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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Joaquim Calado

Department of Genetics

Faculty of Medical Sciences

New University of Lisbon

Lisbon

Portugal

[email]@fcm.unl.pt

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Genetics, Faculty of Medical Sciences, New University of Lisbon, Lisbon, Portugal. 2004 - 2011
  • Departamento de Genética da Faculdade de Ciências Médicas, Instituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa, Lisbon, Portugal. 2008
  • Instituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa, Lisbon, Portugal. 2004

References

  1. Effect of kidney disease on glucose handling (including genetic defects). Calado, J., Santer, R., Rueff, J. Kidney Int. (2011) [Pubmed]
  2. Dapagliflozin, an oral sodium glucose cotransporter type 2 inhibitor for the treatment of type 2 diabetes mellitus. Calado, J. IDrugs (2009) [Pubmed]
  3. 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, M.C., Kattamis, A., Scharf, M., Tasic, V., Greil, J., Brinkert, F., Kemper, M.J., Santer, R. Nephrol. Dial. Transplant. (2008) [Pubmed]
  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. Kidney Int. (2006) [Pubmed]
  5. A novel heterozygous missense mutation in the UMOD gene responsible for Familial Juvenile Hyperuricemic Nephropathy. Calado, J., Gaspar, A., Clemente, C., Rueff, J. BMC Med. Genet. (2005) [Pubmed]
  6. Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria. Calado, J., Soto, K., Clemente, C., Correia, P., Rueff, J. Hum. Genet. (2004) [Pubmed]
  7. Gene Symbol: SLC55A2. Disease: familial renal glucosuria. Calado, J., Soto, K., Clemente, C., Correia, P., Rueff, J. Hum. Genet. (2004) [Pubmed]
 
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