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Prenatal diagnosis of hemoglobinopathies in Tunisia: an 18 years of experience

International journal of laboratory hematology, 2016-06, Vol.38 (3), p.223-232

2016

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Glucose-6-phosphate dehydrogenase deficiency in Tunisia: molecular data and phenotype-genotype association

Molecular biology reports, 2013-02, Vol.40 (2), p.851-856

2013

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Prenatal diagnosis of cystic fibrosis: 10-years experience

Pathologie biologie (Paris), 2015-06, Vol.63 (3), p.126-129

2015

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Contribution of M470V variant to cystic fibrosis: First study in CF and normal Tunisian population

Pathologie biologie (Paris), 2015-09, Vol.63 (4-5), p.169-174

2015

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Association of TGFB1 −509C/T polymorphism gene with clinical variability in cystic fibrosis patients: A case-control study

Pathologie biologie (Paris), 2015-09, Vol.63 (4-5), p.175-178

2015

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Analysis of IVS8 CFTR gene polymorphism in asthmatic children in a Tunisian population

Revue française d'allergologie (2009), 2019-09, Vol.59 (5), p.363-368

2019

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Cystic fibrosis transmembrane conductance regulator mutations and polymorphisms associated with congenital bilateral absence of vas deferens in a restricted group of patients from North Africa

Annals of human biology, 2012-01, Vol.39 (1), p.76-79

2012

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Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients

Molecular biology reports, 2013-11, Vol.40 (11), p.6205-6212

2013

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Association study of apolipoprotein E promoter polymorphism (−427 T/C) and Alzheimer's disease in a Tunisian population

Revue neurologique, 2016-02, Vol.172 (2), p.127-131

2016

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Preliminary study of haplotypes linked to the rare cystic fibrosis E1104X mutation

Acta physiologica Hungarica, 2015-03, Vol.102 (1), p.86-93

2015

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Neonatal screening for hemoglobinopathies in tunisia over a period of 18 years (2005- 2023)

Clinica chimica acta, 2024-05, Vol.558, p.118255, Article 118255

2024

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Implication of polymorphic marker IVS6A GATT in the clinical expression of cystic fibrosis

Clinica chimica acta, 2019-06, Vol.493, p.S573-S573

2019

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A Tunisian neonatal case of co-inheritance of G6PD deficiency and HBC presenting as severe jaundice and hemolytic anemia

Clinica chimica acta, 2019-06, Vol.493, p.S238-S239

2019

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Identification of a mild cystic fibrosis mutation 2789+5 G to a for the first time in Tunisian population

Clinica chimica acta, 2019-06, Vol.493, p.S208-S208

2019

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First study of polymorphic marker MP6D9 in cystic fibrosis Tunisian patients

Clinical biochemistry, 2014-06, Vol.47 (9), p.778-779

2014

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Molecular Characterization of Mycobacterium tuberculosis Strains Resistant to Isoniazid

International journal of mycobacteriology, 2016-12, Vol.5 (5), p.S151-S151

2016

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Novel frameshift mutation in Tunisian cystic fibrosis patient

Clinical biochemistry, 2011-05, Vol.44 (7), p.537-537

2011

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Association between clinical expression and molecular heterogeneity in [beta]-thalassemia Tunisian patients

Molecular biology reports, 2013-11, Vol.40 (11), p.6205

2013

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Up‐to‐date incidence and initial characteristics of cystic fibrosis in Tunisia

Pediatric pulmonology, 2022-10, Vol.57 (10), p.2540-2541

2022

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A gain-of-function mutation in zinc cluster transcription factor Rob1 drives Candida albicans adaptive growth in the cystic fibrosis lung environment

PLoS pathogens, 2024-04, Vol.20 (4), p.e1012154-e1012154

2024

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Efficient and lightweight in-memory computing architecture for hardware security

Journal of parallel and distributed computing, 2024-08, Vol.190, p.104898, Article 104898

2024

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Association between H2 haplotype of microtubule associated protein tau gene (deletion / insertion) with Alzheimer Disease in Tunisian patients

Neurological research (New York), 2022-09, Vol.44 (9), p.814-818

2022

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Catalyzing precision: unraveling the diagnostic conundrum of tunisian familial hypophosphatasia case through integrative clinical and molecular approaches

Molecular genetics and genomics : MGG, 2024-12, Vol.299 (1), p.64, Article 64

2024

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Distribution of rotavirus VP7 and VP4 genotypes circulating in Tunisia from 2009 to 2014: Emergence of the genotype G12

Journal of medical microbiology, 2016-09, Vol.65 (9), p.1028-1037

2016

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FPGA-accelerated anisotropic diffusion filter based on SW/HW-codesign for medical images

Journal of real-time image processing, 2021-12, Vol.18 (6), p.2429-2440

2021

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Prenatal diagnosis of hemoglobinopathies in Tunisia: an 18 years of experience

Glucose-6-phosphate dehydrogenase deficiency in Tunisia: molecular data and phenotype-genotype association

Prenatal diagnosis of cystic fibrosis: 10-years experience

Contribution of M470V variant to cystic fibrosis: First study in CF and normal Tunisian population

Association of TGFB1 −509C/T polymorphism gene with clinical variability in cystic fibrosis patients: A case-control study

Analysis of IVS8 CFTR gene polymorphism in asthmatic children in a Tunisian population

Cystic fibrosis transmembrane conductance regulator mutations and polymorphisms associated with congenital bilateral absence of vas deferens in a restricted group of patients from North Africa

Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients

Association study of apolipoprotein E promoter polymorphism (−427 T/C) and Alzheimer's disease in a Tunisian population

Preliminary study of haplotypes linked to the rare cystic fibrosis E1104X mutation

Neonatal screening for hemoglobinopathies in tunisia over a period of 18 years (2005- 2023)

Implication of polymorphic marker IVS6A GATT in the clinical expression of cystic fibrosis

A Tunisian neonatal case of co-inheritance of G6PD deficiency and HBC presenting as severe jaundice and hemolytic anemia

Identification of a mild cystic fibrosis mutation 2789+5 G to a for the first time in Tunisian population

First study of polymorphic marker MP6D9 in cystic fibrosis Tunisian patients

Molecular Characterization of Mycobacterium tuberculosis Strains Resistant to Isoniazid

Novel frameshift mutation in Tunisian cystic fibrosis patient

Association between clinical expression and molecular heterogeneity in [beta]-thalassemia Tunisian patients

Up‐to‐date incidence and initial characteristics of cystic fibrosis in Tunisia

A gain-of-function mutation in zinc cluster transcription factor Rob1 drives Candida albicans adaptive growth in the cystic fibrosis lung environment

Efficient and lightweight in-memory computing architecture for hardware security

Association between H2 haplotype of microtubule associated protein tau gene (deletion / insertion) with Alzheimer Disease in Tunisian patients

Catalyzing precision: unraveling the diagnostic conundrum of tunisian familial hypophosphatasia case through integrative clinical and molecular approaches

Distribution of rotavirus VP7 and VP4 genotypes circulating in Tunisia from 2009 to 2014: Emergence of the genotype G12

FPGA-accelerated anisotropic diffusion filter based on SW/HW-codesign for medical images

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