Search Results - "Houman, M. H."

Management of Behçet disease: a systematic literature review for the European League Against Rheumatism evidence-based recommendations for the management of Behçet disease by Hatemi, G, Silman, A, Bang, D, Bodaghi, B, Chamberlain, A M, Gul, A, Houman, M H, Kötter, I, Olivieri, I, Salvarani, C, Sfikakis, P P, Siva, A, Stanford, M R, Stübiger, N, Yurdakul, S, Yazici, H

“…To present and analyse the literature sources regarding the management of Behçet disease (BD) identified during the systematic literature research, which…”
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Inflammatory optic neuropathy in Behçet's disease by Khanfir, M S, Belfeki, N, Said, F, Ben Salem, T, Ben Ghorbel, I, Lamloum, M, Hamzaoui, A, Houman, M H

“…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…”
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EULAR recommendations for the management of Behçet disease by Hatemi, G, Silman, A, Bang, D, Bodaghi, B, Chamberlain, A M, Gul, A, Houman, M H, Kötter, I, Olivieri, I, Salvarani, C, Sfikakis, P P, Siva, A, Stanford, M R, Stübiger, N, Yurdakul, S, Yazici, H

“…To develop evidence-based European League Against Rheumatism (EULAR) recommendations for the management of Behçet disease (BD) supplemented where necessary by…”
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Systemic lupus erythematosus in Tunisia: demographic and clinical analysis of 100 patients by Houman, M H, Smiti-Khanfir, M, Ghorbell, I Ben, Miled, M

“…There is a wide variationin the natural history of systemic lupus erythematosus(SLE) among different ethnic and geographicalgroups. Studies in Arabs are few…”
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Thrombophilia in systemic lupus erythematosus: A case-control study by Belfeki, N, Khanfir, M S, Said, F, Houman, M H

“…To investigate the thrombotic tendency in patients with systemic lupus erythematosus (SLE) by evaluating congenital and acquired abnormalities with an…”
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Ischemic Colitis Revealing Polyarteritis Nodosa by Amira, Hamzaoui, Litaiem, Noureddine, Khanfir Monia, Smiti, Ayadi, Sofiene, Nfoussi, Haifa, Mohamed Habib, Houman

“…Ischemic colitis is one of the most common intestinal ischemic injuries. It results from impaired perfusion of blood to the bowel and is rarely caused by…”
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Pathophysiology of Behçet's disease by Houman, M H, Bel Feki, N

“…Although the precise pathogenesis and etiology of Behçet's disease (BD) still remains unknown, current evidence suggests that inflammatory reaction in BD…”
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Intracardiac thrombus in Behçet's disease by Ben Ghorbel, I, Belfeki, N, Houman, M H

“…Behçet's disease (BD) is a multisystem inflammatory disorder. Intracardiac thrombus (ICT) formation is an uncommon but important complication of BD. Of the…”
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Deep vein thrombosis in Behçet's disease by Houman, M H, Ben Ghorbel, I, Khiari Ben Salah, I, Lamloum, M, Ben Ahmed, M, Miled, M

“…We aimed to describe the epidemiological and clinical aspects of deep vein thrombosis (DVT) in Behçet's disease (BD) and to determine the patients at high risk…”
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Successful treatment of refractory adult onset Still's disease with rituximab by Belfeki, N, Smiti Khanfir, M, Said, F, Hamzaoui, A, Ben Salem, T, Ben Ghorbel, I, Lamloum, M, Houman, M H

“…Adult-onset Still's disease (AOSD) is an uncommon inflammatory condition of unknown origin. In chronic disease, joint involvement is often predominant and…”
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Behçet's disease in Tunisia. Demographic, clinical and genetic aspects in 260 patients by Houman, M H, Neffati, H, Braham, A, Harzallah, O, Khanfir, M, Miled, M, Hamzaoui, K

“…To analyze demographic, clinical and genetic features of Behçet's disease (BD) in Tunisia and to compare them with other ethnic and geographic groups. Two…”
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Etiological profile of secondary Raynaud's phenomenon in an internal medicine department. About 121 patients by Ben Salem, T, Tougorti, M, Bziouech, S, Lamloum, M, Khanfir, M, Ben Ghorbel, I, Houman, M H

“…Raynaud's phenomenon is a reversible episodic vasospastic disorder triggered by cold or emotion. Two types of Raynaud's phenomenon were distinguished:…”
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Microscopic polyangiitis presenting with peripheral and central neurological manifestations by Sassi, S. Ben, Ghorbel, I. Ben, Mizouni, H., Houman, M. H., Hentati, F.

“…Although peripheral neuropathy is a common complication of microscopic angiitis, manifestations involving the muscle and the central nervous system have been…”
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Granulomatosis with polyangiitis in Tunisia by Ben Ghorbel, I, Belfeki, N, Baouendi, N, Ben Salem, T, Houman, M H

“…Granulomatosis with polyangiitis (GPA) is more frequent in Northern rather than Southern countries. Very few studies have been conducted in Africa. We have…”
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Headache in a young woman: do not forget Susac's syndrome by Kefi, A, Said, F, Ben Salem, T, Khedher, M, Khanfir, M, Ben Ghorbel, I, Lamloum, M, Houman, M H

“…Susac syndrome is a rare disease characterized by the clinical triad of encephalopathy, branch retinal artery occlusion, and sensorineural hearing loss. This…”
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Polymorphisms of the NOS3 gene in Tunisian patients with Behçet's disease by Kallel, A., Sbaï, M. H., Houman, M. H., Sediri, Y., Ouertani, D., Smiti Khanfir, M., Ben Ghorbel, I., Jemaa, R., Kaabachi, N.

“…Summary Behçet's disease (BD) is a multisystem inflammatory disease characterized by recurrent orogenital ulceration, ocular inflammation and skin lesions…”
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Microscopic polyangiitis associated with primary biliary cirrhosis, sjogren’s syndrome and hashimoto’s thyroiditis by Ghorbel, I. Ben, Feki, N. Bel, Bin Salim, T., Hamzawi, A., Khanfir, M., Lamloum, M., Miled, M., Houman, M. H.

“…The association between microscopic polyangiitis (MPA) and primary biliary cirrhosis (PBC) has seldom been reported. We describe here a patient who presented…”
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Chest pain in patients with undiagnosed Behçet's disease by Hamzaoui, A, Bel Feki, N, Brahem Sfaxi, A, Smiti Khanfir, M, Ben Ghorbel, I, Lamloum, M, Houman, M H

“…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…”
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Amyloidosis in behcet’s disease by Bil Fiki, N., Bin Salim, T., Lamloum, M., Houman, M. H., Bin Ghurbal, I.

“…Behcet’s disease (BD) is a multisystem vasculitis with protean manifestations. It is characterized by a heightened state of inflammation, although the factors…”
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Promising new therapies for Behcet's disease by Houman, M.H., Hamzaoui, K.

“…Improved understanding of the pathogenic mechanisms of Behcet's disease (BD), and especially of the molecular basis involved in its pathogenesis, has sparked a…”
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