Browsing by Author Martins, S

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Issue DateTitleAuthor(s)Type
2019A pipeline to assess disease-associated haplotypes in repeat expansion disorders: The example of MJD/SCA3 locusCosta, IPD; Almeida, B; Sequeiros, J; Amorim, A; Martins, SArtigo em Revista Científica Internacional
2015A triple-biomarker approach for the detection of delayed graft function after kidney transplantation using serum creatinine, cystatin C, and malondialdehydeFonseca, I; Reguengo, H; Oliveira, JC; Martins, S; Malheiro, J; Almeida, M; Santos, J; Dias, L; Pedroso, S; Lobato, L; Henriques, AC; Mendonça, DArtigo em Revista Científica Internacional
2021Apoe variants in an iberian alzheimer cohort detected through an optimized sanger sequencing protocolGonzález, RD; Gomes, I; Gomes, C; Rocha, R; Durães, L; Sousa, P; Figueruelo, M; Rodríguez, M; Pita, C; Hornero, R; Gómez, C; Lopes, AM; Pinto, N; Martins, SArtigo em Revista Científica Internacional
2022Association of thyroid function, within the euthyroid range, with cardiovascular risk: The EPIPorto studyNeves, JS; Fontes-Carvalho, R; Borges-Canha, M; Leite, AR; von Hafe, M; Vale, C; Martins, S; Guimarães, JT; Carvalho, D; Leite-Moreira, A; Azevedo, AArtigo em Revista Científica Internacional
2019Comparison of a rapid test and an automated method for faecal calprotectin measurementMartins, S; Garcia, D; Farinha, R; Guimarães, JTArtigo em Revista Científica Internacional
2015Complement C3c and C4c as predictors of death in heart failureSilva, N; Martins, S; Lourenço, P; Bettencourt, P; Guimarães, JTArtigo em Revista Científica Internacional
2017Contraction of fully expanded FMR1 alleles to the normal range: predisposing haplotype or rare events?Maia, N; Loureiro, JR; Oliveira, B; Marques, I; Santos, R; Jorge, P; Martins, SArtigo em Revista Científica Internacional
2020Diagnosis, treatment, and work impact of iron deficiency anemia in a Portuguese urban communityNorton, P; Araújo, N; Pinho, P; Costa Gomes, J; Silva, C; Gama, C; Barbosa, M; Ferreira, P; Cunha, S; Moreira, S; Martins, S; Faria, S; Sousa, S; Figueiras, Alves, N; Lunet, NArtigo em Revista Científica Nacional
2020Effects of a 16-week recreational team handball intervention on aerobic performance and cardiometabolic fitness markers in postmenopausal women: A randomized controlled trialPereira, R; Krustrup, P; Castagna, C; Coelho, E; Santos, R; Martins, S; Guimarães, JT; Magalhães, J; Póvoas, SArtigo em Revista Científica Internacional
2023Effects of NADPH Oxidase Isoform-2 (NOX2) Inhibition on Behavioral Responses and Neuroinflammation in a Mouse Model of Neuropathic PainTeixeira-Santos, L; Veríssimo, E; Martins, S; Sousa, T; Albino-Teixeira, A; Pinho, DArtigo em Revista Científica Internacional
2023Evaluation of urinary cysteinyl leukotrienes as biomarkers of severity and putative therapeutic targets in COVID-19 patientsReina-Couto, M; Roboredo-Madeira, M; Pereira-Terra, P; Silva-Pereira, C; Martins, S; Teixeira-Santos, L; Pinho, D; Dias, A; Cordeiro, G; Dias, CC; Sarmento, A; Tavares, M; Guimarães, JT; Roncon-Albuquerque, R; Paiva, JA; Albino-Teixeira, A; Sousa, TArtigo em Revista Científica Internacional
2015Family structure and use of prenatal careAlves, E; Silva, S; Martins, S; Barros, HArtigo em Revista Científica Internacional
2022Frailty in Portuguese Older Patients From Convalescence Units: A Cross-Sectional StudyPinto, M; Martins, S; Mesquita, E; Fernandes, LArtigo em Revista Científica Internacional
2021Frailty phenotype and associated nutritional factors in a sample of Portuguese outpatients with heart failureValdiviesso, Rui; Azevedo L; Moreira, E; Ataíde, R; Martins, S; Lia Fernandes; Silva Cardoso, J; Borges, NunoArtigo em Revista Científica Internacional
2023Frailty phenotype in heart failure: A condition that transcends ageValdiviesso, Rui; Moreira, E; Martins, S; Azevedo L; Ataide, R; Lia Fernandes; Silva Cardoso, J; Borges, NunoArtigo em Revista Científica Internacional
2020Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph diseaseAkçimen, F; Martins, S; Liao, C; Bourassa, CV; Catoire, H; Nicholson, GA; Riess, O; Raposo, M; França, MC; Vasconcelos, J; Lima, M; Lopes-Cendes, I; Saraiva-Pereira, ML; Jardim, LB; Sequeiros, J; Dion, PA; Rouleau, GAArtigo em Revista Científica Internacional
2020Genome-wide scan for five brain oscillatory phenotypes identifies a new qtl associated with theta eeg bandRebelo, MÂ; Gómez, C; Gomes, I; Poza, J; Martins, S; Maturana-Candelas, A; Ruiz-Gómez, SJ; Durães, L; Sousa, P; Figueruelo, M; Rodríguez, M; Pita, C; Arenas, M; Alvarez, L; Hornero, R; Pinto, N; Lopes, AMArtigo em Revista Científica Internacional
2019High frequency of CHD7 mutations in congenital hypogonadotropic hypogonadismGonçalves, CI; Patriarca, FM; Aragüés, JM; Carvalho, D; Fonseca, F; Martins, S; Marques, O; Pereira, BD; Martinez-de-Oliveira, J; Lemos, MCArtigo em Revista Científica Internacional
2019Is the high frequency of machado-joseph disease in China due to new mutational orignis?Li, T; Martins, S; Peng, Y; Wang, P; Hou, X; Chen, Z; Wang, C; Tang, Z; Qiu, R; Chen, C; Hu, Z; Xia, K; Tang, B; Sequeiros, J; Jiang, HArtigo em Revista Científica Internacional
2015Machado-Joseph disease in a Nigerian family: mutational origin and review of the literatureOgun, SA; Martins, S; Adebayo, PB; Dawodu, CO; Sequeiros, J; Finkel, MFArtigo em Revista Científica Internacional