Page last updated: 2024-08-26

2,8-dihydroxyadenine and Urinary Lithiasis

2,8-dihydroxyadenine has been researched along with Urinary Lithiasis in 17 studies

Research

Studies (17)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (5.88)29.6817
2010's13 (76.47)24.3611
2020's3 (17.65)2.80

Authors

AuthorsStudies
Bagai, S; Bansal, B; Khullar, D1
Anders, HJ; Boor, P; Djudjaj, S; Edvardsson, VO; Floege, J; Foresto-Neto, O; Hardarson, S; Jahnen-Dechent, W; Klinkhammer, BM; Kunter, U; Moeller, MJ; Mulay, SR; Palsson, R; Thorsteinsdottir, M; Wiech, T1
Edvardsson, VO; Goldfarb, DS; Ketteridge, D; Lin, TL; Michael, M; Palsson, R; Rich, PR; Runolfsdottir, HL; Sayer, JA1
Chen, J; Cheng, Y; Guo, L; Wang, M; Wang, R1
Kimura, T; Kurosawa, A; Nanmoku, K; Shimizu, T; Shinzato, T; Yagisawa, T1
Edvardsson, VO; Eiriksson, F; Goldfarb, DS; Oddsdottir, GS; Palsson, R; Runolfsdottir, HL; Sch Agustsdottir, IM; Thorsteinsdottir, M; Thorsteinsdottir, UA1
Bass, P; Dupont, P; Moochhala, S; Oomatia, A1
Agustsdottir, IM; Edvardsson, VO; Indridason, OS; Palsson, R; Runolfsdottir, HL1
Chan, IHS; Kwok, JSS; Lau, NKC; Ng, KS; Ng, SKW1
Furrow, E; Lulich, JP; Osborne, CA; Pfeifer, RJ1
Hemmilä, U; Kaartinen, K; Kouri, T; Mäkelä, S; Räisänen-Sokolowski, A; Salmela, K1
Haba, T; Koike, H; Yamaguchi, S1
Al-Rushaidan, S; Francis, I; George, SA; Nampoory, MRN; Soonowala, D1
Agustsdottir, IM; Edvardsson, VO; Eiriksson, FF; Hardarson, HK; Kamble, NR; Oddsdottir, S; Palsson, R; Runolfsdottir, HL; Sigurdsson, BB; Sigurdsson, ST; Thorsteinsdottir, M; Thorsteinsdottir, UA1
Ichikawa, K; Kamoda, T; Nozue, H; Saitoh, H; Taniguchi, A1
Bensman, A; Bollée, G; Ceballos-Picot, I; Daudon, M; Harambat, J; Knebelmann, B1
Taniguchi, A1

Reviews

4 review(s) available for 2,8-dihydroxyadenine and Urinary Lithiasis

ArticleYear
Recurrence of 2,8-dihydroxyadenine Crystalline Nephropathy in a Kidney Transplant Recipient: A Case Report and Literature Review.
    Internal medicine (Tokyo, Japan), 2021, Aug-15, Volume: 60, Issue:16

    Topics: Adenine; Adenine Phosphoribosyltransferase; Humans; Kidney Transplantation; Urolithiasis

2021
[A Case Report of 2,8-Dihydroxyadenine Stone].
    Hinyokika kiyo. Acta urologica Japonica, 2015, Volume: 61, Issue:7

    Topics: Adenine; Adenine Phosphoribosyltransferase; Female; Humans; Metabolism, Inborn Errors; Middle Aged; Spectrophotometry, Infrared; Tomography, X-Ray Computed; Treatment Outcome; Ureteral Calculi; Urolithiasis

2015
Adenine phosphoribosyltransferase deficiency.
    Clinical journal of the American Society of Nephrology : CJASN, 2012, Volume: 7, Issue:9

    Topics: Adenine; Adenine Phosphoribosyltransferase; Allopurinol; Animals; Biomarkers; Disease Progression; Enzyme Inhibitors; Genetic Predisposition to Disease; Humans; Kidney Diseases; Metabolism, Inborn Errors; Phenotype; Predictive Value of Tests; Prognosis; Recurrence; Urolithiasis; Xanthine Dehydrogenase

2012
[Adenine phosphoribosyltransferase deficiency and its purine metabolism].
    Nihon rinsho. Japanese journal of clinical medicine, 2008, Volume: 66, Issue:4

    Topics: Adenine; Adenine Phosphoribosyltransferase; Alleles; Asian People; Genotype; Humans; Mutation; Purines; Urolithiasis

2008

Other Studies

13 other study(ies) available for 2,8-dihydroxyadenine and Urinary Lithiasis

ArticleYear
Rare crystalline nephropathy leading to acute graft dysfunction: a case report.
    BMC nephrology, 2019, 11-21, Volume: 20, Issue:1

    Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Allopurinol; Antimetabolites; Biopsy; Crystallization; Humans; Hydrotherapy; Kidney Transplantation; Male; Metabolism, Inborn Errors; Primary Graft Dysfunction; Urolithiasis

2019
Cellular and Molecular Mechanisms of Kidney Injury in 2,8-Dihydroxyadenine Nephropathy.
    Journal of the American Society of Nephrology : JASN, 2020, Volume: 31, Issue:4

    Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Animals; Cohort Studies; Diet; Disease Models, Animal; Female; Humans; Infant; Kidney Diseases; Male; Metabolism, Inborn Errors; Mice; Middle Aged; Urolithiasis

