A case of atypical hemolytic uremic syndrome with a transient decrease in complement factor H. (Q33369638)

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English	A case of atypical hemolytic uremic syndrome with a transient decrease in complement factor H.	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

16362720

retrieved

26 July 2017

title

A case of atypical hemolytic uremic syndrome with a transient decrease in complement factor H. (English)

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Europe PubMed Central

PubMed publication ID

16362720

retrieved

26 July 2017

main subject

atypical hemolytic uremic syndrome

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inferred from title

author name string

Hyewon Hahn

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1

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Europe PubMed Central

PubMed publication ID

16362720

retrieved

26 July 2017

Eun Young Um

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2

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Europe PubMed Central

PubMed publication ID

16362720

retrieved

26 July 2017

Young Seo Park

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3

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Europe PubMed Central

PubMed publication ID

16362720

retrieved

26 July 2017

Hae Il Cheong

series ordinal

4

1 reference

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Europe PubMed Central

PubMed publication ID

16362720

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26 July 2017

publication date

17 December 2005

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stated in

Europe PubMed Central

PubMed publication ID

16362720

retrieved

26 July 2017

published in

Pediatric Nephrology

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stated in

Europe PubMed Central

PubMed publication ID

16362720

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26 July 2017

volume

21

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Europe PubMed Central

PubMed publication ID

16362720

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26 July 2017

issue

2

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Europe PubMed Central

PubMed publication ID

16362720

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26 July 2017

page(s)

295-298

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Europe PubMed Central

PubMed publication ID

16362720

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26 July 2017

cites work

Attempted treatment of factor H deficiency by liver transplantation

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

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12 December 2020

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inferred from PubMed ID database lookup

Genetic studies into inherited and sporadic hemolytic uremic syndrome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial hemolytic uremic syndrome associated with complement factor H deficiency

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atypical (non-diarrhea-associated) hemolytic-uremic syndrome in childhood

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

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12 December 2020

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inferred from PubMed ID database lookup

FHL-1/reconectin: a human complement and immune regulator with cell-adhesive function

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

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12 December 2020

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inferred from PubMed ID database lookup

Familial haemolytic uraemic syndrome and an MCP mutation

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

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12 December 2020

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inferred from PubMed ID database lookup

Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

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12 December 2020

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inferred from PubMed ID database lookup

The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohorts

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in CD46, a complement regulatory protein, predispose to atypical HUS.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemolytic Uremic Syndrome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The risk of recurrence of hemolytic uremic syndrome after renal transplantation in children

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemolytic uremic syndrome

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

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12 December 2020

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inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor H and the pathogenesis of renal diseases

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Control of the complement system.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A favorable outcome of hemolytic uremic syndrome with factor H deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16362720

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00467-005-2108-1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16362720

retrieved

26 July 2017

Dimensions Publication ID

1015769862

0 references

PubMed publication ID

16362720

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16362720

retrieved

26 July 2017

 

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