An update on primary hyperoxaluria (Q38017938)

27 August 2017

title

An update on primary hyperoxaluria (English)

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27 August 2017

Bernd Hoppe

1

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27 August 2017

language of work or name

English

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publication date

12 June 2012

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Nature Reviews Nephrology

27 August 2017

published in

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27 August 2017

volume

8

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27 August 2017

issue

8

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27 August 2017

page(s)

467-475

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Primary hyperoxaluria type 1 in The Netherlands: prevalence and outcome

27 August 2017

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Primary hyperoxaluria type 2 without L-glycericaciduria: is the disease under-diagnosed?

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Mutations in DHDPSL Are Responsible For Primary Hyperoxaluria Type III

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Primary Hyperoxaluria Type III Gene HOGA1 (Formerly DHDPSL) as a Possible Risk Factor for Idiopathic Calcium Oxalate Urolithiasis

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Peculiar morphology of stones in primary hyperoxaluria

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Oxalobacter sp. reduces urinary oxalate excretion by promoting enteric oxalate secretion

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Oxalobacter formigenes gen. nov., sp. nov.: oxalate-degrading anaerobes that inhabit the gastrointestinal tract

21 January 2018

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Hyperoxaluria is reduced and nephrocalcinosis prevented with an oxalate-degrading enzyme in mice with hyperoxaluria

21 January 2018

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Enteric oxalate elimination is induced and oxalate is normalized in a mouse model of primary hyperoxaluria following intestinal colonization withOxalobacter

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Hyperoxaluria: a gut-kidney axis?

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Management of primary hyperoxaluria: efficacy of oral citrate administration

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Renal handling of citrate

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Implications of genotype and enzyme phenotype in pyridoxine response of patients with type I primary hyperoxaluria

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Characteristics and outcomes of children with primary oxalosis requiring renal replacement therapy

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Combined liver-kidney and kidney-alone transplantation in primary hyperoxaluria

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Proteome of human calcium kidney stones

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Role of low native state kinetic stability and interaction of partially unfolded states with molecular chaperones in the mitochondrial protein mistargeting associated with primary hyperoxaluria

21 January 2018

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In vivo and in vitro examination of stability of primary hyperoxaluria-associated human alanine:glyoxylate aminotransferase

21 January 2018

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Changing pattern of primary hyperoxaluria in Switzerland

21 January 2018

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The primary hyperoxalurias

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2012.113

Systemic oxalosis: pathognomonic renal and specific extrarenal findings on US and CT

31 March 2020

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Plasma calcium oxalate supersaturation in children with primary hyperoxaluria and end-stage renal failure

31 March 2020

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Unusual painful sclerotic plaques on the legs of a patient with late diagnosis of primary hyperoxaluria type I

31 March 2020

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Molecular aetiology of primary hyperoxaluria type 1

31 March 2020

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https://api.crossref.org/works/10.1038/NRNEPH.2012.113

Reduction of Plasma Oxalate Levels by Oral Application of Oxalobacter formigenes in 2 Patients With Infantile Oxalosis

31 March 2020

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https://api.crossref.org/works/10.1038/NRNEPH.2012.113

Evidence of true genotype-phenotype correlation in primary hyperoxaluria type 1

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2012.113

Presentation and role of transplantation in adult patients with type 1 primary hyperoxaluria and the I244T AGXT mutation: Single-center experience

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2012.113

The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type 3

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2012.113

Nephrocalcinosis and urolithiasis in children

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2012.113

Plasma Profiles and Dialysis Kinetics of Oxalate in Patients Receiving Hemodialysis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2012.113

Selected exonic sequencing of the AGXT gene provides a genetic diagnosis in 50% of patients with primary hyperoxaluria type 1

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2012.113

Comprehensive mutation screening in 55 probands with type 1 primary hyperoxaluria shows feasibility of a gene-based diagnosis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2012.113

Oxalobacter formigenes: a potential tool for the treatment of primary hyperoxaluria type 1

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2012.113

Results of long-term treatment with orthophosphate and pyridoxine in patients with primary hyperoxaluria

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2012.113

Clearance and removal of oxalate in children on intensified dialysis for primary hyperoxaluria type 1

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2012.113

Oxalate elimination via hemodialysis or peritoneal dialysis in children with chronic renal failure

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2012.113

Long-term results of pre-emptive liver transplantation in primary hyperoxaluria type 1

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2012.113

Liver cell transplantation in severe infantile oxalosis--a potential bridging procedure to orthotopic liver transplantation?

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2012.113

Primary hyperoxaluria: genotype-phenotype correlation

31 March 2020

1 reference

12 December 2020

Oxalate removal in type I hyperoxaluria or acquired oxalosis using HD and equilibration PD

1 reference

12 December 2020

Regulatory aspects of oxalate secretion in enteric oxalate elimination.

1 reference

12 December 2020

Plasma and urine glycolate assays for differentiating the hyperoxaluria syndromes

1 reference

12 December 2020

The primary hyperoxalurias

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12 December 2020

Identifiers

DOI

10.1038/NRNEPH.2012.113

1 reference

27 August 2017

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