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Taieb Ben Messaoud
Observed names:
T Messaoud,
T. Messaoud,
TAIEB MESSAOUD,
Taieb Messaoud,
Taïeb Messaoud
Institution:
Children's Hospital
Observed institutions:
Tunis University,
Hôpital La Rabta,
Institut National de Nutrition et de Technologie Alimentaire,
Hôpital Charles-Nicolle,
Children's Hospital,
Université Montpellier 1,
Tunis El Manar University
show all 7
OpenAlex ID:
A5113811386
Gross genomic rearrangements involving deletions in the CFTR gene: characterization of six new events from a large cohort of hitherto unidentified cystic fibrosis chromosomes and meta-analysis of the underlying mechanisms
2006
·
Claude Férec
, Teresa Casals
, et al.
·
European Journal of Human Genetics
·
93
Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia
2013
·
Chaima Abdelhafidh Sahli
, Amina Bibi
, et al.
·
Clinical Chemistry and Laboratory Medicine (CCLM)
·
47
High APOE epsilon 4 allele frequencies associated with Alzheimer disease in a Tunisian population
2011
·
Afef Achouri Rassas
, Hela Mrabet Khiari
, et al.
·
Neurological Sciences
·
45
Complete ascertainment of intragenic copy number mutations (CNMs) in the CFTR gene and its implications for CNM formation at other autosomal loci
2010
·
Sylvia Quemener
, Jian-Min Chen
, et al.
·
Human Mutation
·
34
PDF
Distribution of CFTR Mutations in Cystic Fibrosis Patients of Tunisian Origin: Identification of Two Novel Mutations
1996
·
Taieb Messaoud
, Claudine Verlingue
, et al.
·
European Journal of Human Genetics
·
32
Cystic Fibrosis Transmembrane Conductance Regulator Mutation Spectrum in Patients with Cystic Fibrosis in Tunisia
2009
·
Sondess Hadj Fredj
, Taïeb Messaoud
, et al.
·
Genetic Testing and Molecular Biomarkers
·
28
Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia
2013
·
Chaima A. Sahli
, Amina Bibi
, et al.
·
Clinical Chemistry and Laboratory Medicine (CCLM)
·
27
Impacts of Iron Metabolism Dysregulation on Alzheimer’s Disease
2021
·
Najla Jouini
, Zakaria Saied
, et al.
·
Journal of Alzheimer s Disease
·
24
Autism in Phenylketonuria Patients
2016
·
Sameh Khemir
, Soumeyya Halayem
, et al.
·
Journal of Child Neurology
·
23
α-Thalassaemia in Tunisia: some epidemiological and molecular data
2008
·
H. Siala
, F. Ouali
, et al.
·
Journal of Genetics
·
22
Cystic fibrosis in Tunisian children: a review of 32 children
2018
·
Khedija Boussetta
, Fatma Khalsi
, et al.
·
African Health Sciences
·
20
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
2011
·
M. Boudaya
, S. Hadj Fredj
, et al.
·
Annals of Human Biology
·
20
First report of molecular characterization of fluoroquinolone-resistant Mycobacterium tuberculosis isolates from a Tunisian hospital
2010
·
A. Soudani
, S. Hadjfredj
, et al.
·
Clinical Microbiology and Infection
·
20
Association between ACE polymorphism, cognitive phenotype and APOE E4 allele in a Tunisian population with Alzheimer disease
2015
·
Afef Achouri-Rassas
, Nadia Ben Ali
, et al.
·
Journal of Neural Transmission
·
16
A new case of congenital atransferrinemia with a novel splice site mutation: c.293-63del
2020
·
Rym Dabboubi
, Yessine Amri
, et al.
·
European Journal of Medical Genetics
·
15
Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients
2013
·
L. Jouini
, C. A. Sahli
, et al.
·
Molecular Biology Reports
·
15
First Description in Tunisia of a Point Mutation at Codon 119 (CCT→TCT) in the α1-Globin Gene: Hb Groene Hart in Association with the − α3.7Deletion
2005
·
Hajer Siala
, Faida Ouali
, et al.
·
Hemoglobin
·
15
Hypodysfibrinogenemia: A novel abnormal fibrinogen associated with bleeding and thrombotic complications
2016
·
Yessine Amri
, Choumous Kallel
, et al.
·
Clinica Chimica Acta
·
14
Prenatal diagnosis of hemoglobinopathies in Tunisia: an 18 years of experience
2016
·
F. Ouali
, H. Siala
, et al.
·
International Journal of Laboratory Hematology
·
13
First report of cystic fibrosis mutations in Libyan cystic fibrosis patients
2011
·
Sondess Hadj Fredj
, Slaheddine Fattoum
, et al.
·
Annals of Human Biology
·
13
A gain-of-function mutation in zinc cluster transcription factor Rob1 drives Candida albicans adaptive growth in the cystic fibrosis lung environment
2024
·
Mayssa Gnaien
, Corinne Maufrais
, et al.
·
PLoS Pathogens
·
12
PDF
Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme
2021
·
Latifa Chkioua
, Yessine Amri
, et al.
·
BMC Medical Genomics
·
12
PDF
Detection of Two Rare β-Thalassemia Alleles Found in the Tunisian Population: Codon 47 (+A) and Codons 106/107 (+G)
2006
·
Amina Bibi
, Taieb Messaoud
, et al.
·
Hemoglobin
·
12
Factor V Leiden G1691A, Prothrombin G20210A, and MTHFR C677T and A1298C Mutations in Patients With Sickle Cell Disease in Tunisia
2018
·
Rim Belhaj Nefissi
, Radhouene Doggui
, et al.
·
Hemoglobin
·
11
Fibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization
2017
·
Y. Amri
, H. Jouini
, et al.
·
Haemophilia
·
11
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Works count:
106
Citation count:
848
H-index:
15
I10-index:
28
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