Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nedia Hentati"'
Autor:
Nadia Kolsi, Fatma Boudaya, Afef Ben Thabet, Manel Charfi, Chiraz Regaieg, Amira Bouraoui, Ridha Regaieg, Nedia Hentati, Amel Ben Hamed, Abdellatif Gargouri
Publikováno v:
Clinical Case Reports, Vol 10, Iss 12, Pp n/a-n/a (2022)
Abstract Treacher Collins syndrome (TCS) is one of the rare genetic syndromes which is specified by symmetrical craniofacial dysmorphism without growth abnormalities or neurological disorders. The inheritance is usually autosomal dominant but sometim
Externí odkaz:
https://doaj.org/article/96a7fa1144504c9ab5c91a3806340fe5
Autor:
Sahar Chakroun, Sana Ben Jemaa, Nadia Kolsi, Hela Zouari, Abdellatif Gargouri, Nedia Hentati, Kaouthar Masmoudi
Publikováno v:
Clinical Neurophysiology. 150:e113-e114
Autor:
Taycir Cheikhrouhou, Ben Dhaou Mahdi, chtourou rahma, Regaieg Chiraz, Manar Hbaieb, Afef Ben Thabet, zouari Mohamed, nedia Hentati, Riadh Mhiri
Total persistent omphalomesenteric canal as a cause of small-bowel obstruction is an exceptional finding. A neonate presented with occlusion due to volvulus of the small bowel around a total persistent omphalomesenteric canal. Remnants of the duct we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5426f44b509560407d67d1139dba0cf
https://doi.org/10.22541/au.167047934.48840301/v1
https://doi.org/10.22541/au.167047934.48840301/v1
Autor:
Sahar Chakroun, Sana Ben Jemaa, Nadia Kolsi, Hela Zouari, Abdellatif Gargouri, Nedia Hentati, Kaouthar Masmoudi
Publikováno v:
Clinical Neurophysiology. 150:e113
Autor:
Sahar Chakroun, Sana Benjemaa, Nadia Kolsi, Nedia Hentati, Hela Zouari, Kaouthar Masmoudi, Abdellatif Gargouri
Publikováno v:
Revue Neurologique. 178:S30