Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1965 1
1968 1
1970 2
1972 1
1975 1
1976 2
1977 1
1979 4
1980 4
1982 3
1983 1
1984 3
1985 4
1986 3
1987 9
1988 3
1989 14
1990 16
1991 12
1992 9
1993 10
1994 6
1995 14
1996 10
1997 18
1998 22
1999 14
2000 11
2001 20
2002 16
2003 20
2004 20
2005 21
2006 15
2007 10
2008 15
2009 26
2010 22
2011 23
2012 32
2013 33
2014 26
2015 37
2016 30
2017 36
2018 33
2019 32
2020 36
2021 36
2022 56
2023 44
2024 16

Text availability

Article attribute

Article type

Publication date

Search Results

762 results

Results by year

Filters applied: . Clear all
Page 1
Pathophysiology and Management of Hyperoxaluria and Oxalate Nephropathy: A Review.
Demoulin N, Aydin S, Gillion V, Morelle J, Jadoul M. Demoulin N, et al. Am J Kidney Dis. 2022 May;79(5):717-727. doi: 10.1053/j.ajkd.2021.07.018. Epub 2021 Sep 9. Am J Kidney Dis. 2022. PMID: 34508834 Review.
Hyperoxaluria results from either inherited disorders of glyoxylate metabolism leading to hepatic oxalate overproduction (primary hyperoxaluria), or increased intestinal oxalate absorption (secondary hyperoxaluria). ...Fortunately, novel promising targeted th …
Hyperoxaluria results from either inherited disorders of glyoxylate metabolism leading to hepatic oxalate overproduction (primary …
Primary hyperoxaluria.
Cochat P, Rumsby G. Cochat P, et al. N Engl J Med. 2013 Aug 15;369(7):649-58. doi: 10.1056/NEJMra1301564. N Engl J Med. 2013. PMID: 23944302 Review. No abstract available.
Clinical practice recommendations for primary hyperoxaluria: an expert consensus statement from ERKNet and OxalEurope.
Groothoff JW, Metry E, Deesker L, Garrelfs S, Acquaviva C, Almardini R, Beck BB, Boyer O, Cerkauskiene R, Ferraro PM, Groen LA, Gupta A, Knebelmann B, Mandrile G, Moochhala SS, Prytula A, Putnik J, Rumsby G, Soliman NA, Somani B, Bacchetta J. Groothoff JW, et al. Nat Rev Nephrol. 2023 Mar;19(3):194-211. doi: 10.1038/s41581-022-00661-1. Epub 2023 Jan 5. Nat Rev Nephrol. 2023. PMID: 36604599 Review.
Primary hyperoxaluria (PH) is an inherited disorder that results from the overproduction of endogenous oxalate, leading to recurrent kidney stones, nephrocalcinosis and eventually kidney failure; the subsequent storage of oxalate can cause life-threatening systemic disease …
Primary hyperoxaluria (PH) is an inherited disorder that results from the overproduction of endogenous oxalate, leading to recurrent …
Primary hyperoxaluria.
Lorenzo V, Torres A, Salido E. Lorenzo V, et al. Nefrologia. 2014 May 21;34(3):398-412. doi: 10.3265/Nefrologia.pre2014.Jan.12335. Epub 2014 Apr 30. Nefrologia. 2014. PMID: 24798559 Free article. Review. English, Spanish.
Primary hyperoxaluria (PH) occurs due to an autosomal recessive hereditary disorder of the metabolism of glyoxylate, which causes excessive oxalate production. ...Diagnosis is based on family history, the presence of urolithiasis and/or nephrocalcinosis, hyperoxaluria …
Primary hyperoxaluria (PH) occurs due to an autosomal recessive hereditary disorder of the metabolism of glyoxylate, which causes exc …
D-glyceric aciduria.
