Results 81 to 90 of about 513,178 (237)
Treatment strategies for interstitial granulomatous dermatitis: Systematic review and expert opinion
Journal of the European Academy of Dermatology and Venereology, EarlyView.Systematic review of 108 studies with a total of 182 patients with interstitial granulomatous dermatitis (IGD). IGD was frequently associated with systemic conditions or drug exposure. Management includes careful medication review and prompt withdrawal of potential triggers. Corticosteroids (systemic and topical) were commonly effective, while biologic
Francesco Bellinato +4 more
wiley +1 more source
Antiphospholipid Antibodies in Patients with Myasthenia Gravis [PDF]
, 1994 We measured antiphospholipid antibodies in sera from 94 patients with myasthenia gravis (MG). We found lgG aCL in 14/94 (14.9 % )lgM aCL in 6/94 (6.4 %) and LA in 4/56 (7.1 %) patients with MG. As a whole 21 of 94 (22.3 % ) patients with MG had some aPL.
Kinoshita, Ikuo +10 more
core
Journal of Internal Medicine, EarlyView.Abstract Background Although systemic lupus erythematosus (SLE) pregnancy frequently results in small for gestational age (SGA) infants, the understanding of underlying mechanisms is limited. We aimed to identify specific histological patterns of placental injury in SGA in SLE and to explore whether an altered balance of angiogenesis‐related proteins ...
Marit Stockfelt +21 more
wiley +1 more source
, 1999 Background: A human IgM monoclonal anticardiolipin antibody–BH1–has previously been described, which has characteristics typical of antiphospholipid antibodies in the serum of patients with antiphospholipid syndrome (APS).
Mackworth-Young, C.G. +2 more
core +1 more source
Antiphospholipid antibodies in Brazilian hepatitis C virus carriers
Brazilian Journal of Medical and Biological Research, 2008 Hepatitis C, a worldwide viral infection, is an important health problem in Brazil. The virus causes chronic infection, provoking B lymphocyte dysfunction, as represented by cryoglobulinemia, non-organ-specific autoantibody production, and non-Hodgkin's ...
A.M. Atta +5 more
doaj
Survival After Catastrophic Antiphospholipid Syndrome With Diffuse Alveolar Hemorrhage
Journal of Investigative Medicine High Impact Case ReportsAntiphospholipid syndrome is a systemic autoimmune disorder characterized by thrombotic events in the presence of antiphospholipid antibodies including lupus anticoagulant, anticardiolipin, and anti-β2-glycoprotein I antibodies.
Edy Quizhpe +6 more
doaj +1 more source
Anetoderma: Is It a Sign of Autoimmunity?
Case Reports in Dermatology, 2009 Anetoderma is a rare elastolytic disorder characterized by circumscribed areas of flaccid skin due to the loss of elastic tissue in the dermis. Primary anetoderma is frequently observed in patients with autoimmune diseases or abnormalities especially ...
Hessa Al Buainain, Mohamed Allam
doaj +1 more source
Veterinary Clinical Pathology, EarlyView.ABSTRACT A 3‐year‐old female‐intact German Shepherd presented for the evaluation of progressive shifting leg lameness, carpal swelling, and weight loss with a poor appetite since adoption about three months prior. Routine blood smear evaluation, lymph node, and synovial fluid cytologies all revealed rare neutrophils with cytoplasmic inclusions ...
Samantha L. Braman +3 more
wiley +1 more source
IgA anti-β2-glycoprotein I as an independent risk factor in acute venous thromboembolism
Frontiers in ImmunologyBackgroundVenous thromboembolism (VTE) is the third most common cause of cardiovascular death. Primary Antiphospholipid Syndrome (P-APS) is a chronic systemic autoimmune disorder characterized by thrombotic events and/or obstetric complications in ...
Raquel Diaz-Simon +34 more
doaj +1 more source
Haematologica, 2008 Background To identify the mechanisms of the hypercoagulability associated with antiphospholipid antibodies, we investigated antibody-mediated platelet activation and interference of antibodies with phospholipid-dependent reactions.Design and Methods We ...
Aurelie Membre +6 more
doaj +1 more source