Results 11 to 20 of about 33,882 (216)

Hemolytic Uremic Syndrome

open access: yesEurasian Journal of Medicine, 2019
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Gülten Tanyeri   +2 more
doaj   +3 more sources

Hemolytic Uremic Syndrome [PDF]

open access: yesEmerging Infectious Diseases, 1995
Mary Beers, Scott Cameron
doaj   +3 more sources

Hemolytic Uremic Syndrome [PDF]

open access: yesJournal of the American Society of Nephrology, 2005
Hemolytic uremic syndrome (HUS) is a thrombotic microangiopathy defined by thrombocytopenia, nonimmune microangiopathic hemolytic anemia, and acute renal failure. The most frequent form is associated with infections by Shiga-like toxin-producing bacteria (STEC-HUS).
Marina, Noris, Giuseppe, Remuzzi
openaire   +4 more sources

Hemolytic uremic syndrome

open access: yesRevista de Nefrología, Diálisis y Trasplante, 2014
Hemolytic uremic syndrome (HUS) is a thrombotic microangiopathy defined by thrombocytopenia, nonimmune microangiopathic hemolytic anemia, and acute renal failure. The most frequent form is associated with infections by Shiga-like toxin-producing bacteria (STEC-HUS).
Marta Lidia Monteverde
doaj   +5 more sources

Hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in a renal transplant recipient case report

open access: yesBrazilian Journal of Nephrology, 2020
Thrombotic microangiopathies are disorders characterized by nonimmune microangiopathic hemolytic anemia, thrombocytopenia, and multi-systemic failure.
John Fredy Nieto-Rios   +7 more
doaj   +2 more sources

Eculizumab in atypical hemolytic-uremic syndrome [PDF]

open access: yesNew England Journal of Medicine, 2013
Kistler, Andreas D
core   +3 more sources

Hemolytic uremic syndrome (HUS) – case report

open access: yesJournal of Education, Health and Sport, 2020
Introduction Hemolytic uremic syndrome (HUS) is characterized by hemolytic anemia, thrombocytopenia and acute renal failure. In 90% of children, HUS most often develops after an intestinal infection caused by verotoxin-producing E. coli. The remaining 10%
Aleksandra Borkowska   +5 more
doaj   +1 more source

A novel missense mutation in complement factor I predisposes patients to atypical hemolytic uremic syndrome: a case report

open access: yesJournal of Medical Case Reports, 2022
Background Atypical hemolytic uremic syndrome, also called the nondiarrheal form of hemolytic uremic syndrome, is a rare disease characterized by the triad of thrombocytopenia, Coomb’s test-negative microangiopathic hemolytic anemia, and acute renal ...
Xin Wei   +5 more
doaj   +1 more source

Infection frequently triggers thrombotic microangiopathy in patients with preexisting risk factors : a single-institution experience [PDF]

open access: yes, 2010
Thrombotic microangiopathies are rare conditions characterized by microangiopathic hemolytic anemia, microthrombi, and multiorgan insult. The disorders, which include hemolytic uremic syndrome and thrombotic thrombocytopenic purpura, are often acute and ...
Catlow, Jamie   +4 more
core   +1 more source

Hyperfunctional complement C3 promotes C5-dependent atypical hemolytic uremic syndrome in mice [PDF]

open access: yes, 2019
Atypical hemolytic uremic syndrome (aHUS) is frequently associated in humans with loss-of-function mutations in complement-regulating proteins or gain-of-function mutations in complement-activating proteins.
Atkinson, John P   +11 more
core   +3 more sources

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