Maria Isabel Jacinto Santana


AuthID: R-000-BR2

Publications Requiring Validation

31
TITLE: Progression of Behavioral Disturbances and Neuropsychiatric Symptoms in Patients With Genetic Frontotemporal Dementia
AUTHORS: 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; ...More
PUBLISHED: 2021, SOURCE: JAMA NETWORK OPEN, VOLUME: 4, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 48
IN MY: ORCID
32
TITLE: Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
AUTHORS: 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; ...More
PUBLISHED: 2021, SOURCE: NATURE GENETICS, VOLUME: 53, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 212
IN MY: ORCID
33
TITLE: HPLC method for the determination of antiepileptic drugs in human saliva and its application in therapeutic drug monitoring
AUTHORS: Carona, A; Bicker, J; Silva, R; Silva, A; Santana, I; Sales, F; Falcao, A; Fortuna, A ;
PUBLISHED: 2021, SOURCE: JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, VOLUME: 197
INDEXED IN: Scopus WOS CrossRef: 9
IN MY: ORCID
34
TITLE: PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice
AUTHORS: 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; ...More
PUBLISHED: 2021, SOURCE: SCIENTIFIC REPORTS, VOLUME: 11, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 2
IN MY: ORCID
35
TITLE: Identification of a novel mutation in MEF2C gene in an atypical patient with frontotemporal lobar degeneration
AUTHORS: Adrião, A; Santana, I; Ribeiro, C; Cancela, ML ; Conceição, N ; Grazina, M;
PUBLISHED: 2021, SOURCE: Neurological Sciences, VOLUME: 43, ISSUE: 1
INDEXED IN: Scopus CrossRef: 2
IN MY: ORCID
36
TITLE: Toulouse-Pieron Cancellation Test: Normative scores for the portuguese population
AUTHORS: Lima, M; Baeta, E; Duro, D; Tabuas Pereira, M; Valerio, D; Freitas, S; Simoes, MR; Santana, I;
PUBLISHED: 2021, SOURCE: APPLIED NEUROPSYCHOLOGY-ADULT, VOLUME: 30, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 7
IN MY: ORCID
37
TITLE: Impairment of episodic memory in genetic frontotemporal dementia: A GENFI study
AUTHORS: Poos, JM; Russell, LL; Peakman, G; Bocchetta, M; Greaves, CV; Jiskoot, LC; van der Ende, EL; Seelaar, H; Papma, JM; van den Berg, E; Pijnenburg, YAL; Borroni, B; Sanchez Valle, R; Moreno, F; Laforce, R; Graff, C; Synofzik, M; Galimberti, D; Rowe, JB; Masellis, M; Tartaglia, C; Finger, E; Vandenberghe, R; de Medonca, A; Tagliavini, F; Butler, CR; Santana, I; Le Ber, I; Gerhard, A; Ducharme, S; Levin, J; Danek, A; Otto, M; Sorbi, S; Pasquier, F; van Swieten, JC; Rohrer, JD; ...More
PUBLISHED: 2021, SOURCE: ALZHEIMER'S & DEMENTIA: DIAGNOSIS, ASSESSMENT & DISEASE MONITORING, VOLUME: 13, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 11 Handle
IN MY: ORCID
38
TITLE: Vitamin D deficiency in a Portuguese epilepsy cohort: who is at risk and how to treat
AUTHORS: Cunha, IA; Saraiva, AMR; Lopes, P; Jesus Ribeiro, J; Duarte, C; Leitao, F; Sales, F; Santana, I; Bento, C;
PUBLISHED: 2021, SOURCE: EPILEPTIC DISORDERS, VOLUME: 23, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 7
IN MY: ORCID
39
TITLE: Knowing how to do it or doing it? A double dissociation between tool-gesture production and tool-gesture knowledge
AUTHORS: Valério, D; Santana, I; Aguiar de Sousa, D; Schu, G; Leal, G; Pavão Martins, I; Almeida, J;
PUBLISHED: 2021, SOURCE: Cortex, VOLUME: 141
INDEXED IN: Scopus CrossRef: 5
IN MY: ORCID
40
TITLE: Serum neurofilament light chain as a surrogate of cognitive decline in sporadic and familial frontotemporal dementia
AUTHORS: Silva Spínola, A; Lima, M; Leitão, MJ; Durães, J; Tábuas Pereira, M; Almeida, MR; Santana, I; Baldeiras, I;
PUBLISHED: 2021, SOURCE: European Journal of Neurology, VOLUME: 29, ISSUE: 1
INDEXED IN: Scopus CrossRef: 15
IN MY: ORCID
Page 4 of 17. Total results: 170.

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