adenine has been researched along with Kidney Calculi in 51 studies
Kidney Calculi: Stones in the KIDNEY, usually formed in the urine-collecting area of the kidney (KIDNEY PELVIS). Their sizes vary and most contains CALCIUM OXALATE.
Excerpt | Relevance | Reference |
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"We report a case of 2,8-dihydroxyadenine (DHA) urolithiasis in a 65-year-old male." | 8.02 | [A Case Report of 2,8-Dihydroxyadenine Urolithiasis]. ( Horiuchi, E; Imamura, T; Miyachi, S, 2021) |
"We have recently encountered patients incorrectly diagnosed with adenine phosphoribosyltransferase (APRT) deficiency due to misidentification of kidney stones as 2,8-dihydroxyadenine (DHA) stones." | 7.96 | Are conventional stone analysis techniques reliable for the identification of 2,8-dihydroxyadenine kidney stones? A case series. ( Edvardsson, VO; Goldfarb, DS; Ketteridge, D; Lin, TL; Michael, M; Palsson, R; Rich, PR; Runolfsdottir, HL; Sayer, JA, 2020) |
"We report a case of 2,8-dihydroxyadenine (DHA) urolithiasis in a 65-year-old male." | 4.02 | [A Case Report of 2,8-Dihydroxyadenine Urolithiasis]. ( Horiuchi, E; Imamura, T; Miyachi, S, 2021) |
"We have recently encountered patients incorrectly diagnosed with adenine phosphoribosyltransferase (APRT) deficiency due to misidentification of kidney stones as 2,8-dihydroxyadenine (DHA) stones." | 3.96 | Are conventional stone analysis techniques reliable for the identification of 2,8-dihydroxyadenine kidney stones? A case series. ( Edvardsson, VO; Goldfarb, DS; Ketteridge, D; Lin, TL; Michael, M; Palsson, R; Rich, PR; Runolfsdottir, HL; Sayer, JA, 2020) |
"Adenine phosphoribosyltransferase (APRT) deficiency is a hereditary purine metabolism disorder that causes kidney stones and chronic kidney disease (CKD)." | 3.91 | Long-term renal outcomes of APRT deficiency presenting in childhood. ( Agustsdottir, IM; Edvardsson, VO; Indridason, OS; Palsson, R; Runolfsdottir, HL, 2019) |
"Adenine phosphoribosyltransferase (APRT) deficiency is a rare, but significant, cause of kidney stones and progressive chronic kidney disease." | 3.88 | Comparison of the effect of allopurinol and febuxostat on urinary 2,8-dihydroxyadenine excretion in patients with Adenine phosphoribosyltransferase deficiency (APRTd): A clinical trial. ( Edvardsson, VO; Eiriksson, F; Goldfarb, DS; Oddsdottir, GS; Palsson, R; Runolfsdottir, HL; Sch Agustsdottir, IM; Thorsteinsdottir, M; Thorsteinsdottir, UA, 2018) |
"Adenine phosphoribosyltransferase deficiency is a rare autosomal recessive disorder manifesting as urolithiasis or crystalline nephropathy." | 3.80 | Adenine phosphoribosyltransferase deficiency as a rare cause of renal allograft dysfunction. ( Hemmilä, U; Kaartinen, K; Kouri, T; Mäkelä, S; Räisänen-Sokolowski, A; Salmela, K, 2014) |
