Isabel Conceição Moreira Pereira Alonso
AuthID: R-000-678
11
TITLE: Large normal alleles of ATXN2 decrease age at onset in transthyretin familial amyloid polyneuropathy Val30Met patients. Large Normal ATXN2
Alleles Full Text
AUTHORS: Diana Santos; Teresa Coelho; Miguel Alves Ferreira; Jorge Sequeiros; Denisa Mendonca ; Isabel Alonso; Alda Sousa; Carolina Lemos ;
PUBLISHED: 2019, SOURCE: ANNALS OF NEUROLOGY, VOLUME: 85, ISSUE: 2
AUTHORS: Diana Santos; Teresa Coelho; Miguel Alves Ferreira; Jorge Sequeiros; Denisa Mendonca ; Isabel Alonso; Alda Sousa; Carolina Lemos ;
PUBLISHED: 2019, SOURCE: ANNALS OF NEUROLOGY, VOLUME: 85, ISSUE: 2
12
TITLE: Proinflammatory and anti-inflammatory cytokines in the CSF of patients with Alzheimer's disease and their correlation with cognitive decline Full Text
AUTHORS: Taipa, R; das Neves, SP; Sousa, AL; Fernandes, J; Pinto, C; Correia, AP; Santos, E; Pinto, PS; Carneiro, P; Costa, P; Santos, D; Alonso, I; Patna, J; Marques, F ; Cavaco, S; Sousa, N ;
PUBLISHED: 2019, SOURCE: NEUROBIOLOGY OF AGING, VOLUME: 76
AUTHORS: Taipa, R; das Neves, SP; Sousa, AL; Fernandes, J; Pinto, C; Correia, AP; Santos, E; Pinto, PS; Carneiro, P; Costa, P; Santos, D; Alonso, I; Patna, J; Marques, F ; Cavaco, S; Sousa, N ;
PUBLISHED: 2019, SOURCE: NEUROBIOLOGY OF AGING, VOLUME: 76
13
TITLE: C1QA and C1QC modify age-at-onset in familial amyloid polyneuropathy patients
AUTHORS: Dias, A; Santos, D; Coelho, T; Alves Ferreira, M; Sequeiros, J; Alonso, I; Sousa, A; Lemos, C ;
PUBLISHED: 2019, SOURCE: ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, VOLUME: 6, ISSUE: 4
AUTHORS: Dias, A; Santos, D; Coelho, T; Alves Ferreira, M; Sequeiros, J; Alonso, I; Sousa, A; Lemos, C ;
PUBLISHED: 2019, SOURCE: ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, VOLUME: 6, ISSUE: 4
16
TITLE: Assessment of patients with hereditary transthyretin amyloidosis–understanding the impact of management and disease progression
AUTHORS: Conceição, I; Coelho, T; Rapezzi, C; Parman, Y; Obici, L; Galán, L; Rousseau, A;
PUBLISHED: 2019, SOURCE: Amyloid, VOLUME: 26, ISSUE: 3
AUTHORS: Conceição, I; Coelho, T; Rapezzi, C; Parman, Y; Obici, L; Galán, L; Rousseau, A;
PUBLISHED: 2019, SOURCE: Amyloid, VOLUME: 26, ISSUE: 3
INDEXED IN: 
Scopus
Scopus17
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
WOS18
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
WOS19
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
WOS20
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
WOS