1. Repositório Científico do Centro Hospitalar do Porto

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Issue DateTitleAuthor(s)TypeAccess Type
2012Nephrogenic diabetes insipidus associated with tenofovir administration: report of a paediatric caseCosta, M.; Teixeira, C.; Costa, A.; Faria, M.; Mota, C.; Marques, L.articleopenAccess
2014Membranoproliferative glomerulonephritis and x-linked agammaglobulinemia: an uncommon associationLavrador, V.; Correia, F.; Sampaio, R.; Candido, C.; Sameiro-Faria, M.; Marques, L.; Mota, C.articleopenAccess
May-2003Homocysteine levels in pediatric renal transplant recipients.Mota, C.; Fonseca, I.; Santos, M.J.; Costa, T.; Faria, M.S.; Henriques, A.C.; Sarmento, A.M.; Pereira, E.; Pereira, M.articleopenAccess
2015D-bifunctional protein deficiency – a cause of neonatal onset seizures and hypotoniaNascimento, J.; Mota, C.; Lacerda, L.; Pacheco, S.; Chorão, R.; Martins, E.; Garrido, C.articleopenAccess
2012Atypical haemolytic-uraemic syndrome caused by factor H mutation: case report and new management strategies in childrenAraújo, L.; Faria, M.; Rocha, L.; Costa, T.; Barbot, J.; Mota, C.articleopenAccess
2000Haemolytic uraemic syndrome, cardiomyopathy, cutaneous vasculopathy and anti-phospholipid activityFaria, M.; Mota, C.; Barbot, J.; Alvares, S.; Jardim, H.; Vilarinho, A.; Pereira, E.articleopenAccess
2015A Novel Noonan Syndrome RAF1 Mutation: Lethal Course in a Preterm InfantRatola, A.; Silva, H.; Guedes, A.; Mota, C.; Braga, A.; Oliveira, D.; Alegria, A.; Carvalho, C.; Álvares, S.; Proença, E.articleopenAccess
2017The Diagnosing Challenge of a Positive ANCA Vasculitis in the Paediatric AgePreto, C.; Silva, A.; Alves, S.; Guedes, M.; Matos, P.; Mota, C.; Rocha, P.; Fernandes, P.articleopenAccess

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