Zobrazeno 1 - 10
of 105
pro vyhledávání: '"Taieb, Messaoud"'
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:
Mayssa Gnaien, Corinne Maufrais, Yasmine Rebai, Aicha Kallel, Laurence Ma, Samia Hamouda, Fatma Khalsi, Khaoula Meftah, Hanen Smaoui, Monia Khemiri, Sondes Hadj Fredj, Sophie Bachellier-Bassi, Imène Najjar, Taieb Messaoud, Khadija Boussetta, Kalthoum Kallel, Helmi Mardassi, Christophe d'Enfert, Marie-Elisabeth Bougnoux, Sadri Znaidi
Publikováno v:
PLoS Pathogens, Vol 20, Iss 4, p e1012154 (2024)
Candida albicans chronically colonizes the respiratory tract of patients with Cystic Fibrosis (CF). It competes with CF-associated pathogens (e.g. Pseudomonas aeruginosa) and contributes to disease severity. We hypothesize that C. albicans undergoes
Externí odkaz:
https://doaj.org/article/3f782e6103b6485eb5a0f45c57ed332f
Autor:
Latifa Chkioua, Yessine Amri, Chayma Sahli, Ferdawes Ben Rhouma, Amel Ben Chehida, Neji Tebib, Taieb Messaoud, Hassen Ben Abdennebi, Sandrine Laradi
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 15, Iss 1, Pp 1-7 (2023)
Abstract Background Glycogen storage disease type 1b (GSD1b) is an autosomal recessive lysosomal storage disease caused by defective glucose-6-phosphate transporter encoded by SLC37A4 leading to the accumulation of glycogen in various tissues. The hi
Externí odkaz:
https://doaj.org/article/5c3a8d027fbc4cf9ba800c73837901e7
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
Autor:
Latifa Chkioua, Yessine Amri, Chayma Saheli, Ferdawes Fenni, Hela Boudabous, Hadhami Ben Turkia, Taieb Messaoud, Neji Tebib, Sandrine Laradi
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-11 (2021)
Abstract Background Fucosidosis is an autosomal recessive lysosomal storage disease caused by defective alpha-l-fucosidase (FUCA1) activity, leading to the accumulation of fucose-containing glycolipids and glycoproteins in various tissues. Clinical f
Externí odkaz:
https://doaj.org/article/05e8d5831c2b44aab94c8e7c13743974
Autor:
Yessine Amri, Sana Aboulkacem, Rym Dabboubi, Manel Ayoub, Oussema Lamine, Mariem Othmani, Zied Aouni, Taieb Messaoud, Chakib Mazigh
Publikováno v:
Annales de Biologie Clinique. 81:204-209
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53aa931986c97b59f61e2c50769e136d
https://doi.org/10.1684/abc.2023.1806
https://doi.org/10.1684/abc.2023.1806
Autor:
Latifa Chkioua, Yessine Amri, Sahli Chaima, Ferdawes Fenni, Hela Boudabous, Hadhami Ben Turkia, Taieb Messaoud, Neji Tebib, Sandrine Laradi
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-1 (2021)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://doaj.org/article/92ffcb6638d14c009fa5b4e80550f66f
Publikováno v:
Journal of genetics. 101
In this study, we investigate the impact of apolipoprotein E epsilon 4 (APOE ε4) as a major risk factor of Alzheimer's disease (AD), based on the clinical presentation of the disease in our population on the one hand, and comparison of the results w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::130fae8fddf4b319b3a27ff3760c2271
https://pubmed.ncbi.nlm.nih.gov/36226340
https://pubmed.ncbi.nlm.nih.gov/36226340
Publikováno v:
Journal of Genetics. 101
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea3a7628ca900fc929a5608bf4a50b07
https://doi.org/10.1007/s12041-022-01384-9
https://doi.org/10.1007/s12041-022-01384-9
Autor:
Taieb Messaoud, Hela Boudabous, Chayma Saheli, Ferdawes Fenni, Sandrine Laradi, Hadhami Ben Turkia, Yessine Amri, Latifa Chkioua, Neji Tebib
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-11 (2021)
BMC Medical Genomics
BMC Medical Genomics
Background Fucosidosis is an autosomal recessive lysosomal storage disease caused by defective alpha-l-fucosidase (FUCA1) activity, leading to the accumulation of fucose-containing glycolipids and glycoproteins in various tissues. Clinical features i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49150142c41f967f1a5d6aab8b1f0a20
https://doaj.org/article/05e8d5831c2b44aab94c8e7c13743974
https://doaj.org/article/05e8d5831c2b44aab94c8e7c13743974