Results 61 to 70 of about 2,311,673 (316)
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT RASopathies are clinically overlapping neurodevelopmental syndromes resulting from germline mutations in genes involved in the rat sarcoma/mitogen‐activated protein kinases (RAS/MAPK) pathway. Historically, RASopathies have been described by clinical phenotypes, such as Noonan syndrome and Neurofibromatosis type I.
Anastasia‐Vasiliki Madenidou +6 more
wiley +1 more source
Catastrophic Antiphospholipid Syndrome: A Case Series
Indian Journal of Radiology and Imaging, 2023 Catastrophic antiphospholipid syndrome (CAPS) is the rare but most severe form of antiphospholipid syndrome with multiple organ ischemia developing over a short period of time.
Navya Christopher +5 more
doaj +1 more source
The Epidemiology of Antiphospholipid Syndrome: A Population‐Based Study
Arthritis & Rheumatology, 2019 To estimate the annual incidence and prevalence of and frequency of mortality associated with antiphospholipid syndrome (APS).
A. Duarte-García +7 more
semanticscholar +1 more source
Arthritis &Rheumatology, EarlyView.Objective International criteria for antiphospholipid syndrome (APS) include lupus anticoagulant (LA), anticardiolipin (aCL) IgG and IgM, and anti–β2‐glycoprotein I (β2GPI) IgG and IgM. However, evidence supporting their prognostic value or treatment efficacy in improving live birth rates is limited.
Megumi Nonobe +8 more
wiley +1 more source
Kehamilan Dengan Sindroma Antifosfolipid [PDF]
, 2016 Antiphospholipid antibody syndrome is disorder of coagulation characterize with vascular thrombosis associated with increase of antiphospholipid (aPL) antibody such as anticardiolipin (aCL) antibodies, lupus anticoagulant (LA), and anti-beta 2 ...
herlambang, H. (herlambang)
core
Laboratory Detection of the Antiphospholipid Syndrome via Calibrated Automated Thrombography [PDF]
, 2009 Lupus anticoagulants (LAC) consist of anti phospholipid antibodies, detected via their anti coagulant properties in vitro. Strong LAC relate to thromboembolic events, a hallmark of the anti-phospholipid syndrome.
arnout, jef +3 more
core +2 more sources
Obstetric antiphospholipid syndrome [PDF]
Lupus Science & Medicine, 2018 The present clinical and laboratory classification criteria for antiphospholipid syndrome (APS) were established in Sydney, Australia, in 2006. In this review, we focus on the obstetric subset of APS (OAPS), defined by persistent positivity for antiphospholipid antibodies together with either early recurrent pregnancy loss, early fetal death ...
Antovic, Aleksandra +3 more
openaire +2 more sources
A Randomized, Placebo‐Controlled Trial of Hydroxychloroquine in Incomplete Lupus
Arthritis &Rheumatology, EarlyView.Objective Patients with features of systemic lupus erythematosus (SLE) who do not fulfill classification criteria can be designated as incomplete lupus erythematosus (ILE). This condition includes individuals with a high risk of progression to SLE. Treatment of ILE may reduce symptoms, severity, and incidence of SLE.
Nancy J. Olsen +14 more
wiley +1 more source
RMD OpenObjective To develop and validate LUPIN, a self-administered, patient-centred questionnaire codesigned by patients and lupus specialists to assess disease activity and patient-reported outcomes in systemic lupus erythematosus (SLE).Methods LUPIN and the ...
+53 more
doaj +1 more source
Síndroma antifosfolípido primária catastrófica.
Acta Médica Portuguesa, 2003 Catastrophic antiphospholipid syndrome develops in a minority of patients with antiphospholipid syndrome, and is characterized by acute thrombotic microvasculopathy with multiorganic involvement (three or more organs).
Paula Casanova +11 more
doaj +1 more source