Results 101 to 110 of about 548 (135)
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Reversible chorea in primary antiphospholipid syndrome

Movement Disorders, 1998
AbstractA 20‐year‐old woman with acute chorea induced by primary antiphospholipid syndrome was studied by using fluorodeoxyglucose and positron emission tomography (PET). PET sessions were conducted during an episode of severe chorea and after recovery.
J, Sundén-Cullberg   +2 more
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Primary antiphospholipid syndrome in monozygotic twins

Lupus, 2012
Monozygotic twins, 27 years old, with primary anti-phospholipid syndrome have been described. The first of the twins had obstetric morbidities (one miscarriage at 12 weeks and premature birth of a growth-restricted fetus at 27 weeks secondary to pre-eclampsia) and the second had venous thrombosis.
V, Ravindran, S, Rajendran, G, Elias
openaire   +2 more sources

Primary Antiphospholipid Syndrome and Thyroid Involvement

JCR: Journal of Clinical Rheumatology, 2010
Data on thyroid involvement in primary antiphospholipid syndrome are scarce and inconclusive.The aim of this study was to evaluate the frequency of thyroid dysfunction and antibodies in patients with primary antiphospholipid syndrome (PAPS) and the association of these alterations with clinical and immunologic features.The study group included 50 PAPS ...
Jozélio Freire, de Carvalho   +1 more
openaire   +2 more sources

Primary antiphospholipid syndrome and neovascular glaucoma.

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie, 2000
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Nijhawan, Navdeep   +4 more
openaire   +2 more sources

Primary antiphospholipid syndrome in stroke in the young

The Indian Journal of Pediatrics, 1998
Antiphospholipid syndrome is an uncommon cause of stroke. A 12 year old girl with this syndrome is reported who presented with thrombotic stroke and high titres of anticardiolipin (aCL) and lupus anticoagulant (LAC). The patient improved subsequently and was put on aspirin.
A, Kakar, P K, Sethi
openaire   +2 more sources

Primary antiphospholipid syndrome: A distinct entity?

Autoimmunity Reviews, 2006
Although antiphospholipid syndrome (APS) was first fully described in the context of connective tissue diseases such as systemic lupus erythematosus (SLE), it was soon recognised that the condition can exist on its own. APS appears to represent a clinical spectrum, both in terms of APS features and the presence of other autoimmune conditions.
openaire   +2 more sources

Lipoprotein (a) and apolipoprotein (a) in primary antiphospholipid syndrome

Clinical Biochemistry, 2007
To investigate whether lipoprotein (a) (Lp(a)) and/or apolipoprotein (a) (apo(a)) may be markers for clinical features of 37 patients with primary antiphospholipid syndrome (PAPS) and to compare with 37 age- and sex-matched controls.Apo(a) and Lp(a) concentrations were determined by ELISA and immunonephelometry, respectively.Only elevated apo(a ...
Mirjana, Bećarević   +2 more
openaire   +2 more sources

The primary antiphospholipid syndrome: Case report

The Italian Journal of Neurological Sciences, 1992
Lupus anticoagulant antibodies and anticardiolipin antibodies are acquired circulating immunoglobulins that interact with phospholipids. These factors may exert anticoagulant properties in vitro and so interfere with coagulation tests that use phospholipids. These antibodies are not, however, associated with a hemorrhagic diathesis.
S, Severi, M, Ghezzi, M, Felici
openaire   +2 more sources

Primary antiphospholipid syndrome

The American Journal of Medicine, 1993
Ronald A. Asherson, Graham R.V. Hughes
openaire   +1 more source

Primary antiphospholipid syndrome

The Italian Journal of Neurological Sciences, 1995
G. Quattrocolo   +5 more
openaire   +1 more source

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