Laura Ferreira Teixeira Vilarinho
AuthID: R-002-GKT
81
TITLE: The mitochondrial DNA A3243G mutation in Portugal: clinical and molecular studies in 5 families Full Text
AUTHORS: Vilarinho, L; Santorelli, FM; Coelho, I; Rodrigues, L; Maia, M; Barata, I; Cabral, P; Dionisio, A; Costa, A; Guimaraes, A; DiMauro, S;
PUBLISHED: 1999, SOURCE: JOURNAL OF THE NEUROLOGICAL SCIENCES, VOLUME: 163, ISSUE: 2
AUTHORS: Vilarinho, L; Santorelli, FM; Coelho, I; Rodrigues, L; Maia, M; Barata, I; Cabral, P; Dionisio, A; Costa, A; Guimaraes, A; DiMauro, S;
PUBLISHED: 1999, SOURCE: JOURNAL OF THE NEUROLOGICAL SCIENCES, VOLUME: 163, ISSUE: 2
82
TITLE: Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes in Portugal: evidences for clinical heterogeneity Full Text
AUTHORS: Vilarinho, L; Santorelli, FM; Coelho, I; Rodrigues, L; Maia, C; Cabral, P; Dionisio, A; Guimaraes, A; DiMauro, S;
PUBLISHED: 1998, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 6
AUTHORS: Vilarinho, L; Santorelli, FM; Coelho, I; Rodrigues, L; Maia, C; Cabral, P; Dionisio, A; Guimaraes, A; DiMauro, S;
PUBLISHED: 1998, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 6
INDEXED IN: 
WOS
WOS83
TITLE: Mitochondrial DNA Analysis in Ocular Myopathy
AUTHORS: Laura Vilarinho; Filippo M Santorelli; Maria Luís Cardoso; Teresa Coelho; António Guimarães; Paula Coutinho;
PUBLISHED: 1998, SOURCE: European Neurology - Eur Neurol, VOLUME: 39, ISSUE: 3
AUTHORS: Laura Vilarinho; Filippo M Santorelli; Maria Luís Cardoso; Teresa Coelho; António Guimarães; Paula Coutinho;
PUBLISHED: 1998, SOURCE: European Neurology - Eur Neurol, VOLUME: 39, ISSUE: 3
INDEXED IN: 
CrossRef
CrossRef84
TITLE: Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS Full Text
AUTHORS: Santorelli, FM; Tanji, K; Kulikova, R; Shanske, S; Vilarinho, L; Hays, AP; DiMauro, S;
PUBLISHED: 1997, SOURCE: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, VOLUME: 238, ISSUE: 2
AUTHORS: Santorelli, FM; Tanji, K; Kulikova, R; Shanske, S; Vilarinho, L; Hays, AP; DiMauro, S;
PUBLISHED: 1997, SOURCE: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, VOLUME: 238, ISSUE: 2
85
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
86
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
