A family with X-linked benign familial hematuria. (Q54453204)

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English	A family with X-linked benign familial hematuria.	scientific article

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scholarly article

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

A family with X-linked benign familial hematuria. (English)

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

Kazunari Kaneko

1

object named as

Kazunari Kaneko

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

author name string

Sachiyo Tanaka

2

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

Masafumi Hasui

3

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

Kandai Nozu

4

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

Rafal Przybyslaw Krol

5

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

Kazumoto Iijima

6

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

Keisuke Sugimoto

7

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

Tsukasa Takemura

8

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

publication date

1 March 2010

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

Pediatric Nephrology

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

25

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

3

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

545-548

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

https://scigraph.springernature.com/pub.10.1007/s00467-009-1370-z

0 references

Somatic mosaicism associated with a mild Alport syndrome phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/19937058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Collagen alpha5 and alpha2(IV) chain coexpression: analysis of skin biopsies of Alport patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19937058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Benign familial hematuria due to mutation of the type IV collagen alpha4 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/19937058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19937058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19937058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in theCOL4A4 and COL4A3 genes cause familial benign hematuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/19937058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrum of mutations in the COL4A5 collagen gene in X-linked Alport syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19937058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19937058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidn

1 reference

https://pubmed.ncbi.nlm.nih.gov/19937058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sixteen novel mutations identified in COL4A3, COL4A4, and COL4A5 genes in Slovenian families with Alport syndrome and benign familial hematuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/19937058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficient detection of Alport syndrome COL4A5 mutations with multiplex genomic PCR-SSCP

1 reference

https://pubmed.ncbi.nlm.nih.gov/19937058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thin basement membrane nephropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19937058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alport syndrome and benign familial hematuria (thin basement membrane disease) in two brothers of a family with hematuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/19937058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nine novel COL4A3 and COL4A4 mutations and polymorphisms identified in inherited membrane diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/19937058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00467-009-1370-Z

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

1 reference

Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/19937058

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