Zobrazeno 1 - 10
of 40
pro vyhledávání: '"N Bel Feki"'
Autor:
I Ben Ghorbel, N Bel Feki, T Ben Salem, A Hamzaoui, M Khanfir, M Lamloum, M Miled, M H Houman
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 26, Iss 2, Pp 359-362 (2015)
The association between microscopic polyangiitis (MPA) and primary biliary cirrhosis (PBC) has seldom been reported. We describe here a patient who presented with sensorimotor neuropathy along with hypothyroidism, renal failure and liver dysfunction.
Externí odkaz:
https://doaj.org/article/7e89f50846cd4241913836fea85a970e
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 26, Iss 1, Pp 132-134 (2015)
Behcet′s disease (BD) is a multisystem vasculitis with protean manifestations. It is characterized by a heightened state of inflammation, although the factors that initiate and sustain this inflammation are not clear. We report some cases of BD-ass
Externí odkaz:
https://doaj.org/article/af0b00f9c3d946e08f790978745c5360
Autor:
M.H. Houman, N. Bel Feki
Publikováno v:
La Revue de Médecine Interne. 35:90-96
Although the precise pathogenesis and etiology of Behcet's disease (BD) still remains unknown, current evidence suggests that inflammatory reaction in BD arises from disruption of homeostasis in genetically susceptible individuals, resulting in alter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f63367e5bb06d1d013ac2a86c8d9c39
https://doi.org/10.1016/j.revmed.2013.10.012
https://doi.org/10.1016/j.revmed.2013.10.012
Publikováno v:
Journal des maladies vasculaires. 41(6)
Summary The lupus anticoagulant-hypoprothrombinemia syndrome (LA-HPS) – the association of acquired factor II deficiency and lupus anticoagulant – is a rare disease that may cause a predisposition not only to thrombosis but also to severe bleedin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c009b51046f03017f294c4178468c90a
https://pubmed.ncbi.nlm.nih.gov/27743753
https://pubmed.ncbi.nlm.nih.gov/27743753
Publikováno v:
La Revue de Médecine Interne. 37:A159-A160
Introduction Le syndrome de Gougerot Sjogren (SGS) est une maladie auto-immune caracterisee par une triade associant fatigue, douleurs et secheresse. L’objectif de notre etude etait de determiner le profil epidemiologique, clinique, biologique, rad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcadbb74aa43ef0d9c7f73c8bc630de6
https://doi.org/10.1016/j.revmed.2016.10.177
https://doi.org/10.1016/j.revmed.2016.10.177
Autor:
T. Ben Salem, I. Ben Ghorbel, M.H. Houman, M. Lamloum, W. Bensalem, A. Hamzaoui, F. Said, M. Khanfir, N. Bel Feki
Publikováno v:
La Revue de Médecine Interne. 36:A158-A159
Introduction Les manifestations cliniques de la sarcoidose sont variees. L’atteinte neurologique est rapportee dans 5 a 10 % des cas. L’objectif de notre etude etait de decrire les manifestations cliniques et radiologiques de la neurosarcoidose a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbb38e55ffc7e8d1ae977073e17a40d5
https://doi.org/10.1016/j.revmed.2015.03.180
https://doi.org/10.1016/j.revmed.2015.03.180
Autor:
M H, Houman, N, Bel Feki
Publikováno v:
La Revue de medecine interne. 35(2)
Although the precise pathogenesis and etiology of Behçet's disease (BD) still remains unknown, current evidence suggests that inflammatory reaction in BD arises from disruption of homeostasis in genetically susceptible individuals, resulting in alte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3fbe5462dceba59d0a941dd4b696dc95
https://pubmed.ncbi.nlm.nih.gov/24210264
https://pubmed.ncbi.nlm.nih.gov/24210264
Autor:
A, Hamzaoui, N, Bel Feki, A, Brahem Sfaxi, M, Smiti Khanfir, I, Ben Ghorbel, M, Lamloum, M H, Houman
Publikováno v:
Clinical and experimental rheumatology. 30(3 Suppl 72)
Behçet's disease (BD) is a systemic inflammatory disease having a chronic and prolonged course with 4 major symptoms: oral and genital ulcerations, eye disease and cutaneous manifestations, as well as other multisystem involvements. Arterial involve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7c1647df8f518d677b7689333564b8dc
https://pubmed.ncbi.nlm.nih.gov/23043972
https://pubmed.ncbi.nlm.nih.gov/23043972
Publikováno v:
Annales d'Endocrinologie. 75:509-510
Syndrome auto-immun multiple (SAM), entite rare, traduit un trouble de regulation de la reponse immunitaire sur un terrain genetique particulier. Nous rapportons l’observation d’une patiente presentant un SAM et discutons les particularites epide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a1460efcfd28613ab71044eba58e047
https://doi.org/10.1016/j.ando.2014.07.818
https://doi.org/10.1016/j.ando.2014.07.818
Autor:
M. Lamloum, Y. Saïid, A. Hamzaoui, Mohamed Miled, T. Ben Salem, N. Bel Feki, I. Ben Ghorbel, M.H. Houman
Publikováno v:
La Revue de Médecine Interne. 34:A133-A134
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1df3f35cb26a23329fab9c8e0726f18d
https://doi.org/10.1016/j.revmed.2013.03.112
https://doi.org/10.1016/j.revmed.2013.03.112