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A Ben Ammar

Showing results (31-40 of 41) with videos related to

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Archives of Virology|May 17, 2008
Profile of drug resistance mutations among HIV-1-infected Tunisian subjects failing antiretroviral therapyA Jlizi, A Ben Ammar El Gaaied, A Slim, et al.
Journal of Human Genetics|October 9, 2007
Contribution of the BRCA1 and BRCA2 mutations to breast cancer in TunisiaWafa Troudi, N Uhrhammer, C Sibille, et al.
International Journal of Immunogenetics|April 14, 2006
HLA class II genetic diversity in southern Tunisia and the Mediterranean areaB Abdennaji Guenounou, B Yacoubi Loueslati, S Buhler, et al.
Pathologie-Biologie|February 4, 2014
Failure to find evidence for deletion of LCE3C and LCE3B genes at PSORS4 contributing to psoriasis susceptibility in Tunisian familiesM Ammar, C Bouchlaka-Souissi, K Soumaya, et al.
La Tunisie Medicale|February 24, 2001
Gastric MALT lymphoma. A clinico-pathological study of 65 cases. Relationship to Helicobacter pyloriA Ben Rejeb, N Kchir, M R Bouali, et al.
Cancer Biomarkers : Section a of Disease Markers|March 13, 2008
Complete mutation screening and haplotype characterization of BRCA1 gene in Tunisian patients with familial breast cancerW Troudi, N Uhrhammer, K Ben Romdhane, et al.
The British Journal of Dermatology|September 28, 2012
Genome-wide linkage scan for psoriasis susceptibility loci in multiplex Tunisian familiesM Ammar, C Bouchlaka-Souissi, C A Helms, et al.
L'Encephale|January 22, 2020
Association of high-sensitivity C-reactive protein with susceptibility to Schizophrenia in Tunisian populationF Ayari, A Ben Chaaben, H Ben Ammar, et al.
Neurology|December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North AfricaP Richard, K Gaudon, H Haddad, et al.
Journal of Neurology|December 17, 2009
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7A Ben Ammar, F Petit, N Alexandri, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Archives of Virology|May 17, 2008
Profile of drug resistance mutations among HIV-1-infected Tunisian subjects failing antiretroviral therapyA Jlizi, A Ben Ammar El Gaaied, A Slim, et al.
Journal of Human Genetics|October 9, 2007
Contribution of the BRCA1 and BRCA2 mutations to breast cancer in TunisiaWafa Troudi, N Uhrhammer, C Sibille, et al.
International Journal of Immunogenetics|April 14, 2006
HLA class II genetic diversity in southern Tunisia and the Mediterranean areaB Abdennaji Guenounou, B Yacoubi Loueslati, S Buhler, et al.
Pathologie-Biologie|February 4, 2014
Failure to find evidence for deletion of LCE3C and LCE3B genes at PSORS4 contributing to psoriasis susceptibility in Tunisian familiesM Ammar, C Bouchlaka-Souissi, K Soumaya, et al.
La Tunisie Medicale|February 24, 2001
Gastric MALT lymphoma. A clinico-pathological study of 65 cases. Relationship to Helicobacter pyloriA Ben Rejeb, N Kchir, M R Bouali, et al.
Cancer Biomarkers : Section a of Disease Markers|March 13, 2008
Complete mutation screening and haplotype characterization of BRCA1 gene in Tunisian patients with familial breast cancerW Troudi, N Uhrhammer, K Ben Romdhane, et al.
The British Journal of Dermatology|September 28, 2012
Genome-wide linkage scan for psoriasis susceptibility loci in multiplex Tunisian familiesM Ammar, C Bouchlaka-Souissi, C A Helms, et al.
L'Encephale|January 22, 2020
Association of high-sensitivity C-reactive protein with susceptibility to Schizophrenia in Tunisian populationF Ayari, A Ben Chaaben, H Ben Ammar, et al.
Neurology|December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North AfricaP Richard, K Gaudon, H Haddad, et al.
Journal of Neurology|December 17, 2009
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7A Ben Ammar, F Petit, N Alexandri, et al.
Pageof 5