Detalhe da pesquisa
1.
Association of the OPRM1 and COMT genes' polymorphisms with the efficacy of morphine in Tunisian cancer patients: Impact of the high genetic heterogeneity in Tunisia?
Therapie
; 71(5): 507-513, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27288213
2.
Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan Africa.
Ann Neurol
; 75(4): 525-32, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24515897
3.
Macrozoospermia: screening for the homozygous c.144delC mutation in AURKC gene in infertile men and estimation of its heterozygosity frequency in the Tunisian population.
J Assist Reprod Genet
; 32(11): 1651-8, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26341096
4.
Multiplex Minisequencing of the HBB Gene: A Rapid Strategy to Confirm the Most Frequent ß-Thalassemia Mutations in the Tunisian Population.
Hemoglobin
; 39(4): 251-5, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26016902
5.
A Systematic Review of Chronic Diseases and Their Prevalence Among the Population of Northern Borders Province (NBP) in Saudi Arabia.
J Multidiscip Healthc
; 16: 1047-1056, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37089278
6.
Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III.
J Hum Genet
; 57(3): 170-5, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22089644
7.
Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11ß hydroxylase deficiency in a Tunisian family.
Gen Comp Endocrinol
; 175(3): 514-8, 2012 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22210247
8.
Familial early-onset diabetes is not a typical MODY in several Tunisian patients.
Tunis Med
; 90(12): 882-7, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23247789
9.
10.
Frequency of HNF4A-P.I463V Variant in the Tunisian North-African Population and Its Relation with Diabetes Mellitus.
Iran J Public Health
; 44(3): 396-403, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25905084
11.
Genetic study in a tunisian family revealed IVS1+1G>A mutation in the CHM gene.
Ann Biol Clin (Paris)
; 73(4): 469-73, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26411914
12.
Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients.
Eur J Paediatr Neurol
; 16(2): 167-74, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21821450
13.
Multiple self-healing palmoplantar carcinoma: a familial predisposition to skin cancer with primary palmoplantar and conjunctival lesions.
J Invest Dermatol
; 135(1): 304-308, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25050600
14.
Challenges for molecular diagnosis of familial early-onset diabetes in unexplored populations.
Iran J Public Health
; 43(7): 1011-3, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25909071