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Cited by 586

The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index.

Primary Hyperoxaluria

Cochat, Pierre, Rumsby, Gill·2013·New England Journal of Medicine

Abstract

The primary hyperoxalurias are a group of autosomal recessive disorders of endogenous oxalate overproduction. This review discusses the major biochemical, genetic, and therapeutic advances that have led to a better understanding of the disease.

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Registry

Crossref · 10.1056/nejmra1301564

Cites

32 of 32 references verified0 citation errors · 0 not checkable

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Citations

Cites

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Cited by

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Metadata

Authors
Cochat, P., & Rumsby, G.
Venue
New England Journal of Medicine
Published
2013-08-15
Volume
369
Issue
7
Pages
649-658
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W4236938577
Cited by
586
References
32
FWCI
22.41
Type
journal article
Language
en
Open access
closed

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This page
CoChat. (2026). Citation check: Primary Hyperoxaluria. https://app.cochat.ai/papers/10.1056/nejmra1301564
The paper
Cochat, P., & Rumsby, G. (2013). Primary Hyperoxaluria. New England Journal of Medicine. https://doi.org/10.1056/nejmra1301564

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.