Ricardo Jorge Ferreira Taipa


AuthID: R-000-FCG

Publications Requiring Validation

11
TITLE: Pseudotumoral Isolated Neurosarcoidosis; Apresentação Pseudotumoral de Neurosarcoidose Isolada
AUTHORS: Ana João Ribeiro Marques; Carolina Azoia; Ricardo Jorge Ferreira Taipa; João Paulo Gabriel;
PUBLISHED: 2024, SOURCE: Sinapse, VOLUME: 24, ISSUE: 4
INDEXED IN: Scopus CrossRef
IN MY: ORCID
12
TITLE: Neurolinfomatose Bilateral do Ângulo Ponto-Cerebeloso
AUTHORS: Carolina Q Azoia; Ana João Marques; André Costa; Ricardo Taipa; Luís Rocha;
PUBLISHED: 2023, SOURCE: Sinapse, VOLUME: 23, ISSUE: 3
INDEXED IN: CrossRef
IN MY: ORCID
13
TITLE: Multisystemic RFC1 -Related Disorder. Expanding the Phenotype Beyond Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome
AUTHORS: Maria João Malaquias; Luis Braz; Cláudia Santos Silva; Joana Damásio; André Jorge; João M Lemos; Catarina F Campos; Daniela Garcez; Miguel Oliveira Santos; Ana G Velon; André Caetano; Margarida Calejo; Preza Fernandes; Ângela Rego; Sandra Castro; Ana P Sousa; Marcio Neves Cardoso; Marco Fernandes; Miguel M Pinto; Ricardo Taipa; Ana M Lopes; Jorge Oliveira; Marina Magalhães; ...More
PUBLISHED: 2023, SOURCE: Neurology Clinical Practice, VOLUME: 13, ISSUE: 5
INDEXED IN: CrossRef: 5
IN MY: ORCID
14
TITLE: Anti-NMDAr Encephalitis and COVID-19 in a Patient With Systemic pANCA-Vasculitis and Recurrent Varicella Zoster Infection
AUTHORS: Moura, J ; Duarte, S; Sardoeira, A; Neves Maia, J; Damasio, J ; Taipa, R; Carneiro, P; Neves, E; Campar, A; Santos, E;
PUBLISHED: 2022, SOURCE: NEUROHOSPITALIST, VOLUME: 12, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
15
TITLE: Structural brain splitting is a hallmark of Granulin-related frontotemporal dementia
AUTHORS: Gazzina, S; Grassi, M; Premi, E; Alberici, A; Benussi, A; Archetti, S; Gasparotti, R; Bocchetta, M; Cash, DM; Todd, EG; Peakman, G; Convery, RS; van Swieten, JC; Jiskoot, LC; Seelaar, H; Sanchez Valle, R; Moreno, F; Laforce, R; Jr; Graff, C; Synofzik, M; Galimberti, D; Rowe, JB; Masellis, M; Tartaglia, MC; Finger, E; Vandenberghe, R; de Mendonça, A; Tagliavini, F; Butler, CR; Santana, I; Gerhard, A; Ber, IL; Pasquier, F; Ducharme, S; Levin, J; Danek, A; Sorbi, S; Otto, M; Rohrer, JD; Borroni, B; Afonso, S; Almeida, MR; Andersson, C; Antonell, A; Arighi, A; Balasa, M; Barandiaran, M; Bargalló, N; Bartha, R; Bender, B; Bertoux, M; Bertrand, A; Bessi, V; Black, S; Borrego Ecija, S; Bouzigues, A; Bras, J; Brice, A; Bruffaerts, R; Camuzat, A; Cañada, M; Cantoni, V; Caroppo, P; Castelo Branco, M; Colliot, O; Cope, T; Deramecourt, V; Fede, GD; Díez, A; Duro, D; Fenoglio, C; Ferrari, C; Ferreira, CB; Fox, N; Freedman, M; Fumagalli, G; Funkiewiez, A; Gabilondo, A; Gauthier, S; Giaccone, G; Gorostidi, A; Greaves, C; Guerreiro, R; Heller, C; Hoegen, T; Indakoetxea, B; Jelic, V; Karnath, O; Keren, R; Kuchcinski, G; Langheinrich, T; Lebouvier, T; Leitão, MJ; Lladó, A; Lombardi, G; Lombardi, J; Loosli, S; Maruta, C; Mead, S; Meeter, L; Miltenberger, G; van Minkelen, R; Mitchell, S; Moore, K; Nacmias, B; Nelson, A; Nicholas, J; Öijerstedt, L; Olives, J; Ourselin, S; Panman, J; Papma, JM; Pijnenburg, Y; Polito, C; Prioni, S; Prix, C; Rademakers, R; Redaelli, V; Rinaldi, D; Rittman, T; Rogaeva, E; Rollin, A; Rosa Neto, P; Rossi, G; Rossor, M; Santiago, B; Saracino, D; Sayah, S; Scarpini, E; Schönecker, S; Shafei, R; Shoesmith, C; Swift, I; Tábuas Pereira, M; Tainta, M; Taipa, R; Tang Wai, D; Thomas, DL; Thompson, P; Thonberg, H; Timberlake, C; Tiraboschi, P; Van Damme, P; Vandenbulcke, M; Veldsman, M; Verdelho, A; Villanua, J; Warren, J; Wilke, C; Woollacott, I; Wlasich, E; Zetterberg, H; Zulaica, M; Genetic Frontotemporal dementia Initiative (GENFI); ...More