"Adenine phosphoribosyltransferase (APRT) deficiency in humans is an autosomal recessive syndrome characterized by the urinary excretion of adenine and the highly insoluble compound 2,8-dihydroxyadenine (DHA) that can produce kidney stones or renal failure." | 3.69 | Adenine phosphoribosyltransferase-deficient mice develop 2,8-dihydroxyadenine nephrolithiasis. ( Boivin, G; Chen, J; Davies, PM; Engle, SJ; Sahota, A; Simmonds, HA; Stambrook, PJ; Stockelman, MG; Tischfield, JA; Ying, MY; Yum, MN, 1996) |
"On May 1986, right percutaneous nephrolithotripsy was performed." | 2.37 | [A case of 2,8-dihydroxyadenine stones with a partial deficiency of adenine phosphoribosyltransferase]. ( Kataoka, K; Kohri, K; Matsuura, T; Tsujihashi, H; Uejima, S; Uemura, T, 1988) |
"Percutaneous nephrolithotomy and cystolithotripsy were performed." | 1.28 | [Two cases of 2.8-dihydroxyadenine stone with a partial deficiency of adenine phosphoribosyltransferase]. ( Komatz, Y; Ohara, T; Osawa, O, 1991) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 23 (45.10) | 18.7374 |
1990's | 13 (25.49) | 18.2507 |
2000's | 9 (17.65) | 29.6817 |
2010's | 4 (7.84) | 24.3611 |
2020's | 2 (3.92) | 2.80 |
Authors | Studies |
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Miyachi, S | 1 |
Imamura, T | 1 |
Horiuchi, E | 1 |
Runolfsdottir, HL | 3 |
Lin, TL | 1 |
Goldfarb, DS | 2 |
Sayer, JA | 1 |
Michael, M | 1 |
Ketteridge, D | 1 |
Rich, PR | 1 |
Edvardsson, VO | 3 |
Palsson, R | 4 |
Thorsteinsdottir, UA | 1 |
Sch Agustsdottir, IM | 1 |
Oddsdottir, GS | 1 |
Eiriksson, F | 1 |
Thorsteinsdottir, M | 1 |
Agustsdottir, IM | 1 |
Indridason, OS | 1 |
Kaartinen, K | 1 |
Hemmilä, U | 1 |
Salmela, K | 1 |
Räisänen-Sokolowski, A | 1 |
Kouri, T | 1 |
Mäkelä, S | 1 |
Ueno, K | 1 |
Shimizu, M | 1 |
Kubo, T | 1 |
Igarashi, N | 1 |
Hatasaki, K | 1 |
Tzortzaki, EG | 1 |
Yang, M | 2 |
Glass, D | 1 |
Deng, L | 4 |
Evan, AP | 3 |
Bledsoe, SB | 2 |
Stambrook, PJ | 5 |
Sahota, A | 10 |
Tischfield, JA | 7 |
Shiba, M | 1 |
Shimizu, K | 1 |
Takatera, H | 1 |
Wilkinson, H | 1 |
Samuell, C | 1 |
Stower, M | 1 |
Cicconi, P | 1 |
Bongiovanni, M | 1 |
Melzi, S | 1 |
Tordato, F | 1 |
d'Arminio Monforte, A | 1 |
Bini, T | 1 |
Liang, L | 3 |
Chen, J | 5 |
Vittal, R | 1 |
Selvanayagam, ZE | 1 |
McAteer, JA | 1 |
Tischfield, J | 1 |
Chin, KV | 1 |
Chung, TG | 1 |
Kanazawa, I | 1 |
Saito, A | 1 |
Takeuchi, N | 1 |
Joost, J | 1 |
Doppler, W | 2 |
Greenwood, MC | 1 |
Dillon, MJ | 1 |
Simmonds, HA | 8 |
Barratt, TM | 4 |
