Works by Messaoud, Taieb

Results: 59

Vitamin D receptor gene BsmI (rs1544410) polymorphism: role in multiple sclerosis and genotype-phenotype correlations.

Published in:

Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09369-w

By:

Jamoussi, Maha;
Alaya, Faten;
Jamoussi, Hela;
Baraket, Ghada;
Achouri, Afef;
Mahmoud, Mariem Ben;
Fray, Saloua;
Ben Ali, Nadia;
Messaoud, Taieb;
Hannachi Salhi, Amel;
Fredj, Mohamed

Publication type:

Article

Complete ascertainment of intragenic copy number mutations (CNMs) in the CFTR gene and its implications for CNM formation at other autosomal loci.

Published in:

Human Mutation, 2010, v. 31, n. 4, p. 421, doi. 10.1002/humu.21196

By:

Quemener, Sylvia;
Chen, Jian-Min;
Chuzhanova, Nadia;
Bénech, Caroline;
Casals, Teresa;
Macek, Milan;
Bienvenu, Thierry;
McDevitt, Trudi;
Farrell, Philip M.;
Loumi, Ourida;
Messaoud, Taieb;
Cuppens, Harry;
Cutting, Garry R.;
Stenson, Peter D.;
Giteau, Karine;
Audrézet, Marie-Pierre;
Cooper, David N.;
Férec, Claude

Publication type:

Article

Clopidogrel utilization in patients with coronary artery disease and diabetes mellitus: should we determine CYP2C19*2 genotype?

Published in:

European Journal of Clinical Pharmacology, 2018, v. 74, n. 12, p. 1567, doi. 10.1007/s00228-018-2530-5

By:

Chouchene, Saoussen;
Dabboubi, Rym;
Raddaoui, Haythem;
Abroug, Hela;
Ben Hamda, Khaldoun;
Hadj Fredj, Sondess;
Abderrazak, Fatma;
Gaaloul, Mayssa;
Rezek, Marwa;
Neffeti, Fadoua;
Hellara, Ilhem;
Sassi, Mouna;
Khefacha, Linda;
Sriha, Asma;
Nouira, Semir;
Najjar, Mohamed Fadhel;
Maatouk, Faouzi;
Messaoud, Taieb;
Hassine, Mohsen

Publication type:

Article

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.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 5, p. 567, doi. 10.1038/sj.ejhg.5201590

By:

Férec, Claude;
Casals, Teresa;
Chuzhanova, Nadia;
Macek Jr., Milan;
Bienvenu, Thierry;
Holubova, Andrea;
King, Caitriona;
McDevitt, Trudi;
Castellani, Carlo;
Farrell, Philip M;
Sheridan, Molly;
Pantaleo, Sarah-Jane;
Loumi, Ourida;
Messaoud, Taieb;
Cuppens, Harry;
Torricelli, Francesca;
Cutting, Garry R;
Williamson, Robert;
Ramos, Maria Jesus Alonso;
Pignatti, Pier Franco

Publication type:

Article

Early psychiatrics symptoms in familial Alzheimer's disease with presenilin 1 mutation (I83T).

Published in:

Journal of Neural Transmission, 2016, v. 123, n. 4, p. 451, doi. 10.1007/s00702-015-1498-x

By:

Fray, Saloua;
Ali, Nadia;
Rassas, Afef;
Kechaou, Meriem;
Oudiaa, Nouria;
Cherif, Aroua;
Echebbi, Slim;
Messaoud, Taieb;
Belal, Samir

Publication type:

Article

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

Published in:

Journal of Neural Transmission, 2016, v. 123, n. 3, p. 317, doi. 10.1007/s00702-015-1468-3

By:

Achouri-Rassas, Afef;
Ali, Nadia;
Cherif, Aroua;
Fray, Saloua;
Siala, Hajer;
Zakraoui, Nouria;
Hadj-Fredj, Sondes;
Kechaou, Mariem;
Anane, Nadia;
Echebi, Slim;
Messaoud, Taieb;
Belal, Samir

Publication type:

Article

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

Published in:

Journal of Neural Transmission, 2013, v. 120, n. 9, p. 1355, doi. 10.1007/s00702-013-0985-1

By:

Rassas, Afef;
Fredj, Sondess;
Khiari, Hela;
Sahnoun, Safa;
Bibi, Amina;
Siala, Hajer;
Mrabet, Amel;
Messaoud, Taieb

Publication type:

Article

Refractory epilepsy in PSEN 1 mutation (I83T).

