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

Year Number of Results
1965 1
1967 3
1968 3
1969 3
1970 6
1971 4
1972 1
1973 9
1974 3
1975 2
1976 6
1977 4
1978 3
1979 7
1980 8
1981 3
1982 8
1983 6
1984 2
1985 3
1986 6
1987 3
1988 4
1989 9
1990 3
1991 4
1992 11
1993 9
1994 8
1995 19
1996 12
1997 12
1998 11
1999 7
2000 13
2001 16
2002 12
2003 28
2004 19
2005 28
2006 26
2007 24
2008 14
2009 21
2010 25
2011 25
2012 26
2013 19
2014 23
2015 26
2016 34
2017 28
2018 17
2019 23
2020 18
2021 18
2022 17
2023 20
2024 8

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678 results

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Page 1
Fanconi Syndrome.
Foreman JW. Foreman JW. Pediatr Clin North Am. 2019 Feb;66(1):159-167. doi: 10.1016/j.pcl.2018.09.002. Pediatr Clin North Am. 2019. PMID: 30454741 Review.
Fanconi syndrome, also known as the DeToni, Debre, Fanconi syndrome is a global dysfunction of the proximal tubule characterized by glucosuria, phosphaturia, generalized aminoaciduria, and type II renal tubular acidosis. ...
Fanconi syndrome, also known as the DeToni, Debre, Fanconi syndrome is a global dysfunction of the proximal tubu …
Renal Tubular Acidosis.
Alexander RT, Bitzan M. Alexander RT, et al. Pediatr Clin North Am. 2019 Feb;66(1):135-157. doi: 10.1016/j.pcl.2018.08.011. Pediatr Clin North Am. 2019. PMID: 30454739 Review.
Further workup is needed to determine the type of renal tubular acidosis and the presumed etiopathogenesis, which informs treatment choices and prognosis. The risk of nephrolithiasis and calcinosis is linked to the presence (proximal renal tubular acidosis, negligib …
Further workup is needed to determine the type of renal tubular acidosis and the presumed etiopathogenesis, which informs treatment c …
Renal Tubular Acidosis.
Bagga A, Sinha A. Bagga A, et al. Indian J Pediatr. 2020 Sep;87(9):733-744. doi: 10.1007/s12098-020-03318-8. Epub 2020 Jun 26. Indian J Pediatr. 2020. PMID: 32591997 Review.
Renal tubular acidosis (RTA) comprises a group of disorders characterized by low capacity for net acid excretion and persistent hyperchloremic metabolic acidosis, despite preserved glomerular filtration rate. ...Management involves correction of acidosis and dyselectrolyte …
Renal tubular acidosis (RTA) comprises a group of disorders characterized by low capacity for net acid excretion and persistent hyper …
Cystinosis: a review.
Elmonem MA, Veys KR, Soliman NA, van Dyck M, van den Heuvel LP, Levtchenko E. Elmonem MA, et al. Orphanet J Rare Dis. 2016 Apr 22;11:47. doi: 10.1186/s13023-016-0426-y. Orphanet J Rare Dis. 2016. PMID: 27102039 Free PMC article. Review.
Cystinosis is the most common hereditary cause of renal Fanconi syndrome in children. It is an autosomal recessive lysosomal storage disorder caused by mutations in the CTNS gene encoding for the carrier protein cystinosin, transporting cystine out of the lys …
Cystinosis is the most common hereditary cause of renal Fanconi syndrome in children. It is an autosomal recessive lyso …
Nephrotoxicity and Chinese Herbal Medicine.
Yang B, Xie Y, Guo M, Rosner MH, Yang H, Ronco C. Yang B, et al. Clin J Am Soc Nephrol. 2018 Oct 8;13(10):1605-1611. doi: 10.2215/CJN.11571017. Epub 2018 Apr 3. Clin J Am Soc Nephrol. 2018. PMID: 29615394 Free PMC article. Review.
The kidney manifestations of nephrotoxicity associated with herbal medicine include acute kidney injury, CKD, nephrolithiasis, rhabdomyolysis, Fanconi syndrome, and urothelial carcinoma. Several factors contribute to the nephrotoxicity of herbal medicines, including …
The kidney manifestations of nephrotoxicity associated with herbal medicine include acute kidney injury, CKD, nephrolithiasis, rhabdomyolysi …
VACTERL/VATER Association.
Solomon BD. Solomon BD. Orphanet J Rare Dis. 2011 Aug 16;6:56. doi: 10.1186/1750-1172-6-56. Orphanet J Rare Dis. 2011. PMID: 21846383 Free PMC article. Review.
VACTERL/VATER association is typically defined by the presence of at least three of the following congenital malformations: vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities. In addition to these core comp …
VACTERL/VATER association is typically defined by the presence of at least three of the following congenital malformations: vertebral defect …
Renal involvement in primary Sjogren syndrome.
François H, Mariette X. François H, et al. Nat Rev Nephrol. 2016 Feb;12(2):82-93. doi: 10.1038/nrneph.2015.174. Epub 2015 Nov 16. Nat Rev Nephrol. 2016. PMID: 26568188 Review.
Electrolyte disturbances may occur in pSS, such as renal distal tubular acidosis, diabetes insipidus, Gitelman syndrome or Fanconi syndrome. ...Appropriate screening must be performed at least once a year in patients with systemic pSS in order to facil …
Electrolyte disturbances may occur in pSS, such as renal distal tubular acidosis, diabetes insipidus, Gitelman syndrome or …
Genotype-phenotype associations in Fanconi anemia: A literature review.
Fiesco-Roa MO, Giri N, McReynolds LJ, Best AF, Alter BP. Fiesco-Roa MO, et al. Blood Rev. 2019 Sep;37:100589. doi: 10.1016/j.blre.2019.100589. Epub 2019 Jul 16. Blood Rev. 2019. PMID: 31351673 Free PMC article. Review.
Fanconi anemia (FA) is a genomic instability syndrome with predisposition to congenital abnormalities, bone marrow failure, and cancer. ...Patients with biallelic or hemizygous null variants had a higher proportion of at least one abnormality, renal malformat …
Fanconi anemia (FA) is a genomic instability syndrome with predisposition to congenital abnormalities, bone marrow failure, an …
Monoclonal Immunoglobulin Deposition Disease and Related Diseases.
Kanzaki G, Okabayashi Y, Nagahama K, Ohashi R, Tsuboi N, Yokoo T, Shimizu A. Kanzaki G, et al. J Nippon Med Sch. 2019;86(1):2-9. doi: 10.1272/jnms.JNMS.2019_86-1. J Nippon Med Sch. 2019. PMID: 30918151 Free article. Review.
In addition, tubulointerstitial diseases with the deposition of monoclonal immunoglobulins or their components are constituted by light chain (myeloma) cast nephropathy, light chain associated Fanconi's syndrome (light chain proximal [crystal] tubulopathy), and crys …
In addition, tubulointerstitial diseases with the deposition of monoclonal immunoglobulins or their components are constituted by light chai …
Glycogen storage diseases: new perspectives.
Ozen H. Ozen H. World J Gastroenterol. 2007 May 14;13(18):2541-53. doi: 10.3748/wjg.v13.i18.2541. World J Gastroenterol. 2007. PMID: 17552001 Free PMC article. Review.
There is no hyperuricemia or hyperlactatemia. Type XI is characterized by hepatic glycogenosis and renal Fanconi syndrome. Type II is a prototype of inborn lysosomal storage diseases and involves many organs but primarily the muscle. ...
There is no hyperuricemia or hyperlactatemia. Type XI is characterized by hepatic glycogenosis and renal Fanconi syndrome …
678 results