Pincott, JR | 1 |
Metreweli, C | 1 |
Gault, MH | 2 |
Snedden, W | 1 |
Dow, D | 1 |
Churchill, DN | 1 |
Penney, H | 1 |
Kuroda, M | 1 |
Miki, T | 1 |
Kiyohara, H | 1 |
Usami, M | 1 |
Nakamura, T | 1 |
Kotake, T | 1 |
Takemoto, M | 1 |
Sonoda, T | 1 |
Webster, DR | 1 |
Van Acker, KJ | 2 |
Cameron, JS | 3 |
Dillon, M | 1 |
Cartier, P | 2 |
Hamet, M | 2 |
Vincens, A | 2 |
Perignon, JL | 1 |
Boyadjiev, SA | 1 |
Winter, P | 1 |
Hesse, A | 2 |
Klocke, K | 1 |
Schaefer, RM | 1 |
Fye, KH | 1 |
Hancock, DC | 1 |
Gelb, AB | 1 |
Sparks, JW | 1 |
Sibley, RK | 1 |
Engle, SJ | 1 |
Stockelman, MG | 1 |
Boivin, G | 1 |
Yum, MN | 1 |
Davies, PM | 1 |
Ying, MY | 1 |
de Jong, DJ | 1 |
Assmann, KJ | 1 |
De Abreu, RA | 1 |
Monnens, LA | 1 |
van Liebergen, FJ | 1 |
Dijkman, HB | 1 |
Huysmans, FT | 1 |
Thomas, J | 1 |
Conort, P | 1 |
Fompeydie, D | 1 |
Bellin, J | 1 |
Rechke, JP | 1 |
Arvis, G | 1 |
Suzuki, K | 1 |
Kobayashi, S | 1 |
Kawamura, K | 1 |
Kuhara, T | 1 |
Tsugawa, R | 1 |
Ohne, T | 1 |
Fujito, A | 1 |
Koga, K | 1 |
Imaide, Y | 1 |
Uchida, M | 1 |
Yagisawa, T | 1 |
Yamazaki, Y | 1 |
Toma, H | 1 |
Kamatani, N | 1 |
Wang, L | 1 |
Raikwar, N | 1 |
Shao, C | 2 |
Connors, BA | 1 |
Fineberg, NS | 1 |
Grynpas, MD | 1 |
Youzhi, S | 1 |
Edvardsson, V | 1 |
Olafsson, I | 1 |
Hjaltadottir, G | 1 |
Laxdal, T | 1 |
Gröbner, W | 1 |
Walter-Sack, I | 1 |
Potter, CF | 2 |
Rose, GA | 2 |
Arkell, DG | 2 |
Williams, DI | 2 |
Reveillaud, RJ | 1 |
Daudon, M | 1 |
Protat, MF | 1 |
Graveleau, D | 1 |
Behzadian, MA | 1 |
Ravindra, R | 1 |
Takeuchi, H | 1 |
Osawa, O | 1 |
Ohara, T | 1 |
Komatz, Y | 1 |
Zöllner, N | 1 |
Gresser, U | 1 |
Leusmann, DB | 1 |
Schmidt, G | 1 |
Hönecke, K | 1 |
Butz, M | 1 |
Coupris, L | 1 |
Champion, G | 1 |
Duverne, C | 1 |
Varlet, F | 1 |
Ratajczak, A | 1 |
Uejima, S | 1 |
Kataoka, K | 1 |
Uemura, T | 1 |
Tsujihashi, H | 1 |
Matsuura, T | 1 |
Kohri, K | 1 |
Glicklich, D | 1 |
Gruber, HE | 1 |
Matas, AJ | 1 |
Tellis, VA | 1 |
Karwa, G | 1 |
Finley, K | 1 |
Salem, C | 1 |
Soberman, R | 1 |
Seegmiller, JE | 1 |
Miersch, WD | 1 |
Classen, A | 1 |
Thon, A | 1 |
Jung, P | 1 |
Becht, E | 1 |
Ziegler, M | 1 |
Bommert, R | 1 |
Bach, K | 1 |
Haas, HJ | 1 |
Brulé, D | 1 |
Sarwar, G | 1 |
Savoie, L | 1 |
Campbell, J | 1 |
Van Zeggelaar, M | 1 |
Nishida, Y | 1 |
Hirano, S | 2 |
Miyamoto, T | 1 |
Ebina, K | 1 |
Someno, T | 1 |
Morita, T | 1 |
Szönyi, P | 1 |
Berényi, M | 1 |
Tóth, J | 1 |
Delbarre, F | 1 |
Auscher, C | 1 |
de Géry, A | 1 |
4 reviews available for adenine and Kidney Calculi
Article | Year |
---|---|
[2,8-dihydroxyadenine urolithiasis due to partial deficiency of adenine phosphoribosyltransferase: a case report].