Published in:

2020

By:

Fray, Saloua;
Rassas, Afef;
Messaoud, Taieb;
Belal, Samir

Publication type:

journal article

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

Published in:

Neurological Research, 2022, v. 44, n. 9, p. 814, doi. 10.1080/01616412.2022.2056338

By:

Fray, Saloua;
Achouri-Rassas, Afef Achouri;
Hadj Fredj, Sondes;
Messaoud, Taieb;
Belal, Samir

Publication type:

Article

Detection of Two Rare β-Thalassemia Alleles Found in the Tunisian Population: Codon 47 (+A) and Codons 106/107 (+G).

Published in:

Hemoglobin, 2006, v. 30, n. 4, p. 437, doi. 10.1080/03630260600867933

By:

Bibi, Amina;
Messaoud, Taieb;
Beldjord, Cherif;
Fattoum, Slaheddine

Publication type:

Article

HAPLOTYPES LINKED TO THREE RARE β-THALASSEMIA MUTATIONS, ORIGINALLY REPORTED IN TUNISIA.

Published in:

Hemoglobin, 2006, v. 30, n. 2, p. 175, doi. 10.1080/03630260600642427

By:

Bibi, Amina;
Messaoud, Taieb;
Fattoum, Slaheddine

Publication type:

Article

First Description in Tunisia of a Point Mutation at Codon 119 ( C CT→ T CT) in the α1-Globin Gene: Hb Groene Hart in Association with the - α 3.7 Deletion.

Published in:

Hemoglobin, 2005, v. 29, n. 4, p. 263, doi. 10.1080/03630260500308053

By:

Siala, Hajer;
Ouali, Faida;
Messaoud, Taieb;
Sfar, Rachida;
Fattoum, Slaheddine

Publication type:

Article

A Novel α-Thalassemia Nonsense Mutation in Codon 23 of the α2-Globin Gene (GAG→TAG) in a Tunisian Family.

Published in:

Hemoglobin, 2004, v. 28, n. 3, p. 249, doi. 10.1081/HEM-120040258

By:

Siala, Hajer;
Fattoum, Slaheddine;
Messaoud, Taieb;
Ouali, Fadiq;
Gerard, Nathalie;
Krishnamoorthy, Rajagopal

Publication type:

Article

Missing apolipoprotein E ɛ4 allele associated with nonamnestic Alzheimer’s disease in a Tunisian population.

Published in:

Journal of Genetics, 2022, v. 101, n. 2, p. 1, doi. 10.1007/s12041-022-01384-9

By:

Fray, Saloua;
Achouri-Rassas, Afef;
Belal, Samir;
Messaoud, Taieb

Publication type:

Article

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

Published in:

Journal of Genetics, 2016, v. 95, n. 1, p. 193, doi. 10.1007/s12041-015-0609-7

By:

OUESLATI, SABRINE;
HADJ FREDJ, SONDESS;
SIALA, HAJER;
BIBI, AMINA;
ALOULOU, HAJER;
BOUGHAMOURA, LAMIA;
BOUSSETTA, KHADIJA;
BARSAOUI, SIHEM;
MESSAOUD, TAIEB

Publication type:

Article

New frameshift CF mutation 3729delAinsTCT in a Tunisian cystic fibrosis patient.

Published in:

Journal of Genetics, 2013, v. 92, n. 1, p. 81, doi. 10.1007/s12041-013-0208-4

By:

FREDJ, SONDESS;
BOUDAYA, MONIA;
OUESLATI, SABRINE;
SAHNOUN, SAFA;
SAHLI, CHAIMA;
SIALA, HAJER;
BOUSSETTA, KHEDIJA;
BIBI, AMINA;
MESSAOUD, TAIEB

Publication type:

Article

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

Published in:

Neurochemical Research, 2014, v. 39, n. 2, p. 244, doi. 10.1007/s11064-013-1213-y

By:

Achouri-Rassas, Afef;
Hadj Fredj, Sondes;
Mrabet Khiari, Hela;
Bibi, Amina;
Siala, Hajer;
Mrabet, Amel;
Messaoud, Taieb

