(Q56658122)

English

Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations

scientific article published on 11 January 2012

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scholarly article

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20 January 2020

Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations (English)

1 reference

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20 January 2020

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Frederik Peters

2

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20 January 2020

Laurence Heidet

5

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20 January 2020

6

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20 January 2020

author name string

Johanna Temme

1

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20 January 2020

Katharina Lange

3

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20 January 2020

Yves Pirson

4

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20 January 2020

Jean-Pierre Grunfeld

7

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20 January 2020

Manfred Weber

8

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20 January 2020

Christoph Licht

9

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20 January 2020

Gerhard-Anton Müller

10

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20 January 2020

Oliver Gross

11

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20 January 2020

language of work or name

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publication date

11 January 2012

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20 January 2020

Kidney International

1 reference

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20 January 2020

81

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20 January 2020

8

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20 January 2020

779-783

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20 January 2020

https://scigraph.springernature.com/pub.10.1038/ki.2011.452

0 references

HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Alport's syndrome, Goodpasture's syndrome, and type IV collagen.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetics of classic Alport's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

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[From the molecular genetics of Alport's syndrome to principles of organo-protection in chronic renal diseases]

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Meta-analysis of genotype-phenotype correlation in X-linked Alport syndrome: impact on clinical counselling

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Genotype-phenotype correlation in X-linked Alport syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Treatment of Alport syndrome: beyond animal models

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Alport syndrome and the X chromosome: implications of a diagnosis of Alport syndrome in females

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Segregation of hematuria in thin basement membrane disease with haplotypes at the loci for Alport syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Novel COL4A4 splice defect and in‐frame deletion in a large consanguine family as a genetic link between benign familial haematuria and autosomal Alport syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Thin GBM nephropathy: premature glomerular obsolescence is associated with hypertension and late onset renal failure

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Signs and symptoms of thin basement membrane nephropathy: a prospective regional study on primary glomerular disease-The Limburg Renal Registry

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Abnormally thin glomerular basement membranes associated with hematuria, proteinuria or renal failure in adults

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Thin-basement-membrane nephropathy in adults with persistent hematuria

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Thin basement membrane nephropathy

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

The clinical features of thin basement membrane nephropathy

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Living donor kidney transplantation from relatives with mild urinary abnormalities in Alport syndrome: long-term risk, benefit and outcome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Chronic renal failure and shortened lifespan in COL4A3+/- mice: an animal model for thin basement membrane nephropathy

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Women and Alport syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

The logrank test

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.452

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/KI.2011.452

1 reference

Europe PubMed Central

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20 January 2020

1 reference

Europe PubMed Central

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20 January 2020

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