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Female; Heterozygote; Humans; Kidney Calculi | 1998 |
[Urolithiasis in 2,8-dihydroxyadeninuria: presentation of 3 additional cases].
Topics: Adenine; Adenine Phosphoribosyltransferase; Adolescent; Humans; Kidney Calculi; Male; Pedigree; Puri | 1990 |
[A case of 2,8-dihydroxyadenine stones with a partial deficiency of adenine phosphoribosyltransferase].
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Female; Humans; Kidney Calculi; Pentosyltransfera | 1988 |
2,8-dihydroxyadenine urolithiasis: report of a case first diagnosed after renal transplant.
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Female; Humans; Kidney Calculi; Kidney Failure, C | 1988 |
47 other studies available for adenine and Kidney Calculi
Article | Year |
---|---|
[A Case Report of 2,8-Dihydroxyadenine Urolithiasis].
Topics: Adenine; Adenine Phosphoribosyltransferase; Aged; Humans; Kidney Calculi; Lithotripsy; Male; Metabol | 2021 |
Are conventional stone analysis techniques reliable for the identification of 2,8-dihydroxyadenine kidney stones? A case series.
Topics: Adenine; Adenine Phosphoribosyltransferase; Adolescent; Adult; Child; Child, Preschool; Female; Huma | 2020 |
Comparison of the effect of allopurinol and febuxostat on urinary 2,8-dihydroxyadenine excretion in patients with Adenine phosphoribosyltransferase deficiency (APRTd): A clinical trial.
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Aged; Allopurinol; Cross-Over Studies; Enzyme Inh | 2018 |
Long-term renal outcomes of APRT deficiency presenting in childhood.
Topics: Acute Kidney Injury; Adenine; Adenine Phosphoribosyltransferase; Adolescent; Adult; Allopurinol; Chi | 2019 |
Adenine phosphoribosyltransferase deficiency as a rare cause of renal allograft dysfunction.
Topics: Adenine; Adenine Phosphoribosyltransferase; Allografts; Humans; Kidney Calculi; Kidney Transplantati | 2014 |
An infant with nephrolithiasis and renal failure: Answers.
Topics: Adenine; Adenine Phosphoribosyltransferase; Allopurinol; Humans; Infant; Kidney Calculi; Renal Insuf | 2016 |
Impaired expression of an organic cation transporter, IMPT1, in a knockout mouse model for kidney stone disease.
Topics: Adenine; Adenine Phosphoribosyltransferase; Animals; Biological Transport; Female; Gene Dosage; Gene | 2003 |
[2,8-dihydoroxyadenine (DHA) urolithiasis: a case report].
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Female; Humans; Kidney Calculi; Ureteral Calculi | 2003 |
2,8-Dihydroxyadenine renal stones in a 41-year-old man.
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Allopurinol; Antimetabolites; Humans; Kidney Calc | 2004 |
Nephrolithiasis and hydronephrosis in an HIV-infected man receiving tenofovir.
Topics: Adenine; Adult; Anti-HIV Agents; Antiretroviral Therapy, Highly Active; HIV Infections; Humans; Hydr | 2004 |
Expression profiling of crystal-induced injury in human kidney epithelial cells.
Topics: Adenine; Calcium Oxalate; Cell Line; Crystallization; Epithelial Cells; Gene Expression Profiling; H | 2006 |
Determination of 2,8-dihydroxyadenine in urine by high-performance anion-exchange liquid chromatography.
Topics: Adenine; Adenine Phosphoribosyltransferase; Anion Exchange Resins; Chromatography, High Pressure Liq | 1983 |
2,8-dihydroxyadenine stone in children.
Topics: Adenine; Adenine Phosphoribosyltransferase; Child; Humans; Kidney Calculi; Male; Pentosyltransferase | 1982 |
Renal failure due to 2,8-dihydroxyadenine urolithiasis.
Topics: Adenine; Adenine Phosphoribosyltransferase; Allopurinol; Child, Preschool; Diet, Vegetarian; Erythro | 1982 |
Urolithiasis due to 2,8-dihydroxyadenine in an adult.
