Works by Hadj-Fredj, Sondess

Results: 13

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

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

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

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

Published in:

Pediatric Pulmonology, 2022, v. 57, n. 10, p. 2540, doi. 10.1002/ppul.26032

By:

Hamouda, Samia;
Hadj Fredj, Sondess;
Messaoud, Taieb;
Scotet, Virginie;
Boussetta, Khadija;
Munck, Anne

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

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

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

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

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

Published in:

Molecular Genetics & Genomics, 2024, v. 299, n. 1, p. 1, doi. 10.1007/s00438-024-02157-y

By:

Amri, Yessine;
Dabboubi, Rym;
Khemiri, Monia;
Jebabli, Elham;
Hadj Fredj, Sondess;
Ahmed, Sarra Ben;
Jouini, Yosr;
Ouali, Faida;
Messaoud, Taieb

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

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

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