Results 191 to 200 of about 12,655 (217)

Skin Involvement in Atypical Hemolytic Uremic Syndrome

American Journal of Kidney Diseases, 2014
Skin involvement in atypical hemolytic uremic syndrome (aHUS) is very uncommon and therefore often unrecognized as a specific symptom of aHUS. We describe 3 cases of patients with aHUS who developed skin lesions that completely recovered when disease-specific treatment was established.
ARDISSINO, GIAN LUIGI, F. Tel, S. Testa, A. V. Marzano, R. Lazzari, S. Salardi, A. Edefonti   +6 more
openaire   +3 more sources

An Atypical Case of Atypical Hemolytic Uremic Syndrome

Journal of Pediatric Hematology/Oncology, 2019
We present the case of a 2-month-old infant presenting with pallor and laboratory results showing: hemoglobin 5.1 (10 to 1.5) g/dL, MCV 94.7 (75 to 105) fL, leukocytes 17.4 (7 to 15) ×103/μL, platelets 259 (150 to 450) ×103/μL, hyperbilirubinemia and renal dysfunction.
Tine, Francois, Johan, Vande Walle, Evelyn, Dhont, Werner, Keenswijk   +3 more
openaire   +2 more sources

Refractory Atypical Hemolytic Uremic Syndrome

Blood, 2012
Abstract Abstract 4635 Atypical hemolytic uremic syndrome is a rare but often lethal disease if not diagnosed and treated early. The mainstay of treatment has been plasma exchange, though eculizumab has recently been approved for treatment.
Ju-Hsien Chao, Beth C. Riley, Rebecca Redman   +2 more
openaire   +1 more source

Atypical hemolytic uremic syndrome: a clinical conundrum

Pediatric Nephrology, 2016
Patients negative for Shiga toxin-producing E. coli (STEC) are categorized as having atypical hemolytic uremic syndrome (HUS) and are associated with an increased risk for complement mutations and poorer prognosis compared with typical HUS. However, STEC identification is limited by the natural history of HUS.The current study is aimed at identifying ...
Prabesh, Bajracharya, Amrish, Jain, Rossana, Baracco, Tej K, Mattoo, Gaurav, Kapur   +4 more
openaire   +2 more sources

Atypical Hemolytic Uremic Syndrome

2023
Michal Malina, Veronique Fremeaux-Bacchi, Sally Johnson   +2 more
openaire   +1 more source

Terminal Complement Inhibitor Eculizumab in Atypical Hemolytic–Uremic Syndrome

New England Journal of Medicine, 2013
Denis Fouque, Bruno Moulin, Giuseppe Remuzzi   +2 more
exaly  

Thrombomodulin Mutations in Atypical Hemolytic–Uremic Syndrome

New England Journal of Medicine, 2009
Marina Noris, Stephane Plaisance, Diether Lambrechts   +2 more
exaly  

von Willebrand Factor–Cleaving Protease in Thrombotic Thrombocytopenic Purpura and the Hemolytic–Uremic Syndrome

New England Journal of Medicine, 1998
Miriam Galbusera, Giuseppe Remuzzi, Bernhard Lämmle   +2 more
exaly  

Improved Survival in Thrombotic Thrombocytopenic Purpura–Hemolytic Uremic Syndrome

New England Journal of Medicine, 1991
Thomas S Kickler
exaly  

Prothrombotic Coagulation Abnormalities Preceding the Hemolytic–Uremic Syndrome

New England Journal of Medicine, 2002
Srdjan Jelacic, Marcia A Ciol, Phillip I Tarr   +2 more
exaly