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TITLE: Association between gait and cognitive functioning in Parkinson's disease  Full Text
AUTHORS: Mendes, A; Goncalves, A; Vila Cha, N; Moreira, I; Cavaco, S ; Bastos Lima, AB;
PUBLISHED: 2013, SOURCE: JOURNAL OF NEUROLOGY, VOLUME: 260
INDEXED IN: WOS
63
TITLE: Genetic and clinical characterization of 45 acute leukemia patients with MLL gene rearrangements from a single institution
AUTHORS: Cerveira, N ; Lisboa, S; Correia, C; Bizarro, S; Santos, J; Torres, L; Vieira, J; Barros Silva, JD; Pereira, D; Moreira, C; Meyer, C; Oliva, T; Moreira, I; Martins, A; Viterbo, L; Costa, V; Marschalek, R; Pinto, A; Mariz, JM; Teixeira, MR ;
PUBLISHED: 2012, SOURCE: MOLECULAR ONCOLOGY, VOLUME: 6, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 16
64
TITLE: Extracting BI-RADS features from Portuguese clinical texts
AUTHORS: Nassif, H; Cunha, F; Moreira, IC; Cruz Correia, R ; Sousa, E; Page, D; Burnside, E ; Dutra, I ;
PUBLISHED: 2012, SOURCE: 2012 IEEE International Conference on Bioinformatics and Biomedicine, BIBM2012 in Proceedings - 2012 IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2012
INDEXED IN: Scopus DBLP CrossRef: 6
65
TITLE: A case of progressive spastic paraparesis, cerebellar ataxia, sensory-motor neuropathy and cognitive decline with thin corpus callosum  Full Text
AUTHORS: Geraldes, R; Lopes L da Silva; Pereira, C; Alonso, I; Pinto Basto, J; Pavao P Martins;
PUBLISHED: 2010, SOURCE: 14th Congress of European-Federation-of-Neurological-Societies in EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 17
INDEXED IN: WOS
66
TITLE: Susceptibility and modifier genes in Portuguese transthyretin V30M amyloid polyneuropathy: complexity in a single-gene disease
AUTHORS: Soares, ML ; Coelho, T; Sousa, A ; Batalov, S; Conceicao, I; Sales Luis, ML; Ritchie, MD; Williams, SM; Nievergelt, CM; Schork, NJ; Saraiva, MJ ; Buxbaum, JN;
PUBLISHED: 2005, SOURCE: HUMAN MOLECULAR GENETICS, VOLUME: 14, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 82
67
TITLE: A missense mutation in a calcium-channel gene causes SCA in a four generation family also with hemiplegic migraine.
AUTHORS: Alonso, I; Tuna, A; Coelho, J; Barros, José ; Sequeiros, J ; Silveira, I; Coutinho, P;
PUBLISHED: 2001, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 69, ISSUE: 4
INDEXED IN: WOS
68
TITLE: Trinucleotide and pentanuclectide repeats in 202 unrelated families with spinocerebellar ataxia.
AUTHORS: Silveira, I; Alonso, I; Miranda, C; Guimaraes, L ; Moreira, MC; Mendonca, P; Ferro, A; Pinto Basto, J; Coelho, J; Ferreirinha, F; Jardim, L; Coutinho, P; Sequeiros, J ;
PUBLISHED: 2001, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 69, ISSUE: 4
INDEXED IN: WOS
69
TITLE: CACNA1A gene polymorphisms in families with episodic ataxia and hemiplegic migraine.
AUTHORS: Alonso, I; Coelho, J; Mendonca, P; Jardim, L; Tuna, A; Barros, José ; Coutinho, P; Sequeiros, J ; Silveira, I;
PUBLISHED: 2000, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 67, ISSUE: 4
INDEXED IN: WOS
70
TITLE: Molecular analysis of the P/Q type Ca2+ channel alpha 1-subunit gene in patients with progressive cerebellar ataxia.
AUTHORS: Alonso, I; Moreira, MC; Mendonca, P; Jardim, L; Barros, José ; Coutinho, P; Sequeiros, J ; Silveira, I;
PUBLISHED: 1999, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 65, ISSUE: 4
INDEXED IN: WOS
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