Results 91 to 100 of about 19,610 (201)

NEWLY DIAGNOSED HEREDITARY FACTOR V DEFICIENCY IN A PATIENT PRESENTING WITH DEEP VEIN THROMBOSIS: A Rare Case

Hematology, Transfusion and Cell Therapy
Objective: Factor V (FV) is a crucial regulator of hemostasis, functioning as both a procoagulant and an anticoagulant glycoprotein within the coagulation cascade. In plasma, FV exists as an inactive precursor, which is activated by thrombin or factor Xa
Songül Beskisiz Dönen, Vehbi Demircan, Abdullah Karakuş, Mehmet Orhan Ayyıldız   +3 more
doaj   +1 more source

PO78 | Acquired hemophilia A as a paraneoplastic syndrome: two cases report on a rare coexistence

Bleeding, Thrombosis and Vascular Biology
Background: Acquired hemophilia, meanwhile, is the most common acquired disease affecting clotting factors. Possible causes that have been empirically described include autoimmune disease (such as rheumatoid arthritis or systemic lupus erythematosus ...
doaj   +1 more source

ACQUIRED HEMOPHILIA A IN A 3-YEAR-OLD PEDIATRIC PATIENT: A CASE REPORT OF RARE AND POTENTIALLY FATAL BLEEDING DISORDER

Hematology, Transfusion and Cell Therapy
Introduction: Acquired hemophilia A (AHA) is a rare severe autoimmune bleeding disorder with significant morbidity and mortality mainly occurring in older adults (average age 75). The condition is extremely rare in children.
Z Alrajhi, LLE Souza, M Carcao
doaj   +1 more source

Ambulatory Care Pharmacy Resident [PDF]

Objectives: 1. Review the background, epidemiology, and diagnostic criteria for the antiphospholipid syndrome 2. List clinical manifestations associated with antiphospholipid syndrome 3.
Jessica Bellone Pharm. D, Pharmacotherapy Rounds   +1 more
core  

Direct Oral Anticoagulants for Thromboprophylaxis in Patients with Antiphospholipid Syndrome [PDF]

, 2018
The current mainstay of the treatment and secondary thromboprophylaxis of thrombotic antiphospholipid syndrome (APS) is anticoagulation with warfarin or other vitamin K antagonists (VKAs).
Cohen, H, Efthymiou, M, Gates, C, Isenberg, D   +3 more
core  

Modern concepts of the platelet in health and disease [PDF]

, 1962
Thesis (M.D.)--Boston ...
Estes, J. Worth
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Acquired inhibitors to coagulation factors in a male patient with systemic lupus erythematosus: A case report and review of the literature

Akkiz koagülasyon faktör inhibitörleri nadirdir ancak koagulasyon faktörlerinin disfonksiyonu veya otoümmün baskılanma nedenli akkiz kanama diyatezi yaşamı tehdit edebilir. Bu hastalıkla ilişkisiz olarak daha sık yaşlı hastalarda ortaya çıkar. Akkiz koagulasyon inhibitörleri aynı zamanda Sistemik Lupus Eritematozus (SLE) ile ilişkili olarak da meydana ...
Erdem, Özgür, Ayyıldız, Orhan, Aybak, Mehmet   +2 more
openaire   +3 more sources

Diagnostics of congenital and acquired hemorrhagic diseases in patients with isolated prolonged activated partial thromboplastin time using laboratory algorithm [PDF]

, 2016
З метою розроблення алгоритму лабораторної діагностики розладів коагуляційного гемостазу і встановлення причини підвищеної схильності до кровотеч у 61 хворого з геморагічним синдромом було виконано скринінгові, 2 групи корекційних тестів (замінні проби ...
Красівська, В.В., Стасишин, О.В.   +1 more
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Erythrocyte Antibodies in AIDS are associated with mycobacteriosis and hypergammaglobulinemia [PDF]

, 1990
A. Matuschke, AP Rapoport, B. Gathof, B. Heinrich, F. -D. Goebel, FJ Raal, J Lelie van der, J. R. Bogner, L Morris, LI Zon, LI Zon, M Adams, MH McGinniss, P Zauber, PT Toy, PT Toy, PY Lepennec, R Perricone, U. Bäcker, V Daniel, Y Inada, Y Schoenfeld   +21 more
core   +1 more source

The Emerging Clinical Usefulness of Complement Measurements [PDF]

, 1977
Not many years ago the main purpose of “complement” seemed to be to drill holes in sheep erythrocytes. In the classic experiment which was part of every medical student’s microbiology laboratory experience, a magic stuff called complement, somewhat ...
Ruddy, Shaun
core   +1 more source