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Search on : CALADO, JOAQUIM [Author]
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 Calado, Joaquim et al. The Kidney Genetics Clinic: delivering precision medicine for kidney patients. Port J Nephrol Hypert, Sept 2021, vol.35, no.3, p.144-152. ISSN 0872-0169
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 Calado, Joaquim. A case of polyuria. Port J Nephrol Hypert, Dec 2020, vol.34, no.4, p.251-253. ISSN 0872-0169
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 Cardoso, Filipa et al. Not the usual suspect. Port J Nephrol Hypert, Dec 2019, vol.33, no.4, p.256-258. ISSN 0872-0169
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 Messias, Ana et al. Nephrotic syndrome in a patient with metastatic melanoma: beyond the obvious. Port J Nephrol Hypert, Dec 2019, vol.33, no.4, p.252-255. ISSN 0872-0169
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 Calado, Joaquim. Alternative pathway complement activation in secondary thrombotic microangiopathies: is genetics the smoking gun?. Port J Nephrol Hypert, Dec 2019, vol.33, no.4, p.238-238. ISSN 0872-0169
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 Azevedo, Ana et al. Portuguese consensus document statement in diagnostic and management of atypical hemolytic uremic syndrome. Port J Nephrol Hypert, Sept 2018, vol.32, no.3, p.1-22. ISSN 0872-0169
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 Calado, Joaquim. Fighting glomerular hegemony: giving the renal tubule the credits it deserves. Port J Nephrol Hypert, Mar 2018, vol.32, no.1, p.9-10. ISSN 0872-0169
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 Costa, Bernardo M et al. Bartter syndrome - report of an unusual late presentation case and brief review. Port J Nephrol Hypert, Mar 2016, vol.30, no.1, p.65-69. ISSN 0872-0169

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 Meneses, Guida et al. Anti-phospholipase A2 receptor antibodies in the diagnosis of idiopathic membranous nephropathy. Port J Nephrol Hypert, Mar 2015, vol.29, no.1, p.44-47. ISSN 0872-0169

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 Aires, Ines et al. Disruption of urate transport in familial renal glucosuria and report on SGLT2 expression in normal and pathological kidney. Port J Nephrol Hypert, Dec 2013, vol.27, no.4, p.261-267. ISSN 0872-0169

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