Maria Teresa Pardal Monteiro Coelho
AuthID: R-000-CPE
1
TITLE: Heterogeneity in families with ATTRV30M amyloidosis: a historical and longitudinal Portuguese case study impact for genetic counselling Full Text
AUTHORS: Pedroto, Maria ; Coelho, Teresa; Fernandes, Joana; Oliveira, Alexandra; Jorge, Alipio ; Mendes Moreira, Joao ;
PUBLISHED: 2024, SOURCE: AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
AUTHORS: Pedroto, Maria ; Coelho, Teresa; Fernandes, Joana; Oliveira, Alexandra; Jorge, Alipio ; Mendes Moreira, Joao ;
PUBLISHED: 2024, SOURCE: AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
2
TITLE: Phenotyping mitochondrial glutamyl-tRNA synthetase deficiency (EARS2 ): A case series and systematic literature review Full Text
AUTHORS: Pelayo, Goncalo; Coelho, Margarida Paiva; Correia, Joana; Bandeira, Anabela; Nogueira, Celia; Vilarinho, Laura; Martins, Esmeralda;
PUBLISHED: 2024, SOURCE: NEUROBIOLOGY OF DISEASE, VOLUME: 200
AUTHORS: Pelayo, Goncalo; Coelho, Margarida Paiva; Correia, Joana; Bandeira, Anabela; Nogueira, Celia; Vilarinho, Laura; Martins, Esmeralda;
PUBLISHED: 2024, SOURCE: NEUROBIOLOGY OF DISEASE, VOLUME: 200
3
TITLE: Tafamidis concentration required for transthyretin stabilisation in cerebrospinal fluid
AUTHORS: Tsai, Felix J.; Jaeger, Marcus; Coelho, Teresa; Powers, Evan T.; Kelly, Jeffery W.;
PUBLISHED: 2023, SOURCE: AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
AUTHORS: Tsai, Felix J.; Jaeger, Marcus; Coelho, Teresa; Powers, Evan T.; Kelly, Jeffery W.;
PUBLISHED: 2023, SOURCE: AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
INDEXED IN: Scopus WOS
4
TITLE: Clinical model for Hereditary Transthyretin Amyloidosis age of onset prediction Full Text
AUTHORS: Pedroto, Maria ; Coelho, Teresa; Jorge, Alipio ; Mendes Moreira, Joao ;
PUBLISHED: 2023, SOURCE: FRONTIERS IN NEUROLOGY, VOLUME: 14
AUTHORS: Pedroto, Maria ; Coelho, Teresa; Jorge, Alipio ; Mendes Moreira, Joao ;
PUBLISHED: 2023, SOURCE: FRONTIERS IN NEUROLOGY, VOLUME: 14
5
TITLE: Optimal practices for the management of hereditary transthyretin amyloidosis: real-world experience from Japan, Brazil, and Portugal Full Text
AUTHORS: Ando, Yukio; Waddington Cruz, Marcia; Sekijima, Yoshiki; Koike, Haruki; Ueda, Mitsuharu; Konishi, Hiroaki; Ishii, Tomonori; Coelho, Teresa;
PUBLISHED: 2023, SOURCE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 18, ISSUE: 1
AUTHORS: Ando, Yukio; Waddington Cruz, Marcia; Sekijima, Yoshiki; Koike, Haruki; Ueda, Mitsuharu; Konishi, Hiroaki; Ishii, Tomonori; Coelho, Teresa;
PUBLISHED: 2023, SOURCE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 18, ISSUE: 1
INDEXED IN: Scopus WOS
6
TITLE: A 15-year consolidated overview of data in over 6000 patients from the Transthyretin Amyloidosis Outcomes Survey (THAOS) Full Text
AUTHORS: Luca Gentile; Teresa Coelho; Angela Dispenzieri; Isabel Conceição; Márcia Waddington Cruz; Arnt Kristen; Jonas Wixner; Igor Diemberger; Juan Gonzalez Moreno; Eve Cariou; Mathew Maurer; Violaine Planté Bordeneuve; Pablo Garcia Pavia; Ivailo Tournev; Jose Gonzalez Costello; Alejandra Gonzalez Duarte; Martha Grogan; Anna Mazzeo; Doug Chapman; Pritam Gupta; ...More
