Luisa Maria Quental Mota Vieira
AuthID: R-000-K6E
61
TITLE: Multiple consanguinity in a large Azorean family affected with spinal muscular atrophy type I: Implication in genetic counselling Full Text
AUTHORS: Mota Vieira, L; Rodrigues, L; Melo, P; Melo, C; Forjaz Sampaio, J; dos Santos, R; Maia, A;
PUBLISHED: 2002, SOURCE: European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 10
AUTHORS: Mota Vieira, L; Rodrigues, L; Melo, P; Melo, C; Forjaz Sampaio, J; dos Santos, R; Maia, A;
PUBLISHED: 2002, SOURCE: European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 10
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ORCID | ResearcherID62
TITLE: Study of genetic diversity by surname analysis of the Azorean population (Portugal).
AUTHORS: Branco, CC; Mota Vieira, L;
PUBLISHED: 2002, SOURCE: 52nd Annual Meeting of the American-Society-of-Human-Genetics in AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 71, ISSUE: 4
AUTHORS: Branco, CC; Mota Vieira, L;
PUBLISHED: 2002, SOURCE: 52nd Annual Meeting of the American-Society-of-Human-Genetics in AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 71, ISSUE: 4
INDEXED IN: WOS
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ORCID | ResearcherID63
TITLE: Parkinsonism phenotype in a large Azorean family affect with Machado-Joseph Disease.
AUTHORS: Mota Vieira, L; Ferro, A; Silveira, I; Sequeiros, J ; Coutinho, P; Lopes, J;
PUBLISHED: 2001, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 69, ISSUE: 4
AUTHORS: Mota Vieira, L; Ferro, A; Silveira, I; Sequeiros, J ; Coutinho, P; Lopes, J;
PUBLISHED: 2001, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 69, ISSUE: 4
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ORCID | ResearcherID64
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
65
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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ORCID66
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
67
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
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ORCID | ResearcherID68
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
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ORCID | ResearcherID69
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
70
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
