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TITLE: Neuroprotective Effects of Creatine in the CMVMJD135 Mouse Model of Spinocerebellar Ataxia Type 3  Full Text
AUTHORS: Duarte Silva, S; Neves Carvalho, A; Soares Cunha, C; Silva, JM; Teixeira Castro, A; Vieira, R; Silva Fernandes, A ; Maciel, P ;
PUBLISHED: 2018, SOURCE: MOVEMENT DISORDERS, VOLUME: 33, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 27 Handle
62
TITLE: Pharmacological Therapies for Machado-Joseph Disease
AUTHORS: Duarte Silva, S; Maciel, P ;
PUBLISHED: 2018, SOURCE: POLYGLUTAMINE DISORDERS, VOLUME: 1049
INDEXED IN: Scopus WOS CrossRef: 17
63
TITLE: Revalorisation of rapeseed pomace extracts: An in vitro study into its anti-oxidant and DNA protective properties
AUTHORS: Pohl, F; Goua, M; Bermano, G; Russell, WR; Scobbie, L; Maciel, P ; Lin, PKT;
PUBLISHED: 2018, SOURCE: FOOD CHEMISTRY, VOLUME: 239
INDEXED IN: Scopus WOS CrossRef: 25
64
TITLE: Tauroursodeoxycholic Acid Improves Motor Symptoms in a Mouse Model of Parkinson's Disease  Full Text
AUTHORS: Rosa, AI; Duarte Silva, S; Silva Fernandes, A ; Nunes, MJ; Carvalho, AN; Rodrigues, E; Gama, MJ ; Rodrigues, CMP ; Maciel, P ; Castro Caldas, M;
PUBLISHED: 2018, SOURCE: MOLECULAR NEUROBIOLOGY, VOLUME: 55, ISSUE: 12
INDEXED IN: Scopus WOS CrossRef: 61
65
TITLE: The contribution of 7q33 copy number variations for intellectual disability
AUTHORS: Lopes, F; Torres, F; Lynch, SA; Jorge, A; Sousa, S; Silva, J; Rendeiro, P; Tavares, P; Fortuna, AM; Maciel, P ;
PUBLISHED: 2018, SOURCE: NEUROGENETICS, VOLUME: 19, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 2
66
TITLE: A novel microduplication of ARID1B: Clinical, genetic, and proteomic findings
AUTHORS: Seabra, CM; Szoko, N; Erdin, S; Ragavendran, A; Stortchevoi, A; Maciel, P ; Lundberg, K; Schlatzer, D; Smith, J; Talkowski, ME; Gusella, JF; Natowicz, MR;
PUBLISHED: 2017, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 173, ISSUE: 9
INDEXED IN: Scopus WOS CrossRef: 6
67
TITLE: Altered striatal endocannabinoid signaling in a transgenic mouse model of spinocerebellar ataxia type-3
AUTHORS: Rodriguez Cueto, C; Hernandez Galvez, M; Hillard, CJ; Maciel, P ; Valdeolivas, S; Ramos, JA; Gomez Ruiz, M; Fernandez Ruiz, J;
PUBLISHED: 2017, SOURCE: PLOS ONE, VOLUME: 12, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 6
68
TITLE: Discovery of Therapeutic Approaches for Polyglutamine Diseases: A Summary of Recent Efforts  Full Text
AUTHORS: Esteves, S; Duarte Silva, S; Maciel, P ;
PUBLISHED: 2017, SOURCE: MEDICINAL RESEARCH REVIEWS, VOLUME: 37, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 17
69
TITLE: Whole gene deletion of EBF3 supporting haploinsufficiency of this gene as a mechanism of neurodevelopmental disease
AUTHORS: Lopes, F; Soares, G; Gonçalves Rocha, M; Pinto Basto, J; Maciel, P ;
PUBLISHED: 2017, SOURCE: Frontiers in Genetics, VOLUME: 8, ISSUE: OCT
INDEXED IN: Scopus CrossRef: 17
70
TITLE: Whole Gene Deletion of EBF3 Supporting Haploinsufficiency of This Gene as a Mechanism of Neurodevelopmental Disease
AUTHORS: Lopes, F; Soares, G; Gonsalves Rocha, M; Pinto Basto, J; Maciel, P ;
PUBLISHED: 2017, SOURCE: FRONTIERS IN GENETICS, VOLUME: 8
INDEXED IN: WOS
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