Results 31 to 40 of about 7,162 (211)

Challenges in classification of novel CFH variants in patients with atypical hemolytic uremic syndrome

open access: yesThrombosis Update, 2020
Atypical hemolytic uremic syndrome (aHUS) is a thrombotic microangiopathy (TMA) characterized by dysregulation of the alternative pathway of complement. Heterozygous variants in complement and complement regulatory proteins may increase risk for aHUS and,
Meera Sridharan   +4 more
doaj   +1 more source

Rapid Resolution of Atypical Hemolytic Uremic Syndrome by Eculizumab Treatment [PDF]

open access: yesChildhood Kidney Diseases, 2020
Atypical hemolytic uremic syndrome (aHUS) is an extremely rare and life-threatening disorder. Typical HUS is often caused by Shiga toxin-positive Escherichia coli, while aHUS is caused by dysregulation of the alternative pathway of the complement system ...
Min Seung Kim   +5 more
doaj   +1 more source

Gain of function mutant of complement factor B K323E mimics pathogenic C3NeF autoantibodies in convertase assays

open access: yesAutoimmunity, 2018
Complement convertases are enzymatic complexes, which play a critical role in propagation and amplification of the complement cascade. Under physiological conditions, convertases decay shortly after being formed in either spontaneous or inhibitor-driven ...
Aleksandra Urban   +6 more
doaj   +1 more source

Case Report: Lipoprotein Glomerulopathy Complicated by Atypical Hemolytic Uremic Syndrome

open access: yesFrontiers in Medicine, 2021
Lipoprotein glomerulopathy (LPG) is a rare inherited disease caused by mutations in the APOE gene, encoding apolipoprotein E (apoE). Atypical hemolytic uremic syndrome (aHUS) is a thrombotic microangiopathy (TMA) characterized by overactivation of the ...
Lara Kollbrunner   +7 more
doaj   +1 more source

Demographic data of Brazilian aHUS cohort patients in renal transplantation.

open access: yes, 2021
Demographic data of Brazilian aHUS cohort patients in renal transplantation.
Hong Si Nga (4592092)   +9 more
core   +1 more source

Epidemiology of Atypical Hemolytic Uremic Syndrome: A Systematic Literature Review

open access: yesClinical Epidemiology, 2020
Kevin Yan,1,2 Kamal Desai,1 Lakshmi Gullapalli,1 Eric Druyts,1 Chakrapani Balijepalli1 1Pharmalytics Group, Vancouver, British Columbia, Canada; 2Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, CanadaCorrespondence ...
Yan K   +4 more
doaj  

The Ahu (Capreolus pygargus) [PDF]

open access: yesAnnals and Magazine of Natural History, 1872
n ...
openaire   +2 more sources

COMPLEMENTing the diagnosis of aHUS

open access: yesBlood, 2014
In this issue of Blood , Noris et al describe a functional complement assay that can be used to diagnose atypical hemolytic-uremic syndrome (aHUS).[1][1] This assay might also be useful in identifying aHUS patients in remission and in detecting asymptomatic carriers of complement gene mutations.
openaire   +3 more sources

Paediatric renal transplantation: Paediatric surgeons' perspective

open access: yesSurgical Practice, EarlyView.
Abstract Renal transplantation is the most effective treatment for paediatric end‐stage renal disease (ESRD), offering advantages in survival, growth and neurocognitive development that surpass other renal replacement therapies (RRT). The paediatric setting, however, introduces distinct complexities that distinguish it from adult practice.
Adrian Chi‐heng Fung   +3 more
wiley   +1 more source

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