2020
Are conventional stone analysis techniques reliable for the identification of 2,8-dihydroxyadenine kidney stones? A case series.
    Urolithiasis, 2020, Volume: 48, Issue:4

    Topics: Adenine; Adenine Phosphoribosyltransferase; Adolescent; Adult; Child; Child, Preschool; Female; Humans; Kidney Calculi; Male; Metabolism, Inborn Errors; Middle Aged; Reproducibility of Results; Retrospective Studies; Urolithiasis; Young Adult

2020
Febuxostat for the Prevention of Recurrent 2,8-dihydroxyadenine Nephropathy due to Adenine Phosphoribosyltransferase Deficiency Following Kidney Transplantation.
    Internal medicine (Tokyo, Japan), 2017, Volume: 56, Issue:11

    Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Febuxostat; Gout Suppressants; Humans; Kidney Transplantation; Male; Metabolism, Inborn Errors; Urolithiasis

2017
Comparison of the effect of allopurinol and febuxostat on urinary 2,8-dihydroxyadenine excretion in patients with Adenine phosphoribosyltransferase deficiency (APRTd): A clinical trial.
    European journal of internal medicine, 2018, Volume: 48

    Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Aged; Allopurinol; Cross-Over Studies; Enzyme Inhibitors; Febuxostat; Female; Humans; Iceland; Kidney Calculi; Male; Metabolism, Inborn Errors; Middle Aged; Pilot Projects; Registries; Treatment Outcome; Urolithiasis

2018
The Case | Shining a light on an unusual case of chronic kidney disease.
    Kidney international, 2018, Volume: 93, Issue:4

    Topics: Adenine; Adenine Phosphoribosyltransferase; Aged; Biopsy; Crystallization; Humans; Kidney; Male; Metabolism, Inborn Errors; Microscopy, Polarization; Renal Insufficiency, Chronic; Urolithiasis

2018
Long-term renal outcomes of APRT deficiency presenting in childhood.
    Pediatric nephrology (Berlin, Germany), 2019, Volume: 34, Issue:3

    Topics: Acute Kidney Injury; Adenine; Adenine Phosphoribosyltransferase; Adolescent; Adult; Allopurinol; Child; Child, Preschool; Disease Progression; Female; Follow-Up Studies; Glomerular Filtration Rate; Humans; Infant; Kidney; Kidney Calculi; Male; Metabolism, Inborn Errors; Recurrence; Registries; Renal Insufficiency, Chronic; Urolithiasis; Xanthine Dehydrogenase; Young Adult

2019
Urinary bladder stone due to adenine phosphoribosyltransferase deficiency: first genetically confirmed case in a Chinese patient.
    Pathology, 2019, Volume: 51, Issue:5

    Topics: Adenine; Adenine Phosphoribosyltransferase; Asian People; Child, Preschool; Early Diagnosis; Humans; Kidney; Male; Metabolism, Inborn Errors; Radiography; Urinary Bladder Calculi; Urolithiasis

2019
An APRT mutation is strongly associated with and likely causative for 2,8-dihydroxyadenine urolithiasis in dogs.
    Molecular genetics and metabolism, 2014, Volume: 111, Issue:3

    Topics: Adenine; Adenine Phosphoribosyltransferase; Animals; Dogs; High-Throughput Nucleotide Sequencing; Homozygote; Humans; Metabolism, Inborn Errors; Mutation, Missense; Urolithiasis

2014
Adenine phosphoribosyltransferase deficiency as a rare cause of renal allograft dysfunction.
    Journal of the American Society of Nephrology : JASN, 2014, Volume: 25, Issue:4

    Topics: Adenine; Adenine Phosphoribosyltransferase; Allografts; Humans; Kidney Calculi; Kidney Transplantation; Male; Metabolism, Inborn Errors; Middle Aged; Risk Factors; Urolithiasis

2014
2,8-Dihydroxyadenine Nephropathy Identified as Cause of End-Stage Renal Disease After Renal Transplant.
    Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, 2017, Volume: 15, Issue:5

    Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Allopurinol; Biomarkers; Biopsy; Enzyme Inhibitors; Female; Humans; Kidney Failure, Chronic; Kidney Transplantation; Metabolism, Inborn Errors; Treatment Outcome; Urolithiasis; Xanthine Dehydrogenase

2017
Quantitative UPLC-MS/MS assay of urinary 2,8-dihydroxyadenine for diagnosis and management of adenine phosphoribosyltransferase deficiency.
    Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2016, Nov-15, Volume: 1036-1037

    Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Chromatography, High Pressure Liquid; Humans; Limit of Detection; Metabolism, Inborn Errors; Tandem Mass Spectrometry; Urinalysis; Urolithiasis

2016
A Japanese boy with adenine phosphoribosyltransferase (APRT) deficiency caused by compound heterozygosity including a novel missense mutation in APRT gene.
    Acta paediatrica (Oslo, Norway : 1992), 2011, Volume: 100, Issue:12

    Topics: Adenine; Adenine Phosphoribosyltransferase; Asian People; Child, Preschool; Humans; Lithotripsy; Male; Metabolism, Inborn Errors; Mutation; Nephritis, Interstitial; Nephrolithiasis; Recurrence; Urinary Tract Infections; Urolithiasis

2011