Endoscopic Retrograde Cholangiopancreatography on Pediatric Patients: Experience of a Portuguese Adult Gastroenterology Department.

Autor: Saraiva, Rita Ornelas, Borges, Verónica Pavão, Silva, Mário Jorge, Loureiro, Rafaela, Capela, Tiago, Ramos, Gonçalo, Canena, Jorge, Mateus Dias, António, Alves, Rui, Coimbra, João

Publikováno v: GE Portuguese Journal of Gastroenterology; 2024, Vol. 31 Issue 2, p110-115, 6p

Exploratory research about playing styles and performance patterns in football teams

Autor: Ramos, Gonçalo Ribeiro

Dissertation presented as the partial requirement for obtaining a Master's degree in Statistics and Information Management, specialization in Marketing Research and CRM The sports industry has grown exponentially over the years and is becoming an inc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1437::52bd6d5b06e781778f122a1d34d4c3c4
https://hdl.handle.net/10362/149106

A multidisciplinary approach in complicated acute pancreatitis

Autor: Paulino, Jorge, Ramos, Gonçalo, Gomes, Filipe Veloso

Publisher Copyright: © 2019 by the authors. Licensee MDPI, Basel, Switzerland. Acute pancreatitis (AP) is an inflammatory condition with a mild course in most patients, but 20–30% evolve to single or multiple organ dysfunction and pancreatic/perip

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1437::3eea3653c5cf89d5a33130cf07340205
https://hdl.handle.net/10362/124964

Bevacizumab for Refractory Gastrointestinal Bleeding in Rendu-Osler-Weber Disease

Autor: Bernardes, Carlos, Santos, Sara, Loureiro, Rafaela, Borges, Verónica, Ramos, Gonçalo

Publikováno v: GE-Portuguese Journal of Gastroenterology v.25 n.2 2018
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
GE-Portuguese Journal of Gastroenterology, Volume: 25, Issue: 2, Pages: 91-95, Published: APR 2018

Rendu-Osler-Weber disease, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant disorder which is often characterized by recurrent epistaxis, mucocutaneous and gastrointestinal telangiectasias, and visceral arteriovenous

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9efa74bde415c3977d12ff4a72e5c883
http://www.scielo.mec.pt/scielo.php?script=sci_arttext&pid=S2341-45452018000200009

O estatuto do muçulmano na Modernidade: na génese de um modelo identitário contemporâneo (estudo de história comparada das representaçÕes).

Autor: Ramos, Gonçalo Matos¹

Publikováno v: Revista da Faculdade de Letras: História. 2014, Vol. 4, p157-166. 10p.