(Q50472643)

English

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

scientific article published on 8 June 2005

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15942778

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

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15942778

Alport syndrome

1 reference

based on heuristic

inferred from title

author name string

Maja Slajpah

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15942778

Anamarija Meglic

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15942778

Polonca Furlan

3

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15942778

Damjan Glavac

4

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15942778

publication date

8 June 2005

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15942778

Pediatric Nephrology

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15942778

20

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15942778

9

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15942778

1260-1264

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15942778

https://scigraph.springernature.com/pub.10.1007/s00467-005-1975-9

0 references

X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15942778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alport syndrome. An inherited disorder of renal, ocular, and cochlear basement membranes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15942778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contemporary diagnostic approach in Alport's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15942778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Erythrocyte deformability and microhematuria in children and adolescents

1 reference

https://pubmed.ncbi.nlm.nih.gov/15942778

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/15942778

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/15942778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alport's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15942778

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/15942778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High mutation detection rate in the COL4A5 collagen gene in suspected Alport syndrome using PCR and direct DNA sequencing.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15942778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alport disease: a review of the diagnostic difficulties

1 reference

https://pubmed.ncbi.nlm.nih.gov/15942778

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/15942778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary nephropathy (Alport syndrome): correlation of clinical data with glomerular basement membrane alterations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15942778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of mutations in the COL4A5 collagen gene in Alport syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15942778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15942778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15942778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00467-005-1975-9

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15942778

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15942778

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q50472643&oldid=1503703194"