(Q51767034)

English

Discordance between skin biopsy and kidney biopsy in an X-linked carrier of Alport syndrome.

scientific article published on 10 February 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17294221

Discordance between skin biopsy and kidney biopsy in an X-linked carrier of Alport syndrome. (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17294221

0 references

Alport syndrome

1 reference

based on heuristic

inferred from title

author name string

Lorraine A Hamiwka

1

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17294221

David H George

2

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17294221

Silviu Grisaru

3

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17294221

Julian P Midgley

4

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17294221

publication date

10 February 2007

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17294221

Pediatric Nephrology

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17294221

22

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17294221

7

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17294221

1050-1053

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17294221

https://scigraph.springernature.com/pub.10.1007/s00467-007-0437-y

0 references

Diagnosis of Alport syndrome without biopsy?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidermal basement membrane alpha 5(IV) expression in females with Alport syndrome and severity of renal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alport syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alport syndrome and thin basement membrane nephropathy: unraveling the tangled strands of type IV collagen.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Persistent familial hematuria in children and the locus for thin basement membrane nephropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The importance of non-invasive genetic analysis in the initial diagnostics of Alport syndrome in young patients.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Histopathology, ultrastructure, and clinical phenotypes in thin glomerular basement membrane disease variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative analysis of glomerular type IV collagen alpha3-5 chain expression in children with thin basement membrane disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Making the diagnosis of Alport's syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294221

12 December 2020

based on heuristic

inferred from PubMed ID 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://pubmed.ncbi.nlm.nih.gov/17294221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of alpha5(IV) collagen chain expression in skin with disease severity in women with X-linked Alport syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alport syndrome and thin glomerular basement membrane disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294221

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00467-007-0437-Y

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17294221

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17294221

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