Clinical characterization of primary hyperoxaluria type 3 in comparison with types 1 and 2
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Title
Clinical characterization of primary hyperoxaluria type 3 in comparison with types 1 and 2
Authors
Keywords
-
Journal
NEPHROLOGY DIALYSIS TRANSPLANTATION
Volume -, Issue -, Pages -
Publisher
Oxford University Press (OUP)
Online
2021-02-03
DOI
10.1093/ndt/gfab027
References
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Related references
Note: Only part of the references are listed.- Endpoints for Clinical Trials in Primary Hyperoxaluria
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- Association of Urinary Oxalate Excretion With the Risk of Chronic Kidney Disease Progression
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- Nine novel HOGA1 gene mutations identified in primary hyperoxaluria type 3 and distinct clinical and biochemical characteristics in Chinese children
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- Urinary oxalate as a potential mediator of kidney disease in diabetes mellitus and obesity
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- Patients with primary hyperoxaluria type 2 have significant morbidity and require careful follow-up
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- Clinical features of genetically confirmed patients with primary hyperoxaluria identified by clinical indication versus familial screening
- (2019) David J. Sas et al. KIDNEY INTERNATIONAL
- Personalized Intervention in Monogenic Stone Formers
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- Metabolite diagnosis of primary hyperoxaluria type 3
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- Molecular basis of primary hyperoxaluria: clues to innovative treatments
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- Systematic assessment of urinary hydroxy-oxo-glutarate for diagnosis and follow-up of primary hyperoxaluria type III
- (2017) Ada Ventzke et al. PEDIATRIC NEPHROLOGY
- An estimated glomerular filtration rate equation for the full age spectrum
- (2016) Hans Pottel et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Predictors of Incident ESRD among Patients with Primary Hyperoxaluria Presenting Prior to Kidney Failure
- (2015) F. Zhao et al. Clinical Journal of the American Society of Nephrology
- Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria
- (2015) K. Hopp et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Nephrocalcinosis is a risk factor for kidney failure in primary hyperoxaluria
- (2015) Xiaojing Tang et al. KIDNEY INTERNATIONAL
- Stone Composition Among First-Time Symptomatic Kidney Stone Formers in the Community
- (2015) Prince Singh et al. MAYO CLINIC PROCEEDINGS
- Renal function can be impaired in children with primary hyperoxaluria type 3
- (2015) Lise Allard et al. PEDIATRIC NEPHROLOGY
- Primary hyperoxalurias: diagnosis and treatment
- (2014) Efrat Ben-Shalom et al. PEDIATRIC NEPHROLOGY
- Kidney Stones in Primary Hyperoxaluria: New Lessons Learnt
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- Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies
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- An update on primary hyperoxaluria
- (2012) Bernd Hoppe Nature Reviews Nephrology
- The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type III
- (2012) B. Hoppe NEPHROLOGY DIALYSIS TRANSPLANTATION
- The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type 3
- (2012) E. L. Williams et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment
- (2012) P. Cochat et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Primary Hyperoxaluria Type III Gene HOGA1 (Formerly DHDPSL) as a Possible Risk Factor for Idiopathic Calcium Oxalate Urolithiasis
- (2011) C. G. Monico et al. Clinical Journal of the American Society of Nephrology
- Mutations in DHDPSL Are Responsible For Primary Hyperoxaluria Type III
- (2010) Ruth Belostotsky et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The primary hyperoxalurias
- (2009) Bernd Hoppe et al. KIDNEY INTERNATIONAL
- Peculiar Morphology of Stones in Primary Hyperoxaluria
- (2008) Michel Daudon et al. NEW ENGLAND JOURNAL OF MEDICINE
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