11
TITLE: Early-onset phenotype of bi-allelic GRN mutations  Full Text
AUTHORS: Neuray, C; Sultan, T; Alvi, JR; Franca, MC; Assmann, B; Wagner, M; Canafoglia, L; Franceschetti, S; Rossi, G; Santana, I; Macario, MC; Almeida, MR; Kamate, M; Parikh, S; Elloumi, HZ; Murphy, D; Efthymiou, S; Maroofian, R; Houlden, H;
PUBLISHED: 2021, SOURCE: BRAIN, VOLUME: 144, ISSUE: 2
INDEXED IN: Scopus WOS
12
TITLE: MRI data-driven algorithm for the diagnosis of behavioural variant frontotemporal dementia
AUTHORS: Ana L Manera; Mahsa Dadar; John Cornelis Van Swieten; Barbara Borroni; Raquel Sanchez Valle; Fermin Moreno; Robert Laforce; Caroline Graff; Matthis Synofzik; Daniela Galimberti; James Benedict Rowe; Mario Masellis; Maria Carmela Tartaglia; Elizabeth Finger; Rik Vandenberghe; Alexandre de Mendonca; Fabrizio Tagliavini; Isabel Santana; Christopher R Butler; Alex Gerhard; Adrian Danek; Johannes Levin; Markus Otto; Giovanni Frisoni; Roberta Ghidoni; Sandro Sorbi; Jonathan Daniel Rohrer; Simon Ducharme; Louis Collins D.; Howard Rosen; Bradford C Dickerson; Kimoko Domoto Reilly; David Knopman; Bradley F Boeve; Adam L Boxer; John Kornak; Bruce L Miller; William W Seeley; Maria Luisa Gorno Tempini; Scott McGinnis; Maria Luisa Mandelli; Sónia Afonso; Maria Rosario Almeida; Sarah Anderl Straub; Christin Andersson; Anna Antonell; Silvana Archetti; Andrea Arighi; Mircea Balasa; Myriam Barandiaran; Nuria Bargalló; Robart Bartha; Benjamin Bender; Alberto Benussi; Luisa Benussi; Valentina Bessi; Giuliano Binetti; Sandra Black; Martina Bocchetta; Sergi Borrego Ecija; Jose Bras; Rose Bruffaerts; Paola Caroppo; David Cash; Miguel Castelo Branco; Rhian Convery; Thomas Cope; Maura Cosseddu; María de Arriba; Giuseppe Di Fede; Zigor Díaz; Diana Duro; Chiara Fenoglio; Camilla Ferrari; Carlos Ferreira; Catarina B Ferreira; Toby Flanagan; Nick Fox; Morris Freedman; Giorgio Fumagalli; Alazne Gabilondo; Roberto Gasparotti; Serge Gauthier; Stefano Gazzina; Giorgio Giaccone; Ana Gorostidi; Caroline Greaves; Rita Guerreiro; Carolin Heller; Tobias Hoegen; Begoña Indakoetxea; Vesna Jelic; Lize Jiskoot; Hans Otto Karnath; Ron Keren; Maria João Leitão; Albert Lladó; Gemma Lombardi; Sandra Loosli; Carolina Maruta; ...More
PUBLISHED: 2021, SOURCE: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, VOLUME: 92, ISSUE: 6
INDEXED IN: Scopus WOS
13
TITLE: Serum neurofilament light chain as a surrogate of cognitive decline in sporadic and familial frontotemporal dementia  Full Text
AUTHORS: Silva Spinola, A; Lima, M; Leitao, MJ; Duraes, J; Tabuas Pereira, M; Almeida, MR; Santana, I; Baldeiras, I;
PUBLISHED: 2021, SOURCE: EUROPEAN JOURNAL OF NEUROLOGY
INDEXED IN: WOS
14
TITLE: NOTCH3 mutations in a cohort of Portuguese patients within CADASIL spectrum phenotype  Full Text
AUTHORS: Almeida, MR; Elias, I; Fernandes, C; Machado, R; Galego, O; Santo, G;
PUBLISHED: 2021, SOURCE: NEUROGENETICS
INDEXED IN: Scopus WOS
15
TITLE: Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease  Full Text
AUTHORS: Irene Rosas; Carmen Martinez; Jordi Clarimon; Alberto Lleo; Ignacio Illan Gala; Oriol Dols Icardo; Barbara Borroni; Maria Rosario Almeida; Julie van der Zee; Christine Van Broeckhoven; Amalia C Bruni; Maria Anfossi; Livia Bernardi; Raffaele Maletta; Maria Serpente; Daniela Galimberti; Elio Scarpini; Giacomina Rossi; Paola Caroppo; Luisa Benussi; Roberta Ghidoni; Giuliano Binetti; Benedetta Nacmias; Sandro Sorbi; Irene Piaceri; Silvia Bagnoli; Anna Antonell; Raquel Sanchez Valle; Beatriz De la Casa Fages; Francisco Grandas; Monica Diez Fairen; Pau Pastor; Raffaele Ferrari; Victoria Alvarez; Manuel Menendez Gonzalez; ...More
PUBLISHED: 2020, SOURCE: NEUROBIOLOGY OF AGING, VOLUME: 87
INDEXED IN: Scopus WOS
16
TITLE: Memory impairment in FTD patients with pathogenic mutations  Full Text
AUTHORS: Lima, M; Baldeiras, I; Almeida, MR; Pereira, M; Duro, D; Gomes, I; Santana, I;
PUBLISHED: 2020, SOURCE: 6th Congress of the European-Academy-of-Neurology (EAN) in EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 27
INDEXED IN: WOS
17
TITLE: APOE epsilon 4-TOMM40L Haplotype Increases the Risk of Mild Cognitive Impairment Conversion to Alzheimer's Disease
AUTHORS: Cardoso, R; Lemos, C ; Oliveiros, B; Almeida, MR; Baldeiras, I; Pereira, CF; Santos, A; Duro, D; Vieira, D; Santana, I; Oliveira, CR;
PUBLISHED: 2020, SOURCE: JOURNAL OF ALZHEIMERS DISEASE, VOLUME: 78, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef
18
TITLE: SQSTM1 gene as a potential genetic modifier of CADASIL phenotype  Full Text
AUTHORS: Maria Rosario Almeida; Ana Rita Silva; Ines Elias; Carolina Fernandes; Rita Machado; Orlando Galego; Gustavo Cordeiro Santo;
PUBLISHED: 2020, SOURCE: JOURNAL OF NEUROLOGY
INDEXED IN: Scopus WOS
19
TITLE: Patients with progranulin mutations overlap with the progressive dysexecutive syndrome: towards the definition of a frontoparietal dementia phenotype
AUTHORS: Tabuas Pereira, M; Almeida, MR; Duro, D; Lima, M; Duraes, J; Guerreiro, R; Bras, J; Baldeiras, I; Santana, I;
PUBLISHED: 2020, SOURCE: BRAIN COMMUNICATIONS, VOLUME: 2, ISSUE: 2
INDEXED IN: WOS
20
TITLE: Increased CSF tau is associated with a higher risk of seizures in patients with Alzheimer's disease  Full Text
AUTHORS: Miguel Tabuas Pereira; Joao Duraes; Joana Lopes; Francisco Sales; Conceicao Bento; Diana Duro; Beatriz Santiago; Maria Rosario Almeida; Maria Joao Leitao; Ines Baldeiras; Isabel Santana;
PUBLISHED: 2019, SOURCE: EPILEPSY & BEHAVIOR, VOLUME: 98, ISSUE: Pt A
INDEXED IN: Scopus WOS
Página 2 de 4. Total de resultados: 34.