Results 51 to 60 of about 2,311,673 (316)

Catastrophic secondary antiphospholipid syndrome with peripheral nervous system involvement: a case report. [PDF]

, 2004
A 34-year-old woman was admitted to our emergency room with a high fever, abdominal pain, dyspnea and confusion. High fever and abdominal pain had first occured after a cystocele operation 5 months earlier.
Erten, Nilgun, Karan, M Akif, Parman, Yesin, Saka, Bulent, Tascioglu, Cemil, Umman, Berrin   +5 more
core   +1 more source

What nephrolopathologists need to know about antiphospholipid syndrome-associated nephropathy: Is it time for formulating a classification for renal morphologic lesions? [PDF]

Journal of Nephropathology, 2014
Context: Antiphospholipid syndrome (APS) is a systemic autoimmune disorder which commonly affects kidneys. Evidence Acquisitions: Directory of Open Access Journals (DOAJ), Google Scholar, PubMed (NLM), LISTA (EBSCO) and Web of Science have been searched.
Muhammed Mubarak, Hamid Nasri
doaj   +1 more source

Leg Ulcers in Antiphospholipid Syndrome Secondary to Systemic Lupus Erythematosus Treated with Intravenous Immunoglobulin [PDF]

, 2014
BACKGROUND: Despite encouraging reports on the efficacy of intravenous immunoglobulin (IVIg) in antiphospholipid syndrome, the clinical value of this treatment is not well established, and most of the data are based on case reports and small series of ...
João, A, Santos, G, Sousa, L
core   +1 more source

Antiphospholipid syndrome: Complement activation, complement gene mutations, and therapeutic implications

Journal of Thrombosis and Haemostasis, 2020
Antiphospholipid syndrome (APS) is an acquired thromboinflammatory disorder characterized by the presence of antiphospholipid antibodies as well as an increased frequency of venous or arterial thrombosis and/or obstetrical morbidity.
Shruti Chaturvedi, Evan M. Braunstein, R. Brodsky   +2 more
semanticscholar   +1 more source

Primary antiphospholipid syndrome presenting with homonymous quadrantanopsia

American Journal of Ophthalmology Case Reports, 2018
Purpose: To report a case of primary antiphospholipid syndrome presenting with isolated homonymous superior quadrantanopsia. Observations: A 50-year-old Korean man presented with subjective visual disturbance for 1 month.
Hee Kyung Yang, Ki Won Moon, Min Jung Ji, Sang Beom Han, Jeong-Min Hwang   +4 more
doaj   +1 more source

Arginine mutation alters binding of a human monoclonal antibody to antigens linked to systemic lupus erythematosus and the antiphospholipid syndrome [PDF]

, 2007
Objective: Previous studies have shown the importance of somatic mutations and arginine residues in the complementarity-determining regions (CDRs) of pathogenic anti-double-stranded DNA (anti-dsDNA) antibodies in human and murine lupus, and in studies of
Giles, I., Ioannou, Y., Isenberg, D.A., Lambrianides, A., Latchman, D.S., Manson, J.J., Mason, L., Rahman, A.   +7 more
core   +1 more source

A probable case of catastrophic antiphospholipid syndrome: Should high-dose steroids be given in the setting of polymicrobial sepsis?

SAGE Open Medical Case Reports, 2019
In this clinical vignette, we present a case of a 59-year-old woman with catastrophic antiphospholipid syndrome likely triggered by polymicrobial sepsis.
Shanna Ariane Tucker, Justin Choi, Dhruv Khullar   +2 more
doaj   +1 more source

An Integrated Soft Computing Approach to Hughes Syndrome Risk Assessment [PDF]

, 2017
The AntiPhospholipid Syndrome (APS) is an acquired autoimmune disorder induced by high levels of antiphospholipid antibodies that cause arterial and veins thrombosis, as well as pregnancy-related complications and morbidity, as clinical manifestations ...
Caldeira, Filomena, Grañeda, José M., Gusmão, Rodrigo, Martins, M. Rosário, Neves, José, Neves, João, Vicente, Henrique, Vilhena, João   +7 more
core   +1 more source

The (non‐)sense of detecting anti‐cardiolipin and anti‐β2glycoprotein I IgM antibodies in the antiphospholipid syndrome

Journal of Thrombosis and Haemostasis, 2020
The antiphospholipid syndrome (APS) is characterized by thrombosis and/or pregnancy morbidity with the persistent presence of lupus anticoagulant (LAC), anti‐cardiolipin (aCL) and/or anti‐β2glycoprotein I (aβ2GPI) antibodies of the immunoglobulin G ...
W. Chayoua, H. Kelchtermans, J. Gris, G. Moore, J. Musial, D. Wahl, P. D. de Groot, B. Laat, K. Devreese   +8 more
semanticscholar   +1 more source

Clinical relevance of silent red blood cell autoantibodies. [PDF]

, 2017
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Alessandri, C, Caputo, Md, Colafigli, G, Coluzzi, S, De Propris, Ms, Foà, R, Giovannetti, G, Girelli, G, Guarini, Ar, Mauro, Fr, Pepe, S, Porrazzo, M, Riemma, C, Trastulli, F, Valesini, G   +14 more
core   +1 more source