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pro vyhledávání: '"Olfa, Hallara"'
Autor:
Olfa Hallara, Labiba Adala, Ali Saad, Lamia Golli, Klaus Brusgaard, Wiem Manoubi, Mahdi Ksiaa, Moez Gribaa, Fahmi Hmila, Lilian Bomme Ousager, Rihab Ben Seghaier, Yosra Halleb, Ameni Kdissa
Publikováno v:
Kdissa, A, Brusgaard, K, Ksiaa, M, Golli, L, Hallara, O, Ousager, L B, Manoubi, W, Seghaier, R B, Adala, L, Halleb, Y, Saad, A, Hmila, F & Gribaa, M 2020, ' c.1227_1228dupGG (p.Glu410Glyfs), a frequent variant in Tunisian patients with MUTYH associated polyposis ', Cancer genetics and cytogenetics, vol. 240, pp. 45-53 . https://doi.org/10.1016/j.cancergen.2019.10.007
INTRODUCTION: Familial adenomatous polyposis (FAP) is an autosomal dominant-inherited disease caused by germline variants in the APC gene. It is characterized by the development of hundreds to thousands of adenomatous polyps in colon and rectum. Rece
Autor:
Soumaya, Mrabet, Olfa, Hallara, Hichem, Loghmari, Wafa, Ben Mansour, Wided, Bouhlel, Leila, Safer
Publikováno v:
La Tunisie medicale. 96(1)
The primary squamous cell carcinoma of the rectum is a rare tumor that presents epidemiological, etiopathogenic and evolutionary characteristics different from those of adenocarcinoma . We report the case of a primary squamous cell carcinoma well dif