Results 11 to 20 of about 12,787 (210)
Atypical hemolytic uremic syndrome [PDF]
Renal Replacement Therapy, 2017 Atypical hemolytic uremic syndrome (aHUS) is a thrombotic microangiopathy (TMA) characterized by microangiopathic hemolytic anemia, thrombocytopenia, and acute renal failure.
Yoko Yoshida +2 more
doaj +2 more sources
Atypical hemolytic uremic syndrome: a case report [PDF]
Journal of Medical Case Reports, 2020 Background Thrombotic microangiopathy is a pathological condition comprised of microvascular thrombosis involving any organ of the body leading to thrombocytopenia, Coombs-negative hemolytic anemia, and end-organ damage.
B. M. D. B. Basnayake +7 more
doaj +3 more sources
Pediatric Atypical Hemolytic Uremic Syndrome Advances [PDF]
Cells, 2021 Atypical hemolytic uremic syndrome (aHUS) is a rare disorder characterized by dysregulation of the alternate pathway. The diagnosis of aHUS is one of exclusion, which complicates its early detection and corresponding intervention to mitigate its high ...
Rupesh Raina +9 more
doaj +3 more sources
Difficulties in diagnosing atypical hemolytic uremic syndrome [PDF]
Сибирский научный медицинский журнал, 2020 The paper presents the case of clinical observation of a patient with atypical hemolytic-uremic syndrome (aHUS). aHUS is a disease characterized by an unfavorable prognosis (severe or catastrophic course with rapid development of terminal renal or multi ...
N. V. Fomina +5 more
doaj +2 more sources
A Case of Severe Pre‐Eclampsia Complicated by HELLP Syndrome and Extensive Hepatic Infarction
Clinical Case ReportsExtensive hepatic infarction is a rare but potentially fatal complication of HELLP syndrome and is often difficult to recognize because of nonspecific clinical manifestations.
Tiange Xia +3 more
doaj +2 more sources
Atypical hemolytic uremic syndrome: a brief review [PDF]
Hematology Reports, 2017 Atypical hemolytic uremic syndrome (aHUS) is a disease characterized by the triad of microangiopathic hemolytic anemia, thrombocytopenia and acute kidney injury.
Kuixing Zhang +3 more
doaj +5 more sources
Eculizumab in atypical hemolytic-uremic syndrome [PDF]
New England Journal of Medicine, 2013 To the Editor: With regard to the article by Legendre et al. (June 6 issue)(1): assessment of the 37 patients with atypical hemolytic-uremic syndrome is difficult, since the process of selection seems opaque, particularly for the 20 patients in trial 2.
Kistler, Andreas D
core +10 more sources
Atypical hemolytic uremic syndrome [PDF]
Hematology, 2016 AbstractAtypical hemolytic uremic syndrome (aHUS) is a thrombotic microangiopathy (TMA) that affects multiple organs and the kidneys in particular. aHUS can be sporadic or familial and is most commonly caused by dysregulation of the alternative complement pathway.
Ali, Nayer, Arif, Asif
openaire +4 more sources
Pregnancy-Induced Atypical Hemolytic Uremic Syndrome. [PDF]
CureusAtypical hemolytic uremic syndrome (aHUS) is a rare form of thrombotic microangiopathy that causes anemia, thrombocytopenia, and acute renal failure. In aHUS, a triggering event can lead to dysregulation of the complement immune system, leading to a cascade of events resulting in clot formation, capillary thrombosis, and renal dysfunction.
Den Boef A +4 more
europepmc +3 more sources
Transplantation in Atypical Hemolytic Uremic Syndrome [PDF]
Seminars in Thrombosis and Hemostasis, 2010 Atypical hemolytic uremic syndrome (aHUS) is a disease characterized by overactivation of complement. Recurrence following renal transplantation is determined by a genetic predisposition. Genetic screening of all individuals with aHUS should be performed prior to listing for transplantation. Individuals with isolated mutations in MCP have a low risk of
Kavanagh D +3 more
openaire +3 more sources