Dimer NW, Schuck PF, Streck EL, Ferreira GC. Dimer NW, et al. An Acad Bras Cienc. 2015 Aug;87(2 Suppl):1409-14. doi: 10.1590/0001-3765201520150021. Epub 2015 Aug 4. An Acad Bras Cienc. 2015. PMID: 26247153 Free article. Review.
Hyperoxaluric calcium nephrolithiasis.
Asplin JR. Asplin JR. Endocrinol Metab Clin North Am. 2002 Dec;31(4):927-49. doi: 10.1016/s0889-8529(02)00030-0. Endocrinol Metab Clin North Am. 2002. PMID: 12474639 Review.
Hyperoxaluria leads to increased calcium oxalate supersaturation and calcium oxalate stone formation. Excess oxalate can arise from endogenous overproduction as in primary hyperoxaluria or from dietary sources. In the last 15 years great strides have been made in th …
Hyperoxaluria leads to increased calcium oxalate supersaturation and calcium oxalate stone formation. Excess oxalate can arise from e …
Secondary oxalate nephropathy and kidney transplantation.
Aziz F, Jorgenson M, Garg N. Aziz F, et al. Curr Opin Organ Transplant. 2023 Feb 1;28(1):15-21. doi: 10.1097/MOT.0000000000001035. Epub 2022 Nov 7. Curr Opin Organ Transplant. 2023. PMID: 36342385 Review.
PURPOSE OF REVIEW: Secondary hyperoxaluria is associated with poor kidney allograft outcomes after the kidney transplant. Calcium oxalate (CaOx) deposition is common in early allograft biopsies leading to acute tubular necrosis and poor kidney allograft function. Though tr …
PURPOSE OF REVIEW: Secondary hyperoxaluria is associated with poor kidney allograft outcomes after the kidney transplant. Calcium oxa …
The primary hyperoxalurias.
Hoppe B, Beck BB, Milliner DS. Hoppe B, et al. Kidney Int. 2009 Jun;75(12):1264-1271. doi: 10.1038/ki.2009.32. Epub 2009 Feb 18. Kidney Int. 2009. PMID: 19225556 Free PMC article. Review.
The primary hyperoxalurias (PHs) are rare disorders of glyoxylate metabolism in which specific hepatic enzyme deficiencies result in overproduction of oxalate. Due to the resulting severe hyperoxaluria, recurrent urolithiasis or progressive nephrocalcinosis are principal m …
The primary hyperoxalurias (PHs) are rare disorders of glyoxylate metabolism in which specific hepatic enzyme deficiencies result in overpro …
Primary Hyperoxaluria.
Xie X, Zhang X. Xie X, et al. N Engl J Med. 2022 Mar 10;386(10):976. doi: 10.1056/NEJMicm2113369. Epub 2022 Mar 5. N Engl J Med. 2022. PMID: 35245013 No abstract available.
PHYOX2: a pivotal randomized study of nedosiran in primary hyperoxaluria type 1 or 2.
Baum MA, Langman C, Cochat P, Lieske JC, Moochhala SH, Hamamoto S, Satoh H, Mourani C, Ariceta G, Torres A, Wolley M, Belostotsky V, Forbes TA, Groothoff J, Hayes W, Tönshoff B, Takayama T, Rosskamp R, Russell K, Zhou J, Amrite A, Hoppe B; PHYOX2 study investigators. Baum MA, et al. Kidney Int. 2023 Jan;103(1):207-217. doi: 10.1016/j.kint.2022.07.025. Epub 2022 Aug 22. Kidney Int. 2023. PMID: 36007597 Free article. Clinical Trial.
Oxalate overproduction is the hallmark of all genetic subtypes of primary hyperoxaluria (PH). In this double-blind, placebo-controlled study, we randomly assigned (2:1) 35 participants with PH1 (n = 29) or PH2 (n = 6) with eGFR 30 mL/min/1.73 m(2) to subcutaneous nedosiran …
Oxalate overproduction is the hallmark of all genetic subtypes of primary hyperoxaluria (PH). In this double-blind, placebo-controlle …
762 results