PUBLISHED: 2022, SOURCE: Neurobiology of Aging, VOLUME: 114
INDEXED IN: Scopus CrossRef: 1 Handle
IN MY: ORCID
16
TITLE: Disease-related cortical thinning in presymptomatic granulin mutation carriers
AUTHORS: Borrego Écija, S; Sala Llonch, R; van Swieten, J; Borroni, B; Moreno, F; Masellis, M; Tartaglia, C; Graff, C; Galimberti, D; Laforce, R; Rowe, JB; Finger, E; Vandenberghe, R; Tagliavini, F; de Mendonça, A; Santana, I; Synofzik, M; Ducharme, S; Levin, J; Danek, A; Gerhard, A; Otto, M; Butler, C; Frisoni, G; Sorbi, S; Heller, C; Bocchetta, M; Cash, DM; Convery, RS; Moore, KM; Rohrer, JD; Sanchez Valle, R; Rossor, MN; Fox, NC; Woollacott, IOC; Shafei, R; Greaves, C; Neason, M; Guerreiro, R; Bras, J; Thomas, DL; Nicholas, J; Mead, S; Meeter, L; Panman, J; Papma, J; van Minkelen, R; Pijnenburg, Y; Indakoetxea, B; Gabilondo, A; TaintaMD, M; de Arriba, M; Gorostidi, A; Zulaica, M; Villanua, J; Diaz, Z; Olives, J; Lladó, A; Balasa, M; Antonell, A; Bargallo, N; Premi, E; Cosseddu, M; Gazzina, S; Padovani, A; Gasparotti, R; Archetti, S; Black, S; Mitchell, S; Rogaeva, E; Freedman, M; Keren, R; Tang Wai, D; Öijerstedt, L; Andersson, C; Jelic, V; Thonberg, H; Arighi, A; Fenoglio, C; Scarpini MD, E; Fumagalli, G; Cope, T; Timberlake, C; Rittman, T; Shoesmith, C; Bartha, R; Rademakers, R; Wilke, C; Bender, B; Bruffaerts, R; Vandamme, P; Vandenbulcke, M; Maruta, C; Ferreira, CB; Miltenberger, G; Verdelho, A; Afonso, S; Taipa, R; Caroppo, P; Di Fede, G; Giaccone, G; Prioni, S; Redaelli, V; Rossi, G; Tiraboschi, P; Duro, D; Rosario Almeida, M; Castelo Branco, M; João Leitão, M; Tabuas Pereira, M; Santiago, B; Gauthier, S; Rosa Neto, P; Veldsman, M; Flanagan, T; Prix, C; Hoegen, T; Wlasich, E; Loosli, S; Schonecker, S; Semler, E; Anderl Straub, S; ...More
PUBLISHED: 2021, SOURCE: NeuroImage: Clinical, VOLUME: 29
INDEXED IN: Scopus CrossRef: 8 Handle
IN MY: ORCID
17
TITLE: Adult polyglucosan body disease-an atypical compound heterozygous with a novel GBE1 mutation
AUTHORS: Carvalho, A; Nunes, J; Taipa, R; Pires, MM; Basto, JP; Barros, P;
PUBLISHED: 2021, SOURCE: NEUROLOGICAL SCIENCES
INDEXED IN: Scopus WOS CrossRef: 2
IN MY: ORCID
18
TITLE: THE GENETIC ANALYSIS OF PORTUGUESE PATIENTS WITH CEREBELLAR ATAXIA, NEUROPATHY, VESTIBULAR AREFLEXIA SYNDROME (CANVAS): A FREQUENT AND GENETICALLY COMPLEX CLINICAL ENTITY  Full Text
AUTHORS: Lopes, A; Malaquias, MJ; Braz, L; Aires, A; Sousa, AL; Sousa, AP; Cruto, C; Alves, C; Costa, C; Coelho, CR; Brandao, E; Nadais, G; Guimaraes, J; Vila Cha, N; Abreu, P; Barbosa, R; Samoes, R; Taipa, R; Araujo, R; Pimentel, T; Cruz, VT ; Caetano, A; Calejo, M; Salgado, P; Marques, B; Damasio, J; Garcez, D; Morais, S; Freixo, JP; Magalhaes, M; Oliveira, J; ...More
PUBLISHED: 2021, SOURCE: 24th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 100, ISSUE: 4
INDEXED IN: WOS
IN MY: ORCID
19
TITLE: T2-FLAIR mismatch sign: a roadmap of pearls and pitfalls
AUTHORS: Pinto, C; Noronha, C; Taipa, R; Ramos, C;
PUBLISHED: 2021, SOURCE: BRITISH JOURNAL OF RADIOLOGY, VOLUME: 95, ISSUE: 1129
INDEXED IN: WOS CrossRef: 9
IN MY: ORCID
20
TITLE: Diagnosis of Aicardi-Goutieres Syndrome in Adults: A Case Series
AUTHORS: Videira, G; Malaquias, MJ; Laranjinha, I; Martins, R; Taipa, R; Magalhaes, M;
PUBLISHED: 2020, SOURCE: MOVEMENT DISORDERS CLINICAL PRACTICE, VOLUME: 7, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 14
IN MY: ORCID
Page 2 of 12. Total results: 115.

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