Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Monia, Smiti Khanfir"'
Autor:
Amira, Gabsi, Akram, Dlala, Fadoua, Missaoui, Bilel, Neili, Alya, Boutaba, Khalil, Ben salem, Monia, Smiti Khanfir, Fatma, Said, Habib, Houman Mohamed, Nathalie, Bardin, Raja, Triki Marrakchi
Publikováno v:
In La Presse Médicale March 2024 53(1)
Publikováno v:
The Pan African Medical Journal, Vol 23, Iss 149 (2016)
La panniculite est une manifestation rare au cours des dermatomyosites (DM). L'apparition d'une panniculite au cours d'un traitement par du méthotrexate (MTX) est exceptionnelle et n'a été décrite que dans 3 cas. Nous rapportons l'observation d'u
Externí odkaz:
https://doaj.org/article/12dc41dcde154c4f984593376fd907a6
Autor:
Amira Hamzaoui, Fatima Jaziri, Thouraya Ben Salem, Fatma Said Imed Ben Ghorbel, Mounir Lamloum, Monia Smiti Khanfir, Habib Houman Mohamed
Publikováno v:
Acta Medica Iranica, Vol 52, Iss 10 (2014)
Behcet's disease (BD) is a multisystemic inflammatory disease that occurs most often between the second and fourth decade of life. Patients have been reported during the first months of life and after 70 years. Our objective was to determine the clin
Externí odkaz:
https://doaj.org/article/4cf74552c2eb40d3a0ce1c90ffbfbb6c
Publikováno v:
La Presse Médicale. 37:e25-e35
Key points Behcet disease is a multisystem inflammatory disorder, the cause of which remains unclear. Vasculitis is its predominant histopathological feature. It remains a source of significant morbidity in affected patients, many of whom become blin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44b8b7324da8f84843b2f1557d889220
https://doi.org/10.1016/j.lpm.2007.03.037
https://doi.org/10.1016/j.lpm.2007.03.037
Autor:
Monia Smiti-Khanfir, Amira Hamzaoui, Thouraya Ben Salem, Mohamed Habib Houman, F. Said, Nabil Bel Feki, M. Lamloum, Imed Ben Ghorbel
Publikováno v:
International Journal of Clinical Case Reports.
Pyoderma gangrenosum occurrence in a familial pattern is extremely rare. We report pyoderma gangrenosum in two Tunisian siblings with onset respectively at 28 and 26 years old. The initial lesion was a pustule that breaks down to form an ulcer with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::352fb45572b5e0a92ed11eb5ba782fac
https://doi.org/10.5376/ijccr.2015.05.0050
https://doi.org/10.5376/ijccr.2015.05.0050
Autor:
Monia Smiti Khanfir, Moncef Feki, Kamel Hamzaoui, Imed Ben Ghorbal, Habib Houman, Agnes Hamzaoui
Publikováno v:
Mediators of Inflammation, Vol 13, Iss 4, Pp 247-253 (2004)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::e62d90e998c01c1dd77aa372714cff2a
https://doaj.org/article/74a73a2fc6e542ce906f3242f14318c7
https://doaj.org/article/74a73a2fc6e542ce906f3242f14318c7
Autor:
Melika Ben Ahmed, Nadia Belhadj Hmida, Mohamed Habib Houman, Maha Abdeladhim, Monia Smiti-Khanfir, Nadine Cerf-Bensussan, Asma Elbeldi-Ferchiou, Hechmi Louzir
Publikováno v:
Journal of Clinical Immunology
Journal of Clinical Immunology, Springer Verlag, 2011, epub ahead of print. ⟨10.1007/s10875-011-9531-9⟩
Journal of Clinical Immunology, Springer Verlag, 2011, epub ahead of print. 〈10.1007/s10875-011-9531-9〉
Journal of Clinical Immunology, Springer Verlag, 2011, epub ahead of print. ⟨10.1007/s10875-011-9531-9⟩
Journal of Clinical Immunology, Springer Verlag, 2011, epub ahead of print. 〈10.1007/s10875-011-9531-9〉
International audience; BACKGROUND: The mechanisms underlying the loss of self-tolerance in systemic lupus erythematosus (SLE) are incompletely deciphered. TGF-β plays a key role in self-tolerance demonstrated by the onset of a fatal autoimmune synd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79ebe0aa4a2f2c35f528b81afbcaf374
https://hal-riip.archives-ouvertes.fr/pasteur-00606434
https://hal-riip.archives-ouvertes.fr/pasteur-00606434
Autor:
Monia Smiti, Khanfir, Imene, Ben Hafsa, Hajer, Neffati, Imed, Ben Ghorbel, Monunir, Lamloum, Mohamed H, Houman
Publikováno v:
Presse medicale (Paris, France : 1983). 37(9)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6cdf571b29ec18cf58ab205c68a9e657
https://pubmed.ncbi.nlm.nih.gov/18424061
https://pubmed.ncbi.nlm.nih.gov/18424061
Publikováno v:
Presse medicale (Paris, France : 1983). 37(2 Pt 2)
Behçet disease is a multisystem inflammatory disorder, the cause of which remains unclear. Vasculitis is its predominant histopathological feature. It remains a source of significant morbidity in affected patients, many of whom become blind. Treatme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::661c9e2e388bd636a6c2c4d86770433c
https://pubmed.ncbi.nlm.nih.gov/17544613
https://pubmed.ncbi.nlm.nih.gov/17544613
Autor:
Kamel Hamzaoui, Mehdi Ghannouchi, Neziha Kaabachi, Abderraouf Mebazaa, Moncef Feki, Habib Houman, Leila El Matri, Monia Smiti-Khanfir
Publikováno v:
Clinical chemistry and laboratory medicine. 42(12)
Plasma homocysteine was assessed in Behcet's disease (BD) patients in order to determine the prevalence of hyperhomocysteinaemia in BD and to test its association with clinical manifestations of the disease. The study included 59 patients with BD and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f085beff0f3277d3e045aa84695deb37
https://pubmed.ncbi.nlm.nih.gov/15576305
https://pubmed.ncbi.nlm.nih.gov/15576305