Publication type:

Article

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

Published in:

Electrophoresis, 2017, v. 38, n. 17, p. 2210, doi. 10.1002/elps.201600423

By:

Doggui, Radhouene;
Abdelhafidh Sahli, Chaïma;
Aissa, Wassef Lotfi;
Hammami, Maroua;
Ben Sedrine, Maha;
Mahjoub, Rahma;
Zouaoui, Khemais;
Daboubi, Rim;
Siala, Hajer;
Messaoud, Taieb;
Bibi, Amina

Publication type:

Article

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

Published in:

2016

By:

Sahli, Chaima Abdelhafidh;
Ben Salem, Ikbel;
Jouini, Latifa;
Laouini, Naouel;
Dabboubi, Rym;
Hadj Fredj, Sondes;
Siala, Hajer;
Othmeni, Rym;
Dakhlaoui, Boutheina;
Fattoum, Slaheddine;
Bibi, Amina;
Messaoud, Taieb

Publication type:

journal article

Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients.

Published in:

Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 10, p. 1, doi. 10.1002/mgg3.2048

By:

Mahmoud, Taher;
Sahli, Chaima;
Hadj Fredj, Sondess;
Amri, Yessine;
Othmani, Rim;
Mohamed, Ghaber S.;
Zein, Ekhtelbenina;
Messaoud, Taieb

Publication type:

Article

High APOE epsilon 4 allele frequencies associated with Alzheimer disease in a Tunisian population.

Published in:

Neurological Sciences, 2012, v. 33, n. 1, p. 33, doi. 10.1007/s10072-011-0663-8

By:

Rassas, Afef;
Mrabet Khiari, Hela;
Hadj Fredj, Sondes;
Sahnoun, Safa;
Batti, Hend;
Zakraoui, Nouria;
Cherif, Aroua;
Anane, Nadia;
Ben Ali, Nadia;
Messaoud, Taieb;
Mrabet, Amel

Publication type:

Article

Obsessive-compulsive disorder: a new risk factor for Alzheimer disease?

Published in:

Neurological Sciences, 2011, v. 32, n. 5, p. 959, doi. 10.1007/s10072-011-0480-0

By:

Mrabet Khiari, Hela;
Achouri, Afef;
Ben Ali, Nadia;
Cherif, Aroua;
Batti, Hend;
Messaoud, Taieb;
Mrabet, Amel

Publication type:

Article

Autism in Phenylketonuria Patients.

Published in:

Journal of Child Neurology, 2016, v. 31, n. 7, p. 843, doi. 10.1177/0883073815623636

By:

Khemir, Sameh;
Halayem, Soumeyya;
Azzouz, Hatem;
Siala, Hajer;
Ferchichi, Maherzia;
Guedria, Asma;
Bedoui, Amel;
Abdelhak, Sonia;
Messaoud, Taieb;
Tebib, Neji;
Belhaj, Ahlem;
Kaabachi, Naziha

Publication type:

Article

Epidemiological and clinical characteristics of 66 Tunisian Sickle cell syndrome patients.

Published in:

African Health Sciences, 2023, v. 23, n. 3, p. 213, doi. 10.4314/ahs.v23i3.26

By:

Sahli, Ahlem;
Ouali, Faida;
Dabboubi, Rym;
Fredj, Sondess Hadj;
Meddeb, Nabila;
Mzoughi, Naila;
Messaoud, Taieb

Publication type:

Article

Preliminary national report on cystic fibrosis epidemiology in Tunisia: the actual state of affairs.

Published in:

African Health Sciences, 2020, v. 20, n. 1, p. 444, doi. 10.4314/ahs.v20i1.51

By:

Hamouda, Samia;
Fredj, Sondess Hadj;
Hilioui, Sonia;
Khalsi, Fatma;
Ameur, Salma Ben;
Bouguila, Jihene;
Boussoffara, Raoudha;
Besbes, Habib;
Ajmi, Houda;
Mattoussi, Nadia;
Messaoud, Taieb;
Mehrezi, Ahmed;
Hachicha, Mongia;
Boughamoura, Lamia;
Sfar, Mohamed Taher;
Gueddiche, Neji;
Abroug, Saoussen;
Becheur, Saida Ben;
Barsaoui, Sihem;
Tebib, Neji

Publication type:

Article

Cystic fibrosis in Tunisian children: a review of 32 children.

