Primary hyperoxaluria in populations of Pakistan origin: results from a literature review and two major registries
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Title
Primary hyperoxaluria in populations of Pakistan origin: results from a literature review and two major registries
Authors
Keywords
Primary hyperoxaluria, Consanguinity, Oxalate stones, Oxalosis, End-stage renal disease, Pakistan origin, Oxalate crystals, Mutation analysis
Journal
Urolithiasis
Volume 46, Issue 2, Pages 187-195
Publisher
Springer Nature
Online
2017-06-28
DOI
10.1007/s00240-017-0996-8
References
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Related references
Note: Only part of the references are listed.- An Investigational RNAi Therapeutic Targeting Glycolate Oxidase Reduces Oxalate Production in Models of Primary Hyperoxaluria
- (2016) Abigail Liebow et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
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- (2016) Oliver Clifford-Mobley et al. ANNALS OF CLINICAL BIOCHEMISTRY
- 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
- Data from a large European study indicate that the outcome of primary hyperoxaluria type 1 correlates with the AGXT mutation type
- (2014) Giorgia Mandrile et al. KIDNEY INTERNATIONAL
- Ethnic differences inGRHPRmutations in patients with primary hyperoxaluria type 2
- (2013) T. Takayama et al. CLINICAL GENETICS
- Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies
- (2012) Bodo B Beck et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- 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
- Ayurvedic medicine and NADPH oxidase: a possible approach to the prevention of ESRD in hyperoxaluria
- (2011) G. Gambaro et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Pre-emptive liver transplantation for primary hyperoxaluria (PH-I) arrests long-term renal function deterioration
- (2010) M. T. P. Perera et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Primary hyperoxaluria type 1: update and additional mutation analysis of theAGXTgene
- (2009) Emma L. Williams et al. HUMAN MUTATION
- Late diagnosis of primary hyperoxaluria after failed kidney transplantation
- (2009) Goce Spasovski et al. INTERNATIONAL UROLOGY AND NEPHROLOGY
- Genotype–phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome
- (2009) Jérôme Harambat et al. KIDNEY INTERNATIONAL
- Calcium oxalate crystals in the bone marrow
- (2008) Raihan Sajid et al. BRITISH JOURNAL OF HAEMATOLOGY
- Consanguinity and its relevance to clinical genetics
- (2003) AH Bittles CLINICAL GENETICS
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