Luisa Maria Quental Mota Vieira
AuthID: R-000-K6E
61
TITLE: Disease knowledge and attitudes toward predictive testing and prenatal diagnosis in families with Machado-Joseph disease from the Azores Islands (Portugal)
AUTHORS: Lima, M ; Kay, T; Vasconcelos, J; Mota Vieira, L; Gonzalez, C; Peixoto, A; Abade, A; MacLeod, P; Graca, R; Santos, J;
PUBLISHED: 2001, SOURCE: Community Genetics, VOLUME: 4, ISSUE: 1
AUTHORS: Lima, M ; Kay, T; Vasconcelos, J; Mota Vieira, L; Gonzalez, C; Peixoto, A; Abade, A; MacLeod, P; Graca, R; Santos, J;
PUBLISHED: 2001, SOURCE: Community Genetics, VOLUME: 4, ISSUE: 1
62
TITLE: Transcriptional and translational mechanisms of cytochrome b<sub>5</sub> reductase isoenzyme generation in humans
AUTHORS: Leroux, A; Vieira, LM; Kahn, A;
PUBLISHED: 2001, SOURCE: BIOCHEMICAL JOURNAL, VOLUME: 355, ISSUE: 2
AUTHORS: Leroux, A; Vieira, LM; Kahn, A;
PUBLISHED: 2001, SOURCE: BIOCHEMICAL JOURNAL, VOLUME: 355, ISSUE: 2
INDEXED IN: 
Scopus 
WOS
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ORCID
ORCID63
TITLE: Transcriptional and translational mechanisms of cytochrome b5 reductase isoenzyme generation in humans
AUTHORS: Alena LEROUX; Luisa MOTA VIEIRA; Axel KAHN;
PUBLISHED: 2001, SOURCE: Biochem. J. - Biochemical Journal, VOLUME: 355, ISSUE: 2
AUTHORS: Alena LEROUX; Luisa MOTA VIEIRA; Axel KAHN;
PUBLISHED: 2001, SOURCE: Biochem. J. - Biochemical Journal, VOLUME: 355, ISSUE: 2
64
TITLE: Genetic variation of serotonin system genes in a sample of autism families from Portugal.
AUTHORS: Vicente, AM; Coutinho, A; Mota Vieira, L; Marques, C; Oliveira, G;
PUBLISHED: 2000, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 67, ISSUE: 4
AUTHORS: Vicente, AM; Coutinho, A; Mota Vieira, L; Marques, C; Oliveira, G;
PUBLISHED: 2000, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 67, ISSUE: 4
INDEXED IN: WOS
WOS IN MY: ORCID | ResearcherID
ORCID | ResearcherID65
TITLE: Charcot-Marie-Tooth neuropathy and Duchenne muscular dystrophy segregating in the same family: clinical and genetic studies.
AUTHORS: Mota Vieira, L; Martins, F; Vieira, E; Tardieu, S; Guimaraes, A; Pires, MM; Medeiros, E; Lopes, J; Santos, MR; LeGuern, E; Santos, J;
PUBLISHED: 1999, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 65, ISSUE: 4
AUTHORS: Mota Vieira, L; Martins, F; Vieira, E; Tardieu, S; Guimaraes, A; Pires, MM; Medeiros, E; Lopes, J; Santos, MR; LeGuern, E; Santos, J;
PUBLISHED: 1999, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 65, ISSUE: 4
INDEXED IN: WOS
WOS IN MY: ORCID | ResearcherID
ORCID | ResearcherID66
TITLE: Absence of mutation in the β- and γ-synuclein genes in familial autosomal dominant parkinson's disease
AUTHORS: Lavedan, C; Buchholtz, S; Auburger, G; Albin, RL; Athanassiadou, A; Blancato, J; Burguera, JA; Ferrell, RE; Kostic, V; Leroy, E; Leube, B; Mota Vieira, L; Papapetropoulos, T; Pericak Vance, MA; Pinkus, J; Scott, WK; Ulm, G; Vasconcelos, J; Vilchez, JJ; Nussbaum, RL; ...More
PUBLISHED: 1998, SOURCE: DNA Research, VOLUME: 5, ISSUE: 6
AUTHORS: Lavedan, C; Buchholtz, S; Auburger, G; Albin, RL; Athanassiadou, A; Blancato, J; Burguera, JA; Ferrell, RE; Kostic, V; Leroy, E; Leube, B; Mota Vieira, L; Papapetropoulos, T; Pericak Vance, MA; Pinkus, J; Scott, WK; Ulm, G; Vasconcelos, J; Vilchez, JJ; Nussbaum, RL; ...More
PUBLISHED: 1998, SOURCE: DNA Research, VOLUME: 5, ISSUE: 6
67
TITLE: Physical Mapping of 49 Microsatellite Markers on Chromosome 19 and Correlation with the Genetic Linkage Map Full Text
AUTHORS: Reguigne-Arnould, I; Faure, S; Chery, M; Mota-Vieira, L; Mollicone, R; J.J Candelier; Oriol, R; Couillin, P;
PUBLISHED: 1996, SOURCE: Genomics, VOLUME: 32, ISSUE: 3
AUTHORS: Reguigne-Arnould, I; Faure, S; Chery, M; Mota-Vieira, L; Mollicone, R; J.J Candelier; Oriol, R; Couillin, P;
PUBLISHED: 1996, SOURCE: Genomics, VOLUME: 32, ISSUE: 3
68
TITLE: Neurological degeneration due to CAG expansions in the gene for Machado-Joseph disease [UNE AUTRE MALADIE NEURODEGENERATIVE DUE A L'EXPANSION DU TRIPLET CAG: LA MALADIE DE MACHADO-JOSEPH]
AUTHORS: Mota Vieira, L;
PUBLISHED: 1995, SOURCE: Medecine/Sciences, VOLUME: 11, ISSUE: 1
AUTHORS: Mota Vieira, L;
PUBLISHED: 1995, SOURCE: Medecine/Sciences, VOLUME: 11, ISSUE: 1
INDEXED IN: Scopus
Scopus IN MY: ORCID
ORCID69
TITLE: 4 NEW MUTATIONS IN THE NADH-CYTOCHROME B5 REDUCTASE GENE FROM PATIENTS WITH RECESSIVE CONGENITAL METHEMOGLOBINEMIA TYPE-II
AUTHORS: VIEIRA, LM; KAPLAN, JC; KAHN, A; LEROUX, A;
PUBLISHED: 1995, SOURCE: BLOOD, VOLUME: 85, ISSUE: 8
AUTHORS: VIEIRA, LM; KAPLAN, JC; KAHN, A; LEROUX, A;
PUBLISHED: 1995, SOURCE: BLOOD, VOLUME: 85, ISSUE: 8
INDEXED IN: Scopus WOS
Scopus WOS IN MY: ORCID | ResearcherID
ORCID | ResearcherID70
TITLE: Heterogeneity of the rat NADH-cytochrome-b5-reductase transcripts resulting from multiple alternative first exons
AUTHORS: Mota Vieira, L; Kaplan, JC; Kahn, A; Leroux, A;
PUBLISHED: 1994, SOURCE: European Journal of Biochemistry, VOLUME: 220, ISSUE: 3
AUTHORS: Mota Vieira, L; Kaplan, JC; Kahn, A; Leroux, A;
PUBLISHED: 1994, SOURCE: European Journal of Biochemistry, VOLUME: 220, ISSUE: 3
INDEXED IN: Scopus
Scopus