Results 91 to 100 of about 28,211 (255)
Clinical Case Reports, Volume 14, Issue 1, January 2026.ABSTRACT DiGeorge syndrome (22q11.2 deletion syndrome) is a congenital disorder typically identified in infancy, but adult presentations may feature autoimmune and thrombotic complications. We report a 30‐year‐old woman with known DiGeorge syndrome who presented with progressive right lower extremity pain.
Aziz‐ur‐Rahman Khalid +7 more
wiley +1 more source
Microangiopatía trombótica en paciente con síndrome antisintetasa : a propósito de un caso [PDF]
, 2015 Las microangiopatías trombóticas se caracterizan por presentar anemia hemolítica microangiopática asociada a plaquetopenia, fallo renal y lesión neurológica. El Síndrome anti-sintetasa es una entidad poco frecuente perteneciente al grupo de las miopatías
Carena, José Alberto +4 more
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Drug‐Induced Immune Thrombocytopenia Secondary to Trimethoprim–Sulfamethoxazole
Case Reports in Infectious Diseases, Volume 2026, Issue 1, 2026.We report the case of a 55‐year‐old male with AIDS who developed severe thrombocytopenia following initiation of trimethoprim–sulfamethoxazole. Despite drug discontinuation and supportive measures, thrombocytopenia persisted, leading to the patient’s death.
Christopher Cimperman +7 more
wiley +1 more source
Plasma von Willebrand factor levels predict in-hospital survival in patients with acute-on-chronic liver failure [PDF]
, 2016 BACKGROUND AND AIMS: Circulating levels of von Willebrand factor (vWF) predict mortality in patients with cirrhosis. We hypothesized that systemic inflammation in acute-on-chronic liver failure (ACLF) will stimulate endothelium, increase vWF levels, and ...
Amirtharaj, GJ +9 more
core +1 more source
Complete Recovery of Ischemic Cardiomyopathy from Thrombotic Thrombocytopenic purpura
Clinical Medicine Insights: Cardiology, 2011 A 50 year old male HIV patient on antiretroviral therapy was admitted for chest pain. Upon admission, the patient was found to have elevated cardiac enzymes, acute thrombocytopenia, hemolytic anemia, acute pancreatitis and acute renal failure.
Sainath Gaddam +7 more
doaj +1 more source
Delayed‐Onset Hemolysis in a Case of Hemolytic Uremic Syndrome: A Diagnostic Challenge
Case Reports in Hematology, Volume 2026, Issue 1, 2026.Background Hemolytic uremic syndrome is a rare thrombotic microangiopathy characterized by hemolytic anemia, thrombocytopenia, and acute kidney injury. While commonly reported in children, adult‐onset presentations are less frequent and often atypical, leading to diagnostic delays.
Muhammad Younas +4 more
wiley +1 more source
Severe Acral Necrosis Complicating Thrombotic Microangiopathy in Two Toddlers
Case Reports in Pediatrics, 2020 Acral ischemia/necrosis is one of the rarest but most dreadful complications of thrombotic microangiopathy in pediatric patients. It is more reported with thrombotic thrombocytopenic purpura than with hemolytic and uremic syndrome.
H. Nassih, Z. Lazrak, S. Younous
doaj +1 more source
Advanced Therapeutics, Volume 8, Issue 12, December 2025.This review explores how antibody engineering and display technologies are driving therapeutic advances against mosquito‐borne orthoflaviviruses such as Zika, dengue, and yellow fever viruses. It highlights diverse neutralizing targets on the envelope protein, including the conserved fusion loop, and discusses how Fc engineering, rational antigen ...
Ana Clara Barbosa Antonelli +5 more
wiley +1 more source
Modern concepts of the platelet in health and disease [PDF]
, 1962 Thesis (M.D.)--Boston ...
Estes, J. Worth
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