Topics: Adenine; Adult; Allopurinol; Female; Humans; Kidney Calculi; Kidney Pelvis; Purine-Pyrimidine Metabo | 1981 |
[Urolithiasis composed of 2,8-dihydroxyadenine due to partial deficiency of adenine phosphoribosyltransferase. Report of a case (author's transl)].
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Humans; Kidney Calculi; Male; Pentosyltransferase | 1980 |
Spectrum of 2,8-dihydroxyadenine urolithiasis in complete APRT deficiency.
Topics: Adenine; Adenine Phosphoribosyltransferase; Child; Child, Preschool; Creatinine; Female; Humans; Kid | 1980 |
Complete adenine phosphoribosyltransferase (APRT) deficiency in two siblings: report of a new case.
Topics: Adenine; Adenine Phosphoribosyltransferase; Allopurinol; Child, Preschool; Female; Humans; Kidney Ca | 1980 |
Missense mutation in the adenine phosphoribosyltransferase gene causing 2,8-dihydroxyadenine urolithiasis.
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Female; Genes; Humans; Kidney Calculi; Male; Poin | 1994 |
Scanning electron microscopy of 2,8-dihydroxyadenine crystals and stones.
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Allopurinol; Chromatography, High Pressure Liquid | 1993 |
Adenine phosphoribosyltransferase deficiency with renal deposition of 2,8-dihydroxyadenine leading to nephrolithiasis and chronic renal failure.
Topics: Adenine; Adenine Phosphoribosyltransferase; Heterozygote; Humans; Kidney; Kidney Calculi; Kidney Fai | 1993 |
Adenine phosphoribosyltransferase-deficient mice develop 2,8-dihydroxyadenine nephrolithiasis.
Topics: Adenine; Adenine Phosphoribosyltransferase; Alleles; Animals; Erythrocytes; Fibrosis; Homozygote; Hu | 1996 |
2,8-Dihydroxyadenine stone formation in a renal transplant recipient due to adenine phosphoribosyltransferase deficiency.
Topics: Adenine; Adenine Phosphoribosyltransferase; Humans; Kidney Calculi; Kidney Transplantation; Male; Mi | 1996 |
[A case of lithiasis caused by 2,8 dihydroxyadenine. Evolutive characteristics. Therapeutic problems].
Topics: Adenine; Adult; Female; Humans; Kidney Calculi; Lithotripsy; Nephrectomy; Nephrostomy, Percutaneous; | 1996 |
Family study of 2,8-dihydroxyadenine stone formation: report of two cases of a compound heterozygote for adenine phosphoribosyltransferase deficiency (APRT*J/APRT*Q0).
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Family Health; Female; Genotype; Humans; Kidney C | 1997 |
Radiopaque 2,8-dihydroxyadenine lithiasis.
Topics: Adenine; Adenine Phosphoribosyltransferase; Female; Humans; Kidney Calculi; Middle Aged; Radiography | 1999 |
Altered gene expression in kidneys of mice with 2,8-dihydroxyadenine nephrolithiasis.
Topics: Adenine; Adenine Phosphoribosyltransferase; Age Factors; Animals; Disease Models, Animal; DNA Primer | 2000 |
Sequential analysis of kidney stone formation in the Aprt knockout mouse.
Topics: Adenine; Adenine Phosphoribosyltransferase; Age Factors; Animals; Female; Genotype; Kidney Calculi; | 2001 |
Clinical features and genotype of adenine phosphoribosyltransferase deficiency in iceland.
Topics: Acute Kidney Injury; Adenine; Adenine Phosphoribosyltransferase; Adolescent; Adult; Biopsy; Child; C | 2001 |
[Hyperuricemia and gout--diagnosis].
Topics: Adenine; Adult; Diagnosis, Differential; Drug-Related Side Effects and Adverse Reactions; Female; Go | 2002 |
Complete deficiency of adenine phosphoribosyltransferase: a third case presenting as renal stones in a young child.
