Results 101 to 110 of about 8,636 (197)

Extra-Renal manifestations of atypical hemolytic uremic syndrome in children [PDF]

, 2018
Atypical hemolytic uremic syndrome (aHUS) is a chronic disease characterized by thrombotic microangiopathy and a high risk of end-stage kidney disease.
Fatih Ozaltin, Oguz Soylemezoglu, Fidan, Kibriya, Goknar, Nilufer, Nilüfer Göknar, Zeynep Y. Yıldırım, Baskin, Esra, Yildirim, Zeynep Y., Gulleroglu, Kaan, ÖZALTIN, FATİH, MELEK, ENGİN, HAYRAN, KADİR MUTLU, GÜLHAN, BORA, Zeynep B. Özçakar, Engin Melek, Kaan Gülleroglu, Kibriya Fidan, Soylemezoglu, Oguz, Esra Baskın, Bora Gülhan, Mutlu Hayran, Ozcakar, Zeynep B.   +21 more
core   +1 more source

Postoperative atypical hemolytic uremic syndrome in nontransplant setting: A case report with review of literature

Global Journal of Transfusion Medicine, 2018
Atypical hemolytic uremic syndrome (aHUS) is a clinical diagnosis characterized by a triad of microangiopathic hemolytic anemia, thrombocytopenia, and renal dysfunction. Postoperative aHUS in nontransplant patients is a rare entity.
Anil Khetarpal, Vidhi Gupta, Urvershi Kotwal   +2 more
doaj   +1 more source

Differential complement activation by alloantibodies in sickle cell hyperhaemolysis syndrome may influence disease course

British Journal of Haematology, Volume 208, Issue 6, Page 2311-2314, June 2026.
Mamie M. Thant, Jahnavi Gollamudi, Stefanie W. Benoit, Satheesh Chonat, Jose A. Cancelas   +4 more
wiley   +1 more source

Concurrent Atypical Hemolytic Uremic Syndrome and Autoimmune Hemolytic Anemia: a case report

Caspian Journal of Pediatrics, 2018
Background: Atypical hemolytic uremic syndrome (aHUS) is a life-threatening and scarce disorder characterized by acute renal failure and disease, non-immune microangiopathic hemolytic anemia and thrombocytopenia, leading to end-stage renal failure or ...
Sayed Yousef Mojtahedi, Mohammad Kaji Yazdi   +1 more
doaj  

Atypical Hemolytic Uremic Syndrome

Advances in Pediatrics, 2014
Kaan GÜLLEROĞLU, Başak GÜLLEROĞLU, Esra BASKIN   +2 more
  +6 more sources

A Case of Severe Pre‐Eclampsia Complicated by HELLP Syndrome and Extensive Hepatic Infarction

Clinical Case Reports
Extensive 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, Fei Gao, Fengming Liang, Yang Shao   +3 more
doaj   +1 more source

Factor I Autoantibodies in Patients with Atypical Hemolytic Uremic Syndrome: Disease-Associated or an Epiphenomenon? [PDF]

Background and objectivesAtypical hemolytic uremic syndrome is a disease associated with mutations in the genes encoding the complement regulators factors H and I.
Bennaceur K, Pappworth IY, Strain L, Marchbank KJ, Lea S, Kavanagh D, Roversi P, Ward R, Plant N, Moore I, Hayes CM, Hunze EM, Goodship TH, Nailescu C, Anderson H   +14 more
core  

Poster Sessions

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Atypical hemolytic uremic syndrome in a child: A rare case report

Clinical Case Reports
Key Clinical Message Atypical hemolytic uremic syndrome, a rare thrombotic microangiopathy, necessitates early diagnosis and comprehensive care due to its potential severity, emphasizing the importance of a multidisciplinary approach to improve outcomes.
Bishal Kunwor, Bishal Sharma, Suchit Thapa Chhetri, Prerana Joshi, Dipendra Pradhan   +4 more
doaj   +1 more source

Publication Only

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source