Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Sondess, Hadj Fredj"'
Autor:
Sarra Tombari, Yessine Amri, Yosra Hasni, Sondess Hadj Fredj, Yesmine Salem, Salima Ferchichi, Leila Essaddam, Taieb Messaoud, Rym Dabboubi
Publikováno v:
Heliyon, Vol 10, Iss 14, Pp e34947- (2024)
Introduction: Growth Hormone Deficiency (GHD) is a rare disease marked by a complete or partial reduction in the production of growth hormone. Vitamin D deficiency is frequent and may be associated with several pathologies. However, the association b
Externí odkaz:
https://doaj.org/article/01af9c3f89184630bb3f14d3ea0c7f2c
Autor:
Taher Mahmoud, Chaima Sahli, Sondess Hadj Fredj, Yessine Amri, Rim Othmani, Ghaber S. Mohamed, Ekhtelbenina Zein, Taieb Messaoud
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 10, Pp n/a-n/a (2022)
Abstract Background Hemoglobinopathies, inherited disorders of hemoglobin (Hb), are the most common hereditary monogenic diseases of the red cell in the world. Few studies have been conducted on hemoglobinopathies in Mauritania. Therefore, the aim of
Externí odkaz:
https://doaj.org/article/6382c27ae37a4ff2b7770ed6b61bdab7
Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations
Autor:
Sana Hammami, Sabrine Oueslati, Malek Dabboussi, Chaima Kasmi, Sondess Hadj-Fredj, Faika Ben Mami, Amina Bibi, Imen Aljane, Yessine Amri, Henda Jamoussi, Rahma Mahjoub, Taieb Messaoud
Publikováno v:
Molecular Biology Reports. 48:5923-5933
Thalassemia is one of the most prevalent worldwide autosomal recessive disorders characterized by a great molecular and clinical expression heterogeneity. Alpha and beta-thalassemia are the main two types observed in case of mutations affecting alpha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::690663f937edb5e8789e174ce38d5c16
https://doi.org/10.1007/s11033-021-06592-7
https://doi.org/10.1007/s11033-021-06592-7
Autor:
Samia Hamouda, Sondess Hadj Fredj, Taieb Messaoud, Virginie Scotet, Khadija Boussetta, Anne Munck
Publikováno v:
Pediatric pulmonologyREFERENCES. 57(10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce3c10a2482647ab927ce5a10fe09def
https://pubmed.ncbi.nlm.nih.gov/35668039
https://pubmed.ncbi.nlm.nih.gov/35668039
Publikováno v:
Biological Research For Nursing. 23:408-417
Background: This study investigated the association of BglII polymorphism in α2β1 integrin gene ( ITGA2) and eNOS (894G/T and –786T/C) polymorphisms with ischemic stroke (IS) in Tunisian patients. Methods: The study comprised 210 patients with IS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86cb5747df251edafea617a45873c407
https://doi.org/10.1177/1099800420977685
https://doi.org/10.1177/1099800420977685
Autor:
Pascale Fanen, K. Boussetta, Sondess Hadj Fredj, Rym Dabboubi, R. Othmani, Malek Nefzi, Imen Wahabi, Taieb Messaoud
Publikováno v:
Journal of Asthma. 59:1-11
This study aims to describe the molecular variability in theWe used direct sequencing for the genotyping of theThe molecular study revealed 26 variants including 24 intronic variations and 2 exonic variations (T138N and S186N) with respective frequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e8fb72ffe240e7f8208f0188b29ced2
https://doi.org/10.1080/02770903.2020.1827419
https://doi.org/10.1080/02770903.2020.1827419
Autor:
W. Bahri, K. Bousseta, Sondess Hadj Fredj, Chaima Abdelhafidh Sahli, Rym Dabboubi, A. Mehrzi, Taieb Messaoud
Publikováno v:
Russian Journal of Genetics. 55:756-761
The aim of this study was to determine a possible association of IVS3 poly A and IVS10 CA microsatellites with CF in case–control Tunisian groups and to compare the results with the findings in Italian population. Both microsatellites were analyzed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec5c5cd83fd5468be5bb71cb45847076
https://doi.org/10.1134/s1022795419060139
https://doi.org/10.1134/s1022795419060139
Autor:
F. Khalsi, Malek Nefzi, Khedija Bousetta, Hajer Siala, Sondess Hadj Fredj, Imen Wahabi, Rym Dabboubi, Taieb Messaoud
Publikováno v:
Allergologia et Immunopathologia. 47:159-165
Introduction and Objectives Asthma is a complex genetic disorder. Several genes have been found associated with asthma. The cystic fibrosis transmembrane conductance regulator (CFTR) gene is one of them. The aim of this study was to perform a compara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d310d45b25dcf574bb68bc18f4b14d31
https://doi.org/10.1016/j.aller.2018.06.007
https://doi.org/10.1016/j.aller.2018.06.007
Autor:
Taieb Messaoud, Yessine Amri, Sondess Hadj Fredj, Rym Dabboubi, Leila Essaddam, Saida Ben Becher, Chaima Abdelhafidh Sahli, Ala Zoghlami
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM). 57:e226-e229
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77130c1593b05c5930a47b1838082d08
https://doi.org/10.1515/cclm-2018-1133
https://doi.org/10.1515/cclm-2018-1133
Autor:
Sondess Hadj Fredj, Malek Nefzi, Neji Tebib, K. Boussetta, S. Hamouda, Taieb Messaoud, Rym Dabboubi
Publikováno v:
Annales de biologie clinique. 79(1)
BACKGROUND & OBJECTIVES Cystic fibrosis (CF) is caused by mutations in the gene encoding the CF transmembrane regulator (CFTR) protein, a chloride channel located in the epithelial cell membrane. Over than 2,000 CFTR mutations have been identified, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dc16d437eac2ee9386ffbbadb70b944
https://pubmed.ncbi.nlm.nih.gov/33589413
https://pubmed.ncbi.nlm.nih.gov/33589413