Teresinha Maria Dias Evangelista
AuthID: R-001-F3V
11
TITLE: Commonly used endocrine drugs
AUTHORS: Rosa, MM; Dias, T;
PUBLISHED: 2014, SOURCE: Handbook of Clinical Neurology, VOLUME: 120
AUTHORS: Rosa, MM; Dias, T;
PUBLISHED: 2014, SOURCE: Handbook of Clinical Neurology, VOLUME: 120
INDEXED IN: 
Scopus 
CrossRef
Scopus CrossRef12
TITLE: Atypical phenotype in two patients with LAMA2 mutations Full Text
AUTHORS: Joana Marques; Sofia T Duarte; Sonia Costa; Sandra Jacinto; Jorge Oliveira; Marcia E Oliveira; Rosario Santos; Bronze-da-Rocha E; Bronze E; Bronze-Rocha E ; Ana Rita Silvestre; Eulalia Calado; Teresinha Evangelista;
PUBLISHED: 2014, SOURCE: NEUROMUSCULAR DISORDERS, VOLUME: 24, ISSUE: 5
AUTHORS: Joana Marques; Sofia T Duarte; Sonia Costa; Sandra Jacinto; Jorge Oliveira; Marcia E Oliveira; Rosario Santos; Bronze-da-Rocha E; Bronze E; Bronze-Rocha E ; Ana Rita Silvestre; Eulalia Calado; Teresinha Evangelista;
PUBLISHED: 2014, SOURCE: NEUROMUSCULAR DISORDERS, VOLUME: 24, ISSUE: 5
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TITLE: New variants, challenges and pitfalls in DMD genotyping: implications in diagnosis, prognosis and therapy Full Text
AUTHORS: Rosario Santos; Ana Goncalves; Jorge Oliveira; Emilia Vieira; Jose Pedro Vieira; Teresinha Evangelista; Teresa Moreno; Manuela Santos; Isabel Fineza; Bronze-da-Rocha E; Bronze E; Bronze-Rocha E ;
PUBLISHED: 2014, SOURCE: JOURNAL OF HUMAN GENETICS, VOLUME: 59, ISSUE: 8
AUTHORS: Rosario Santos; Ana Goncalves; Jorge Oliveira; Emilia Vieira; Jose Pedro Vieira; Teresinha Evangelista; Teresa Moreno; Manuela Santos; Isabel Fineza; Bronze-da-Rocha E; Bronze E; Bronze-Rocha E ;
PUBLISHED: 2014, SOURCE: JOURNAL OF HUMAN GENETICS, VOLUME: 59, ISSUE: 8
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TITLE: A family with 2 different hereditary diseases leading to early cardiac involvement
AUTHORS: Nzwalo, H; Conceicao, I; Pereira, P; Santos, R; Evangelista, T;
PUBLISHED: 2013, SOURCE: Journal of Clinical Neuromuscular Disease, VOLUME: 14, ISSUE: 4
AUTHORS: Nzwalo, H; Conceicao, I; Pereira, P; Santos, R; Evangelista, T;
PUBLISHED: 2013, SOURCE: Journal of Clinical Neuromuscular Disease, VOLUME: 14, ISSUE: 4
INDEXED IN: Scopus CrossRef
Scopus CrossRef15
TITLE: Intermittent rhabdomyolysis with adult onset associated with a mutation in the ACADVL Gene
AUTHORS: Antunes, AP; Nogueira, C; Rocha, H; Vilarinho, L; Evangelista, T;
PUBLISHED: 2013, SOURCE: Journal of Clinical Neuromuscular Disease, VOLUME: 15, ISSUE: 2
AUTHORS: Antunes, AP; Nogueira, C; Rocha, H; Vilarinho, L; Evangelista, T;
PUBLISHED: 2013, SOURCE: Journal of Clinical Neuromuscular Disease, VOLUME: 15, ISSUE: 2
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TITLE: "Double-trouble" or digenic disorder in complex I deficiency Full Text
