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

Year Number of Results
1966 1
1967 1
1969 1
1978 1
1980 1
1987 3
1990 1
1991 1
1992 1
1996 1
1999 1
2000 1
2001 6
2002 2
2003 2
2004 5
2005 2
2006 4
2007 4
2008 3
2009 7
2010 6
2011 7
2012 4
2013 8
2014 9
2015 8
2016 8
2017 7
2018 4
2019 4
2020 2
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Similar Articles for PMID: 14569097

99 results
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Page 1
Molecular analysis of the SGLT2 gene in patients with renal glucosuria.
Santer R, Kinner M, Lassen CL, Schneppenheim R, Eggert P, Bald M, Brodehl J, Daschner M, Ehrich JH, Kemper M, Li Volti S, Neuhaus T, Skovby F, Swift PG, Schaub J, Klaerke D. Santer R, et al. J Am Soc Nephrol. 2003 Nov;14(11):2873-82. doi: 10.1097/01.asn.0000092790.89332.d2. J Am Soc Nephrol. 2003. PMID: 14569097 Free article.
Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2).
van den Heuvel LP, Assink K, Willemsen M, Monnens L. van den Heuvel LP, et al. Hum Genet. 2002 Dec;111(6):544-7. doi: 10.1007/s00439-002-0820-5. Epub 2002 Sep 27. Hum Genet. 2002. PMID: 12436245
A novel missense mutation in SLC5A2 encoding SGLT2 underlies autosomal-recessive renal glucosuria and aminoaciduria.
Magen D, Sprecher E, Zelikovic I, Skorecki K. Magen D, et al. Kidney Int. 2005 Jan;67(1):34-41. doi: 10.1111/j.1523-1755.2005.00053.x. Kidney Int. 2005. PMID: 15610225 Free article.
Renal glucosuria due to SGLT2 mutations.
Kleta R, Stuart C, Gill FA, Gahl WA. Kleta R, et al. Mol Genet Metab. 2004 May;82(1):56-8. doi: 10.1016/j.ymgme.2004.01.018. Mol Genet Metab. 2004. PMID: 15110322
Abnormal expression and dysfunction of novel SGLT2 mutations identified in familial renal glucosuria patients.
Yu L, Lv JC, Zhou XJ, Zhu L, Hou P, Zhang H. Yu L, et al. Hum Genet. 2011 Mar;129(3):335-44. doi: 10.1007/s00439-010-0927-z. Epub 2010 Dec 17. Hum Genet. 2011. PMID: 21165652
Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting.
Calado J, Loeffler J, Sakallioglu O, Gok F, Lhotta K, Barata J, Rueff J. Calado J, et al. Kidney Int. 2006 Mar;69(5):852-5. doi: 10.1038/sj.ki.5000194. Kidney Int. 2006. PMID: 16518345 Free article.
Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion.
Calado J, Sznajer Y, Metzger D, Rita A, Hogan MC, Kattamis A, Scharf M, Tasic V, Greil J, Brinkert F, Kemper MJ, Santer R. Calado J, et al. Nephrol Dial Transplant. 2008 Dec;23(12):3874-9. doi: 10.1093/ndt/gfn386. Epub 2008 Jul 12. Nephrol Dial Transplant. 2008. PMID: 18622023
Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria.
Calado J, Soto K, Clemente C, Correia P, Rueff J. Calado J, et al. Hum Genet. 2004 Feb;114(3):314-6. doi: 10.1007/s00439-003-1054-x. Epub 2003 Nov 12. Hum Genet. 2004. PMID: 14614622
Familial renal glucosuria: a clinicogenetic study of 23 additional cases.
Lee H, Han KH, Park HW, Shin JI, Kim CJ, Namgung MK, Kim KH, Koo JW, Chung WY, Lee DY, Kim SY, Cheong HI. Lee H, et al. Pediatr Nephrol. 2012 Jul;27(7):1091-5. doi: 10.1007/s00467-012-2109-9. Pediatr Nephrol. 2012. PMID: 22314875
Genetic analysis and literature review of Chinese patients with familial renal glucosuria: Identification of a novel SLC5A2 mutation.
Wang X, Yu M, Wang T, Zhang H, Ping F, Zhang Q, Xu J, Feng K, Xiao X. Wang X, et al. Clin Chim Acta. 2017 Jun;469:105-110. doi: 10.1016/j.cca.2017.03.027. Epub 2017 Mar 29. Clin Chim Acta. 2017. PMID: 28365451
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