António Jorge dos Santos Pereira de Sequeiros
AuthID: R-000-23K
61
TITLE: Twenty Years of a Pre-Symptomatic Testing Protocol for Late-Onset Neurological Diseases in Portugal Full Text
AUTHORS: Paneque, M ; Felix, J; Mendes, A; Lemos, C ; Ledo, S; Silva, J; Sequeiros, J;
PUBLISHED: 2019, SOURCE: ACTA MEDICA PORTUGUESA, VOLUME: 32, ISSUE: 4
AUTHORS: Paneque, M ; Felix, J; Mendes, A; Lemos, C ; Ledo, S; Silva, J; Sequeiros, J;
PUBLISHED: 2019, SOURCE: ACTA MEDICA PORTUGUESA, VOLUME: 32, ISSUE: 4
62
TITLE: Diabetic patients need higher loop diuretic doses: a report on acute and chronic heart failure patients
AUTHORS: Cunha, FM; Pereira, J; Marques, P; Ribeiro, A; Bettencourt, P ; Lourenco, P ;
PUBLISHED: 2019, SOURCE: EUROPEAN JOURNAL OF HEART FAILURE, VOLUME: 21
AUTHORS: Cunha, FM; Pereira, J; Marques, P; Ribeiro, A; Bettencourt, P ; Lourenco, P ;
PUBLISHED: 2019, SOURCE: EUROPEAN JOURNAL OF HEART FAILURE, VOLUME: 21
INDEXED IN: 
WOS
WOS63
TITLE: A formula to calculate discharge furosemide dose after an acute heart failure hospitalization
AUTHORS: Lourenco, P ; Cunha, F; Pereira, J; Carreira, M; Marques, P; Ribeiro, A; Araujo, JP; Bettencourt, P;
PUBLISHED: 2019, SOURCE: EUROPEAN JOURNAL OF HEART FAILURE, VOLUME: 21
AUTHORS: Lourenco, P ; Cunha, F; Pereira, J; Carreira, M; Marques, P; Ribeiro, A; Araujo, JP; Bettencourt, P;
PUBLISHED: 2019, SOURCE: EUROPEAN JOURNAL OF HEART FAILURE, VOLUME: 21
INDEXED IN: WOS
WOS64
TITLE: The role of Neurexin (NRXN2) genetic network in migraine susceptibility Full Text
AUTHORS: Miguel Alves Ferreira; Joao Luis Neto; Jose Pereira Monteiro; Jorge Sequeiros; Isabel Alonso; Alda Sousa; Carolina Lemos ;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
AUTHORS: Miguel Alves Ferreira; Joao Luis Neto; Jose Pereira Monteiro; Jorge Sequeiros; Isabel Alonso; Alda Sousa; Carolina Lemos ;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
INDEXED IN: WOS
WOS65
TITLE: Patients' Voices in Portugal - when rare becomes common Full Text
AUTHORS: Catarina Costa; Isabel Alonso; Jorge Sequeiros; Milena Paneque ;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
AUTHORS: Catarina Costa; Isabel Alonso; Jorge Sequeiros; Milena Paneque ;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
INDEXED IN: WOS
WOS66
TITLE: A Portuguese Tool for Quality Assessment of Genetic Counselling by Genetics Healthcare Professionals Full Text
AUTHORS: Catarina Costa; Marina S Lemos; Carolina Lemos ; Miguel Alves Ferreira; Jorge Sequeiros; Milena Paneque ;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
AUTHORS: Catarina Costa; Marina S Lemos; Carolina Lemos ; Miguel Alves Ferreira; Jorge Sequeiros; Milena Paneque ;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
INDEXED IN: WOS
WOS67
TITLE: Interpreting sequence variants: a daily challenge in a clinical molecular genetics laboratory Full Text
AUTHORS: Rita Bastos Ferreira; Ana Filipa Brandao; Ana Margarida Lopes; Susana Sousa; Patricia Arinto; Sara Morais; Paulo Silva; Susana Barbosa; Diana Santos; Isabel Alonso; Jorge Sequeiros;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
AUTHORS: Rita Bastos Ferreira; Ana Filipa Brandao; Ana Margarida Lopes; Susana Sousa; Patricia Arinto; Sara Morais; Paulo Silva; Susana Barbosa; Diana Santos; Isabel Alonso; Jorge Sequeiros;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
INDEXED IN: WOS
WOS68
TITLE: Ancestral Origin and diffusion of Va150Met mutation in Transthyretin-Related Familial Amyloid Polyneuropathy (ATTRV50M) in the Portuguese populations Full Text
AUTHORS: Catia Leal; Teresa Coelho; Diana Santos; Jorge Sequeiros; Isabel Alonso; Alda Sousa; Miguel Alves Ferreira; Carolina Lemos ;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
AUTHORS: Catia Leal; Teresa Coelho; Diana Santos; Jorge Sequeiros; Isabel Alonso; Alda Sousa; Miguel Alves Ferreira; Carolina Lemos ;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
INDEXED IN: WOS
WOS69
TITLE: Detection of copy number variations in rare Mendelian disorders using whole exome sequencing Full Text
AUTHORS: Susana Sousa; Paulo Silva; Susana Barbosa; Ana Lopes; Ana Filipa Brandao; Patricia Arinto; Sara Morais; Isabel Alonso; Jorge Sequeiros;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
AUTHORS: Susana Sousa; Paulo Silva; Susana Barbosa; Ana Lopes; Ana Filipa Brandao; Patricia Arinto; Sara Morais; Isabel Alonso; Jorge Sequeiros;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
INDEXED IN: WOS
WOS70
TITLE: Parkin truncating variants result in a loss-of-function phenotype Full Text
AUTHORS: Santos, M; Morais, S; Pereira, C; Sequeiros, J; Alonso, I;
PUBLISHED: 2019, SOURCE: SCIENTIFIC REPORTS, VOLUME: 9, ISSUE: 1
AUTHORS: Santos, M; Morais, S; Pereira, C; Sequeiros, J; Alonso, I;
PUBLISHED: 2019, SOURCE: SCIENTIFIC REPORTS, VOLUME: 9, ISSUE: 1