PUBLISHED: 2023, SOURCE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 18, ISSUE: 1
AUTHORS: Luca Gentile; Teresa Coelho; Angela Dispenzieri; Isabel Conceição; Márcia Waddington Cruz; Arnt Kristen; Jonas Wixner; Igor Diemberger; Juan Gonzalez Moreno; Eve Cariou; Mathew Maurer; Violaine Planté Bordeneuve; Pablo Garcia Pavia; Ivailo Tournev; Jose Gonzalez Costello; Alejandra Gonzalez Duarte; Martha Grogan; Anna Mazzeo; Doug Chapman; Pritam Gupta; ...More
PUBLISHED: 2023, SOURCE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 18, ISSUE: 1
INDEXED IN: Scopus WOS
7
TITLE: Clinical and Genotype Characteristics and Symptom Migration in Patients With Mixed Phenotype Transthyretin Amyloidosis from the Transthyretin Amyloidosis Outcomes Survey
AUTHORS: Gonzalez Moreno, Juan; Dispenzieri, Angela; Grogan, Martha; Coelho, Teresa; Tournev, Ivailo; Waddington Cruz, Marcia; Wixner, Jonas; Diemberger, Igor; Garcia Pavia, Pablo; Chapman, Doug; Gupta, Pritam; Glass, Oliver;
PUBLISHED: 2023, SOURCE: CARDIOLOGY AND THERAPY
AUTHORS: Gonzalez Moreno, Juan; Dispenzieri, Angela; Grogan, Martha; Coelho, Teresa; Tournev, Ivailo; Waddington Cruz, Marcia; Wixner, Jonas; Diemberger, Igor; Garcia Pavia, Pablo; Chapman, Doug; Gupta, Pritam; Glass, Oliver;
PUBLISHED: 2023, SOURCE: CARDIOLOGY AND THERAPY
INDEXED IN: Scopus WOS
8
TITLE: Mitochondrial uncoupling proteins (UCPs) are metabolic modulators in human sertoli cells Full Text
AUTHORS: David F Carrageta ; Freire Brito, L.; Monteiro, B. S.; Guerra Carvalho, B. ; Bernardino, R. L. ; Oliveira, P. F.; Monteiro, M. P.; Alves, M. G. ;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, VOLUME: 52
AUTHORS: David F Carrageta ; Freire Brito, L.; Monteiro, B. S.; Guerra Carvalho, B. ; Bernardino, R. L. ; Oliveira, P. F.; Monteiro, M. P.; Alves, M. G. ;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, VOLUME: 52
INDEXED IN: WOS
9
TITLE: A natural history analysis of asymptomatic TTR gene carriers as they develop symptomatic transthyretin amyloidosis in the Transthyretin Amyloidosis Outcomes Survey (THAOS)
AUTHORS: Coelho, Teresa; Conceicao, Isabel; Waddington Cruz, Marcia; Keohane, Denis; Sultan, Marla B.; Chapman, Doug; Amass, Leslie;
PUBLISHED: 2022, SOURCE: AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
AUTHORS: Coelho, Teresa; Conceicao, Isabel; Waddington Cruz, Marcia; Keohane, Denis; Sultan, Marla B.; Chapman, Doug; Amass, Leslie;
PUBLISHED: 2022, SOURCE: AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
INDEXED IN: Scopus WOS
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TITLE: Gait Characterization and Analysis of Hereditary Amyloidosis Associated with Transthyretin Patients: A Case Series
AUTHORS: Vilas Boas, Maria do Carmo ; Pereira Fonseca, Pedro Filipe; Sousa, Ines Martins; Cardoso, Marcio Neves; Silva Cunha, Joao Paulo ; Coelho, Teresa;
PUBLISHED: 2022, SOURCE: JOURNAL OF CLINICAL MEDICINE, VOLUME: 11, ISSUE: 14
AUTHORS: Vilas Boas, Maria do Carmo ; Pereira Fonseca, Pedro Filipe; Sousa, Ines Martins; Cardoso, Marcio Neves; Silva Cunha, Joao Paulo ; Coelho, Teresa;
PUBLISHED: 2022, SOURCE: JOURNAL OF CLINICAL MEDICINE, VOLUME: 11, ISSUE: 14