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Title
Genetic determinants of urolithiasis
Authors
Keywords
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Journal
Nature Reviews Nephrology
Volume 8, Issue 3, Pages 151-162
Publisher
Springer Nature
Online
2011-12-20
DOI
10.1038/nrneph.2011.211
References
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Note: Only part of the references are listed.- 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
- Association Between the T-593A and C6982T Polymorphisms of the Osteopontin Gene and Risk of Developing Nephrolithiasis
- (2010) Bülent Gögebakan et al. ARCHIVES OF MEDICAL RESEARCH
- The impact of osteopontin promoter polymorphisms on the risk of calcium urolithiasis
- (2010) Chia-Chu Liu et al. CLINICA CHIMICA ACTA
- Phenotype and Genotype Characterization of Adenine Phosphoribosyltransferase Deficiency
- (2010) G. Bollee et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Crystalline nephropathy due to 2,8-dihydroxyadeninuria: an under-recognized cause of irreversible renal failure
- (2010) S. H. Nasr et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Risk Factors for CKD in Persons With Kidney Stones: A Case-Control Study in Olmsted County, Minnesota
- (2009) Nathan A. Saucier et al. AMERICAN JOURNAL OF KIDNEY DISEASES
- Primary hyperoxaluria type 1: update and additional mutation analysis of theAGXTgene
- (2009) Emma L. Williams et al. HUMAN MUTATION
- Hypophosphatemic Rickets with Hypercalciuria due to Mutation inSLC34A3/Type IIc Sodium-Phosphate Cotransporter: Presentation as Hypercalciuria and Nephrolithiasis
- (2009) Amanda L. Tencza et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Large rearrangements detected by MLPA, point mutations, and survey of the frequency of mutations within the SLC3A1 and SLC7A9 genes in a cohort of 172 cystinuric Italian patients
- (2009) Luigi Bisceglia et al. MOLECULAR GENETICS AND METABOLISM
- Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density
- (2009) Gudmar Thorleifsson et al. NATURE GENETICS
- TRPV5 gene polymorphisms in renal hypercalciuria
- (2009) K. Y. Renkema et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Claudin-16 and claudin-19 interaction is required for their assembly into tight junctions and for renal reabsorption of magnesium
- (2009) J. Hou et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Lithiases rénales héréditaires monogéniques : récents acquis diagnostiques et thérapeutiques
- (2008) Paul Jungers et al. Nephrologie & Therapeutique
- CLDN16 Genotype Predicts Renal Decline in Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis
- (2007) M. Konrad et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
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