Clara Gomes

Case Report - Port J Nephrol Hypert 2022; 36(1): 7-10

Membranoproliferative glomerulonephritis: A rare pediatric nephropathy

Andreia Marinhas, Telma Luís, Catarina Neves, Carmen Carmo, Clara Gomes

Case Report - Port J Nephrol Hypert 2017; 31(3): 305-309

Alport Syndrome – A rare presentation

Catarina Neves, Ana Carolina Cordinhã, Carmen Ferreira, Vítor Sousa, Clara Gomes, António Jorge Correia

Case Report - Port J Nephrol Hypert 2012; 26(1): 55-60

Membranous nephropathy in three paediatric patients

Susana Nobre, Raquel Santos, Clara Gomes, Fernanda X. Cunha, António J. Correia

Case Report - Port J Nephrol Hypert 2010; 24(3): 239-242

Lowe Syndrome. Case report of a patient with a missense mutation in the OCRL1 gene

Ana Marques, Lina Ramos, Clara Gomes, António J. Correia

Original Article - Port J Nephrol Hypert 2015; 29(4): 49-53

Idiopathic nephrotic syndrome – Deflazacort, an alternative?

Catarina Neves, Ana Carolina Cordinhã, Carmen Ferreira, Clara Gomes, António Jorge Correia

Original Article - Port J Nephrol Hypert 2013; 27(4): 283-288

Clinical evolution in adults with nephrotic syndrome diagnosed in paediatric ages – a single-centre experience

Marta Neves, Luís Escada, Luís Rodrigues, Clara Gomes, Jorge Pratas, António Jorge Correia, Mário Campos

Original Article - Port J Nephrol Hypert 2012; 26(1): 41-46

Multicystic dysplastic kidney: a review of eleven years (2000 – 2010)

Helena Rios, Raquel Santos, Clara Gomes, António Jorge Correia

Original Article - Port J Nephrol Hypert 2012; 26(4): 278-284

Hereditary hypophosphataemic rickets: experience from a paediatric nephrology unit

Joana S. Caetano, Carolina Cordinhã, Clara Gomes, António J. Correia

Original Article - Port J Nephrol Hypert 2007; 21(2): 77-82

Paediatric nephrolithiasis and nephrocalcinosis: a 20 year retrospective analysis

Sofia A Martins, Clara Gomes, A Jorge Correia