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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1954 1
1963 1
1964 5
1965 2
1966 3
1967 4
1968 5
1969 3
1970 3
1971 3
1972 8
1973 7
1974 7
1975 3
1976 6
1977 3
1978 6
1979 7
1980 4
1981 7
1982 7
1983 5
1984 10
1985 6
1986 7
1987 9
1988 7
1989 10
1990 9
1991 15
1992 6
1993 8
1994 11
1995 18
1996 13
1997 11
1998 16
1999 18
2000 16
2001 15
2002 15
2003 21
2004 18
2005 22
2006 27
2007 22
2008 31
2009 30
2010 34
2011 44
2012 46
2013 48
2014 52
2015 46
2016 53
2017 67
2018 60
2019 33
2020 50
2021 55
2022 74
2023 52
2024 27

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1,098 results

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Page 1
Nephrocalcinosis in Neonates.
Oh GJ, Butani L. Oh GJ, et al. Neoreviews. 2024 Feb 1;25(2):e88-e98. doi: 10.1542/neo.25-2-e88. Neoreviews. 2024. PMID: 38296790 Review.
Nephrocalcinosis occurs in as many as 40% of preterm neonates. Many causes and contributors predispose neonates to develop nephrocalcinosis, including metabolic, genetic, and iatrogenic factors. ...In this article, we review the epidemiology, pathogenesis, diagnosis …
Nephrocalcinosis occurs in as many as 40% of preterm neonates. Many causes and contributors predispose neonates to develop nephroc …
Nephrocalcinosis.
Alon US. Alon US. Curr Opin Pediatr. 1997 Apr;9(2):160-5. Curr Opin Pediatr. 1997. PMID: 9204244 Review.
The routine use of ultrasonography has resulted in an explosion in the number of conditions reported to be associated with nephrocalcinosis. It has also been increasingly recognized that urolithiasis and nephrocalcinosis can coexist in the same patient. ...Among the …
The routine use of ultrasonography has resulted in an explosion in the number of conditions reported to be associated with nephrocalcinos …
AhR activation attenuates calcium oxalate nephrocalcinosis by diminishing M1 macrophage polarization and promoting M2 macrophage polarization.
Yang X, Liu H, Ye T, Duan C, Lv P, Wu X, Liu J, Jiang K, Lu H, Yang H, Xia D, Peng E, Chen Z, Tang K, Ye Z. Yang X, et al. Theranostics. 2020 Oct 25;10(26):12011-12025. doi: 10.7150/thno.51144. eCollection 2020. Theranostics. 2020. PMID: 33204326 Free PMC article.
Calcium oxalate (CaOx) crystal can trigger kidney injury, which contributes to the pathogenesis of nephrocalcinosis. The phenotypes of infiltrating macrophage may impact CaOx-mediated kidney inflammatory injury as well as crystal deposition. How aryl hydrocarbon receptor ( …
Calcium oxalate (CaOx) crystal can trigger kidney injury, which contributes to the pathogenesis of nephrocalcinosis. The phenotypes o …
Enamel-Renal-Syndrome: case report.
Torres LHS, de-Azevedo-Vaz SL, Barroso DRC, Silva DN, Velloso TRG, de Barros LAP. Torres LHS, et al. Spec Care Dentist. 2018 May;38(3):172-175. doi: 10.1111/scd.12288. Epub 2018 Apr 19. Spec Care Dentist. 2018. PMID: 29672880
AIMS: to describe a case in which dental changes were observed and investigation proceeded to consider Enamel-Renal-Syndrome (ERS), a rare disorder that associates amelogenesis imperfecta with nephrocalcinosis. CASE REPORT: an 11-year-old male patient upon intraoral examin …
AIMS: to describe a case in which dental changes were observed and investigation proceeded to consider Enamel-Renal-Syndrome (ERS), a rare d …
Primary Hyperoxaluria.
Xie X, Zhang X. Xie X, et al. N Engl J Med. 2022 Mar 10;386(10):976. doi: 10.1056/NEJMicm2113369. Epub 2022 Mar 5. N Engl J Med. 2022. PMID: 35245013 No abstract available.
Renal impairment in hypophosphatasia.
Bacchetta J. Bacchetta J. Arch Pediatr. 2017 May;24(5S2):5S93-5S95. doi: 10.1016/S0929-693X(18)30023-X. Arch Pediatr. 2017. PMID: 29405941 Review.
Renal impairment in hypophosphatasia (HPP) has been described but remains poorly understood: hypercalciuria, nephrocalcinosis and sometimes even chronic kidney failure secondary to chronic hypercalcemia/hypercalciuria or exposure to toxic agents. ...
Renal impairment in hypophosphatasia (HPP) has been described but remains poorly understood: hypercalciuria, nephrocalcinosis and som …
Nephrocalcinosis.
Adams ND, Rowe JC. Adams ND, et al. Clin Perinatol. 1992 Mar;19(1):179-95. Clin Perinatol. 1992. PMID: 1576767 Review.
Inherited conditions resulting in nephrolithiasis.
Hoppe B, Martin-Higueras C. Hoppe B, et al. Curr Opin Pediatr. 2020 Apr;32(2):273-283. doi: 10.1097/MOP.0000000000000848. Curr Opin Pediatr. 2020. PMID: 31789978 Review.
In hypercalcuria, for example, the commonly used definition of idiopathic hypercalciuria was adopted to the genetic background, here three autosomal recessive hereditary forms of CYP24A1, SLC34A1 and SLC34A3 associated nephrocalcinosis/urolithiasis with elevated 1.25-dihyd …
In hypercalcuria, for example, the commonly used definition of idiopathic hypercalciuria was adopted to the genetic background, here three a …
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.
Diagnosis and management of pediatric nephrolithiasis/nephrocalcinosis is a very complex and challenging task for every pediatrician. ...Herein we will review clinical, biochemical, metabolic and genetic characteristics of the inherited diseases which lead to nephrolithias …
Diagnosis and management of pediatric nephrolithiasis/nephrocalcinosis is a very complex and challenging task for every pediatrician. …
Research progress on renal calculus associate with inborn error of metabolism.
Song Y, Zhao C, Li D. Song Y, et al. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2023 Apr 25;52(2):169-177. doi: 10.3724/zdxbyxb-2022-0698. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2023. PMID: 37283101 Free PMC article. Review. Chinese, English.
The hereditary conditions associated with renal calculus include primary hyperoxaluria, cystinuria, Dent disease, familial hypomagnesemia with hypercalciuria and nephrocalcinosis, Bartter syndrome, primary distal renal tubular acidosis, infant hypercalcemia, hereditary hyp …
The hereditary conditions associated with renal calculus include primary hyperoxaluria, cystinuria, Dent disease, familial hypomagnesemia wi …
1,098 results