Joaquim Fernando Tomaz Rodrigues Moita Calado


AuthID: R-000-7HS

Confirmed Publications: 15



1
TITLE: Hypouricaemia and hyperuricosuria in familial renal glucosuria
AUTHORS: Aires, I; Santos, AR; Pratas, J; Nolasco, F ; Calado, J ;
PUBLISHED: 2013, SOURCE: Clinical Kidney Journal, VOLUME: 6, ISSUE: 5
INDEXED IN: Scopus CrossRef
IN MY: ORCID
2
TITLE: Effect of kidney disease on glucose handling (including genetic defects)  Full Text
AUTHORS: Calado, J ; Santer, R; Rueff, J ;
PUBLISHED: 2011, SOURCE: KIDNEY INTERNATIONAL, VOLUME: 79, ISSUE: SUPPL. 120
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
3
TITLE: BI-10773, a sodium-glucose cotransporter 2 inhibitor for the potential oral treatment of type 2 diabetes mellitus
AUTHORS: Ines Aires; Joaquim Calado ;
PUBLISHED: 2010, SOURCE: CURRENT OPINION IN INVESTIGATIONAL DRUGS, VOLUME: 11, ISSUE: 10
INDEXED IN: Scopus WOS
4
TITLE: Familial Renal Glucosuria and SGLT2: From a Mendelian Trait to a Therapeutic Target
AUTHORS: Rene Santer; Joaquim Calado ;
PUBLISHED: 2010, SOURCE: CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, VOLUME: 5, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
5
TITLE: Secondary Amyloidosis in a Patient with Long Duration Crohn's Disease Treated with Infliximab  Full Text
AUTHORS: Catarina Fidalgo; Joaquim Calado ; Marilia Cravo ;
PUBLISHED: 2010, SOURCE: BIODRUGS, VOLUME: 24, ISSUE: SUPPL. 1
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
6
TITLE: Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion
AUTHORS: Calado, J ; Sznajer, Y; Metzger, D; Rita, A; Hogan, MC; Kattamis, A; Scharf, M; Tasic, V; Greil, J; Brinkert, F; Kemper, MJ; Santer, R;
PUBLISHED: 2008, SOURCE: NEPHROLOGY DIALYSIS TRANSPLANTATION, VOLUME: 23, ISSUE: 12
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
7
TITLE: Unusual adult-onset manifestation of an attenuated Bartter's syndrome type IV renal phenotype caused by a mutation in BSND
AUTHORS: Sandra Brum; Jose Rueff ; Joao R Santos; Joaquim Calado ;
PUBLISHED: 2007, SOURCE: NEPHROLOGY DIALYSIS TRANSPLANTATION, VOLUME: 22, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
8
TITLE: Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting  Full Text
AUTHORS: Calado, J ; Loeffler, J; Sakallioglu, O; Gok, F; Lhotta, K; Barata, J; Rueff, J ;
PUBLISHED: 2006, SOURCE: KIDNEY INTERNATIONAL, VOLUME: 69, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
9
TITLE: A novel heterozygous missense mutation in the UMOD gene responsible for Familial Juvenile Hyperuricemic Nephropathy
AUTHORS: Calado, J ; Gaspar, A; Clemente, C; Rueff, J ;
PUBLISHED: 2005, SOURCE: BMC MEDICAL GENETICS, VOLUME: 6, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 13 Handle
IN MY: ORCID
10
TITLE: Gene Symbol: SLC55A2. Disease: familial renal glucosuria.
AUTHORS: Calado, J ; Soto, K; Clemente, C; Correia, P; Rueff, J ;
PUBLISHED: 2004, SOURCE: Human genetics, VOLUME: 115, ISSUE: 2
INDEXED IN: Scopus
IN MY: ORCID
Page 1 of 2. Total results: 15.

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