Results 101 to 110 of about 38,539 (238)

Antiphospholipid Antibodies and Acute-Phase Response in Non-Metastatic Colorectal Cancer Patients

The International Journal of Biological Markers, 2008
Aim To investigate the plasma levels and prevalence of the most common antiphospholipid antibodies, as well as their relationships with several plasma markers of inflammation, in order to characterize some aspects of cancer thrombophilia.
S. Battistelli, M. Stefanoni, R. Petrioli, A. Genovese, R. Dell'Avanzato, G. Donati, A. Vittoria, F. Roviello   +7 more
doaj   +1 more source

The diagnosis and management of the haematologic manifestations of lupus [PDF]

, 2016
Haematological manifestations in systemic lupus erythematosus (SLE) are frequently observed. They are diverse and range from mild to severe.
Castro, SG, Isenberg, DA, Velo-García, A   +2 more
core   +1 more source

The Role of Extracorporeal Membrane Oxygenation in Cardiopulmonary Dysfunction Due to Rheumatologic Diseases: A Systematic Review

ACR Open Rheumatology, Volume 8, Issue 4, April 2026.
Objective This systematic review documents the current status of extracorporeal membrane oxygenation (ECMO) use in patients with complications of rheumatologic diseases. Methods Following Preferred Reporting Items for Systematic Reviews and Meta Analyses 2020 guidelines, we conducted a systematic review of studies published from January 2019 to ...
Kari L. Falaas, Lyubov Y. Tiegs, Nicole Theis‐Mahon, Elie Gertner   +3 more
wiley   +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, P. Estevam, R. Paraná, C.M. Pereira, B.C.O. Leite, M.L.B. Sousa-Atta   +5 more
doaj  

Isolated IgA Anti-β2 Glycoprotein I Antibodies in Patients with Clinical Criteria for Antiphospholipid Syndrome

Journal of Immunology Research, 2014
Seronegative antiphospholipid syndrome (SNAPS) is an autoimmune disease present in patients with clinical manifestations highly suggestive of Antiphospholipid Syndrome (APS) but with persistently negative consensus antiphospholipid antibodies (a-PL). IgA
Raquel Ruiz-García, Manuel Serrano, José Ángel Martínez-Flores, Sergio Mora, Luis Morillas, María Ángeles Martín-Mola, José M. Morales, Estela Paz-Artal, Antonio Serrano   +8 more
doaj   +1 more source

Clinical and neuroimaging correlates of antiphospholipid antibodies in multiple sclerosis: a preliminary study [PDF]

, 2007
Background The presence of antiphospholipid antibodies (APLA) in multiple sclerosis (MS) patients has been reported frequently but no clear relationship between APLA and the clinical and neuroimaging features of MS have heretofore been shown. We assessed
Carlos J Bidot, Lawrence L Horstman, Wenche Jy, Joaquin J Jimenez, Carlos Bidot, Yeon S Ahn, J Steven Alexander, Eduardo Gonzalez-Toledo, Roger E Kelley, Alireza Minagar, SL Hauser, EM Froman, JH Noseworthy, AG Kermode, A Minagar, A Minagar, CL Conley, CL Conley, GRV Hughes, GRV Hughes, JS Levine, JA McIntyre, JA McIntyre, H Shan, DA Kandiah, CJ Bidot, RC Hinton, RL Brey, D Karussis, JW Ijdo, GRV Hughes, MJ Cuadrado, S Ferreira, T Fukazawa, MA Cordoliani, A Tourbah, Y Sugiyama, CJ Bidot, CJ Bidot, CH Polman, A Tincani, G Reber, N Garg, LD Notarangelo, N DelPapa, J Constans, R Simantov, SS Pierangeli, PL Meroni, JJ Jimenez, W Jy, A Minagar, HH Versteeg   +52 more
core   +1 more source

Concomitant Immune‐Mediated Thrombotic Thrombocytopenic Purpura and Evans Syndrome With Multiple Cerebral Infarctions in an Elderly Patient

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT We report a rare case of concomitant immune thrombotic thrombocytopenic purpura (iTTP) and Evans syndrome, complicated by multiple cerebral infarctions. The patient presented with severe thrombocytopenia and hemolytic anemia, as well as a positive direct Coombs test. The initial diagnosis was Evans syndrome.
Shinichi Ogawa, Yangsu Kim, Takayoshi Ito   +2 more
wiley   +1 more source

Catastrophic antiphospholipid syndrome presenting as fever of unknown origin

Saudi Journal of Kidney Diseases and Transplantation, 2012
Antiphospholipid syndrome is characterized by the presence of antiphospholipid antibodies with characteristic clinical manifestation, which include venous, arterial thrombosis, thrombotic microangiopathy, and recurrent fetal loss.
Fatma I Al-Beladi
doaj   +1 more source

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

Stent Thrombosis: A Narrative Review From Pathophysiology to Therapy

Clinical Cardiology, Volume 49, Issue 4, April 2026.
Stent thrombosis remains a life‐threatening complication of PCI driven by complex interactions between stent design, procedural factors, thrombogenic milieu, and inflammation. This review integrates pathophysiological mechanisms with contemporary and emerging therapeutic strategies, highlighting optimized PCI, tailored antithrombotic therapy, and novel
Emanuele Cecchi, Andrea Grasso Granchietti, Ruggero Mazzotta, Manuel Garofalo, Giorgia Panichella, Giuseppe Iula, Francesca Maria Di Muro, Silvia Menale, Rossella Marcucci   +8 more
wiley   +1 more source