Inherited factor H deficiency and collagen type III glomerulopathy (Q49287293)

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scientific article published in February 1995

Language	Label	Description	Also known as
English	Inherited factor H deficiency and collagen type III glomerulopathy	scientific article published in February 1995

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/7742208

Inherited factor H deficiency and collagen type III glomerulopathy (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/7742208

2

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/7742208

author name string

B A Vogt

1

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/7742208

B A Burke

3

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/7742208

S C Simonton

4

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/7742208

C E Kashtan

5

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/7742208

publication date

1 February 1995

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/7742208

Pediatric Nephrology

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/7742208

9

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/7742208

1

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/7742208

11-15

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/7742208

Combined homozygous factor H and heterozygous C2 deficiency in an Italian family

1 reference

https://pubmed.ncbi.nlm.nih.gov/7742208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunofluorescence studies of dense deposit disease. The presence of railroad tracks and mesangial rings

1 reference

https://pubmed.ncbi.nlm.nih.gov/7742208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ISOLATION OF BETA IF-GLOBULIN FROM HUMAN SERUM AND ITS CHARACTERIZATION AS THE FIFTH COMPONENT OF COMPLEMENT.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7742208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Collagen Type III Glomerulopathy: A New Idiopathic Glomerular Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/7742208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary, complete deficiency of complement factor H associated with recurrent meningococcal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/7742208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Collagen type III glomerulopathy: a new type of hereditary nephropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7742208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary glomerular fibrosis: a new nephropathy caused by diffuse intra-glomerular increase in atypical type III collagen fibers

1 reference

https://pubmed.ncbi.nlm.nih.gov/7742208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of collagenofibrotic glomerulopathy associated with hepatic perisinusoidal fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7742208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glomerular localization of type III collagen in human kidney disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/7742208

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

https://pubmed.ncbi.nlm.nih.gov/7742208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Control of serum C3 levels by beta 1H and C3b inactivator

1 reference

https://pubmed.ncbi.nlm.nih.gov/7742208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/7742208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial H (beta 1H) deficiency and glomerulonephritis in two families

1 reference

https://pubmed.ncbi.nlm.nih.gov/7742208

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/7742208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephrotic syndrome with massive accumulation of type I and type III collagen in the glomeruli

1 reference

https://pubmed.ncbi.nlm.nih.gov/7742208

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00858956

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/7742208

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/7742208

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