Published in:

African Health Sciences, 2018, v. 18, n. 3, p. 664, doi. 10.4314/ahs.v18i3.24

By:

Boussetta, Khedija;
Khalsi, Fatma;
Bahri, Yasmine;
Belhadj, Imen;
Tinsa, Faten;
Ben Messaoud, Taieb;
Hamouda, Samia

Publication type:

Article

Association analysis of the surfactant protein-C gene to childhood asthma.

Published in:

Journal of Asthma, 2022, v. 59, n. 1, p. 1, doi. 10.1080/02770903.2020.1827419

By:

Nefzi, Malek;
Wahabi, Imen;
Hadj Fredj, Sondess;
Othmani, Rym;
Dabboubi, Rym;
Boussetta, Khedija;
Fanen, Pascale;
Messaoud, Taieb

Publication type:

Article

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

Published in:

PLoS Pathogens, 2024, v. 20, n. 4, p. 1, doi. 10.1371/journal.ppat.1012154

By:

Gnaien, Mayssa;
Maufrais, Corinne;
Rebai, Yasmine;
Kallel, Aicha;
Ma, Laurence;
Hamouda, Samia;
Khalsi, Fatma;
Meftah, Khaoula;
Smaoui, Hanen;
Khemiri, Monia;
Hadj Fredj, Sondes;
Bachellier-Bassi, Sophie;
Najjar, Imène;
Messaoud, Taieb;
Boussetta, Khadija;
Kallel, Kalthoum;
Mardassi, Helmi;
d'Enfert, Christophe;
Bougnoux, Marie-Elisabeth;
Znaidi, Sadri

Publication type:

Article

Vitamin D receptor gene BsmI (rs1544410) polymorphism: role in multiple sclerosis and genotype-phenotype correlations.

Published in:

Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09369-w

By:

Jamoussi, Maha;
Alaya, Faten;
Jamoussi, Hela;
Baraket, Ghada;
Achouri, Afef;
Mahmoud, Mariem Ben;
Fray, Saloua;
Ben Ali, Nadia;
Messaoud, Taieb;
Hannachi Salhi, Amel;
Fredj, Mohamed

Publication type:

Article

Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations.

Published in:

Molecular Biology Reports, 2021, v. 48, n. 8, p. 5923, doi. 10.1007/s11033-021-06592-7

By:

Kasmi, Chaima;
Amri, Yessine;
Hadj-Fredj, Sondess;
Oueslati, Sabrine;
Dabboussi, Malek;
Mahjoub, Rahma;
Hammami, Sana;
Aljane, Imen;
Mami, Faika Ben;
Jamoussi, Henda;
Messaoud, Taieb;
Bibi, Amina

Publication type:

Article

Contribution of β-globin cluster polymorphisms to raise fetal hemoglobin levels in normal adults.

Published in:

Molecular Biology Reports, 2012, v. 39, n. 4, p. 4619, doi. 10.1007/s11033-011-1253-9

By:

Jouini, Latifa;
Bibi, Amina;
Ouali, Faida;
Hadj Fredj, Sondess;
Ouennich, Fekria;
Siala, Hajer;
Messaoud, Taieb;
Fattoum, Slaheddine

Publication type:

Article

Molecular characterization of Mycobacterium tuberculosis strains resistant to isoniazid.

Published in:

International Journal of Mycobacteriology, 2016, v. 5, p. S151, doi. 10.1016/j.ijmyco.2016.09.070

By:

Smaoui, Salma;
Siala, Mariem;
Hadj Fredj, Sondes;
Kammoun, Sana;
Marouane, Chema;
Hachicha, Salma;
Ghorbel, Asma;
Gdoura, Radhouane;
Slim, Leila;
Ben Messaoud, Taieb;
Messadi, Férièle

Publication type:

Article

Inherited bisalbuminemia with growth hormone deficiency.

Published in:

2019

By:

Dabboubi, Rym;
Amri, Yessine;
Sahli, Chaima;
Fredj, Sondess Hadj;
Essaddam, Leila;
Zoghlami, Ala;
Ben Becher, Saida;
Messaoud, Taieb

Publication type:

Case Study

First study of angiotensin converting enzyme in cystic fibrosis Tunisian patients.

