Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Carmen Pais"'
Publikováno v:
Galicia Clínica, Vol 78, Iss 1, Pp 42-45 (2017)
RESUMO: A coagulação intravascular disseminada (CID) é uma entidade clínica relativamente incomum, caraterizada por extensa ativação da coagulação que resulta na deposição intravascular de fibrina em vasos de pequeno e médio calibre. Podem
Externí odkaz:
https://doaj.org/article/dedd7078ef3d4284909f4216a876e514
Publikováno v:
Cureus.
Autor:
Emília Pinto, Mónica Pinho, Ana Sofia Patrão, Francisco Rafael Ribeiro Soares, Sergio Azevedo, Helena Magalhães, Li Bei, Eduarda Couto, Lúcia Guedes, Luís Antunes, A. V. R. Silva, Andreia Costa, Maria João Silva, Carmen Pais, Carolina Sales, Ana Raquel Monteiro, Joana Reis, Diana Paula Nobre Fernandes, José António Ferraz-Gonçalves
Publikováno v:
SN Comprehensive Clinical Medicine. 3:2520-2524
The aim of this work was to study the prevalence of hypocalcemia in cancer patients based on ionized calcium and, as a secondary aim, the influence that hypocalcemia may have on survival. For this retrospective study, a representative sample of all t
Publikováno v:
European Journal of Case Reports in Internal Medicine
European Journal of Case Reports in Internal Medicine (2018)
European Journal of Case Reports in Internal Medicine (2018)
Tracheobronchomalacia is defined as loss of the structural integrity of airway wall cartilaginous structures with hyperdynamic airway collapse during respiration. It is a common finding in chronic obstructive pulmonary disease (COPD) but is not alway
Publikováno v:
Revista portuguesa de cirurgia cardio-toracica e vascular : orgao oficial da Sociedade Portuguesa de Cirurgia Cardio-Toracica e Vascular. 24(1-2)
Paget-Schröetter Syndrome, or effort thrombosis of the subclavian vein, is an uncommon condition that affects young, active, healthy individuals. It's a type of Thoracic Outlet Syndrome (TOS), consequence of compression and repetitive injury of the
Publikováno v:
European Journal of Case Reports in Internal Medicine
European Journal of Case Reports in Internal Medicine, Vol 4, Iss 3 (2017)
European Journal of Case Reports in Internal Medicine, Vol 4, Iss 3 (2017)
Light-chain deposition disease (LCDD) is a rare monoclonal gammopathy that involves the deposition of light chains (LC) in multiple organs, leading to progressive dysfunction. The kidney is usually the most affected organ and responsible for the init
Publikováno v:
International Journal of Case Reports and Images. 8:86
Publikováno v:
Acta Médica Portuguesa, Vol 31, Iss 10, Pp 593-596 (2018)
Systemic lupus erythematosus is a heterogeneous and unpredictable autoimmune disease which can be complicated to approach and treat. Hemophagocytic lymphohistiocytosis and diffuse alveolar hemorrhage are rare disease complications. The authors descri
Externí odkaz:
https://doaj.org/article/33670f6909a04f9fbfd8ef9d76b13e05