(Q33392114)

English

Recurrent haemolytic uraemic syndrome and acquired hypomorphic variant of the third component of complement

scientific article

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scholarly article

1 reference

Europe PubMed Central

26 July 2017

Recurrent haemolytic uraemic syndrome and acquired hypomorphic variant of the third component of complement (English)

1 reference

Europe PubMed Central

26 July 2017

author name string

Roodhooft AM

1

1 reference

Europe PubMed Central

26 July 2017

McLean RH

2

1 reference

Europe PubMed Central

26 July 2017

Elst E

3

1 reference

Europe PubMed Central

26 July 2017

Van Acker KJ

4

1 reference

Europe PubMed Central

26 July 2017

publication date

1 November 1990

1 reference

Europe PubMed Central

26 July 2017

Pediatric Nephrology

1 reference

Europe PubMed Central

26 July 2017

4

1 reference

Europe PubMed Central

26 July 2017

6

1 reference

Europe PubMed Central

26 July 2017

597-599

1 reference

Europe PubMed Central

26 July 2017

https://scigraph.springernature.com/pub.10.1007/bf00858631

0 references

Hypomorphic variant of C3, arthritis, and chronic glomerulonephritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2088459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2088459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma exchanges in frequently recurrent hemolytic-uremic syndrome in a child

1 reference

https://pubmed.ncbi.nlm.nih.gov/2088459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasmapheresis in the haemolytic-uraemic syndrome in children

1 reference

https://pubmed.ncbi.nlm.nih.gov/2088459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemolytic uremic syndrome with recurrent episodes: an important subset

1 reference

https://pubmed.ncbi.nlm.nih.gov/2088459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ANTIGEN-ANTIBODY CROSSED ELECTROPHORESIS

1 reference

https://pubmed.ncbi.nlm.nih.gov/2088459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C4 uremic variant: an acquired C4 allotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/2088459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetically determined variation in the complement system: relationship to disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/2088459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent haemolytic-uraemic syndrome with hypocomplementaemia: a case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/2088459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypocomplementaemia due to a genetic deficiency of beta 1H globulin

1 reference

https://pubmed.ncbi.nlm.nih.gov/2088459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent hemolytic-uremic syndrome with the hypomorphic fast allele of the third component of complement

1 reference

https://pubmed.ncbi.nlm.nih.gov/2088459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00858631

1 reference

Europe PubMed Central

26 July 2017

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

26 July 2017

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