Laura Ferreira Teixeira Vilarinho
AuthID: R-002-GKT
91
TITLE: The mitochondrial A3243G mutation presenting as severe cardiomyopathy
AUTHORS: Vilarinho, L; Santorelli, FM; Rosas, MJ; Tavares, C; MeloPires, M; DiMauro, S;
PUBLISHED: 1997, SOURCE: JOURNAL OF MEDICAL GENETICS, VOLUME: 34, ISSUE: 7
AUTHORS: Vilarinho, L; Santorelli, FM; Rosas, MJ; Tavares, C; MeloPires, M; DiMauro, S;
PUBLISHED: 1997, SOURCE: JOURNAL OF MEDICAL GENETICS, VOLUME: 34, ISSUE: 7
92
TITLE: L-2-hydroxyglutaric aciduria: Clinical, biochemical and magnetic resonance imaging in six Portuguese pediatric patients Full Text
AUTHORS: Barbot, C ; Fineza, I; Diogo, L; Maia, M; Melo, J; Guimaraes, A; Pires, MM ; Cardoso, ML; Vilarinho, L;
PUBLISHED: 1997, SOURCE: BRAIN & DEVELOPMENT, VOLUME: 19, ISSUE: 4
AUTHORS: Barbot, C ; Fineza, I; Diogo, L; Maia, M; Melo, J; Guimaraes, A; Pires, MM ; Cardoso, ML; Vilarinho, L;
PUBLISHED: 1997, SOURCE: BRAIN & DEVELOPMENT, VOLUME: 19, ISSUE: 4
