Results 81 to 90 of about 548 (135)
Some of the next articles are maybe not open access.

Atherosclerosis in primary antiphospholipid syndrome

Expert Review of Clinical Immunology, 2006
Antiphospholipid syndrome (APS) is the most common cause of acquired thrombophilia, but experimental and clinical evidence accumulated over the years suggest that the clinical manifestations of APS go beyond those of a simple hypercoagulable state.
Paul R J, Ames   +6 more
openaire   +2 more sources

Chorea in primary antiphospholipid syndrome

Clinical Neurology and Neurosurgery, 1996
A 12-year-old girl with chorea, thrombocytopenia and false positive VDRL had negative serological tests for SLE, but high titre of antiocardiolipine antibodies. Primary antiphospholipid antibody syndrome is rarely complicated by chorea, but should be taken into consideration in patients who do not fulfill the diagnostic criteria for SLE.
C. Masala   +3 more
openaire   +3 more sources

Belimumab in primary antiphospholipid syndrome

Lupus, 2016
[No abstract available]
Yazici, A., Yazirli, B., Erkan, D.
openaire   +3 more sources

Primary antiphospholipid syndrome with and without Sneddon’s syndrome

Rheumatology International, 2009
The main objective of this study was to compare clinical and laboratory data obtained from patients with primary antiphospholipid syndrome (PAPS) with and without Sneddon's syndrome (SS). A transverse study with 54 (85.2% female) PAPS patients (Sapporo criteria) was performed.
Cezar Augusto Muniz, Caldas   +1 more
openaire   +2 more sources

Primary Antiphospholipid Syndrome

2006
PAPS has emerged as an important disease entity. Depending on the organ systems involved, it can produce a highly variable clinical picture, with severity ranging from mild asymptomatic disease (often undiagnosed) to major life-threatening events. It may be regarded as the pure form of a condition which is also frequently seen in the context of other ...
Tonia L. Vincent   +1 more
openaire   +1 more source

Primary Antiphospholipid Syndrome and Pulmonary Hypertension

Current Pharmaceutical Design, 2014
Primary antiphospholipid syndrome (APS) is a disease characterized by the presence of autoantibodies reacting with proteins bound to phospholipids, leading to thrombosis and gestation abnormalities. Prothrombotic states and impaired clot dissolution are believed to contribute to the occurrence of chronic thromboembolic pulmonary hypertension (CTEPH) in
Aibek E, Mirrakhimov, Nicholas S, Hill
openaire   +2 more sources

The Primary Antiphospholipid Syndrome

2000
The emergence of the antiphospholipid syndrome (APS) over the last thirty-odd years has been one of the most striking developments in clinical autoimmunity. The identification of a pure or “primary” variant of the syndrome has been central to this story, not least in enabling us to establish the place of this remarkable condition in the wide spectrum ...
T. Vincent, C. Mackworth-Young
openaire   +1 more source

Familial Occurrence of Primary Antiphospholipid Syndrome

Thrombosis Research, 1999
venom (dRVV) were prolonged. LA was found positive according to the criteria of the scientific subcommittee for LA [11]. ACAs were also positive (Table 1).
A, Cantalapiedra   +3 more
openaire   +2 more sources

Subclinical Atherosclerosis in Primary Antiphospholipid Syndrome

Annals of the New York Academy of Sciences, 2007
Abstract:  To test the atherosclerosis hypothesis in primary antiphospholipid syndrome (PAPS) we measured intima media thickness (IMT) of carotid arteries and other cardiovascular risk factors in 44 patients with PAPS (mean age 35 ± 12 years), in 25 patients with inherited thrombophilia (mean age 40 ± 10 years), and in 34 normal controls (mean age 38 ±
Annamaria, Margarita   +7 more
openaire   +2 more sources

IgA deficiency in primary antiphospholipid syndrome

Joint Bone Spine, 2014
Joint Bone Spine - In Press.Proof corrected by the author Available online since mercredi 26 juin ...
Camila Cristina, Bonin   +2 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy