Background: The antiphospholipid syndrome (APS) is a systemic autoimmune disorder characterized by a combination of arterial and/or venous thrombosis and recurrent fetal loss, and can be an ...

Prader-Willi syndrome is caused by changes in gene expression in a specific portion of chromosome 15. Starting in childhood, it often leads to extreme, insatiable hunger.(Image credit: Catherine ...

Biologic Therapy Significantly Improves Pregnancy Outcomes in Women with Antiphospholipid Syndrome at High Risk for Serious Complications According to Hospital for Special Surgery A landmark ...

Antiphospholipid Antibody Syndrome (APS) is an autoimmune condition where the immune system of the body mistakenly forms antibodies that target healthy tissues. Scroll down to learn how this ...

Catastrophic antiphospholipid syndrome (CAPS) is a rare and life threatening complication of antiphospholipid syndrome. Up to half of people with CAPS die, so timely treatment is essential ...

Primary antiphospholipid syndrome presenting with a branch retinal artery occlusion in a 15-year-old boy. J Child Neurol. 2002;17 (5):392-4. 8 Garcia-Carrasco M, Galarza-Maldonado C, Mendoza-Pinto C, ...

Haematological abnormalities are common in systemic lupus erythematosus. Anaemia is found in about 50% of patients, with anaemia of chronic disease being the most common form. Impaired erythropoietin ...

Antiphospholipe antibody syndrome (APS) is a rare cause, and its association with thrombocytosis is exceptional. We report a case of stenosing TBI secondary to APS associated with thrombocytosis ...

Neutrophil glucose flux as a therapeutic target in antiphospholipid syndrome. Journal of Clinical Investigation, 2024; 134 (15) DOI: 10.1172/JCI169893 ...