Published in:

2014

By:

Sahli, Chaîma;
Hadj Fredj, Sondess;
Siala, Hajer;
Bibi, Amina;
Messaoud, Taieb

Publication type:

Letter to the Editor

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

Published in:

Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 11, p. 2115, doi. 10.1515/cclm-2013-0354

By:

Sahli, Chaima Abdelhafidh;
Bibi, Amina;
Ouali, Faida;
Fredj, Sondess Hadj;
Dakhlaoui, Boutheina;
Othmani, Rym;
Laouini, Naouel;
Jouini, Latifa;
Ouenniche, Fekria;
Siala, Hajer;
Touhami, Imed;
Becher, Mariem;
Fattoum, Slaheddine;
Toumi, Nour El Houda;
Messaoud, Taieb

Publication type:

Article

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

Published in:

Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 8, p. 1595, doi. 10.1515/cclm-2012-0842

By:

Sahli, Chaima A.;
Bibi, Amina;
Ouali, Faida;
Fredj, Sondess Hadj;
Dakhlaoui, Boutheina;
Othmani, Rym;
Laaouini, Naouel;
Jouini, Latifa;
Ouenniche, Fekria;
Siala, Hajer;
Touhami, Imed;
Becher, Mariem;
Fattoum, Slaheddine;
Toumi, Nour El Houda;
Messaoud, Taieb

Publication type:

Article

δ0-Thalassemia in cis of βKnossos globin gene: first homozygous description in thalassemia intermedia Libyans and first combination with codon 39 (C→T) in thalassemia intermedia Tunisian patients.

Published in:

Clinical Chemistry & Laboratory Medicine, 2012, v. 50, n. 10, p. 1743, doi. 10.1515/cclm-2012-0102

By:

Sahli, Chaima Abdelhafidh;
Bibi, Amina;
Ouali, Faida;
Siala, Hajer;
Fredj, Sondess Hadj;
Othmani, Rym;
Ouenniche, Fekria;
Cheour, Mondher;
Fitouri, Zohra;
Becher, Saida Ben;
Messaoud, Taieb

Publication type:

Article

Comprehensive analysis of a novel LYST mutation in a Tunisian patient with Chediak-Higashi syndrome.

Published in:

BMC Medical Genomics, 2025, v. 18, n. 1, p. 1, doi. 10.1186/s12920-025-02145-0

By:

Amri, Yessine;
Chouchene, Saoussen;
Foddha, Hajer;
Abderahmene, Amani;
Kooli, Ikbel;
Toumi, Adnen;
Hadj Khalifa, Kawthar;
Mezrigui, Rihem;
Messaoud, Taieb;
Hassine, Mohsen;
Dabboubi, Rym

Publication type:

Article

Factor V Leiden G1691A, Prothrombin G20210A, and MTHFR C677T and A1298C Mutations in Patients With Sickle Cell Disease in Tunisia.

Published in:

Hemoglobin, 2018, v. 42, n. 2, p. 96, doi. 10.1080/03630269.2018.1451340

By:

Belhaj Nefissi, Rim;
Doggui, Radhouene;
Ouali, Faida;
Messaoud, Taieb;
Gritli, Nasreddine

Publication type:

Article

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

Published in:

Hemoglobin, 2016, v. 40, n. 6, p. 411, doi. 10.1080/03630269.2016.1252386

By:

Mejri, Awatef;
Mansri, Marwa;
Hadj Fredj, Sondess;
Ouali, Faida;
Bibi, Amina;
Hafsia, Raouf;
Messaoud, Taieb;
Siala, Hajer

Publication type:

Article

First report of cystic fibrosis mutations in Libyan cystic fibrosis patients.

Published in:

Annals of Human Biology, 2011, v. 38, n. 5, p. 561, doi. 10.3109/03014460.2011.557090

By:

Hadj Fredj, Sondess;
Fattoum, Slaheddine;
Chabchoub, Abdelraouf;
Messaoud, Taieb

Publication type:

Article

Association of Bgl II Polymorphism in ITGA2 and (894G/T and −786T/C) Polymorphisms in eNOS Gene With Stroke Susceptibility in Tunisian Patients α2 Gene Polymorphism in α2β1 Integrin and eNOS Gene Variants and Stroke.

