Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Olfa, Khayat"'
Autor:
Cherine Charfeddine, Nadia Laroussi, Rahma Mkaouar, Raja Jouini, Olfa Khayat, Aladin Redissi, Amor Mosbah, Hamza Dallali, Achraf Chedly Debbiche, Anissa Zaouak, Sami Fenniche, Sonia Abdelhak, Houda Hammami-Ghorbel
Publikováno v:
PLoS ONE, Vol 16, Iss 10 (2021)
Erythrokeratodermia variabilis (EKV) is a rare disorder of cornification usually associated with dominant mutations in the GJB3 and GJB4 genes encoding connexins (Cx)31 and 30.3. Genetic heterogeneity of EKV has already been suggested. We investigate
Externí odkaz:
https://doaj.org/article/5567076a693f4cf28b9af24a2bae6cf6
Autor:
Leila Bouhajja, Raja Jouini, Olfa Khayat, Wafa Koubâa, Chiraz Mbarek, Ehsen Ben Brahim, Achraf Chedly-Debbiche
Publikováno v:
Case Reports in Otolaryngology, Vol 2017 (2017)
Intranodal palisaded myofibroblastoma (IPM), also known as “intranodal hemorrhagic spindle cell tumor with amianthoid fibers,” is a rare benign mesenchymal tumor originating from smooth muscle cells and myofibroblasts, often with the presence of
Externí odkaz:
https://doaj.org/article/e55e12e687234f488d35a323fc417abd
Autor:
Salsabil Attafi Sehli, Mariem Bel Haj Salah, Ines Smichi, Wafa Koubaa, Olfa Khayat, Aschraf Chadli Debbiche
Publikováno v:
Nasza Dermatologia Online, Vol 6, Iss 2, Pp 170-172 (2015)
Elastofibroma dorsi is a rare soft tissue pseudotumor, slow-growing, sitting in 99% of cases at the subscapular region and occurring in the elderly active people. Its pathogenesis is unclear. It is often asymptomatic. However, the diagnosis can be ma
Externí odkaz:
https://doaj.org/article/8f6fd5bd3153468ea93ffdb4a14914b4
Autor:
Anissa Zaouak, Hamza Dallali, Houda Hammami-Ghorbel, Amor Mosbah, Sonia Abdelhak, S. Fenniche, Cherine Charfeddine, Olfa Khayat, Nadia Laroussi, Achraf Chedly Debbiche, Aladin Redissi, Rahma Mkaouar, Raja Jouini
Publikováno v:
PLoS ONE, Vol 16, Iss 10 (2021)
PLoS ONE, Vol 16, Iss 10, p e0258777 (2021)
PLoS ONE
PLoS ONE, Vol 16, Iss 10, p e0258777 (2021)
PLoS ONE
Erythrokeratodermia variabilis (EKV) is a rare disorder of cornification usually associated with dominant mutations in the GJB3 and GJB4 genes encoding connexins (Cx)31 and 30.3. Genetic heterogeneity of EKV has already been suggested. We investigate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::873b5d0f9dfbdfc55c4459bcdcc01832
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528321/?tool=EBI
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528321/?tool=EBI
Publikováno v:
Nasza Dermatologia Online, Vol 6, Iss 2, Pp 356-357 (2015)
Externí odkaz:
https://doaj.org/article/f5533dde43bb4c08af53422f74a6bbff
Autor:
Salsabil Attafi Sehli, Mariem Bel Haj Salah, Olfa Khayat, Ines Smichi, Aschraf Chadli Debbiche
Publikováno v:
Nasza Dermatologia Online, Vol 6, Iss 2, Pp 244-245 (2015)
Externí odkaz:
https://doaj.org/article/2aea666f26154e8c80534924d2e9180d
Autor:
Fatma Khanchel, Olfa Khayat, Samy Fenniche, Houda Hammami, Ehsen Ben Brahim, Anissa Zaouak, Azima Ben Tanfous, Hafsa Touati
Publikováno v:
International Journal of Dermatology. 61:46-47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94d885e64cad568481fe3d343146ebac
https://doi.org/10.1111/ijd.15745
https://doi.org/10.1111/ijd.15745
Autor:
Raja, Jouini, Raoueh, Hedhli, Fatma, Khanchel, Mèriem, Sabbah, Dorra, Trad, Imen, Hlel, Wafa, Koubaa, Olfa, Khayat, Ehsen, Ben Brahim, Achraf Chadli, Debbiche
Publikováno v:
La Tunisie medicale. 97(12)
Anguillulosis is a ubiquitous digestive parasitosis. Rare in Tunisia, it is due to a round worm, strongyloid stercoralis, whose natural lodging is the duodeno-jejunal mucosa. Its malignant form is rare but it represents a potentially life-threatening
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fd49518ecb5e61fe3469679c542a0978
https://pubmed.ncbi.nlm.nih.gov/32173814
https://pubmed.ncbi.nlm.nih.gov/32173814
Autor:
Ehsen Ben Brahim, Leila Bouhajja, Achraf Chedly-Debbiche, Chiraz Mbarek, Raja Jouini, W. Koubâa, Olfa Khayat
Publikováno v:
Case Reports in Otolaryngology, Vol 2017 (2017)
Case Reports in Otolaryngology
Case Reports in Otolaryngology
Intranodal palisaded myofibroblastoma (IPM), also known as “intranodal hemorrhagic spindle cell tumor with amianthoid fibers,” is a rare benign mesenchymal tumor originating from smooth muscle cells and myofibroblasts, often with the presence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2052f949f3279aeb07b6d2cc5192a32
https://doi.org/10.1155/2017/7121485
https://doi.org/10.1155/2017/7121485
Autor:
Mar Llamas-Velasco, Fatma Khanchel, Olfa Khayat, Talel Badri, Ehsen Ben Brahim, Imen Helel, Thomas Mentzel, Aschraf Chadli, Raja Jouini, Wafa Koubaa Mahjoub
Publikováno v:
Journal of cutaneous pathology. 46(3)
Neuroblastoma-like schwannoma (NLS) is a rare variant of a common tumor. The aim of this study is to discuss, through a literature review, the differential diagnoses of NLS while emphasizing the importance of ancillary studies. So far, 24 cases have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecee04567efddba14d6e232fad6d43e6
https://pubmed.ncbi.nlm.nih.gov/30582192
https://pubmed.ncbi.nlm.nih.gov/30582192