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TITLE: The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families. Portuguese MSH2 founder mutation  Full Text
AUTHORS: Pinheiro, M; Pinto, C; Peixoto, A; Veiga, I; Mesquita, B; Henrique, R ; Lopes, P; Sousa, O; Fragoso, M; Dias, LM ; Baptista, M; Marinho, C; Mangold, E; Vaccaro, C; Evans, DG; Farrington, S; Dunlop, MG; Teixeira, MR ;
PUBLISHED: 2013, SOURCE: CLINICAL GENETICS, VOLUME: 84, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 13
15
TITLE: Endoscopic submucosal dissection of solitary duodenal somatostatinoma  Full Text
AUTHORS: Ines Marques; Mario Dinis Ribeiro ; Pedro Pimentel Nunes ; Antonio Pereira Coutinho; Analisa Ribeiro; Luis Afonso; Margarida Caldas; Luis Moreira Dias ; Beatriz Costa Neves;
PUBLISHED: 2012, SOURCE: GASTROINTESTINAL ENDOSCOPY, VOLUME: 76, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 1
16
TITLE: Increased hepatic expression of TLR2 and TLR4 in the hepatic inflammation-fibrosis-carcinoma sequence
AUTHORS: Soares, JB; Pimentel Nunes, P ; Afonso, L; Rolanda, C ; Lopes, P; Roncon Albuquerque, R ; Goncalves, N ; Boal Carvalho, I; Pardal, F; Lopes, S; Macedo, G ; Lara Santos, L ; Henrique, R ; Moreira Dias, L ; Goncalves, R; Dinis Ribeiro, M ; Leite Moreira, AF ;
PUBLISHED: 2012, SOURCE: INNATE IMMUNITY, VOLUME: 18, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 51 Handle
17
TITLE: Tracheobronchial Polyflex stents for the management of benign refractory hypopharyngeal strictures  Full Text
AUTHORS: Rui Almeida Silva ; Nuno Mesquita; Pedro Pimentel Nunes ; Elisabete Cardoso; Ricardo Marcos Pinto ; Luis Moreira Dias ;
PUBLISHED: 2012, SOURCE: WORLD JOURNAL OF GASTROENTEROLOGY, VOLUME: 18, ISSUE: 6
INDEXED IN: Scopus WOS CrossRef: 2
18
TITLE: Use of cardiac septal occluder device on upper GI anastomotic dehiscences: a new endoscopic approach  Full Text
AUTHORS: Elisabete Cardoso; Rui Almeida Silva ; Luis Moreira Dias ;
PUBLISHED: 2012, SOURCE: GASTROINTESTINAL ENDOSCOPY, VOLUME: 76, ISSUE: 6
INDEXED IN: Scopus WOS CrossRef
19
TITLE: A novel exonic rearrangement affecting MLH1 and the contiguous LRRFIP2 is a founder mutation in Portuguese Lynch syndrome families
AUTHORS: Manuela Pinheiro; Carla Pinto; Ana Peixoto; Isabel Veiga; Barbara Mesquita; Rui Henrique ; Manuela Baptista; Maria Fragoso; Olga Sousa; Helena Pereira; Carla Marinho; Luis Moreira Dias ; Manuel R Teixeira ;
PUBLISHED: 2011, SOURCE: GENETICS IN MEDICINE, VOLUME: 13, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef: 21
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