Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Carmélia Rodrigues"'
Autor:
Isabel Tarrio, Marta Moreira, Tarcísio Araújo, Emília Guerreiro, Carmélia Rodrigues, Luís Lopes
Publikováno v:
GE: Portuguese Journal of Gastroenterology, Pp 1-6 (2022)
Introduction: Eosinophilic gastrointestinal disorders are rare idiopathic conditions characterized by eosinophilic infiltration of any area of the gastrointestinal tract. The clinical presentation is variable and depends on the location and depth of
Externí odkaz:
https://doaj.org/article/e4d675e16f3a43f1b8954cdf4f74223b
Autor:
António Ferreira, Cátia Barreiros, Duarte Silva, Lúcia Meireles-Brandão, Edgar Torre, Carmélia Rodrigues
Publikováno v:
Galicia Clínica, Vol 79, Iss 3, Pp 76-80 (2018)
Resumo: Introdução: A embolia cardíaca por Fibrilhação Auricular (FA) paroxística não diagnosticada é responsável por uma parte substancial dos Acidentes Vasculares Cerebrais (AVC) isquémicos classificados como criptogénicos. As atuais or
Externí odkaz:
https://doaj.org/article/8aa058d7078d4c108c89608d5a2fa9c5
Publikováno v:
European Journal of Case Reports in Internal Medicine, Vol 5, Iss 2 (2017)
Sarcoidosis is a risk factor for the development of cryptococcal infection due to dysfunction at T-cell level. Its rarity may, however, delay diagnosis and treatment. We describe the case of a 60-year-old man, diagnosed with sarcoidosis since 1999. H
Externí odkaz:
https://doaj.org/article/deb889e786554b7ca0a52f774c2c56bb
Autor:
André Miranda, Ramy Abdelnaby, André Araújo, Marta Rodrigues, Valeria Battistella, José Mário Roriz, Carmélia Rodrigues, Martin Wiesmann, Jörg B. Schulz, Omid Nikoubashman, Arno Reich, Manuel Ribeiro, João Pinho
Publikováno v:
Clinical neuroradiology 33(1), 65-72 (2023). doi:10.1007/s00062-022-01183-w
Clinical neuroradiology (2022). doi:10.1007/s00062-022-01183-w
Published by Urban & Vogel, München
Published by Urban & Vogel, München
Autor:
Danúbia Rodrigues Novaes Carvalho, Heberton Solano Rodrigues Novaes Leite, Jainara Rodrigues Novaes de Sá, Nery Freire Novaes Sobrinha, Thiago Emanuel Rodrigues Novaes, Erik Fabiano Silva, Polivânia Gomes Nunes, Natanael Alves de Lima, Ana Selia Rodrigues Novaes, Julia Maria Guimarães Fortuna, Nathyelle Maria de Oliveira Cândido, Carmélia Rodrigues Novaes Carvalho
Publikováno v:
Extensão Universitária nas Ciências da Saúde no Brasil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6735b74cb18c741b645135cced2bfdbc
https://doi.org/10.22533/at.ed.2632003036
https://doi.org/10.22533/at.ed.2632003036
Publikováno v:
European Journal of Case Reports in Internal Medicine (2019)
European Journal of Case Reports in Internal Medicine
European Journal of Case Reports in Internal Medicine
Tuberous sclerosis complex (TSC) is a rare, autosomal dominant disorder with a recognized phenotypic variability with clinical manifestations developing continuously throughout life. The follow-up of TSC patients is challenging. The authors present a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4698c3b0393f4c92a1ef18bc864ab1c
https://www.ejcrim.com/index.php/EJCRIM/article/view/1264
https://www.ejcrim.com/index.php/EJCRIM/article/view/1264
Autor:
C Barreiros, Lúcia Meireles-Brandão, Duarte Silva, Edgar Torre, A.L. Ferreira, Carmélia Rodrigues
Publikováno v:
Galicia Clínica, Vol 79, Iss 3, Pp 76-80 (2018)
Resumo: Introdução: A embolia cardíaca por Fibrilhação Auricular (FA) paroxística não diagnosticada é responsável por uma parte substancial dos Acidentes Vasculares Cerebrais (AVC) isquémicos classificados como criptogénicos. As atuais ori
Publikováno v:
European Journal of Case Reports in Internal Medicine, Vol 5, Iss 2 (2017)
European Journal of Case Reports in Internal Medicine
European Journal of Case Reports in Internal Medicine
Sarcoidosis is a risk factor for the development of cryptococcal infection due to dysfunction at T-cell level. Its rarity may, however, delay diagnosis and treatment. We describe the case of a 60-year-old man, diagnosed with sarcoidosis since 1999. H
Publikováno v:
European Journal of Case Reports in Internal Medicine (2019)
Tuberous sclerosis complex (TSC) is a rare, autosomal dominant disorder with a recognized phenotypic variability with clinical manifestations developing continuously throughout life. The follow-up of TSC patients is challenging. The authors present a
Externí odkaz:
https://doaj.org/article/6572689ae5af45a5b8dab29ef7cb4b0e