Results 1 to 10 of about 35 (32)

Primary antiphospholipid syndrome in a hemodialysis patient with recurrent thrombosis of arteriovenous fistulas [PDF]

open access: yesBrazilian Journal of Nephrology, 2019
Introduction: The antiphospholipid syndrome is a systemic autoimmune disease defined by recurrent vascular and/or obstetrical morbidity that occurs in patients with persistent antiphospholipid antibodies.
Nikola Gjorgjievski   +1 more
doaj   +2 more sources

Consensus on the investigation of thrombophilia in women and clinical management [PDF]

open access: yesEinstein (São Paulo), 2019
Objective To standardize the investigation and clinical management of women with laboratory and/or clinical abnormalities suggestive of thrombophilia, in order to optimize antithrombotic approach and indication of laboratory tests.
Claudia Mac Donald Bley Nascimento   +9 more
doaj   +2 more sources

Neurovascular complications of antiphospholipid syndrome: a narrative review [PDF]

open access: yesArquivos de Neuro-Psiquiatria
Background Antiphospholipid syndrome (APS) is a systemic autoimmune disorder characterized by thrombosis, pregnancy complications, and other nonthrombotic manifestations in the presence of antiphospholipid antibodies.
George Nilton Nunes Mendes   +6 more
doaj   +2 more sources

Síndrome Antifosfolipídica: Uma Revisão a Propósito de Três Casos Clínicos

open access: yesGazeta Médica, 2018
A síndrome antifosfolipídica é uma doença autoimune e sistémica que se define com base em achados clínicos e laboratoriais, ou seja, presença de tromboses recorrentes, arteriais ou venosas em pessoas jovens, abortos espontâneos recorrentes ...
Joana Sotto Mayor   +4 more
doaj   +1 more source

Síndrome Antifosfolipídica Primária: Uma Apresentação Incomum

open access: yesGazeta Médica, 2019
A síndrome antifosfolipídica caracteriza-se por eventos trombóticos, morte fetal recorrente e presença de anticorpos antifosfolipídicos circulantes.
Andreia Sofia Rocha Costa   +3 more
doaj   +1 more source

An unusual case of pacemaker endocarditis in a patient with antiphospholipid syndrome

open access: yesRevista Portuguesa de Cardiologia, 2012
We report the case of a 50-year-old woman with systemic lupus erythematosus who had previously undergone pacemaker implantation. She developed recurrent pulmonary thromboembolism and was diagnosed with antiphospholipid syndrome.
Miguel Correia   +5 more
doaj   +1 more source

Correlação entre a síndrome antifosfolipídica e a crioglobulinemia: série de quatro casos e revisão da literatura

open access: yesRevista Brasileira de Reumatologia, 2016
Resumo Introdução: A crioglobulinemia é uma vasculite de pequenos vasos mediada por imunocomplexos que normalmente envolvem a pele, os rins e os nervos periféricos. A síndrome antifosfolipídica (SAF) é um transtorno da hipercoagulabilidade autoimune que
Shiber Shachaf, Molad Yair
doaj   +1 more source

Síndrome de imunização antifosfolipídica e trombose.

open access: yesActa Médica Portuguesa, 1994
The designation of Antiphospholipid Syndrome was first applied by Harris in 1987, to a clinical status characterized by the detection of anticardiolipin and/or lupus anticoagulant with clinical thromboembolic manifestations.
J C de Sousa, F Carriço
doaj   +1 more source

Antiphospholipid syndrome and acute myocardial infarction: Treatment with thrombectomy and abciximab

open access: yesRevista Portuguesa de Cardiologia, 2014
Antiphospholipid syndrome (APS) is an autoimmune coagulation disorder that manifests clinically as venous and arterial thrombosis, and may affect any tissue or organ. Coronary artery involvement, however, is very rare.
Vicens Martí   +3 more
doaj   +1 more source

Síndrome antifosfolípide e dermatomiosite/polimiosite: uma rara associação Antiphospholipid syndrome and dermatomyositis/polymyositis: a rare association

open access: yesRevista Brasileira de Reumatologia, 2012
A associação entre a síndrome antifosfolípide e as miopatias inflamatórias idiopáticas tem sido raramente descrita na literatura. No presente trabalho relatamos dois pacientes com síndrome antifosfolípide diagnosticados com dermatomiosite ou polimiosite.
Fernando Henrique Carlos de Souza   +2 more
doaj   +1 more source

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