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Autor:
Pereira, Diana, Salgado, Catarina, Fradique, Emília, Sobral, Filipa, Teixeira, Inês, Palaré, Maria João
Publikováno v:
Portuguese Journal of Pediatrics; Vol. 54 No. 2 (2023)
Portuguese Journal of Pediatrics; Vol. 54 N.º 2 (2023)
Portuguese Journal of Pediatrics; Vol. 54 N.º 2 (2023)
Introduction: Complex chronic diseases have been responsible for about a third of all pediatric deaths in Portugal in recent years. Early referral and implantation of an advance care plan are strategies that result in greater preparation on the part
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fdedb611914959f3255bac252650992
Publikováno v:
Acta Médica Portuguesa; May2023, Vol. 36 Issue 5, p326-335, 10p
Normal levels of coagulation factors in neonates are generally lower, which lead to prolonged clotting times, namely prothrombin time and activated partial thromboplastin time. These tests are frequently requested in neonatal intensive care units, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c359fc7e373cbbd95b05c7b5c71531b8
Publikováno v:
Portuguese Journal of Pediatrics; Vol. 53 No. 2 (2022)
Portuguese Journal of Pediatrics; Vol. 53 N.º 2 (2022)
Portuguese Journal of Pediatrics; Vol. 53 N.º 2 (2022)
Normal levels of coagulation factors in neonates are generally lower, which lead to prolonged clotting times, namelyprothrombin time and activated partial thromboplastin time. These tests are frequently requested in neonatal intensive care units, and
Publikováno v:
Revista Portuguesa de Pedopsiquiatria; N.º 46 (2020)
Segundo a definição da Organização Mundial de Saúde, os Cuidados Paliativos Pediátricos (CPP) destinam-se a crianças com doenças ameaçadoras de vida e abrangem elementos físicos, emocionais, sociais e espirituais. As crianças e adolescente
Publikováno v:
Portuguese Journal of Pediatrics; Vol. 52 No. 4 (2021)
Portuguese Journal of Pediatrics; Vol. 52 N.º 4 (2021)
Portuguese Journal of Pediatrics; Vol. 52 N.º 4 (2021)
Fanconi anemia is the most common of the rare inherited bone marrow failure syndromes. It is caused by genetic mutations that lead to genomic instability, the hallmark of the disorder. Therefore, patients are extremely vulnerable to bone marrow failu
Publikováno v:
Portuguese Journal of Pediatrics, Vol 51, Iss 4 (2020)
Portuguese Journal of Pediatrics (former Acta Pediátrica Portuguesa); Vol. 51 No. 4 (2020)
Portuguese Journal of Pediatrics; vol. 51 n.º 4 (2020)
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Portuguese Journal of Pediatrics (former Acta Pediátrica Portuguesa); Vol. 51 No. 4 (2020)
Portuguese Journal of Pediatrics; vol. 51 n.º 4 (2020)
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Thromboembolism is infrequent in children, nonetheless, whenever malignancy is present, there is an increased risk, around 7% to 25%. Rhabdomyosarcomas are typically asymptomatic masses, but patients can become symptomatic due to mass overgrowth and
Akademický článek
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Publikováno v:
BMJ Case Reports; 3/5/2021, Vol. 14, p1-4, 4p