AUTHORS: Ligia S Almeida; Mariana Ferreira; Celia Nogueira; Fatima Furtado; Teresinha Evangelista; Filippo M Santorelli; Laura Vilarinho;
PUBLISHED: 2012, SOURCE: MITOCHONDRION, VOLUME: 12, ISSUE: 5
AUTHORS: Ligia S Almeida; Mariana Ferreira; Celia Nogueira; Fatima Furtado; Teresinha Evangelista; Filippo M Santorelli; Laura Vilarinho;
PUBLISHED: 2012, SOURCE: MITOCHONDRION, VOLUME: 12, ISSUE: 5
INDEXED IN: 
WOS CrossRef
WOS CrossRef17
TITLE: Liver and Muscle in Morbid Obesity: The Interplay of Fatty Liver and Insulin Resistance Full Text
AUTHORS: Mariana Verdelho Machado; Duarte M S Ferreira; Rui E Castro ; Ana Rita Silvestre; Teresinha Evangelista; Joao Coutinho; Fatima Carepa; Adilia Costa; Cecilia M P Rodrigues ; Helena Cortez Pinto;
PUBLISHED: 2012, SOURCE: PLOS ONE, VOLUME: 7, ISSUE: 2
AUTHORS: Mariana Verdelho Machado; Duarte M S Ferreira; Rui E Castro ; Ana Rita Silvestre; Teresinha Evangelista; Joao Coutinho; Fatima Carepa; Adilia Costa; Cecilia M P Rodrigues ; Helena Cortez Pinto;
PUBLISHED: 2012, SOURCE: PLOS ONE, VOLUME: 7, ISSUE: 2
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TITLE: ENDOMUS: "Clinical and diagnostic characterization of patients with neuromuscular disorders" - Epidemiologic study Full Text
AUTHORS: Evangelista, T; Lacerda, L; Santos, R;
PUBLISHED: 2011, SOURCE: 16th International Congress of the World-Muscle-Society in NEUROMUSCULAR DISORDERS, VOLUME: 21, ISSUE: 9-10
AUTHORS: Evangelista, T; Lacerda, L; Santos, R;
PUBLISHED: 2011, SOURCE: 16th International Congress of the World-Muscle-Society in NEUROMUSCULAR DISORDERS, VOLUME: 21, ISSUE: 9-10
INDEXED IN: WOS CrossRef
WOS CrossRef19
TITLE: Autosomal dominant chronic progressive ophthalmoplegia (adPEO) and lung adenocarcinoma showing compound heterozygous POLGI mutations Full Text
AUTHORS: Pires, C; Silvestre, AR; Vilarinho, L; Evangelista, T;
PUBLISHED: 2011, SOURCE: 16th International Congress of the World-Muscle-Society in NEUROMUSCULAR DISORDERS, VOLUME: 21, ISSUE: 9-10
AUTHORS: Pires, C; Silvestre, AR; Vilarinho, L; Evangelista, T;
PUBLISHED: 2011, SOURCE: 16th International Congress of the World-Muscle-Society in NEUROMUSCULAR DISORDERS, VOLUME: 21, ISSUE: 9-10
INDEXED IN: WOS CrossRef
WOS CrossRef20
TITLE: Adult onset intermittent rhabdomyolysis Full Text
AUTHORS: Antunes, AP; Nogueira, C; Rocha, H; Vilarinho, L; Evangelista, T;
PUBLISHED: 2011, SOURCE: 16th International Congress of the World-Muscle-Society in NEUROMUSCULAR DISORDERS, VOLUME: 21, ISSUE: 9-10
AUTHORS: Antunes, AP; Nogueira, C; Rocha, H; Vilarinho, L; Evangelista, T;
PUBLISHED: 2011, SOURCE: 16th International Congress of the World-Muscle-Society in NEUROMUSCULAR DISORDERS, VOLUME: 21, ISSUE: 9-10
INDEXED IN: WOS CrossRef
WOS CrossRef