Results 91 to 100 of about 548 (135)
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Anetoderma associated with primary antiphospholipid syndrome

Journal of the American Academy of Dermatology, 2007
We report the case of a 34-year-old white man with a 7-year history of nodules on the face, neck, upper torso, and arms which evolved to anetodermic lesions. After onset of these lesions, deep vein thrombosis developed in the patient's right arm and leg in association with circulating antiphospholipid antibodies.
Elemir Macedo, de Souza   +2 more
openaire   +2 more sources

Fibromyalgia in primary antiphospholipid (Hughes) syndrome

Lupus, 2011
Fibromyalgia (FM) is a syndrome that can be associated with several rheumatic diseases. However, no study has evaluated its frequency in patients with primary antiphospholipid syndrome (PAPS). The objective of this study was to analyze the frequency of FM in PAPS patients compared with healthy controls, to determine the possible associations between FM
S P, Costa   +3 more
openaire   +2 more sources

Primary antiphospholipid syndrome.

The Journal of rheumatology, 1989
An antiphospholipid antibody (APLA) syndrome has been proposed for those patients with systemic lupus erythematosus (SLE) or with other connective tissue diseases who have APLA and manifestations that seem related to their effect (venous thrombosis, arterial occlusions, thrombocytopenia, hemolytic anemia, recurrent fetal loss, leg ulcers, and livedo ...
D, Alarcón-Segovia, J, Sanchez-Guerrero
openaire   +1 more source

Melanoderma Revealing Primary Antiphospholipid Syndrome

Dermatology, 2009
Acute adrenal insufficiency is a rare complication of the primary antiphospholipid syndrome. We report a case of melanoderma of rapid onset revealing an addisonian crisis associated with primary antiphospholipid syndrome, which was associated with life-threatening hypercalcemia.
F, Guibal   +6 more
openaire   +2 more sources

Lung cavitation in primary antiphospholipid syndrome

Lupus, 2002
Pulmonary complications of primary antiphospholipid syndrome are common and diverse, with thromboembolic events counting as the most frequent manifestation. We present the case of a female patient with a diagnosis of primary antiphospholipid syndrome, pulmonary thromboembolism and infarction followed by lung cavitation.
A M, Bertoli   +5 more
openaire   +2 more sources

Fibrinolytic treatment in primary antiphospholipid syndrome

Lupus, 1996
We document a 30 y old man with Primary Antiphospholipid Syndrome (PAPS) and thrombosis of the common femoral vein and both the external and common iliac veins, extending to the lower vena cava, which failed to respond to high dose heparin. After three days of fibrinolytic treatment with urokinase there was complete venous recanalization.
M T, Camps García   +5 more
openaire   +2 more sources

Sleep disorders in primary antiphospholipid syndrome

Clinical Rheumatology, 2018
The objective of this study was to evaluate the sleep quality, the presence of sleep disorders in patients with primary antiphospholipid syndrome (pAPS), and their possible clinical and laboratory associations. This was a cross-sectional study of 40 consecutive pAPS patients and 211 healthy age- and sex-matched controls.
Luana Viana de Oliveira   +4 more
openaire   +2 more sources

[Primary antiphospholipid syndrome].

Oftalmologia (Bucharest, Romania : 1990), 2008
Antiphospholipid syndrome (APS) is a disorder characterised by recurrent arterial or venous thrombosis and/or pregnancy losses, in the presence of persistently elevated levels of anticardiolipin antibodies and/or evidence of circulating lupus anticoagulant (these abnormalities are detected by blood tests).
Angela, Popa   +6 more
openaire   +1 more source

Renal involvement in primary antiphospholipid syndrome

Journal of Nephrology, 2016
Antiphospholipid syndrome is an autoimmune disorder characterized by recurrent venous or arterial thrombosis and/or pregnancy-related problems associated with persistently elevated levels of antiphospholipid antibodies. The kidney is a major target organ in both primary and secondary antiphospholipid syndrome.
Marcantoni, Carmelita   +2 more
openaire   +3 more sources

Atherosclerosis in thrombotic primary antiphospholipid syndrome

Journal of Thrombosis and Haemostasis, 2009
Primary antiphospholipid syndrome (PAPS) is characterized by arterial and venous thrombosis, pregnancy loss, often recurrent, in the presence and persistence on antiphospholipid antibodies (aPL). The issue of early atherosclerosis, as evaluated by measuring carotid intima media thickness (IMT), associated with aPL, has been limitedly explored in PAPS ...
AMES PR   +5 more
openaire   +2 more sources

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