(Q46551809)

English

Intra-familial clinical heterogeneity: absence of genotype-phenotype correlation in primary hyperoxaluria type 1 in Israel

scientific article published in May 2005

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

Intra-familial clinical heterogeneity: absence of genotype-phenotype correlation in primary hyperoxaluria type 1 in Israel (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

0 references

1 reference

based on heuristic

inferred from title

genotype-phenotype correlation

1 reference

based on heuristic

inferred from title

primary hyperoxaluria

1 reference

based on heuristic

inferred from title

primary hyperoxaluria type I

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Ronald J A Wanders

8

object named as

Ronald J A Wanders

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

author name string

Yaacov Frishberg

1

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

Choni Rinat

2

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

Adel Shalata

3

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

Ihab Khatib

4

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

Sofia Feinstein

5

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

Rachel Becker-Cohen

6

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

Irit Weismann

7

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

Gill Rumsby

9

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

Frank Roels

10

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

Hanna Mandel

11

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

publication date

1 May 2005

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

American Journal of Nephrology

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

25

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

3

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

269-275

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

End-stage renal disease of the Tunisian child: epidemiology, etiologies, and outcome

1 reference

https://api.crossref.org/works/10.1159%2F000086357

21 January 2018

Characterization and chromosomal mapping of a genomic clone encoding human alanine:glyoxylate aminotransferase

1 reference

https://api.crossref.org/works/10.1159%2F000086357

21 January 2018

Genetic heterogeneity in primary hyperoxaluria type 1: impact on diagnosis

1 reference

https://api.crossref.org/works/10.1159%2F000086357

21 January 2018

Primary hyperoxaluria type 1: improved outcome with timely liver transplantation: a single-center report of 36 children

1 reference

https://api.crossref.org/works/10.1159%2F000086357

21 January 2018

Evaluation of mutation screening as a first line test for the diagnosis of the primary hyperoxalurias.

1 reference

https://api.crossref.org/works/10.1159%2F000086357

21 January 2018

Genetic analysis--a diagnostic tool for primary hyperoxaluria type I.

1 reference

https://api.crossref.org/works/10.1159%2F000086357

21 January 2018

Clinical implications of mutation analysis in primary hyperoxaluria type 1.

1 reference

https://api.crossref.org/works/10.1159%2F000086357

21 January 2018

Why mutation analysis does not always predict clinical consequences: explanations in the era of genomics

1 reference

https://api.crossref.org/works/10.1159%2F000086357

21 January 2018

Maneuvering in the complex path from genotype to phenotype

1 reference

https://api.crossref.org/works/10.1159%2F000086357

21 January 2018

Identifiers

10.1159/000086357

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/15961946

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