med Res. 2008 Feb;39(2):236-41. doi: 10.1016/j.arcmed.2007.09.006. Arch Med Res. 2008. PMID: 18164971

7

Genotype determination in Moroccan hepatitis B chronic carriers.

Ezzikouri S, Chemin I, Chafik A, Wakrim L, Nourlil J, Malki AE, Marchio A, Dejean A, Hassar M, Trepo C, Pineau P, Benjelloun S. Ezzikouri S, et al. Among authors: hassar m. Infect Genet Evol. 2008 May;8(3):306-12. doi: 10.1016/j.meegid.2008.01.010. Epub 2008 Feb 3. Infect Genet Evol. 2008. PMID: 18372221

8

The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population.

Naamane H, El Maataoui O, Ailal F, Barakat A, Bennani S, Najib J, Hassar M, Saile R, Bousfiha AA. Naamane H, et al. Among authors: hassar m. Eur J Pediatr. 2010 Sep;169(9):1069-74. doi: 10.1007/s00431-010-1179-6. Epub 2010 Apr 23. Eur J Pediatr. 2010. PMID: 20414676

9

The Pro variant of the p53 codon 72 polymorphism is associated with hepatocellular carcinoma in Moroccan population.

Ezzikouri S, El Feydi AE, Chafik A, Benazzouz M, El Kihal L, Afifi R, Hassar M, Pineau P, Benjelloun S. Ezzikouri S, et al. Among authors: hassar m. Hepatol Res. 2007 Sep;37(9):748-54. doi: 10.1111/j.1872-034X.2007.00126.x. Epub 2007 Jun 15. Hepatol Res. 2007. PMID: 17573955

10

PCR detection of Leishmania in skin biopsies.

Lemrani M, Hamdi S, Laamrani A, Hassar M. Lemrani M, et al. Among authors: hassar m. J Infect Dev Ctries. 2009 Sep 15;3(2):115-22. doi: 10.3855/jidc.511. J Infect Dev Ctries. 2009. PMID: 19755741 Free article.

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