Haemolytic uraemic syndrome

F Fakhouri, J Zuber, V Frémeaux-Bacchi, C Loirat - The Lancet, 2017 - thelancet.com
Haemolytic uraemic syndrome is a form of thrombotic microangiopathy affecting
predominantly the kidney and characterised by a triad of thrombocytopenia, mechanical …

[HTML][HTML] An update for atypical haemolytic uraemic syndrome: diagnosis and treatment. A consensus document

JM Campistol, M Arias, G Ariceta, M Blasco… - Nefrología (English …, 2015 - Elsevier
Haemolytic uraemic syndrome (HUS) is a clinical entity defined as the triad of nonimmune
haemolytic anaemia, thrombocytopenia, and acute renal failure, in which the underlying …

Eculizumab in secondary atypical haemolytic uraemic syndrome

T Cavero, C Rabasco, A López… - Nephrology Dialysis …, 2017 - academic.oup.com
Background. Complement dysregulation occurs in thrombotic microangiopathies (TMAs)
other than primary atypical haemolytic uraemic syndrome (aHUS). A few of these patients …

Infections associated with the use of eculizumab: recommendations for prevention and prophylaxis

E Benamu, JG Montoya - Current opinion in infectious diseases, 2016 - journals.lww.com
Eculizumab has opened new horizons in the treatment of complement-mediated disorders.
Prophylactic and immunization strategies against the risk of Nesseria spp. infections are …

Spectrum of complement-mediated thrombotic microangiopathies: pathogenetic insights identifying novel treatment approaches

M Riedl, F Fakhouri, M Le Quintrec… - … in thrombosis and …, 2014 - thieme-connect.com
Thrombotic microangiopathy (TMA) is a rare but severe disorder characterized by
endothelial cell activation and thrombus formation. It manifests with the triad of hemolytic …

Atypical hemolytic uremic syndrome in the setting of complement-amplifying conditions: case reports and a review of the evidence for treatment with eculizumab

A Asif, A Nayer, CS Haas - Journal of nephrology, 2017 - Springer
Atypical hemolytic uremic syndrome (aHUS) is a rare, genetic, progressive, life-threatening
form of thrombotic microangiopathy (TMA) predominantly caused by dysregulation of the …

De novo thrombotic microangiopathy after kidney transplantation

N Garg, HG Rennke, M Pavlakis, K Zandi-Nejad - Transplantation Reviews, 2018 - Elsevier
Thrombotic microangiopathy (TMA) is a serious complication of transplantation that
adversely affects kidney transplant recipient and allograft survival. Post-transplant TMA is …

[PDF][PDF] Actualización en síndrome hemolítico urémico atípico: diagnóstico y tratamiento. Documento de consenso

JM Campistol, M Arias, G Ariceta, M Blasco… - Nefrología …, 2015 - SciELO Espana
El síndrome hemolítico urémico (SHU) es una entidad clínica definida por la tríada anemia
hemolítica no inmune, trombocitopenia e insuficiencia renal aguda, en la que las lesiones …

Thrombotic microangiopathy after kidney transplantation: an underdiagnosed and potentially reversible entity

A Ávila, E Gavela, A Sancho - Frontiers in Medicine, 2021 - frontiersin.org
Thrombotic microangiopathy is a rare but serious complication that affects kidney transplant
recipients. It appears in 0.8–14% of transplanted patients and negatively affects graft and …

[HTML][HTML] Thrombotic microangiopathy after renal transplantation: current insights in de novo and recurrent disease

F Abbas, M El Kossi, JJ Kim, A Sharma… - World journal of …, 2018 - ncbi.nlm.nih.gov
Thrombotic microangiopathy (TMA) is one of the most devastating sequalae of kidney
transplantation. A number of published articles have covered either de novo or recurrent …