Results 41 to 50 of about 59,490 (296)

Consensus regarding diagnosis and management of atypical hemolytic uremic syndrome

The Korean Journal of Internal Medicine, 2020
Thrombotic microangiopathy (TMA) is defined by specific clinical characteristics, including microangiopathic hemolytic anemia, thrombocytopenia, and pathologic evidence of endothelial cell damage, as well as the resulting ischemic end-organ injuries.
Hajeong Lee, E. Kang, H. Kang, Y. Kim, Jin Seok Kim, Hee-Jin Kim, K. Moon, T. Ban, S. Oh, S. Jo, Heeyeon Cho, B. Choi, Junshik Hong, H. Cheong, D. Oh   +14 more
semanticscholar   +1 more source

Atypical hemolytic uremic syndrome in high-risk neuroblastoma patient: case report

Онкогематология, 2021
Atypical hemolytic uremic syndrome is a rare disorder uncontrolled complement activation, which is classically manifested by anemia, thrombocytopenia and renal failure.
A. Yu. Smirnova, Yu. V. Dinikina, A. A. Tereshina, E. P. Evsutina, M. B. Belogurova   +4 more
doaj   +1 more source

How I treat thrombotic thrombocytopenic purpura and atypical haemolytic uraemic syndrome [PDF]

, 2014
Thrombotic thrombocytopenic purpura (TTP) and atypical haemolytic uraemic syndrome (aHUS) are acute, rare life-threatening thrombotic microangiopathies that require rapid diagnosis and treatment.
Goodship, T, Scully, M
core   +1 more source

Cutaneous and renal glomerular vasculopathy as a cause of acute kidney injury in dogs in the UK [PDF]

, 2015
To describe the signalment, clinicopathological findings and outcome in dogs presenting with acute kidney injury (AKI) and skin lesions between November 2012 and March 2014, in whom cutaneous and renal glomerular vasculopathy (CRGV) was suspected and ...
ARDISSINO, ARDISSINO, ARONSON, BIRNBAUM, BLOMBERY, BOURHY, BOYCE, BURNENS, CARPENTER, CHANTREY, COWAN, DELL'ORCO, DICKINSON, EUBIG, FERRER, FISCHER, FOURNEL, GARCIA, GOLDFARB, GREENE, HENDRICKS, HERTZKE, HOLLOWAY, KAVANAGH, LI, MILFORD, MONAHAN, MOORE, MORRIS, MUNDAY, NORIS, PASS, REBAR, RENTKO, ROBY, ROTERMUND, RUGGENENTI, SALVADORI, SYKES, TANGEMAN, TARR, TARR, UCHIDA, VAN DEN INGH, VICTORIA, WAIKAR, WALKER   +46 more
core   +1 more source

Prevalence and antimicrobial susceptibility of Escherichia coli O157 in beef at butcher shops and restaurants in central Ethiopia [PDF]

, 2017
Background: Ethiopia bears the largest burden of foodborne diseases in Africa, and diarrheal diseases are the second leading causes of premature deaths.
Beyene, Takele, Beyene, Tariku Jibat, Beyi, Ashenafi Feyisa, Cox, Eric, De Zutter, Lieven, Fite, Akafete Teklu, Genu, Tadele, Goddeeris, Bruno, Kaba, Tamirat, Korsa, Mesula Geloye, Tadesse, Fanos, Tafese, Asdesach, Tora, Ephrem   +12 more
core   +2 more sources

Atypical Hemolytic‐Uremic Syndrome: An Update on Pathophysiology, Diagnosis, and Treatment

Therapeutic apheresis and dialysis, 2018
Atypical hemolytic uremic syndrome (aHUS), a rare variant of thrombotic microangiopathy, is characterized by microangiopathic hemolytic anemia, thrombocytopenia, and renal impairment.
R. Raina, Vinod Krishnappa, T. Blaha, T. Kann, W. Hein, Linda Burke, A. Bagga   +6 more
semanticscholar   +1 more source

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

, 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, Douglas, Kenneth W., Green, Rachel, Pollock, Kevin G.J., Young, David   +4 more
core   +1 more source

Atypical Hemolytic Uremic Syndrome [PDF]

Seminars in Nephrology, 2013
Hemolytic uremic syndrome (HUS) is a triad of microangiopathic hemolytic anemia, thrombocytopenia, and acute renal failure. The atypical form of HUS is a disease characterized by complement overactivation. Inherited defects in complement genes and acquired autoantibodies against complement regulatory proteins have been described.
Kavanagh D, Goodship TH, Richards A
openaire   +3 more sources

RpoS impacts global gene expression and carbon source utilization in Escherichia coli O104:H4

Frontiers in Microbiology
BackgroundEscherichia coli (E. coli) O104:H4 caused the 2011 enterohemorrhagic E. coli (EHEC) outbreak in Germany, which remains the outbreak with the highest incidence of hemolytic uremic syndrome worldwide. We recently identified an E.
Petya Berger, Petya Berger, Karla Bosse-Plois, Wolfgang Pölking, David Loewe, Ian U. Kouzel, Michael Berger, Ulrich Dobrindt, Alexander Mellmann, Alexander Mellmann   +9 more
doaj   +1 more source

Genotypic Characterization of Non-O157 Shiga Toxin–Producing Escherichia coli in Beef Abattoirs of Argentina [PDF]

, 2011
The non-O157 Shiga toxin-producing Escherichia coli (STEC) contamination in carcasses and feces of 811 bovines in nine beef abattoirs from Argentina was analyzed during a period of 17 months.
Carbonari, Claudia Carolina, del Castillo, Lourdes Leonor, D´Astek, B. A., Galli, Lucía, Irino, K., Leotta, Gerardo Anibal, Masana, Marcelo, Palladino, Pablo Martín, Rivas, M., Vilacoba, Elisabet   +9 more
core   +2 more sources