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Allopurinol; Child; Diagnosis, Differential; Fema | 1979 |
[2,8-dihydroxyadenine lithiasis: a new case detected by infra-red analysis].
Topics: Adenine; Adenine Phosphoribosyltransferase; Child, Preschool; Humans; Kidney Calculi; Male; Spectrop | 1979 |
Adenine phosphoribosyltransferase deficiency presenting with supposed 'uric acid' stones: pitfalls of diagnosis.
Topics: Adenine; Adenine Phosphoribosyltransferase; Diagnosis, Differential; Female; Humans; Infant; Kidney | 1978 |
2,8-Dihydroxyadenine lithiasis in a Japanese patient heterozygous at the adenine phosphoribosyltransferase locus.
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Genetic Carrier Screening; Heterozygote; Humans; | 1991 |
[Two cases of 2.8-dihydroxyadenine stone with a partial deficiency of adenine phosphoribosyltransferase].
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Female; Humans; Kidney Calculi; Lithotripsy; Male | 1991 |
Nephrolithiasis in twins with APRT-deficiency. Stones as a marker of an inborn error of metabolism.
Topics: Adenine; Adenine Phosphoribosyltransferase; Adolescent; Diseases in Twins; Humans; Kidney; Kidney Ca | 1990 |
[2,8-dihydroxyadenine urinary calculus: the significance of exact physical calculus analysis].
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Chromatography, High Pressure Liquid; Erythrocyte | 1989 |
[2,8-dihydroxyadenine lithiasis. 2 new pediatric cases of this misdiagnosed metabolic abnormality. The value of extracorporeal lithotripsy].
Topics: Adenine; Child; Diagnosis, Differential; Humans; Infant; Kidney Calculi; Male; Metabolism, Inborn Er | 1989 |
2,8-Dihydroxyadeninuria: laboratory diagnosis and therapy control.
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Allopurinol; Chemistry, Physical; Child; Circadia | 1988 |
New diagnostic and therapeutic aspects of 2,8-dihydroxyadenine lithiasis. Another case of complete adenine phosphoribosyltransferase deficiency.
Topics: Adenine; Adenine Phosphoribosyltransferase; Adolescent; Chromatography, High Pressure Liquid; Female | 1988 |
Differences in uricogenic effects of dietary purine bases, nucleosides and nucleotides in rats.
Topics: Adenine; Allantoin; Animals; Creatinine; Diet; Kidney Calculi; Kidney Tubules; Male; Microscopy, Ele | 1988 |
2,8-Dihydroxyadenine lithiasis--epidemiology, pathogenesis and therapy.
Topics: Adenine; Adenine Phosphoribosyltransferase; Cross-Sectional Studies; Female; Humans; Kidney Calculi; | 1986 |
A mutant adenine phosphoribosyltransferase in 2,8-dihydroxyadenine urolithiasis.
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Erythrocytes; Genetic Variation; Humans; Kidney C | 1986 |
2,8-Dihydroxyadenine lithiasis.
Topics: Adenine; Adenine Phosphoribosyltransferase; Allopurinol; Diagnosis, Differential; Humans; Kidney Cal | 1986 |
[A case of 2,8-dihydroxy adenine renal stones with familial inheritance of partial deficiency of adenine phosphoribosyltransferase].
Topics: Adenine; Adenine Phosphoribosyltransferase; Adult; Allopurinol; Genetic Diseases, Inborn; Humans; Ki | 1986 |
A rare enzyme deficiency causing formation of 2,8-dihydroxyadenine (purine body) calculi.
Topics: Adenine; Adenine Phosphoribosyltransferase; Allopurinol; Child, Preschool; Female; Humans; Kidney Ca | 1985 |
[Enzymopathic gout. Dyspurinia due to hypoxanthine-guanine-phosphoribosyl-transferase deficiency. Occurrence and clinical characteristics of enzyme repression].
Topics: Adenine; Adult; Age Factors; Allopurinol; Enzyme Repression; Female; Gout; Guanine; Humans; Hypoxant | 1970 |