Maria Teresa Pardal Monteiro Coelho
AuthID: R-000-CPE
21
TITLE: Diagnosis, management, and follow-up of mitochondrial disorders in childhood: a personalized medicine in the new era of genome sequence Full Text
AUTHORS: Margarida Paiva Coelho; Esmeralda Martins ; Laura Vilarinho;
PUBLISHED: 2019, SOURCE: EUROPEAN JOURNAL OF PEDIATRICS, VOLUME: 178, ISSUE: 1
AUTHORS: Margarida Paiva Coelho; Esmeralda Martins ; Laura Vilarinho;
PUBLISHED: 2019, SOURCE: EUROPEAN JOURNAL OF PEDIATRICS, VOLUME: 178, ISSUE: 1
22
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
23
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
24
TITLE: A pair of peptides inhibits seeding of the hormone transporter transthyretin into amyloid fibrils
AUTHORS: Lorena Saelices; Binh A Nguyen; Kevin Chung; Yifei F Wang; Alfredo Ortega; Ji H Lee; Teresa Coelho; Johan Bijzet; Merrill D Benson; David S Eisenberg;
PUBLISHED: 2019, SOURCE: JOURNAL OF BIOLOGICAL CHEMISTRY, VOLUME: 294, ISSUE: 15
AUTHORS: Lorena Saelices; Binh A Nguyen; Kevin Chung; Yifei F Wang; Alfredo Ortega; Ji H Lee; Teresa Coelho; Johan Bijzet; Merrill D Benson; David S Eisenberg;
PUBLISHED: 2019, SOURCE: JOURNAL OF BIOLOGICAL CHEMISTRY, VOLUME: 294, ISSUE: 15
INDEXED IN: 
Scopus 
WOS
Scopus WOS25
TITLE: Predictive model of response to tafamidis in hereditary ATTR polyneuropathy
AUTHORS: Ceclia Monteiro; Jaleh S Mesgazardeh; Joao Anselmo; Joana Fernandes; Marta Novais; Carla Rodrigues; Gabriel J Brighty; David L Powers; Evan T Powers; Teresa Coelho; Jeffery W Kelly;
PUBLISHED: 2019, SOURCE: JCI INSIGHT, VOLUME: 4, ISSUE: 12
AUTHORS: Ceclia Monteiro; Jaleh S Mesgazardeh; Joao Anselmo; Joana Fernandes; Marta Novais; Carla Rodrigues; Gabriel J Brighty; David L Powers; Evan T Powers; Teresa Coelho; Jeffery W Kelly;
PUBLISHED: 2019, SOURCE: JCI INSIGHT, VOLUME: 4, ISSUE: 12
INDEXED IN: Scopus WOS
Scopus WOS26
TITLE: Hereditary transthyretin amyloidosis: a model of medical progress for a fatal disease
AUTHORS: David Adams; Haruki Koike; Michel Slama; Teresa Coelho;
PUBLISHED: 2019, SOURCE: NATURE REVIEWS NEUROLOGY, VOLUME: 15, ISSUE: 7
AUTHORS: David Adams; Haruki Koike; Michel Slama; Teresa Coelho;
PUBLISHED: 2019, SOURCE: NATURE REVIEWS NEUROLOGY, VOLUME: 15, ISSUE: 7
INDEXED IN: Scopus WOS
Scopus WOS27
TITLE: The diagnostic utility of neurophysiologic tests for early diagnostic of transthyretin familial amyloid polyneuropathy Full Text
AUTHORS: Ana P Sousa; Katia Valdrez; Marcio Cardoso; Joao Anselmo; Monica Freitas; Helder Ferreira; Teresa Coelho;
PUBLISHED: 2019, SOURCE: 16th International Symposium on Amyloidosis (ISA) in AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, VOLUME: 26, ISSUE: sup1
AUTHORS: Ana P Sousa; Katia Valdrez; Marcio Cardoso; Joao Anselmo; Monica Freitas; Helder Ferreira; Teresa Coelho;
PUBLISHED: 2019, SOURCE: 16th International Symposium on Amyloidosis (ISA) in AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, VOLUME: 26, ISSUE: sup1
INDEXED IN: Scopus WOS
Scopus WOS28
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
Scopus29
TITLE: Assessment of patients with hereditary transthyretin amyloidosis - understanding the impact of management and disease progression Full Text
AUTHORS: Isabel Conceicao; Teresa Coelho; Claudio Rapezzi; Yesim Parman; Laura Obici; Lucia Galan; Antoine Rousseau;
PUBLISHED: 2019, SOURCE: AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, VOLUME: 26, ISSUE: 3
AUTHORS: Isabel Conceicao; Teresa Coelho; Claudio Rapezzi; Yesim Parman; Laura Obici; Lucia Galan; Antoine Rousseau;
PUBLISHED: 2019, SOURCE: AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, VOLUME: 26, ISSUE: 3
INDEXED IN: WOS
WOS30
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