Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Maria Adília Costa"'
Autor:
Fátima Serejo, Ingrid Emerit, Paulo Manuel Filipe, Afonso Camilo Fernandes, Maria Adília Costa, João Pedro Freitas, Miguel Carneiro de Moura
Publikováno v:
Canadian Journal of Gastroenterology, Vol 17, Iss 11, Pp 644-650 (2003)
AIMS: To evaluate the oxidative stress parameters before, during and after interferon treatment.
Externí odkaz:
https://doaj.org/article/4fd241841e9a403cb9ad81cfefe4e24c
Autor:
Paula Catarino Costa, Celeste Canha Barreto, Luisa Pereira, Maria Luisa Lobo, Maria Adília Costa, Ana Isabel Gouveia Lopes
Publikováno v:
Pediatric Reports, Vol 3, Iss 3, Pp e21-e21 (2011)
Prospective studies concerning liver disease in pediatric cystic fibrosis patients are scarce. The present study aimed to describe the prevalence and clinical expression of cystic fibrosis - related liver disease, in a cohort of 62 pediatric patients
Externí odkaz:
https://doaj.org/article/278b747bb5764d57bf1f5105b9c7219a
Autor:
C. Baldaia, Graça Esteves, Fernando Silva Ramalho, Maria Adília Costa, Sara Ferreira, Estela Monteiro, Narcisa Fatela, Delfina Brito
Publikováno v:
Scandinavian Journal of Gastroenterology. 43:375-379
We report the case of a 68-year-old African woman who presented with jaundice, hepatomegaly and anasarca. Clinical investigation disclosed severe intrahepatic cholestasis, nephrotic syndrome, erythrocytosis and hypoglycemia. Diagnosis of systemic AL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2fb44735e1bd226a14a782e9e492198
https://doi.org/10.1080/00365520701679298
https://doi.org/10.1080/00365520701679298
Autor:
Afonso Fernandes, Maria Adília Costa, Joao Freitas, Fátima Serejo, Ingrid Emerit, Paulo Filipe, Miguel Carneiro de Moura
Publikováno v:
Canadian Journal of Gastroenterology, Vol 17, Iss 11, Pp 644-650 (2003)
AIMS: To evaluate the oxidative stress parameters before, during and after interferon treatment.PATIENTS/METHODS: Twenty patients were treated with interferon α2b 5 MU, three times a week, subcutaneously, for 12 months. Liver biopsy was performed si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b9a30c6bc4763743ca26ebb6d0b7699
https://doi.org/10.1155/2003/710693
https://doi.org/10.1155/2003/710693
Autor:
Maria Adília Costa, Maria Luisa Lobo, Luísa Pereira, Celeste Barreto, Paula Catarino Costa, Ana Isabel Gouveia Lopes
Publikováno v:
Pediatric Reports
Pediatric Reports, Vol 3, Iss 3, Pp e21-e21 (2011)
Pediatric Reports; Volume 3; Issue 3; Pages: e21
Pediatric Reports, Vol 3, Iss 3, Pp e21-e21 (2011)
Pediatric Reports; Volume 3; Issue 3; Pages: e21
Prospective studies concerning liver disease in pediatric cystic fibrosis patients are scarce. The present study aimed to describe the prevalence and clinical expression of cystic fibrosis - related liver disease, in a cohort of 62 pediatric patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19bd54fbbaf9f981b3ad9438593998b9
https://doi.org/10.4081/pr.2011.e21
https://doi.org/10.4081/pr.2011.e21