Zobrazeno 1 - 10
of 593
pro vyhledávání: '"I, Ben Ghorbel"'
Autor:
A. Kefi, F. Said, T. Ben Salem, M. Khedher, M. Khanfir, I. Ben Ghorbel, M. Lamloum, M.H. Houman
Publikováno v:
Reumatismo, Vol 69, Iss 3, Pp 122-125 (2017)
Susac syndrome is a rare disease characterized by the clinical triad of encephalopathy, branch retinal artery occlusion, and sensorineural hearing loss. This underdiagnosed condition needs to be considered in the differential diagnosis of a broad var
Externí odkaz:
https://doaj.org/article/ba052314ab674556b7d71c1e434ee169
Publikováno v:
Reumatismo, Vol 69, Iss 1, Pp 23-29 (2017)
Granulomatosis with polyangiitis (GPA) is more frequent in Northern rather than Southern countries. Very few studies have been conducted in Africa. We have performed a retrospective descriptive study including clinical and laboratory profiles of 30 T
Externí odkaz:
https://doaj.org/article/19c79249f3d240c9877dea5058a497ae
Autor:
N. Belfeki, M. Smiti Khanfir, F. Said, A. Hamzaoui, T. Ben Salem, I. Ben Ghorbel, M. Lamloum, M.H. Houman
Publikováno v:
Reumatismo, Vol 68, Iss 3, Pp 159-162 (2016)
Adult-onset Still’s disease (AOSD) is an uncommon inflammatory condition of unknown origin. In chronic disease, joint involvement is often predominant and erosions are noted in one third of patients. Therapeutic strategies derive from observational
Externí odkaz:
https://doaj.org/article/326d9544725e487197d03ccbf67a7c53
Publikováno v:
Reumatismo, Vol 68, Iss 3, Pp 148-153 (2016)
Behçet’s disease (BD) is a multisystem inflammatory disorder. Intracardiac thrombus (ICT) formation is an uncommon but important complication of BD. Of the cases of Behçet’s disease, we selected those with ICT. All patients fulfilled the diagno
Externí odkaz:
https://doaj.org/article/ba43b31f58104571ab0dbcf988a7f586
Autor:
M. S. Khanfir, N. Belfeki, F. Said, T. Ben Salem, I. Ben Ghorbel, M. Lamloum, A. Hamzaoui, M. H. Houman
Publikováno v:
Reumatismo, Vol 67, Iss 4, Pp 156-160 (2016)
Inflammatory optic neuropathy (ON) is a rare event in Behçet’s disease (BD). We report herein a series of ten BD Tunisian patients with ON and describe its clinical features among them. A retrospective review of BD patients (International Study Gr
Externí odkaz:
https://doaj.org/article/fde9f689fcf14056b81809e98d5b24ef
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:
H. Abida, I. Naceur, T. Ben Achour, M. Khanfir, I. Ben Ghorbel, M. Lamloum, F. Said, M.H. Houman
Publikováno v:
La Revue de Médecine Interne. 43:A455-A456
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fac4ba76d492ecb5b3969efa2e8d9379
https://doi.org/10.1016/j.revmed.2022.10.217
https://doi.org/10.1016/j.revmed.2022.10.217
Autor:
H. Abida, T. Ben Achour, I. Naceur, M. Khanfir, I. Ben Ghorbel, M. Lamloum, F. Said, M.H. Houman
Publikováno v:
La Revue de Médecine Interne. 43:A514-A515
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14d66c3c9127e3f86df8688b57d5c9bc
https://doi.org/10.1016/j.revmed.2022.10.305
https://doi.org/10.1016/j.revmed.2022.10.305
Autor:
A. Abid, I. Naceur, T. Ben Achour, A. Baya Chatti, M. Khanfir, I. Ben Ghorbel, M. Lamloum, F. Said, M.H. Houman
Publikováno v:
La Revue de Médecine Interne. 43:A492-A493
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11ec47de2b726748d08f88af143b71f2
https://doi.org/10.1016/j.revmed.2022.10.263
https://doi.org/10.1016/j.revmed.2022.10.263