51
TITLE: Genetic variation at the CY2C19 gene associated with Metabolic Syndrome susceptibility in a South Portuguese population
AUTHORS: Vania Gaio; Baltazar Nunes; Aida Fernandes; Francisco Mendonça; Filomena Horta Correia; Álvaro Beleza; Ana P Gil; Mafalda Bourbon; A.M. Vicente; Carlos M Dias; Marta Barreto da Silva;
PUBLISHED: 2013, SOURCE: 63rd Annual Meeting of The American Society of Human Genetics (ASHG), 22-26 October, 2013
INDEXED IN: Handle
52
TITLE: Inquérito Europeu de Saúde com Exame Físico em Portugal: avaliação das fases de planeamento e implementação
AUTHORS: Ana P Gil; Marta Barreto; Ausenda Machado; Filomena Horta Correia; Carlos M Dias;
PUBLISHED: 2012, SOURCE: 3º Congresso Nacional de Saúde Pública, CHUC, 25-26 outubro 2012
INDEXED IN: Handle
53
TITLE: Prevalence of alpha-1 antitrypsin deficiency and hereditary hemochromatosis gene mutations in Algarve, Portugal
AUTHORS: Marta Barreto da Silva; Vânia Gaio; Aida Fernandes; Francisco Mendonça; Filomena Horta Correia; Álvaro Beleza; Ana P Gil; Mafalda Bourbon; A.M. Vicente; Carlos M Dias;
PUBLISHED: 2012, SOURCE: 62nd Annual Meeting of the American Society of Human Genetics, 6-10 November 2012
INDEXED IN: Handle
54
TITLE: Prevalence of diabetes-associated gene variants and its association with blood glucose levels in the Algarve population, Portugal
AUTHORS: Vania Gaio; Aida Fernandes; Francisco Mendonça; Filomena Horta Correia; Álvaro Beleza; Ana P Gil; Mafalda Bourbon; A.M. Vicente; Marta Barreto da Silva; Carlos M Dias;
PUBLISHED: 2012, SOURCE: Annual Meeting of the American Society of Human Genetics, 25 October 2015
INDEXED IN: Handle
55
TITLE: Biochemical and genetic evaluation of dyslipidemia in a population sample from São Brás de Alportel- Algarve
AUTHORS: Vânia Francisco; Marta Barreto da Silva; Catarina Alves; Paula Rasteiro; Eduardo Sousa; A.M. Vicente; Ana P Gil;
PUBLISHED: 2011, SOURCE: 15º Congresso Português de Genética Humana, 10, 11 e 12 de Novembro de 2011
INDEXED IN: Handle
56
TITLE: Slc25a12 Disruption Alters Myelination and Neurofilaments: A Model for a Hypomyelination Syndrome and Childhood Neurodevelopmental Disorders
AUTHORS: Sakurai, T; Ramoz, N; Barreto, M; Gazdoiu, M; Takahashi, N; Gertner, M; Dorr, N; Sosa, MAG; De Gasperi, R; Perez, G; Schmeidler, J; Mitropoulou, V; Le, HC; Lupu, M; Hof, PR; Elder, GA; Buxbaum, JD;
PUBLISHED: 2010, SOURCE: BIOLOGICAL PSYCHIATRY, VOLUME: 67, ISSUE: 9
INDEXED IN: Scopus WOS CrossRef Handle
IN MY: ORCID
57
TITLE: A Remarkable Depletion of Both Naïve CD4+ and CD8+ with High Proportion of Memory T Cells in an IPEX Infant with a FOXP3 Mutation in the Forkhead Domain  Full Text
AUTHORS: Costa-Carvalho, BT; de Moraes-Pinto, MI; de Almeida, LC; de Seixas Alves, MT; Maia, RP; de Souza, RL; Barreto, M; Lourenço, L; Vicente, AM; Coutinho, A; Carneiro-Sampaio, M;
PUBLISHED: 2008, SOURCE: Scand J Immunol - Scandinavian Journal of Immunology, VOLUME: 68, ISSUE: 1
INDEXED IN: CrossRef
IN MY: ORCID
Page 6 of 6. Total results: 57.