Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Taieb Massoud"'
Autor:
Latifa Chkioua, Houda El Fissi, Yessine Amri, Chayma Sahli, Fadoua Bouzid, Hela Boudabous, Neji Tbib, Salima Ferchichi, Taieb Massoud, Najat Alif, Sandrine Laradi, Hassen Ben Abdennebi
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-9 (2024)
Abstract Background Mucopolysaccharidosis type I is a lysosomal storage disease resulting from a deficiency in alpha-L-iduronidase (IDUA), which causes the accumulation of partially degraded dermatan sulfate and heparan sulfate. This retrospective st
Externí odkaz:
https://doaj.org/article/15bce9b578064770b9c19476d24d775b
Autor:
Latifa Chkioua, Yessine Amri, Chaima Saheli, Wassila Mili, Sameh Mabrouk, Imen Chabchoub, Hela Boudabous, Wissem Ben Azzouz, Hadhami Ben Turkia, Salima Ferchichi, Neji Tebib, Taieb Massoud, Mohamed Ghorbel, Sandrine Laradi
Publikováno v:
Diagnostic Pathology, Vol 17, Iss 1, Pp 1-11 (2022)
Abstract Background Ocular cystinosis is a rare autosomal recessive disorder characterized by intralysosomal cystine accumulation in renal, ophthalmic (cornea, conjunctiva), and other organ abnormalities. Patients with ocular cystinosis are mostly as
Externí odkaz:
https://doaj.org/article/719f2484eacd45bd80f7b8a19e31bbfd
Autor:
Latifa Chkioua, Hadhami Ben Turkia, Chayma Saheli, Hela Boudabous, Imen Chabchoub, Sameh Mabrouk, Taieb Massoud, Mohamed Ghorbel, Wissem Ben Azzouz, Sandrine Laradi, Neji Tebib, Wassila Mili, Salima Ferchichi, Yessine Amri
Background: Ocular cystinosis is a rare autosomal recessive disorder characterized by intralysosomal cystine accumulation in renal, ophthalmic (cornea, conjunctiva), and other organ abnormalities. Patients with ocular cystinosis are mostly asymptomat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0152e7ff4c46bee6e0d47d342ec6076a
https://doi.org/10.21203/rs.3.rs-1027134/v1
https://doi.org/10.21203/rs.3.rs-1027134/v1
Autor:
Latifa Chkioua, Imen Chabchoub, Wissem Ben Azzouz, Mohamed Ghorbel, Neji Tebib, Salima Ferchichi, Chayma Saheli, Taieb Massoud, Hadhami Ben Turkia, Yessine Amri, Sandrine Laradi, Wassila Mili, Sameh Mabrouk, Hela Boudabous
Background: Ocular cystinosis is a rare autosomal recessive disorder characterized by intralysosomal cystine accumulation in renal, ophthalmic (cornea, conjunctiva), and other organ abnormalities. Patients with ocular cystinosis are mostly asymptomat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2dd4d1baabf7f1eda2c8a552cccdc621
https://doi.org/10.21203/rs.3.rs-933169/v1
https://doi.org/10.21203/rs.3.rs-933169/v1
Autor:
Latifa Chkioua, Yessine Amri, Chayma Saheli, Ferdawes Fenni, Hela Boudabous, Hadhami Ben Turkia, Taieb Massoud, Neji Tebib, Sandrine Laradi
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55ccb583a1f7146f74da85c2db010a6b
https://doi.org/10.21203/rs.3.rs-228088/v1
https://doi.org/10.21203/rs.3.rs-228088/v1
Autor:
Zina Kobbi, Samir Boubaker, Balkiss Bouhaouala-Zahar, Nadia Fenina, Zakaria Benlasfar, Ammar Marouani, Taieb Massoud, Hazar Kraiem
Publikováno v:
Regulatory Toxicology and Pharmacology
Regulatory Toxicology and Pharmacology, Elsevier, 2017, 84, pp.9-17. ⟨10.1016/j.yrtph.2016.12.003⟩
Regulatory Toxicology and Pharmacology, Elsevier, 2017, 84, pp.9-17. ⟨10.1016/j.yrtph.2016.12.003⟩
International audience; Enoxaparin is a low-molecular-weight heparin widely used for the prevention and treatment of thromboembolism. With the development of several enoxaparin biosimilars, real medical concerns about their safety and efficacy have b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5851e657fb147e0912b8ae9dce218979
https://hal.archives-ouvertes.fr/hal-01513613
https://hal.archives-ouvertes.fr/hal-01513613
Autor:
Asma Omezzine, Ibtihel Ben HadjMbarek, Kaouther Kchok, Taieb Massoud, Nabila Ben Rejeb, Essia Boughzala, Ahmed Ben Abdelaziz, Jihen Rejeb, Amina Bibi, Naoufel Nabli, Ali Bouslama, R. Belkahla, Lamia Rebhi
Publikováno v:
Clinical Chemical Laboratory Medicine. 46
BACKGROUND Studies that considered apolipoprotein B (APOB) gene polymorphisms as risk factors for coronary artery disease (CAD) have reported conflicting results. We sought to analyze the association between 5' ins/del and 3' VNTR polymorphisms of AP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d75205d3dae71d56bbcc55071e8d10a
https://doi.org/10.1515/cclm.2008.067
https://doi.org/10.1515/cclm.2008.067