Maria Isabel Ginestal Tavares Almeida
AuthID: R-000-BQS
31
TITLE: Pyruvate dehydrogenase complex: mRNA and protein expression patterns of E1 alpha subunit genes in human spermatogenesis Full Text
AUTHORS: Ana Pinheiro; Maria Joao Silva; Ines Graca; Joaquina Silva; Rosalia Sa ; Mario Sousa ; Alberto Barros ; Isabel Tavares de Almeida; Isabel Rivera ;
PUBLISHED: 2012, SOURCE: GENE, VOLUME: 506, ISSUE: 1
AUTHORS: Ana Pinheiro; Maria Joao Silva; Ines Graca; Joaquina Silva; Rosalia Sa ; Mario Sousa ; Alberto Barros ; Isabel Tavares de Almeida; Isabel Rivera ;
PUBLISHED: 2012, SOURCE: GENE, VOLUME: 506, ISSUE: 1
32
TITLE: Asymmetric dimethylarginine in adults with cystathionine beta-synthase deficiency Full Text
AUTHORS: Monica S Rocha; Tom Teerlink; Mirian C H Janssen; Leo A J Kluijtmans; Yvo Smulders; Cornelis Jakobs; Isabel Tavares de Almeida; Isabel Rivera ; Rita Castro ; Henk J Blom;
PUBLISHED: 2012, SOURCE: ATHEROSCLEROSIS, VOLUME: 222, ISSUE: 2
AUTHORS: Monica S Rocha; Tom Teerlink; Mirian C H Janssen; Leo A J Kluijtmans; Yvo Smulders; Cornelis Jakobs; Isabel Tavares de Almeida; Isabel Rivera ; Rita Castro ; Henk J Blom;
PUBLISHED: 2012, SOURCE: ATHEROSCLEROSIS, VOLUME: 222, ISSUE: 2
33
TITLE: Stability of Zn-Ni-TiO2 and Zn-TiO2 nanocomposite coatings in near-neutral sulphate solutions Full Text
AUTHORS: Gomes, A ; Almeida, I; Frade, T; Tavares, AC;
PUBLISHED: 2012, SOURCE: JOURNAL OF NANOPARTICLE RESEARCH, VOLUME: 14, ISSUE: 2
AUTHORS: Gomes, A ; Almeida, I; Frade, T; Tavares, AC;
PUBLISHED: 2012, SOURCE: JOURNAL OF NANOPARTICLE RESEARCH, VOLUME: 14, ISSUE: 2
34
TITLE: Phenylalanine hydroxylase deficiency: Molecular epidemiology and predictable BH4-responsiveness in South Portugal PKU patients Full Text
AUTHORS: Isabel Rivera ; Dina Mendes; Angela Afonso; Madalena Barroso; Ruben Ramos; Patricia Janeiro; Anabela Oliveira; Ana Gaspar; Isabel Tavares de Almeida;
PUBLISHED: 2011, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 104, ISSUE: SUPPL.
AUTHORS: Isabel Rivera ; Dina Mendes; Angela Afonso; Madalena Barroso; Ruben Ramos; Patricia Janeiro; Anabela Oliveira; Ana Gaspar; Isabel Tavares de Almeida;
PUBLISHED: 2011, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 104, ISSUE: SUPPL.
35
TITLE: Inhibition of 3-methylcrotonyl-CoA carboxylase explains the increased excretion of 3-hydroxyisovaleric acid in valproate-treated patients Full Text
AUTHORS: Paula B M Luís; Jos P Ruiter; Lodewijk IJlst; Luísa Diogo; Paula Garcia; Isabel Tavares de Almeida; Marinus Duran; Ronald J Wanders; Margarida F B Silva;
PUBLISHED: 2011, SOURCE: Journal of Inherited Metabolic Disease - J Inherit Metab Dis, VOLUME: 35, ISSUE: 3
AUTHORS: Paula B M Luís; Jos P Ruiter; Lodewijk IJlst; Luísa Diogo; Paula Garcia; Isabel Tavares de Almeida; Marinus Duran; Ronald J Wanders; Margarida F B Silva;
PUBLISHED: 2011, SOURCE: Journal of Inherited Metabolic Disease - J Inherit Metab Dis, VOLUME: 35, ISSUE: 3
36
TITLE: Valproic acid utilizes the isoleucine breakdown pathway for its complete β-oxidation Full Text
AUTHORS: Paula B.M Luís; Jos P Ruiter; Rob Ofman; Lodewijk IJlst; Marco Moedas; Luísa Diogo; Paula Garcia; Isabel Tavares de Almeida; Marinus Duran; Ronald J Wanders; Margarida F.B Silva;
PUBLISHED: 2011, SOURCE: Biochemical Pharmacology, VOLUME: 82, ISSUE: 11
AUTHORS: Paula B.M Luís; Jos P Ruiter; Rob Ofman; Lodewijk IJlst; Marco Moedas; Luísa Diogo; Paula Garcia; Isabel Tavares de Almeida; Marinus Duran; Ronald J Wanders; Margarida F.B Silva;
PUBLISHED: 2011, SOURCE: Biochemical Pharmacology, VOLUME: 82, ISSUE: 11
37
TITLE: Pyruvate dehydrogenase deficiency: identification of a novel mutation in the PDHA1 gene which responds to amino acid supplementation Full Text
AUTHORS: Maria Joao Silva; Ana Pinheiro; Filomena Eusebio; Ana Gaspar; Isabel Tavares de Almeida; Isabel Rivera ;
PUBLISHED: 2009, SOURCE: EUROPEAN JOURNAL OF PEDIATRICS, VOLUME: 168, ISSUE: 1
AUTHORS: Maria Joao Silva; Ana Pinheiro; Filomena Eusebio; Ana Gaspar; Isabel Tavares de Almeida; Isabel Rivera ;
PUBLISHED: 2009, SOURCE: EUROPEAN JOURNAL OF PEDIATRICS, VOLUME: 168, ISSUE: 1
38
TITLE: 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: initial presentation in a young adult.
AUTHORS: Reimao, S; Morgado, C; Almeida, IT; Silva, M ; Corte Real, H; Campos, J;
PUBLISHED: 2009, SOURCE: Journal of inherited metabolic disease, VOLUME: 32 Suppl 1
AUTHORS: Reimao, S; Morgado, C; Almeida, IT; Silva, M ; Corte Real, H; Campos, J;
PUBLISHED: 2009, SOURCE: Journal of inherited metabolic disease, VOLUME: 32 Suppl 1
INDEXED IN: 
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ORCID39
TITLE: 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: Initial presentation in a young adult
AUTHORS: Reimao, S; Morgado, C; Almeida, IT; Silva, M; Real, HC; Campos, J;
PUBLISHED: 2009, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 32, ISSUE: 1
AUTHORS: Reimao, S; Morgado, C; Almeida, IT; Silva, M; Real, HC; Campos, J;
PUBLISHED: 2009, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 32, ISSUE: 1
40
TITLE: Modulation of the Activity of Newly Synthesized Human Phenylalanine Hydroxylase Mutant Proteins by Low-Molecular-Weight Compounds
AUTHORS: Catia Nascimento; Joao Leandro ; Isabel Tavares de Almeida; Paula Leandro ;
PUBLISHED: 2008, SOURCE: PROTEIN JOURNAL, VOLUME: 27, ISSUE: 6
AUTHORS: Catia Nascimento; Joao Leandro ; Isabel Tavares de Almeida; Paula Leandro ;
PUBLISHED: 2008, SOURCE: PROTEIN JOURNAL, VOLUME: 27, ISSUE: 6
