21
TÍTULO: Whole-exome sequencing reveals PSEN1 and ATP7B combined variants as a possible cause of early-onset Lewy body dementia: a case study of genotype-phenotype correlation
AUTORES: Tabuas Pereira, Miguel; Guerreiro, Rita; Kun Rodrigues, Celia; Almeida, Maria Rosario; Bras, Jose; Santana, Isabel;
PUBLICAÇÃO: 2022, FONTE: NEUROGENETICS, VOLUME: 23, NÚMERO: 4
INDEXADO EM: Scopus WOS CrossRef: 1
NO MEU: ORCID
23
TÍTULO: Estimates of Geriatric Delirium Frequency in Noncardiac Surgeries and Its Evaluation Across the Years: A Systematic Review and Meta-Analysis
AUTORES: Silva, AR; Regueira, P; Albuquerque, E; Baldeiras, I; Cardoso, AL; Santana, I; Cerejeira, J;
PUBLICAÇÃO: 2021, FONTE: JOURNAL OF THE AMERICAN MEDICAL DIRECTORS ASSOCIATION, VOLUME: 22, NÚMERO: 3
INDEXADO EM: Scopus WOS CrossRef: 22
NO MEU: ORCID
24
TÍTULO: Neuropsychological features of progranulin-associated frontotemporal dementia: a nested case-control study
AUTORES: Lima, M; Tabuas Pereira, M; Duro, D; Duraes, J; Vieira, D; Baldeiras, I; Almeida, MR; Santana, I;
PUBLICAÇÃO: 2021, FONTE: NEURAL REGENERATION RESEARCH, VOLUME: 16, NÚMERO: 5
INDEXADO EM: Scopus WOS CrossRef: 2
NO MEU: ORCID
25
TÍTULO: Protective effects of cognitive and brain reserve in multiple sclerosis: Differential roles on social cognition and 'classic cognition'
AUTORES: Machado, R; Lima, C; D'Almeida, OC; Afonso, A; Macario, C; Castelo Branco, M; Sousa, L; Santana, I; Batista, S;
PUBLICAÇÃO: 2021, FONTE: MULTIPLE SCLEROSIS AND RELATED DISORDERS, VOLUME: 48
INDEXADO EM: Scopus WOS CrossRef: 1
NO MEU: ORCID
26
TÍTULO: Development and application of an HPLC-DAD technique for human plasma concentration monitoring of perampanel and lamotrigine in drug-resistant epileptic patients
AUTORES: Sabença, R; Bicker, J; Silva, R; Carona, A; Silva, A; Santana, I; Sales, F; Falcão, A; Fortuna, A;
PUBLICAÇÃO: 2021, FONTE: Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences, VOLUME: 1162
INDEXADO EM: Scopus CrossRef: 10
NO MEU: ORCID
27
TÍTULO: Progression of Behavioral Disturbances and Neuropsychiatric Symptoms in Patients With Genetic Frontotemporal Dementia
AUTORES: Benussi, A; Premi, E; Gazzina, S; Brattini, C; Bonomi, E; Alberici, A; Jiskoot, L; van Swieten, JC; Sanchez Valle, R; Moreno, F; Laforce, R; Graff, C; Synofzik, M; Galimberti, D; Masellis, M; Tartaglia, C; Rowe, JB; Finger, E; Vandenberghe, R; de Mendonca, A; Tagliavini, F; Santana, I; Ducharme, S; Butler, CR; Gerhard, A; Levin, J; Danek, A; Otto, M; Frisoni, G; Ghidoni, R; Sorbi, S; Le Ber, I; Pasquier, F; Peakman, G; Todd, E; Bocchetta, M; Rohrer, JD; Borroni, B; ...Mais
PUBLICAÇÃO: 2021, FONTE: JAMA NETWORK OPEN, VOLUME: 4, NÚMERO: 1
INDEXADO EM: Scopus WOS CrossRef: 48
NO MEU: ORCID
28
TÍTULO: Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
