Calado J - Search Results

1

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

2

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

3

Gene Symbol: SLC55A2. Disease: familial renal glucosuria.

Calado J, Soto K, Clemente C, Correia P, Rueff J. Calado J, et al. Hum Genet. 2004 Jul;115(2):170. Hum Genet. 2004. PMID: 15300967 No abstract available.

4

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.

5

Familial renal glucosuria and SGLT2: from a mendelian trait to a therapeutic target.

Santer R, Calado J. Santer R, et al. Among authors: calado j. Clin J Am Soc Nephrol. 2010 Jan;5(1):133-41. doi: 10.2215/CJN.04010609. Epub 2009 Nov 5. Clin J Am Soc Nephrol. 2010. PMID: 19965550 Review.

6

Effect of kidney disease on glucose handling (including genetic defects).

Calado J, Santer R, Rueff J. Calado J, et al. Kidney Int Suppl. 2011 Mar;(120):S7-13. doi: 10.1038/ki.2010.510. Kidney Int Suppl. 2011. PMID: 21358700 Review.

7

Determination of the renal threshold for glucose excretion in Familial Renal Glucosuria.

Aires I, Fila M, Polidori D, Santos AR, Costa AB, Calado J. Aires I, et al. Among authors: calado j. Nephron. 2015;129(4):300-4. doi: 10.1159/000381677. Epub 2015 Apr 18. Nephron. 2015. PMID: 25896487

8

MAP17 Is a Necessary Activator of Renal Na+/Glucose Cotransporter SGLT2.

Coady MJ, El Tarazi A, Santer R, Bissonnette P, Sasseville LJ, Calado J, Lussier Y, Dumayne C, Bichet DG, Lapointe JY. Coady MJ, et al. Among authors: calado j. J Am Soc Nephrol. 2017 Jan;28(1):85-93. doi: 10.1681/ASN.2015111282. Epub 2016 Jun 10. J Am Soc Nephrol. 2017. PMID: 27288013 Free PMC article.

9

A novel heterozygous missense mutation in the UMOD gene responsible for Familial Juvenile Hyperuricemic Nephropathy.

Calado J, Gaspar A, Clemente C, Rueff J. Calado J, et al. BMC Med Genet. 2005 Jan 27;6:5. doi: 10.1186/1471-2350-6-5. BMC Med Genet. 2005. PMID: 15673476 Free PMC article.

10

Hypouricaemia and hyperuricosuria in familial renal glucosuria.

Aires I, Santos AR, Pratas J, Nolasco F, Calado J. Aires I, et al. Among authors: calado j. Clin Kidney J. 2013 Oct;6(5):523-5. doi: 10.1093/ckj/sft100. Clin Kidney J. 2013. PMID: 26064518 Free PMC article.

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