The genetics of atypical hemolytic uremic syndrome (Q92730532)

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1 May 2020

title

The genetics of atypical hemolytic uremic syndrome (English)

1 reference

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atypical hemolytic uremic syndrome

1 May 2020

main subject

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Wouter J C Feitz

1

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1 May 2020

Nicole C A J van de Kar

2

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1 May 2020

Dorothea Orth-Höller

3

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1 May 2020

Lambert P J W van den Heuvel

4

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1 May 2020

Christoph Licht

5

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1 May 2020

publication date

21 December 2018

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1 May 2020

1 reference

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1 May 2020

volume

30

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1 May 2020

issue

4

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1 May 2020

page(s)

400-409

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Anticomplement Treatment in Atypical and Typical Hemolytic Uremic Syndrome

1 May 2020

cites work

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[Human genetics in atypical hemolytic uremic syndrome-its role in diagnosis and treatment]

11 February 2021

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Clinical and genetic predictors of atypical hemolytic uremic syndrome phenotype and outcome

11 February 2021

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Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (CFH) gene family.

11 February 2021

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Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy.

11 February 2021

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Atypical Hemolytic Uremic Syndrome: A Meta-Analysis of Case Reports Confirms the Prevalence of Genetic Mutations and the Shift of Treatment Regimens

11 February 2021

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Thrombotic Microangiopathy and the Kidney

11 February 2021

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Factor H Competitor Generated by Gene Conversion Events Associates with Atypical Hemolytic Uremic Syndrome

11 February 2021

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Haemolytic uraemic syndrome

11 February 2021

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Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies Conference.

11 February 2021

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Thrombotic Microangiopathy in Inverted Formin 2-Mediated Renal Disease

11 February 2021

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Serological and genetic complement alterations in infection-induced and complement-mediated hemolytic uremic syndrome

11 February 2021

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11 February 2021

All Things Complement

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The alternative pathway of complement and the thrombotic microangiopathies

11 February 2021

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A De Novo Deletion in the Regulators of Complement Activation Cluster Producing a Hybrid Complement Factor H/Complement Factor H-Related 3 Gene in Atypical Hemolytic Uremic Syndrome.

11 February 2021

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11 February 2021

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An international consensus approach to the management of atypical hemolytic uremic syndrome in children

11 February 2021

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Syndromes of thrombotic microangiopathy

11 February 2021

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

11 February 2021

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A novel atypical hemolytic uremic syndrome-associated hybrid CFHR1/CFH gene encoding a fusion protein that antagonizes factor H-dependent complement regulation

11 February 2021

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Genetics of atypical hemolytic uremic syndrome (aHUS).

11 February 2021

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Atypical hemolytic uremic syndrome

11 February 2021

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Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome

11 February 2021

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A novel hybrid CFHR1/CFH gene causes atypical hemolytic uremic syndrome

11 February 2021

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Complement factor H related proteins (CFHRs)

11 February 2021

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Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome

11 February 2021

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Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype

11 February 2021

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Complement disorders and hemolytic uremic syndrome

11 February 2021

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Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome

11 February 2021

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Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults

11 February 2021

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Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristics

11 February 2021

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A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome

11 February 2021

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Atypical hemolytic uremic syndrome

11 February 2021

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A novel deletion in the RCA gene cluster causes atypical hemolytic uremic syndrome.

11 February 2021

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Glomerular diseases: genetic causes and future therapeutics.

11 February 2021

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Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype

11 February 2021

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Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome

11 February 2021

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Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome

11 February 2021

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Atypical hemolytic-uremic syndrome

11 February 2021

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Complement regulators and inhibitory proteins

11 February 2021

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Thrombomodulin mutations in atypical hemolytic-uremic syndrome

11 February 2021

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Atypical haemolytic uraemic syndrome associated with a hybrid complement gene

11 February 2021

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Thrombotic Microangiopathies

11 February 2021

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Genetic studies into inherited and sporadic hemolytic uremic syndrome

11 February 2021

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Hypocomplementaemia due to a genetic deficiency of beta 1H globulin

11 February 2021

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10.1007/S11825-018-0216-0

11 February 2021

Identifiers

DOI

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1 May 2020

1 reference

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1 May 2020

PubMed publication ID

30930551

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