Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Foued Slama"'
Autor:
Elyes Bouajina, Hala Zeglaoui, Adel Almogren, Latifa Guaddah, Nejla Elamri, Asma Boumiza, Jihen Sahli, Hana Benhassine, Rim Sghiri, Zahid Shakoor, Imed Harrabi, Foued Slama
Publikováno v:
Clinical Rheumatology. 40:4879-4887
Autoantibodies such as IgM rheumatoid factor (RF) and anti-citrullinated proteins/peptides antibodies (ACPA) have previously been incriminated in systemic bone loss in rheumatoid arthritis (RA). There are, however, no data describing association of I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8dbe39ee65c0df73b93c872ebbac7033
https://doi.org/10.1007/s10067-021-05814-4
https://doi.org/10.1007/s10067-021-05814-4
Autor:
Rim Sghiri, Hana Benhassine, Khadija Baccouche, Meriem Ghozzi, Sarra Jriri, Zahid Shakoor, Adel Almogren, Foued Slama, Nadia Idriss, Zeineb Benlamine, Elyes Bouajina, Ramzi Zemni
Publikováno v:
Clinical rheumatology. 41(6)
Little is known about genes predisposing to systemic bone loss (SBL) in rheumatoid arthritis (RA). Therefore, we examined the association between SBL and variants of genes playing a critical role in both immune response and bone homeostasis among pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::349616663cf3b778d62740b79c4c0ac8
https://pubmed.ncbi.nlm.nih.gov/35107652
https://pubmed.ncbi.nlm.nih.gov/35107652
Autor:
Ramzi Zemni, Nadia Idriss, A. Mzabi, Foued Slama, Elyes Chabchoub, Neirouz Ghannouchi, Rim Sghiri, Asma Boumiza, Elyes Bouajina, Hana Ben Hassine
Publikováno v:
Clinical Rheumatology. 39:419-424
Interleukin-1 receptor-associated kinases (IRAKs) are serine-threonine kinases involved in toll-like receptor and interleukin-1 signaling pathways. They play a key role in inflammation and innate immunity. IRAKs have been previously incriminated in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b63567f1a40de99bbf5811f980c237b5
https://doi.org/10.1007/s10067-019-04781-1
https://doi.org/10.1007/s10067-019-04781-1
Autor:
Foued Slama, Mariem Ben Ahmed, A. Jemaa, Ayda Ben Slama, Azza Baccouche, Zeineb Ben Lamine, Ibtissem Ghedira, Amani Mankaï, Ilhem Ben Jazia
Publikováno v:
Arab journal of gastroenterology : the official publication of the Pan-Arab Association of Gastroenterology. 22(4)
Background and study aims To determine the sensitivity and specificity of anti-gp210 and anti-Sp100 autoantibodies in primary biliary cholangitis (PBC) Patients and Methods Sera of 106 PBC patients with positive anti-mitochondrial antibodies and 58 h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6f02990ede620a3298ac5af3d392d47
https://pubmed.ncbi.nlm.nih.gov/34090832
https://pubmed.ncbi.nlm.nih.gov/34090832
Autor:
S. Jriri, A. Almorgen, Foued Slama, E. Boujina, Zahid Shakoor, N. El Amri, H. Benhassine, Hala Zaglaoui, Rim Sghiri, Asma Boumiza
Publikováno v:
Revue du Rhumatisme. 88:A160
Introduction Le facteur rhumatoide (FR) d’isotype IgM et les anticorps anti-peptides cycliques citrullines (anti-CCP) ont deja ete incrimines dans la perte osseuse systemique (POS) observee au cours de la polyarthrite rhumatoide (PR). Cependant, Il
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8650d1433c9964ad24fd95ba981f2fe
https://doi.org/10.1016/j.rhum.2021.10.254
https://doi.org/10.1016/j.rhum.2021.10.254
Autor:
Foued Slama, Hana Ben Hassine, Elyes Bouajina, Adel Almogren, Zahid Shakoor, Khadija Baccouche, Asma Boumiza, Rim Sghiri, Ramzi Zemni, Christina Mary Mariaselvam, Ryad Tamouza, Elyes Chabchoub
Publikováno v:
Clinical Rheumatology. 37:927-933
This study was performed to investigate the association of the single nucleotide polymorphisms of interleukin-1 receptor-associated kinase 2 (IRAK2) rs3844283 and rs708035 with rheumatoid arthritis (RA). IRAK2 rs3844283 and rs708035genotyping was det
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7497fa27300054d1fd9644d5a21f2ba
https://doi.org/10.1007/s10067-017-3906-0
https://doi.org/10.1007/s10067-017-3906-0
Autor:
Hana Ben Hassine, Ramzi Zemni, Imen Ben Nacef, Khadija Baccouche, Asma Boumiza, Zahid Shakoor, Elyes Bouajina, Foued Slama, Rim Sghiri, Sarra Melayah, Najla Amri, Adel Almogren
Publikováno v:
Clinical rheumatology. 38(4)
This study was aimed to investigate the association of the single nucleotide polymorphism of tumor necrosis factor receptor associated factor 6 (TRAF6), rs540386, with low bone mineral density (BMD) among patients with rheumatoid arthritis (RA). TRAF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21547ff75c518979e63b9e91e31e6f99
https://pubmed.ncbi.nlm.nih.gov/30506403
https://pubmed.ncbi.nlm.nih.gov/30506403
Autor:
Imen Boussaid, Ramzi Zemni, Ines Slim, Foued Slama, Elyes Chabchoub, Asma Boumiza, Latifa Gueddah
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 30
Background:Enteroviral infections have long been suspected in having a role in β cell destruction and therefore leading to the onset of clinical type 1 diabetes (T1D). The frequency of enterovirus (EV)-related T1D in North Africa is still unknown. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a21222e346f1477b829b67c4b3d42af4
https://doi.org/10.1515/jpem-2017-0044
https://doi.org/10.1515/jpem-2017-0044
Publikováno v:
Journal of Genetics. 90:303-307
Coronary heart disease (CHD) is now the leading cause ofdeath worldwide: each year, 3.8 million men and 3.4 millionwomen die from CHD (World Health Organization 2008).The main causal risk factors of CHD include hypertension,dyslipidemia, diabetes mel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c4d8621fea355cf7e4df792b0798446
https://doi.org/10.1007/s12041-011-0058-x
https://doi.org/10.1007/s12041-011-0058-x
Autor:
Ramzi Zemni, Neila Belguith, Dorsaf Moalla, Nacim Louhichi, Faiza Fakhfakh, Chahnez Triki, Nourhene Fendri-Kriaa, Emna Mkaouar-Rebai, Foued Slama
Publikováno v:
Journal of Child Neurology. 25:1042-1046
Rett syndrome is a severe disorder characterized by loss of acquired skills after a period of normal development in infant girls. It is caused mainly by mutations in the MECP2 gene. In this study, we reported mutations in the MECP2 gene in 7 Tunisian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c8a935d23f3fb8002fbe6ec26cf760c
https://doi.org/10.1177/0883073809356353
https://doi.org/10.1177/0883073809356353