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Circulating cell-free DNA levels in Portuguese patients with psoriasis vulgaris...

Coimbra, S; Catarino, C; Costa, E; Oliveira, H; Figueiredo, A; Rocha-Pereira, P; Santos-Silva, A

associated with inflammation. OBJECTIVES: We aimed to understand the relation of CFD levels with psoriasis severity, defined by the Psoriasis Area and Severity Index (PASI), with inflammation and with psoriasis therapy. METHODS: Forty-six patients with psoriasis vulgaris were evaluated before (T0) and after 12 weeks (T12) of treatment with narrowband ultraviolet light B (NB-UVB; n = 17), psoralen plus UVA (PUVA...


Body Fat Percentage Is a Major Determinant of Total Bilirubin Independently of ...

Belo, L; Nascimento, H; Kohlova, M; Bronze-da-Rocha, E; Fernandes, J; Costa, E; Catarino, C; Aires, L; Mansilha, HF; Rocha-Pereira, P; Quintanilha, A

OBJECTIVES: Bilirubin has potential antioxidant and anti-inflammatory properties. The UGT1A1*28 polymorphism (TA repeats in the promoter region) is a major determinant of bilirubin levels and recent evidence suggests that raised adiposity may also be a contributing factor. We aimed to study the interaction between UGT1A1 polymorphism, hematological and anthropometric variables with total bilirubin levels in you...

Data: 2014   |   Origem: Repositório Comum

Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic v...

Kasperavičiute, D.; Catarino, C.B.; Matarin, M.; Leu, C.; Novy, J.; Tostevin, A.; Leal, B.; Hessel, E.V.S.; Hallmann, K.; Hildebrand, M.S.; Dahl, H-H.M.

Epilepsy comprises several syndromes, amongst the most common being mesial temporal lobe epilepsy with hippocampal sclerosis. Seizures in mesial temporal lobe epilepsy with hippocampal sclerosis are typically drug-resistant, and mesial temporal lobe epilepsy with hippocampal sclerosis is frequently associated with important co-morbidities, mandating the search for better understanding and treatment. The cause o...


The Use of Recombinant Activated FVII (rFVIIa, Novoseven®) in the Treatment of ...

Diniz, MJ; Galvão, M; Tavares, A; Vieira, A; Falcão, MT; Catarino, C; Cruz, C


Tromboembolias Múltiplas Associadas a Défice de Anti-Trombina III

Catarino, C; Marques da Silva, P; Quininha, J; Serra, J; Nogueira da Silva, M; Antunes, E; Cruz Ferreira, R; Moura de Oliveira; Gracias, R; Prates, A

A deficiência congénita de anti-trombina III é considerada como um estado de hipercoagulabilidade primária. Os autores apresentam um caso de deficiência de anti-trombina III num jovem do sexo masculino, de 28 anos de idade, com doença valvular aórtica e múltiplos episódios de fenómenos tromboembólicos. Ao discutirem os seus aspectos diagnósticos e terapêuticos, procuram sensibilizar para a necessidade de se ras...


Multiple thromboembolism associated with anti-thrombin III deficiency.

Catarino, C; Serviços de Cardiologia, Hospital de Santa Marta, Lisboa.; Silva, P M; Quininha, J; Serra, J; da Silva, N; Antunes, E; Ferreira, R

Congenital deficiency of antithrombin III is considered as one serious primary hypercoagulable state. The authors present a case of deficiency of antithrombin III in a 28 years old young male, with aortic valve disease and several thromboembolic events. When discussing their diagnostical and therapeutical aspects they call the attention to the need for investigation of the situations in which thrombophilia pres...

Data: 1970   |   Origem: Acta Médica Portuguesa

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    Financiadores do RCAAP

Fundação para a Ciência e a Tecnologia Universidade do Minho   Governo Português Ministério da Educação e Ciência Programa Operacional da Sociedade do Conhecimento União Europeia