81
TITLE: Freezing of gait – First motor manifestation in late infantile variant neuronal ceroid lipofuscinosis  Full Text
AUTHORS: Damásio, J; Taipa, R; Melo-Pires, M; Guimarães, A; K.P Bhatia; Santos, M; Carrilho, I;
PUBLISHED: 2014, SOURCE: Parkinsonism & Related Disorders, VOLUME: 20, ISSUE: 2
INDEXED IN: CrossRef
IN MY: ORCID
82
TITLE: Acute Ischemic Stroke Secondary to Glioblastoma. A Case Report
AUTHORS: Sofia Pina; Ângelo Carneiro; Tiago Rodrigues; Raquel Samões; Ricardo Taipa; Manuel Melo-Pires; Cláudia Pereira;
PUBLISHED: 2014, SOURCE: Neuroradiol J - The Neuroradiology Journal, VOLUME: 27, ISSUE: 1
INDEXED IN: CrossRef
IN MY: ORCID
83
TITLE: Multiple cerebral infarcts and intravascular central nervous system lymphoma: A rare but potentially treatable association  Full Text
AUTHORS: Catarina Cruto; Ricardo Taipa; Cecilia Monteiro; Isabel Moreira; Manuel Melo Pires ; Manuel Correia;
PUBLISHED: 2013, SOURCE: JOURNAL OF THE NEUROLOGICAL SCIENCES, VOLUME: 325, ISSUE: 1-2
INDEXED IN: Scopus WOS CrossRef: 4
IN MY: ORCID
84
TITLE: Novel TTC19 mutation in a family with severe psychiatric manifestations and complex III deficiency  Full Text
AUTHORS: Celia Nogueira; Barros, José ; Maria Jose Sa ; Luisa Azevedo ; Ricardo Taipa; Alessandra Torraco; Maria Chiara Meschini; Daniela Verrigni; Claudia Nesti; Teresa Rizza; Joao Teixeira; Rosalba Carrozzo; Manuel Melo Pires ; Laura Vilarinho; Filippo M Santorelli;
PUBLISHED: 2013, SOURCE: NEUROGENETICS, VOLUME: 14, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 40
IN MY: ORCID
85
TITLE: Expanding the MTM1 mutational spectrum: novel variants including the first multi-exonic duplication and development of a locus-specific database
AUTHORS: Oliveira, J; Oliveira, ME; Kress, W; Taipa, R; Pires, MM ; Hilbert, P; Baxter, P; Santos, M; Buermans, H; den Dunnen, JT; Santos, R;
PUBLISHED: 2013, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 21, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef Handle
IN MY: ORCID
86
TITLE: Genetic Analysis of Inherited Leukodystrophies Genotype-Phenotype Correlations in the CSF1R Gene
AUTHORS: Rita Guerreiro; Eleanna Kara; Isabelle Le Ber; Jose Bras; Jonathan D Rohrer; Ricardo Taipa; Tammaryn Lashley; Celine Dupuits; Nicole Gurunlian; Fanny Mochel; Jason D Warren; Didier Hannequin; Frederic Sedel; Christel Depienne; Agnes Camuzat; Veronique Golfier; Foucaud Du Boisgueheneuc; Lucia Schottlaender; Nick C Fox; Jonathan Beck; Simon Mead; Martin N Rossor; John Hardy; Tamas Revesz; Alexis Brice; Henry Houlden; ...More
PUBLISHED: 2013, SOURCE: JAMA NEUROLOGY, VOLUME: 70, ISSUE: 7
INDEXED IN: Scopus WOS
87
TITLE: Genetic Analysis of Inherited Leukodystrophies. Genotype-Phenotype Correlations in the CSF1R Gene
AUTHORS: Rita Guerreiro; Eleanna Kara; Isabelle Le Ber; Jose Bras; Jonathan D Rohrer; Ricardo Taipa; Tammaryn Lashley; Céline Dupuits; Nicole Gurunlian; Fanny Mochel; Jason D Warren; Didier Hannequin; Frédéric Sedel; Christel Depienne; Agnès Camuzat; Véronique Golfier; Foucaud Du Boisguéheneuc; Lucia Schottlaender; Nick C Fox; Jonathan Beck; Simon Mead; Martin N Rossor; John Hardy; Tamas Revesz; Alexis Brice; Henry Houlden; ...More
PUBLISHED: 2013, SOURCE: JAMA Neurology - JAMA Neurol, VOLUME: 70, ISSUE: 7
INDEXED IN: CrossRef
IN MY: ORCID
88
TITLE: Hereditary Neuropathy with Liability to Pressure Palsy: A Recurrent and Bilateral Foot Drop Case Report  Full Text
AUTHORS: Filipa Flor-de-Lima ; Liliana Macedo; Ricardo Taipa; Manuel Melo-Pires; Maria Lurdes Rodrigues;
PUBLISHED: 2013, SOURCE: Case Reports in Pediatrics, VOLUME: 2013
INDEXED IN: CrossRef
IN MY: ORCID
89
TITLE: TTC7B emerges as a novel risk factor for ischemic stroke through the convergence of several genome-wide approaches
AUTHORS: Tiago Krug; Joao Paulo Gabriel; Ricardo Taipa; Benedita V Fonseca; Sophie Domingues Montanari; Israel Fernandez Cadenas; Helena Manso ; Liliana O Gouveia; Joao Sobral; Isabel Albergaria; Gisela Gaspar; Jordi Jimenez Conde; Raquel Rabionet; Jose M Ferro ; Joan Montaner; Astrid M Vicente ; Mario Rui Silva; Ilda Matos; Gabriela Lopes; Sofia A Oliveira ;
PUBLISHED: 2012, SOURCE: JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, VOLUME: 32, ISSUE: 6
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
90
TITLE: Permanent dysphagia in familial amyloid polyneuropathy (ATTRVal30Met)  Full Text
AUTHORS: Cecilia Monteiro; Marina Magalhaes; Carlos Correia; Ricardo Taipa;
PUBLISHED: 2012, SOURCE: AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, VOLUME: 19, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 2
IN MY: ORCID
Page 9 of 12. Total results: 115.