Výsledky vyhledávání - "Ghazi Chabchoub"

A 20year history of clinical and genetic study of thyroid autoimmunity in a Tunisian multigenerational family: Evidence for gene interaction

Autor: Noura Bougacha-Elleuch, Nadia Charfi, Mohamed Abid, Maha Kammoun-Krichen, Ghazi Chabchoub, Salima Belguith-Maalej, Fatma Ayadi, Najla Kharrat, Hammadi Ayadi, Abdellatif Maalej, Mouna Mnif, Ahmed Rebai

Publikováno v: Meta Gene

Autoimmune thyroid diseases (AITD), which include Hashimoto thyroiditis (HT), Graves' disease (GD) and primary idiopathic myxoedema (PIM), are recognized by their clinical and genetic heterogeneity. In this study, we have carried on a global approach

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Association study of CARD8 (p.C10X) and NLRP3 (p.Q705K) variants with rheumatoid arthritis in French and Tunisian populations

Autor: Elisabeth Petit-Teixeira, Ghazi Chabchoub, M. Ben Hamad, Ahmed Rebai, Zouhir Bahloul, Sameh Marzouk, Abdellatif Maalej, H. Ayadi, Faiza Fakhfakh, François Cornelis

Publikováno v: International Journal of Immunogenetics. 39:131-136

The objective of the study was to investigate the association of caspase activating and recruitment domain 8 (CARD8) and nucleotide-binding oligomerization domain, leucine-rich repeat and pyrin domain containing 3 (NLRP3) polymorphisms with rheumatoi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::27d64a3d39224abd1bd365d3318fbe9e
https://doi.org/10.1111/j.1744-313x.2011.01070.x

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The first genome-wide scan in a tunisian family with generalized epilepsy with febrile seizure plus (GEFS+)

Autor: Fatma Kammoun, Ahmed Rebai, Chahnez Triki, Nourhene Fendri-Kriaa, Emna Mkaouar-Rebai, Ghazi Chabchoub, Faiza Fakhfakh, Nacim Louhichi, Ikhlass Hadj Salem

Publikováno v: Journal of child neurology. 25(11)

Generalized epilepsy with febrile seizure plus (GEFS+) is an autosomal dominant disorder. In the literature, 5 responsible genes were identified and 2 novel susceptibility loci for GEFS+ at 2p24 and 8p23-p21 were reported, indicating the genetic hete

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c94c91fa4c810c01507d4aa0e532e5ff
https://pubmed.ncbi.nlm.nih.gov/20382841

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Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases

Autor: Chigdem A. Mustafa, Mouna Mnif, Abdellatif Maalej, Tayfun Ozcelik, Zouheir Bahloul, Elif Uz, Hammadi Ayadi, Nadir R. Farid, Ghazi Chabchoub, Ahmed Rebai

Publikováno v: Arthritis Research and Therapy
Arthritis Research & Therapy
Chabchoub, G, Uz, E, Maalej, A, Mustafa, C A, Rebai, A, Mnif, M, Bahloul, Z, Farid, N R, Ozcelik, T & Ayadi, H 2009, ' Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases ', Arthritis Research and Therapy, vol. 11, no. 4 . https://doi.org/10.1186/ar2759

IntroductionThe majority of autoimmune diseases such as rheumatoid arthritis (RA) and autoimmune thyroid diseases (AITDs) are characterized by a striking female predominance superimposed on a predisposing genetic background. The role of extremely ske

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a72954e4d7c42b368f3b8510ba5eb2b
https://hdl.handle.net/11693/22696

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The R620W Polymorphism of the Protein Tyrosine Phosphatase 22 Gene in Autoimmune Thyroid Diseases and Rheumatoid Arthritis in the Tunisian Population

Autor: Hammadi Ayadi, Abdellatif Maalej, François Cornelis, Zouheir Bahloul, Mariem Ben Hamad, Elisabeth Petit Teixiera, Ghazi Chabchoub

Publikováno v: Annals of Human Biology
Annals of Human Biology, 2009, 36 (3), pp.342--349. ⟨10.1080/03014460902817968⟩

International audience; Background: Protein tyrosine phosphatase (PTPN22) is involved in the negative regulation of T-cell responsiveness. The association of a coding variant of the PTPN22 gene (R620W) with a number of autoimmune diseases has been de

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3db83ea66e78a07b2b9c929eff9fb2a8
https://hal.archives-ouvertes.fr/hal-02084392

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Lack of association of VDR gene polymorphisms with thyroid autoimmune disorders: familial and case/control studies

Autor: Nadir R. Farid, Ghazi Chabchoub, Abdellatif Maalej, Ahmed Rebai, Mariam Ben Hamad, Hammadi Ayadi, François Cornélis, Elisabeth Petit-Teixeira

Publikováno v: Journal of Clinical Immunology
Journal of Clinical Immunology, 2008, 28 (1), pp.21--25. ⟨10.1007/s10875-007-9124-9⟩
Journal of Clinical Immunology, Springer Verlag, 2008, 28 (1), pp.21--25. ⟨10.1007/s10875-007-9124-9⟩

International audience; We study the association between three Vitamin D receptor gene polymorphisms (rs10735810, rs1544410, rs731236) and susceptibility to thyroid autoimmune diseases. Seventy-six affected subjects, belonging to a large family, as w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93cca5f246f45cf6cf93191ec335c391
https://pubmed.ncbi.nlm.nih.gov/17943423

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