Percorrer por autor Januário, C

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DataTítuloAutor(es)TipoAcesso
2008Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2.Brás, JM; Guerreiro, RJ; Morgadinho, A; Januário, C; Dias, M; Calado, A; Semedo, C; Oliveira, CR; Hardy, J; Singleton, Aarticle-
2006Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort.Guerreiro, RJ; Brás, JM; Santana, I; Januário, C; Morgadinho, A; Ribeiro, MH; Hardy, J; Singleton, A; Oliveira, CRarticle-
2011Bioenergetic dysfunction in Huntington's disease human cybridsFerreira, IL; Cunha-Oliveira, T; Nascimento, MV; Ribeiro, M; Proença, MT; Januário, C; Oliveira, CR; Rego, ACarticleopenAccess
2009Complete screening for glucocerebrosidase mutations in Parkinson disease patients from PortugalBrás, JM; Paisan-Ruiz, C; Guerreiro, C; Ribeiro, MH; Morgadinho, A; Januário, C; Sidransky, E; Oliveira, CR; Singleton, AarticleopenAccess
1999Encefalite do tronco e mielite por listeria num jovem adulto previamente saudávelBento, C; Januário, C; Silva, S; Oliveira, CRarticle-
2005G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort.Brás, JM; Guerreiro, RJ; Ribeiro, MH; Januário, C; Morgadinho, A; Oliveira, CR; Hardy, J; Singleton, Aarticle-
2005Independent patterns of damage within magno-, parvo- and koniocellular pathways in Parkinson's diseaseSilva, MF; Regateiro, FS; Forjaz, V; Januário, C; Freire-Gonçalves, A; Castelo-Branco, MarticleopenAccess
2008Mitochondrial function in Parkinson's disease cybrids containing an nt2 neuron-like nuclear backgroundEsteves, AR; Domingues, AF; Ferreira, IL; Januário, C; Swerdlow, RH; Oliveira, CR; Cardoso, SMarticleopenAccess
2010Mitochondrial-dependent apoptosis in Huntington's disease human cybridsFerreira, IL; Nascimento, MV; Ribeiro, MH; Almeida, S; Cardoso, SM; Grazina, M; Pratas, J; Santos, MJ; Januário, C; Oliveira, CR; Rego, ACarticleopenAccess
2003Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practiceCosta, MC; Magalhães, P; Ferreirinha, F; Guimarães, L; Januário, C; Gaspar, I; Loureiro, L; Vale, J; Garrett, C; Regateiro, FJ; Magalhães, M; Sousa, A; Maciel, P; Sequeiros, Jarticle-
2003Parkinson’s Disease and Mitochondrial DNA NADH Dehydrogenase Subunit 1 Nucleotides 3337–3340: Study in a Population from the Central Region of Portugal (Coimbra)Grazina, M; Silva, F; Januário, C; Oliveira, M; Cunha, L; Oliveira, CRarticleopenAccess
1985Proposta de classificação dos quadros parkinsónicosCunha, L; Freire-Gonçalves, A; Dinis, MA; Oliveira, CR; Ferro, MA; Amaral, R; Januário, CarticleopenAccess
2011Qualidade de vida na doença de Huntington: que sintomas a influenciamJanuário, F; Júlio, F; Januário, CarticleopenAccess
2001Results of a multicenter SPECT study with [123I]-Iodolisuride in extrapyramidal syndromes.Ribeiro, MJ; Januário, C; Prunier, C; Chossat, F; Santos, AC; Mauclaire, L; Bekhechi, D; Marchand, J; Catela, L; Cunha, L; Pedroso de Lima, JJ; Baulieu, JLarticle-
2012Scanning Patterns of Faces do not Explain Impaired Emotion Recognition in Huntington Disease: Evidence for a High Level Mechanismvan Asselen, M; Júlio, F; Januário, C; Campos, EB; Almeida, I; Cavaco, S; Castelo-Branco, MarticleopenAccess
Set-2014Tourette's syndrome and associated disorders: a systematic reviewFerreira, BR; Pio-Abreu, JL; Januário, CarticleopenAccess
2002Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locusSilveira, I; Miranda, C; Guimarães, L; Moreira, MC; Alonso, I; Mendonça, P; Ferro, A; Pinto-Basto, J; Coelho, J; Ferreirinha, F; Poirier, J; Vale, J; Januário, C; Barbot, C; Tuna, A; Barros, Jarticle-