Renal disease associated with inherited disorders of the complement system (Q37310948)

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scientific article published on 29 October 2008

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English	Renal disease associated with inherited disorders of the complement system	scientific article published on 29 October 2008

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18958500

retrieved

19 August 2017

review article

1 reference

stated in

Europe PubMed Central

title

Renal disease associated with inherited disorders of the complement system (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18958500

retrieved

19 August 2017

main subject

kidney disease

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based on heuristic

inferred from title

author name string

Thomas R Welch

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18958500

retrieved

19 August 2017

Lisa W Blystone

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18958500

retrieved

19 August 2017

publication date

29 October 2008

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18958500

retrieved

19 August 2017

published in

Pediatric Nephrology

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stated in

Europe PubMed Central

PubMed publication ID

18958500

retrieved

19 August 2017

volume

24

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stated in

Europe PubMed Central

PubMed publication ID

18958500

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19 August 2017

issue

8

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stated in

Europe PubMed Central

PubMed publication ID

18958500

retrieved

19 August 2017

page(s)

1439-1444

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Europe PubMed Central

PubMed publication ID

18958500

retrieved

19 August 2017

cites work

Nephritic factors predispose to chronic glomerulonephritis

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS00467-008-1027-3

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21 January 2018

Molecular basis of human complement C1s deficiency

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary deficiency of the fifth component of complement in man. I. Clinical, immunochemical, and family studies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary C1q deficiency and systemic lupus erythematosus.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement factor I deficiency associated with recurrent infections, vasculitis and immune complex glomerulonephritis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Selective deficiency of the second component of complement in a patient with anaphylactoid purpura

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Major histocompatibility complex extended haplotypes in systemic lupus erythematosus

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary C2 deficiency and systemic lupus erythematosus associated with severe glomerulonephritis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Kidney transplantation in patients suffering from hereditary complete complement C4 deficiency

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited complement deficiency states: implications for immunity and immunological disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficient alternative complement pathway activation due to factor D deficiency by 2 novel mutations in the complement factor D gene in a family with meningococcal infections

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glomerulonephritis associated with complete deficiency of the fourth component of complement. Response to intravenous immunoglobulin

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restricted genetic defects underlie human complement C6 deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C1q and systemic lupus erythematosus

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe systemic lupus erythematosus with nephritis in a boy with deficiency of the fourth component of complement

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement. First of two parts

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The pathophysiology of hereditary angioedema

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic analysis of complement C1s deficiency associated with systemic lupus erythematosus highlights alternative splicing of normal C1s gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

H deficiency in two brothers with atypical dense intramembranous deposit disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial C1q deficiency in 3 siblings with glomerulonephritis and Rothmund-Thomson syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of the second component of complement. Its occurrence with membranoproliferative glomerulonephritis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary deficiency of C3 in animals and humans

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An inherited defect in the C3 convertase, C3b,Bb, associated with glomerulonephritis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor H genotype-phenotype correlations: lessons from aHUS, MPGN II, and AMD.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The phenotype of SLE associated with complete deficiency of complement isotype C4A

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IgA nephropathy in patients with congenital C9 deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C7 deficiency and persistent haematuria

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms of complement receptor 1 and interleukin-10 genes and systemic lupus erythematosus: a meta-analysis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term follow-up of non-systemic lupus erythematosus glomerulonephritis in patients with hereditary angioedema: report of four cases

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement. Second of two parts

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meningococcal disease in a kidney transplant recipient with mannose-binding lectin deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Does complement factor B have a role in the pathogenesis of atypical HUS?

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor H and the pathogenesis of renal diseases

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pediatric systemic lupus erythematosus with C1q deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous deficiency of C4 in a child with a lupus erythematosus syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A polymorphism in the type one complement receptor (CR1) involves an additional cysteine within the C3b/C4b binding domain that inhibits ligand binding.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effect of null C4 alleles on complement function.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement and the atypical hemolytic uremic syndrome in children.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of C4B deficiency in IgA nephropathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish family

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glomerulonephritis in a patient with complement factor I deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18958500

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00467-008-1027-3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18958500

retrieved

19 August 2017

Fatcat ID

release_2h26bnqbx5g7xolts25ndxq3zm

1 reference

stated in

Fatcat

reference URL

https://api.fatcat.wiki/v0/release/2h26bnqbx5g7xolts25ndxq3zm

retrieved

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

18958500

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18958500

retrieved

19 August 2017

 

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