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Page 1
Nephrolithiasis.
Scheinman SJ. Scheinman SJ. Semin Nephrol. 1999 Jul;19(4):381-8. Semin Nephrol. 1999. PMID: 10435676 Review.
Idiopathic hypercalciuria is the most common stone risk factor, and evidence in humans and in a rat model indicates that hypercalciuria is a complex, polygenic trait. Some candidate genes for idiopathic hypercalciuria are suggested by the known …
Idiopathic hypercalciuria is the most common stone risk factor, and evidence in humans and in a rat model indicates that hy …
Idiopathic hypercalciuria.
Lemann J Jr, Gray RW. Lemann J Jr, et al. J Urol. 1989 Mar;141(3 Pt 2):715-8. doi: 10.1016/s0022-5347(17)40993-1. J Urol. 1989. PMID: 2645429 Review.
Idiopathic hypercalciuria, defined as the urinary excretion of more than 300 mg. calcium per day in men or more than 250 mg. calcium per day in women, or more than 4 mg. calcium per kg. per day, is observed in about 50 per cent of the patients with calcium oxalate/a …
Idiopathic hypercalciuria, defined as the urinary excretion of more than 300 mg. calcium per day in men or more than 250 mg. c …
Role of claudins in idiopathic hypercalciuria and renal lithiasis.
Negri AL, Del Valle EE. Negri AL, et al. Int Urol Nephrol. 2022 Sep;54(9):2197-2204. doi: 10.1007/s11255-022-03119-2. Epub 2022 Jan 27. Int Urol Nephrol. 2022. PMID: 35084652 Review.
Paracellular transport in the kidney is mediated by a family of proteins located in the tight junctions called claudins which confers its ionic selectivity. ...A greater knowledge of the paracellular pathway controlled by claudins and its regulation will allow us to develo …
Paracellular transport in the kidney is mediated by a family of proteins located in the tight junctions called claudins which confers …
[Idiopathic hypercalciuria. Diagnosis and treatment].
Olefir YV, Yavorskii AN, Butnaru DV, Shatalova OV, Gorbatenko VS, Gerasimenko AS. Olefir YV, et al. Urologiia. 2017 Dec;(6):112-119. Urologiia. 2017. PMID: 29376607 Review. Russian.
Most patients with idiopathic hypercalciuria and calcium nephrolithiasis have a family history of the disease. Idiopathic hypercalciuria is a metabolic abnormality with various causes and developmental pathways. ...
Most patients with idiopathic hypercalciuria and calcium nephrolithiasis have a family history of the disease. Idiop …
[Hypercalciuria].
Périmenis P, Wémeau JL, Vantyghem MC. Périmenis P, et al. Ann Endocrinol (Paris). 2005 Dec;66(6):532-9. doi: 10.1016/s0003-4266(05)82114-6. Ann Endocrinol (Paris). 2005. PMID: 16357816 Review. French.
The frequency of hypercalciuria is increasing in western countries with an incidence of nephrolithiasis which can reach 13%. ...If no cause is identified, persistence of hypercalciuria after instituting a correct diet is defined as idiopathic hypercalciuri …
The frequency of hypercalciuria is increasing in western countries with an incidence of nephrolithiasis which can reach 13%. ...If no …
Personalized Intervention in Monogenic Stone Formers.
Policastro LJ, Saggi SJ, Goldfarb DS, Weiss JP. Policastro LJ, et al. J Urol. 2018 Mar;199(3):623-632. doi: 10.1016/j.juro.2017.09.143. Epub 2017 Oct 20. J Urol. 2018. PMID: 29061541 Free PMC article. Review.
Although nephrolithiasis is roughly 50% heritable, the presence of a family history usually does not affect treatment since most stone disease is regarded as polygenic, ie not attributable to a single gene. ...Several genes first reported in association with rare disease m …
Although nephrolithiasis is roughly 50% heritable, the presence of a family history usually does not affect treatment since most ston …
Phosphaturia in kidney stone formers: Still an enigma.
Walker V. Walker V. Adv Clin Chem. 2019;90:133-196. doi: 10.1016/bs.acc.2019.01.004. Epub 2019 Apr 19. Adv Clin Chem. 2019. PMID: 31122608 Review.
Calcium kidney stones are common worldwide. Most are idiopathic and composed of calcium oxalate. Calcium phosphate is present in around 80% and may initiate stone formation. ...In monogenic defects stones develop when phosphaturia is associated with hypercalciuria, …
Calcium kidney stones are common worldwide. Most are idiopathic and composed of calcium oxalate. Calcium phosphate is present in arou …
Nephrolithiasis and Nephrocalcinosis in Children - Metabolic and Genetic Factors.
Tasic V, Gucev Z. Tasic V, et al. Pediatr Endocrinol Rev. 2015 Sep;13(1):468-76. Pediatr Endocrinol Rev. 2015. PMID: 26540764 Review.
Herein we will review clinical, biochemical, metabolic and genetic characteristics of the inherited diseases which lead to nephrolithiasis/nephrocalcinosis, such as: idiopathic hypercalciuria, renal hypophosphatemia, renal tubular acidosis, idiopathic infanti …
Herein we will review clinical, biochemical, metabolic and genetic characteristics of the inherited diseases which lead to nephrolithiasis/n …
Nephrolithiasis in renal tubular acidosis.
Buckalew VM Jr. Buckalew VM Jr. J Urol. 1989 Mar;141(3 Pt 2):731-7. doi: 10.1016/s0022-5347(17)40997-9. J Urol. 1989. PMID: 2645431 Review.
In other cases familial idiopathic hypercalciuria causes nephrocalcinosis and nephrolithiasis resulting in distal tubular damage and type I renal tubular acidosis. In these latter cases hypercalciuria is present in complete and incomplete type I renal …
In other cases familial idiopathic hypercalciuria causes nephrocalcinosis and nephrolithiasis resulting in distal tubul …
[Genetic approach to nephrolithiasis].
Marangella M, Marcuccio C, Vitale C. Marangella M, et al. G Ital Nefrol. 2015;32 Suppl 64:gin/32.S64.7. G Ital Nefrol. 2015. PMID: 26479054 Review. Italian.
Namely, Dents syndrome, calcium sensing receptor mutations, familial hypopomagnesiemic hypercalciuria (FHHNC), hypophosphatemic rickets (HHRH), renal tubular acidosis (dRTA), primary hyperoxaluria (PH), cystinuria, 2-8 dihydroxyadeninuria (2-8 DHA). ...Lastly, a bet …
Namely, Dents syndrome, calcium sensing receptor mutations, familial hypopomagnesiemic hypercalciuria (FHHNC), hypophosphatemi …
26 results