(Q43990085)

English

Primary hyperoxaluria type 1, a too often missed diagnosis and potentially treatable cause of end-stage renal disease in adults: results of the Dutch cohort

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

Primary hyperoxaluria type 1, a too often missed diagnosis and potentially treatable cause of end-stage renal disease in adults: results of the Dutch cohort (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

primary hyperoxaluria

1 reference

based on heuristic

inferred from title

primary hyperoxaluria type I

1 reference

based on heuristic

inferred from title

author name string

S M van der Hoeven

1

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

C S van Woerden

2

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

J W Groothoff

3

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

language of work or name

0 references

publication date

27 July 2012

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

Nephrology Dialysis Transplantation

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

27

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

3855-3862

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

Molecular etiology of primary hyperoxaluria type 1: new directions for treatment

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

Cardiac abnormalities in primary hyperoxaluria

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT gene.

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

Pyridoxine effect in type I primary hyperoxaluria is associated with the most common mutant allele

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

Clinical implications of mutation analysis in primary hyperoxaluria type 1.

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

Partial trypsin digestion as an indicator of mis-folding of mutant alanine:glyoxylate aminotransferase and chaperone effects of specific ligands. Study of a spectrum of missense mutants.

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

Genotype-phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

Primary hyperoxaluria: clinical course, diagnosis, and treatment after kidney failure

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

Primary hyperoxaluria type 1 in The Netherlands: prevalence and outcome

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

Management of primary hyperoxaluria: efficacy of oral citrate administration

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

International registry for primary hyperoxaluria

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

Primary hyperoxaluria--the German experience

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

Primary hyperoxaluria type 1 in Japan

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

Primary hyperoxaluria type 1: still challenging!

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

Is there a genotype-phenotype correlation in primary hyperoxaluria type 1?

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

Effect of conservative treatment on the renal outcome of children with primary hyperoxaluria type 1.

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

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/10.1093%2FNDT%2FGFS320

21 January 2018

Primary hyperoxaluria type 1 in the Canary Islands: a conformational disease due to I244T mutation in the P11L-containing alanine:glyoxylate aminotransferase

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFS320

21 January 2018

Identifiers

10.1093/NDT/GFS320

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

ResearchGate publication ID

0 references

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