Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Achraf Chedly-Debbiche"'
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:
Mohamed Moncef Hamdane, Ehsen Ben Brahim, Mariam belhaj Salah, Nooman Haouas, Ahmed Bouhafa, Achraf Chedly-Debbiche
Publikováno v:
The Pan African Medical Journal, Vol 13, Iss 16 (2012)
Authors report the case of a 51-year-old man, presenting with epigastralgia of recent onset. Physical exam was unremarkable. Endoscopy revealed a large, ulcerated, submucosal, antral tumor. CT scan reveals an antral mass with fat attenuation. The pat
Externí odkaz:
https://doaj.org/article/e669f6d66e4c463987ed18dd02f13ac3
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
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:
Olfa, Khayat, Afef, Kilani, Achraf, Chedly-Debbiche, Abdelfattah, Zeddini, Dalila, Gargouri, Jamel, Kharrat, Adnene, Souissi, Abdel Jabbar, Ghorbel, Mohamed, Ben Ayed, Habib, Ben Khelifa
Publikováno v:
La Tunisie medicale. 84(6)
It's a prospective study leaded between September 1997 and july 1999 (23 months ) in 75 patients with duodenal ulcer and positif for Helicobacter pylori. All patients had a first endoscopy with antral, fundic and duodenal biopsies, followed one month
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5865e3724d25b4124260c3601a9b9ffb
https://pubmed.ncbi.nlm.nih.gov/17042205
https://pubmed.ncbi.nlm.nih.gov/17042205
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