Atypical hemolytic uremic syndrome in the Tunisian population. (Q33389773)

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3 February 2020

title

Atypical hemolytic uremic syndrome in the Tunisian population (English)

1 reference

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atypical hemolytic uremic syndrome

3 February 2020

main subject

1 reference

based on heuristic

inferred from title

author

Margarita López-Trascasa

9

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3 February 2020

author name string

Nadia Leban

1

1 reference

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3 February 2020

Sabra Aloui

2

1 reference

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3 February 2020

Dalel Touati

3

1 reference

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3 February 2020

Ramzy Lakhdhar

4

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3 February 2020

Habib Skhiri

5

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3 February 2020

Gerard Lefranc

6

1 reference

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3 February 2020

Abdellatif Achour

7

1 reference

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3 February 2020

Mezri Elmay

8

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3 February 2020

Pilar Sanchez-Corral

10

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3 February 2020

Jemni Chibani

11

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3 February 2020

Amel Haj Khelil

12

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3 February 2020

publication date

25 May 2010

1 reference

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International Urology and Nephrology

3 February 2020

published in

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volume

43

1 reference

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issue

2

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page(s)

559-564

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A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders

3 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Hemolytic Uremic Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Thrombotic Microangiopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome

21 January 2018

1 reference

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Familial relapsing haemolytic uraemic syndrome and complement factor H deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Familial haemolytic uraemic syndrome and an MCP mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Complement amplification revisited

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Atypical hemolytic-uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome

21 January 2018

1 reference

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Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals.

21 January 2018

1 reference

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Insights into hemolytic uremic syndrome: segregation of three independent predisposition factors in a large, multiple affected pedigree

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Screening for complement system abnormalities in patients with atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Recurrence of hemolytic uremic syndrome after live related renal transplantation associated with subsequent de novo disease in the donor

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Familial hypocomplementemic hemolytic uremic syndrome with HLA-A3,B7 haplotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: prognostic significance of genetic background

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11255-010-9754-3

Human complement factor H deficiency associated with hemolytic uremic syndrome.

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20499172

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Inherited complete factor I deficiency associated with systemic lupus erythematosus, higher susceptibility to infection and low levels of factor H

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20499172

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S11255-010-9754-3

1 reference

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3 February 2020

1 reference