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

Year Number of Results
1975 1
1977 2
1978 1
1979 2
1980 2
1981 1
1982 1
1983 1
1985 2
1986 1
1987 2
1990 2
1991 3
1992 4
1993 1
1994 3
1995 2
1998 1
1999 2
2000 2
2001 2
2002 1
2003 1
2004 3
2005 1
2007 1
2008 3
2010 1
2011 2
2012 2
2013 4
2014 4
2015 2
2016 4
2017 3
2019 1
2020 1
2022 1
2024 1

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69 results

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Page 1
Renal tubular acidosis.
Rothstein M, Obialo C, Hruska KA. Rothstein M, et al. Endocrinol Metab Clin North Am. 1990 Dec;19(4):869-87. Endocrinol Metab Clin North Am. 1990. PMID: 2081516 Review.
It is frequently accompanied by diffuse proximal tubule transport defects with aminoaciduria, glycosuria, hyperphosphaturia, and so forth (Fanconi syndrome). dRTA is associated with a high incidence of nephrolithiasis, nephrocalcinosis, osteodystrophy, and growth retardati …
It is frequently accompanied by diffuse proximal tubule transport defects with aminoaciduria, glycosuria, hyperphosphaturia, and so f …
Interactions of vitamin D and the proximal tubule.
Chesney RW. Chesney RW. Pediatr Nephrol. 2016 Jan;31(1):7-14. doi: 10.1007/s00467-015-3050-5. Epub 2015 Jan 25. Pediatr Nephrol. 2016. PMID: 25618772 Review.
Severe vitamin D deficiency (reduction in serum 25(OH)D concentration) in infants and children can cause features of the Fanconi syndrome, including phosphaturia, glycosuria, aminoaciduria, and renal tubular acidosis. This indicates that vitamin D and its metabolites influ …
Severe vitamin D deficiency (reduction in serum 25(OH)D concentration) in infants and children can cause features of the Fanconi syndrome, i …
Cadmium nephropathy.
Kazantzis G. Kazantzis G. Contrib Nephrol. 1979;16:161-6. doi: 10.1159/000402891. Contrib Nephrol. 1979. PMID: 223811
In a group of 12 cadmium workers some of whom were followed for up to 16 years, tubular proteinuria, renal glycosuria, aminoaciduria, hypercalciuria and defects of concentration and acidification have been observed. ...
In a group of 12 cadmium workers some of whom were followed for up to 16 years, tubular proteinuria, renal glycosuria, aminoaciduria, …
Anticancer drug-induced kidney disorders.
Kintzel PE. Kintzel PE. Drug Saf. 2001 Jan;24(1):19-38. doi: 10.2165/00002018-200124010-00003. Drug Saf. 2001. PMID: 11219485 Review.
Additional signs of streptozocin-induced nephrotoxicity include hypophosphataemia, hypokalaemia, hypouricaemia, renal tubular acidosis, glucosuria, aceturia and aminoaciduria. Cisplatin and carboplatin cause dose-related renal dysfunction. ...
Additional signs of streptozocin-induced nephrotoxicity include hypophosphataemia, hypokalaemia, hypouricaemia, renal tubular acidosis, gluc …
Tenofovir and Severe Symptomatic Hypophosphatemia.
Kichloo A, Chugh SS, Gupta S, Panday J, Goldar GE. Kichloo A, et al. J Investig Med High Impact Case Rep. 2019 Jan-Dec;7:2324709619848796. doi: 10.1177/2324709619848796. J Investig Med High Impact Case Rep. 2019. PMID: 31142127 Free PMC article.
Subsequently, the mitochondrial injury caused by Tenofovir can lead to the development of Fanconi's syndrome which causes renal tubular acidosis, phosphaturia, aminoaciduria, glucosuria with normoglycemia, and tubular proteinuria. ...
Subsequently, the mitochondrial injury caused by Tenofovir can lead to the development of Fanconi's syndrome which causes renal tubular acid …
Metabolic disorders of fetal life: glycogenoses and mitochondrial defects of the mitochondrial respiratory chain.
Dimauro S, Garone C. Dimauro S, et al. Semin Fetal Neonatal Med. 2011 Aug;16(4):181-9. doi: 10.1016/j.siny.2011.04.010. Epub 2011 May 28. Semin Fetal Neonatal Med. 2011. PMID: 21620786 Review.
General conclusions are that: (i) disorders of glycogen metabolism are more likely to cause 'fetal disease' than defects of the respiratory chain; (ii) mitochondrial encephalomyopathies, especially those due to defects of the nuclear genome, are frequent causes of neonatal or inf …
General conclusions are that: (i) disorders of glycogen metabolism are more likely to cause 'fetal disease' than defects of the respiratory …
Hereditary pancreatitis.
Perrault J. Perrault J. Gastroenterol Clin North Am. 1994 Dec;23(4):743-52. Gastroenterol Clin North Am. 1994. PMID: 7698830 Review.
Hereditary pancreatitis is a clinical condition in which typical pancreatitis is associated with an inheritance pattern strongly suggestive of an autosomal dominant trait. Different variants have been described, some with aminoaciduria and some with ductal anomalies. Recur …
Hereditary pancreatitis is a clinical condition in which typical pancreatitis is associated with an inheritance pattern strongly suggestive …
Lysinuric protein intolerance: update and extended mutation analysis of the SLC7A7 gene.
Sperandeo MP, Andria G, Sebastio G. Sperandeo MP, et al. Hum Mutat. 2008 Jan;29(1):14-21. doi: 10.1002/humu.20589. Hum Mutat. 2008. PMID: 17764084 Review.
Lysinuric protein intolerance (LPI) is an inherited aminoaciduria caused by defective cationic amino acid (CAA) transport at the basolateral membrane of epithelial cells in the intestine and kidney. ...
Lysinuric protein intolerance (LPI) is an inherited aminoaciduria caused by defective cationic amino acid (CAA) transport at the baso …
Lysinuric protein intolerance: reviewing concepts on a multisystem disease.
Sebastio G, Sperandeo MP, Andria G. Sebastio G, et al. Am J Med Genet C Semin Med Genet. 2011 Feb 15;157C(1):54-62. doi: 10.1002/ajmg.c.30287. Epub 2011 Feb 9. Am J Med Genet C Semin Med Genet. 2011. PMID: 21308987 Review.
Lysinuric protein intolerance (LPI) is an inherited aminoaciduria caused by defective cationic amino acid transport at the basolateral membrane of epithelial cells in intestine and kidney. ...
Lysinuric protein intolerance (LPI) is an inherited aminoaciduria caused by defective cationic amino acid transport at the basolatera …
69 results