AUTORES: Chia, R; Sabir, MS; Bandres Ciga, S; Saez Atienzar, S; Reynolds, RH; Gustavsson, E; Walton, RL; Ahmed, S; Viollet, C; Ding, JH; Makarious, MB; Diez Fairen, M; Portley, MK; Shah, Z; Abramzon, Y; Hernandez, DG; Blauwendraat, C; Stone, DJ; Eicher, J; Parkkinen, L; Ansorge, O; Clark, L; Honig, LS; Marder, K; Lemstra, A; St George Hyslop, P; Londos, E; Morgan, K; Lashley, T; Warner, TT; Jaunmuktane, Z; Galasko, D; Santana, I; Tienari, PJ; Myllykangas, L; Oinas, M; Cairns, NJ; Morris, JC; Halliday, GM; Van Deerlin, VM; Trojanowski, JQ; Grassano, M; Calvo, A; Mora, G; Canosa, A; Floris, G; Bohannan, RC; Brett, F; Gan Or, Z; Geiger, JT; Moore, A; May, P; Kruger, R; Goldstein, DS; Lopez, G; Tayebi, N; Sidransky, E; Norcliffe Kaufmann, L; Palma, JA; Kaufmann, H; Shakkottai, VG; Perkins, M; Newell, KL; Gasser, T; Schulte, C; Landi, F; Salvi, E; Cusi, D; Masliah, E; Kim, RC; Caraway, CA; Monuki, ES; Brunetti, M; Dawson, TM; Rosenthal, LS; Albert, MS; Pletnikova, O; Troncoso, JC; Flanagan, ME; Mao, QW; Bigio, EH; Rodriguez Rodriguez, E; Infante, J; Lage, C; Gonzalez Aramburu, I; Sanchez Juan, P; Ghetti, B; Keith, J; Black, SE; Masellis, M; Rogaeva, E; Duyckaerts, C; Brice, A; Lesage, S; Xiromerisiou, G; Barrett, MJ; Tilley, BS; Gentleman, S; Logroscino, G; Serrano, GE; Beach, TG; McKeith, IG; Thomas, AJ; Attems, J; Morris, CM; Palmer, L; Love, S; Troakes, C; Al Sarraj, S; Hodges, AK; Aarsland, D; Klein, G; Kaiser, SM; Woltjer, R; Pastor, P; Bekris, LM; Leverenz, JB; Besser, LM; Kuzma, A; Renton, AE; Goate, A; Bennett, DA; Scherzer, CR; Morris, HR; Ferrari, R; Albani, D; Pickering Brown, S; Faber, K; Kukull, WA; Morenas Rodriguez, E; Lleo, A; Fortea, J; Alcolea, D; Clarimon, J; Nalls, MA; Ferrucci, L; Resnick, SM; Tanaka, T; Foroud, TM; Graff Radford, NR; Wszolek, ZK; Ferman, T; Boeve, BF; Hardy, JA; Topol, EJ; Torkamani, A; Singleton, AB; Ryten, M; Dickson, DW; Chio, A; Ross, OA; Gibbs, JR; Dalgard, CL; Traynor, BJ; Scholz, SW; ...Mais
PUBLICAÇÃO: 2021, FONTE: NATURE GENETICS, VOLUME: 53, NÚMERO: 3
INDEXADO EM: Scopus WOS CrossRef: 212
NO MEU: ORCID
29
TÍTULO: HPLC method for the determination of antiepileptic drugs in human saliva and its application in therapeutic drug monitoring
AUTORES: Carona, A; Bicker, J; Silva, R; Silva, A; Santana, I; Sales, F; Falcao, A; Fortuna, A;
PUBLICAÇÃO: 2021, FONTE: JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, VOLUME: 197
INDEXADO EM: Scopus WOS CrossRef: 9
NO MEU: ORCID
30
TÍTULO: PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice
AUTORES: Messerschmidt, C; Foddis, M; Blumenau, S; Muller, S; Bentele, K; Holtgrewe, M; Kun Rodrigues, C; Alonso, I; Macario, MD; Morgadinho, AS; Velon, AG; Santo, G; Santana, I; Monkare, S; Kuuluvainen, L; Schleutker, J; Poyhonen, M; Myllykangas, L; Senatore, A; Berchtold, D; Winek, K; Meisel, A; Pavlovic, A; Kostic, V; Dobricic, V; Lohmann, E; Hanagasi, H; Guven, G; Bilgic, B; Bras, J; Guerreiro, R; Beule, D; Dirnagl, U; Sassi, C; ...Mais
PUBLICAÇÃO: 2021, FONTE: SCIENTIFIC REPORTS, VOLUME: 11, NÚMERO: 1
INDEXADO EM: Scopus WOS CrossRef: 2
NO MEU: ORCID
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