Percorrer por assunto Hyperbilirubinemia
Mostrar resultados 1-3 de 3.
| Data | Título | Autor(es) | Tipo | Acesso |
| 2006 | Analysis of the UDP-glucuronosyltransferase gene in Portuguese patients with a clinical diagnosis of Gilbert and Crigler–Najjar syndromes | Costa, Elísio; Vieira, Emília; Martins, Marcia; Saraiva, Jorge; Cancela, Eugénia; Costa, Miguel; Bauerle, Roswitha; Freitas, Teresa; Carvalho, João; Santos-Silva, Ermelinda; Barbot, José; Santos, Rosário | article |  |
| 2005 | Hematologically important mutations: bilirubin UDP-glucuronosyltransferase gene mutations in Gilbert and Crigler-Najjar syndromes. | Costa, Elísio | article | |
| 2004 | A new case of (TA)8 allele in the UGT1A1 gene promoter in a caucasian girl with Gilbert' syndrome | Coelho, Henrique; Costa, Elísio; Branca, Rosa; Santos, Rosário; Barbot, José | article | |
