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A lower-cost protocol for sickle cell disease neonatal screening in Tunisia

Annals of Saudi medicine, 2012-01, Vol.32 (1), p.49-52

2012

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Mental skills comparison between elite sprint and endurance track and field runners according to their genetic polymorphism: a pilot study

Journal of sports medicine and physical fitness, 2017-09, Vol.57 (9), p.1217

2017

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Prenatal Diagnosis of Hemoglobinopathies: A Case Study on Tunisia

Journal of blood disorders & transfusion, 2015, Vol.6 (3)

Hajer Siala, Faida Ouali

2015

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Is there a difference between power and endurance track and field runners according to their genetic predisposition in motivation and self-esteem?

Medicina dello sport, 2021-03, Vol.74 (1)

2021

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Identification of candidate genes involved in clinical variability among Tunisian patients with β-thalassemia

Gene, 2012-09, Vol.506 (1), p.166-172

2012

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Autism in Phenylketonuria Patients: From Clinical Presentation to Molecular Defects

Journal of child neurology, 2016-06, Vol.31 (7), p.843-849

2016

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Capillarys 2 Flex Piercing: Analytical performance assessment according to CLSI protocols for HbA 1c quantification

Electrophoresis, 2017-09, Vol.38 (17), p.2210-2218

2017

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Determination of glucose-6-phosphate dehydrogenase cut-off values in a Tunisian population

Clinical chemistry and laboratory medicine, 2017-07, Vol.55 (8), p.1193-1201

2017

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Capillarys 2 Flex Piercing: Analytical performance assessment according to CLSI protocols for HbA1c quantification

Electrophoresis, 2017-09, Vol.38 (17), p.2210-2218

2017

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Association of M470V polymorphism of CFTR gene with variability of clinical expression of asthma: Case-report study

Allergologia et immunopathologia, 2019-03, Vol.47 (2), p.159-165

2019

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Genetic advantageous predisposition of angiotensin converting enzyme id polymorphism in Tunisian athletes

The Journal of sports medicine and physical fitness, 2016-06, Vol.56 (6), p.724

2016

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Association between ACE polymorphism, cognitive phenotype and APOE E4 allele in a Tunisian population with Alzheimer disease

Journal of Neural Transmission, 2016-03, Vol.123 (3), p.317-321

2016

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First study of angiotensin converting enzyme in cystic fibrosis Tunisian patients

Clinical chemistry and laboratory medicine, 2014-09, Vol.52 (9), p.e211

2014

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First description of the rs45496295 polymorphism of the C/EBPE gene in β-thalassemia intermedia patients

Hemoglobin, 2016-11, Vol.40 (6), p.411-416

2016

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No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a Tunisian population

Journal of Neural Transmission, 2013-09, Vol.120 (9), p.1355-1358

2013

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Association between angiotensin-converting enzyme gene polymorphism and competitive anxiety in Tunisian athlete

Sport sciences for health, 2016-08, Vol.12 (2), p.233-238

2016

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Association Between Alzheimer Disease and the −491T Allele of Regulatory Region Polymorphism of Apolipoprotein E in a Tunisian Population

Neurochemical research, 2014-02, Vol.39 (2), p.244-247

2014

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Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia

Clinical chemistry and laboratory medicine, 2013-11, Vol.51 (11), p.2115-2124

2013

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Setup of a Protocol of Molecular Diagnosis of [beta]-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC)

Journal of clinical laboratory analysis, 2016-09, Vol.30 (5), p.392

2016

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Angiotensin-converting enzyme insertion/deletion gene polymorphism in cystic fibrosis patients

Journal of genetics, 2016-03, Vol.95 (1), p.193-196

2016

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Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC)

Journal of clinical laboratory analysis, 2016-09, Vol.30 (5), p.392-398

2016

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Identification of a cystic fibrosis mutation W19X in Tunisia

Annales de biologie clinique (Paris), 2013-03, Vol.71 (2), p.223-226

2013

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Fortuitous description of haemoglobin A2' [δ16 (A13) Gly→Arg (GGC→CGC)] in a Tunisian family: study of the molecular defect and its origin

Annales de biologie clinique (Paris), 2015-05, Vol.73 (3), p.353-358

2015

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Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia

Clinical chemistry and laboratory medicine, 2013-08, Vol.51 (8), p.1595-1603

2013

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Detection of a novel splicing mutation causing analbuminemia in a Libyan family

Clinical biochemistry, 2012-10, Vol.45 (15), p.1183-1186

2012

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A lower-cost protocol for sickle cell disease neonatal screening in Tunisia

Mental skills comparison between elite sprint and endurance track and field runners according to their genetic polymorphism: a pilot study

Prenatal Diagnosis of Hemoglobinopathies: A Case Study on Tunisia

Is there a difference between power and endurance track and field runners according to their genetic predisposition in motivation and self-esteem?

Identification of candidate genes involved in clinical variability among Tunisian patients with β-thalassemia

Autism in Phenylketonuria Patients: From Clinical Presentation to Molecular Defects

Capillarys 2 Flex Piercing: Analytical performance assessment according to CLSI protocols for HbA 1c quantification

Determination of glucose-6-phosphate dehydrogenase cut-off values in a Tunisian population

Capillarys 2 Flex Piercing: Analytical performance assessment according to CLSI protocols for HbA1c quantification

Association of M470V polymorphism of CFTR gene with variability of clinical expression of asthma: Case-report study

Genetic advantageous predisposition of angiotensin converting enzyme id polymorphism in Tunisian athletes

Association between ACE polymorphism, cognitive phenotype and APOE E4 allele in a Tunisian population with Alzheimer disease

First study of angiotensin converting enzyme in cystic fibrosis Tunisian patients

First description of the rs45496295 polymorphism of the C/EBPE gene in β-thalassemia intermedia patients

No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a Tunisian population

Association between angiotensin-converting enzyme gene polymorphism and competitive anxiety in Tunisian athlete

Association Between Alzheimer Disease and the −491T Allele of Regulatory Region Polymorphism of Apolipoprotein E in a Tunisian Population

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia

Setup of a Protocol of Molecular Diagnosis of [beta]-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC)

Angiotensin-converting enzyme insertion/deletion gene polymorphism in cystic fibrosis patients

Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC)

Identification of a cystic fibrosis mutation W19X in Tunisia

Fortuitous description of haemoglobin A2' [δ16 (A13) Gly→Arg (GGC→CGC)] in a Tunisian family: study of the molecular defect and its origin

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia

Detection of a novel splicing mutation causing analbuminemia in a Libyan family

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