Published in:

Biological Research for Nursing, 2021, v. 23, n. 3, p. 408, doi. 10.1177/1099800420977685

By:

Jalel, Akrem;
Midani, Fatma;
Fredj, Sondess Hadj;
Messaoud, Taieb;
Hentati, Fayçal;
Soualmia, Hayet

Publication type:

Article

Genotypic and phenotypic characteristics of tunisian isoniazid-resistant Mycobacterium tuberculosis strains.

Published in:

Journal of Microbiology, 2011, v. 49, n. 3, p. 413, doi. 10.1007/s12275-011-0268-1

By:

Soudani, Alya;
Hadjfredj, Sondess;
Zribi, Meriem;
Messaadi, Feriel;
Messaoud, Taieb;
Masmoudi, Afef;
Zribi, Mohamed;
Fendri, Chedlia

Publication type:

Article

Congenital analbuminemia associated with compound heterozygous novel nucleotide variations in a young adult with coronary thrombosis.

Published in:

Annales de Biologie Clinique, 2023, v. 81, n. 2, p. 204, doi. 10.1684/abc.2023.1806

By:

Amri, Yessine;
Aboulkacem, Sana;
Dabboubi, Rym;
Ayoub, Manel;
Lamine, Oussema;
Othmani, Mariem;
Aouni, Zied;
Messaoud, Taieb;
Mazigh, Chakib

Publication type:

Article

Contribution of common CFTR variants (M470V, T854, and Q1463) to cystic fibrosis in Tunisia: haplotype analysis.

Published in:

Annales de Biologie Clinique, 2021, v. 79, n. 1, p. 63, doi. 10.1684/abc.2021.1614

By:

Nefzi, Malek;
Fredj, Sondess Hadj;
Dabboubi, Rym;
Hamouda, Samia;
Tebib, Neji;
Boussetta, Khedija;
Messaoud, Taieb

Publication type:

Article

Glucose-6-phosphate dehydrogenase deficiency in Tunisian jaundiced neonates.

Published in:

Annales de Biologie Clinique, 2020, v. 78, n. 4, p. 411, doi. 10.1684/abc.2020.1558

By:

Dabboubi, Rym;
Amri, Yessine;
Hamdi, Soumaya;
Jouini, Hamida;
Sahli, Chaima;
Fredj, Sondess Hadj;
Salem, Kamel Ben;
ElhoudaToumi, Nour;
Messaoud, Taieb

Publication type:

Article

Association of IVS6A GATT polymorphism of CFTR gene with cystic fibrosis: first study in CF and normal Tunisian population.

Published in:

Annales de Biologie Clinique, 2020, v. 78, n. 3, p. 314, doi. 10.1684/abc.2020.1555

By:

Chaima, Sahli;
Sondess, Hadj Fredj;
Khedija, Boussetta;
Ahmed, Mehrezi;
Taieb, Messaoud

Publication type:

Article

Pseudo-Bartter syndrome as the sole manifestation of cystic fibrosis in a child with 711+G>T/IVS8-5T mutation: a new face of an old disease.

Published in:

Annales de Biologie Clinique, 2017, v. 75, n. 4, p. 466, doi. 10.1684/abc.2017.1268

By:

Tinsa, Faten;
Fredj, Sondes Hadj;
Hadj, Imen Bel;
Khalsi, Fatma;
Abdelhak, Sonia;
Boussetta, Khadija;
Messaoud, Taieb

Publication type:

Article

The MNS blood group system in Tunisian blood donors: common and rare alleles.

Published in:

Molecular Biology Reports, 2025, v. 52, n. 1, p. 1, doi. 10.1007/s11033-025-10552-w

By:

Sellami, Mohamed Hichem;
Ghazouani, Eya;
Hadj Fredj, Sondess;
Ferchichi, Hamida;
Chaabane, Manel;
Kaabi, Houda;
Messaoud, Taieb;
Hmida, Slama

Publication type:

Article

The epidemiology of abnormal hemoglobins in Mediterranean high-level athletes.

Published in:

2010

By:

Touhami, Imed;
Fattoum, Slaheddine;
Bibi, Amina;
Siala, Hajer;
Messaoud, Taieb;
Koubaa, Donia;
Mankai, Rafik;
Bartagi, Zakia;
Le Gallais, Daniel

Publication type:

journal article