21
TITLE: Freeze the Stroke Public Awareness Program for Immediate Detection of First Symptoms
AUTHORS: Vitor Tedim Cruz ; Isabel Araujo; Ivania Alves; Aldiro Magano; Paula Coutinho;
PUBLISHED: 2012, SOURCE: STROKE, VOLUME: 43, ISSUE: 9
INDEXED IN: Scopus WOS CrossRef: 12
22
TITLE: Two novel mutations in the tmprss6 gene associated with iron-refractory iron-deficiency anaemia (irida) and partial expression in the heterozygous form  Full Text
AUTHORS: Rosa M Pellegrino; Maria Coutinho; Domenico D'Ascola; Ana M Lopes; Antonietta Palmieri; Francesca Carnuccio; Monica Costa; Gabriella Zecchina; Giuseppe Saglio; Emilia Costa; Jose Barbot; Graca Porto ; Jorge P Pinto ; Antonella Roetto;
PUBLISHED: 2012, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 158, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef
23
TITLE: Presenting the vibratory stimulus as a neurorehabilitation tool - a tolerability test  Full Text
AUTHORS: Tedim Cruz, VT ; Ferro Bento, VF; Cunha, JP ; Coutinho, P;
PUBLISHED: 2011, SOURCE: 21st Meeting of the European-Neurological-Society in JOURNAL OF NEUROLOGY, VOLUME: 258
INDEXED IN: WOS
24
TITLE: G2019S mutation is a very important cause of Parkinson's disease in Portugal  Full Text
AUTHORS: Morgadinho, A; Almeida, MR; Coutinho, P;
PUBLISHED: 2010, SOURCE: 14th Congress of European-Federation-of-Neurological-Societies in EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 17
INDEXED IN: WOS
25
TITLE: CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5  Full Text
AUTHORS: Boukhris, A; Goizet, C; Durr, A; Tsaousidou, M; Guyant Marechal, L; Guimaraes, J; Chazouilleres, O; Chinnery, P; Coutinho, P; Crosby, A; Mhiri, C; Brice, A; Stevanin, G;
PUBLISHED: 2009, SOURCE: 13th Congress of the European-Federation-of-Neurological-Societies in EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 16
INDEXED IN: WOS
26
TITLE: Pathological crying in patients with Machado-Joseph disease  Full Text
AUTHORS: João Guimarães; Paulo Bugalho; Paula Coutinho;
PUBLISHED: 2008, SOURCE: Movement Disorders - Mov Disord., VOLUME: 23, ISSUE: 3
INDEXED IN: CrossRef
IN MY: ORCID
27
TITLE: Population Genetics of Wild-Type CAG Repeats in the <i>Machado-Joseph Disease</i> Gene in Portugal
AUTHORS: Lima, M; M.C Costa; Montiel, R; Ferro, A; Santos, C; Silva, C; Bettencourt, C; Sousa, A; Sequeiros, J; Coutinho, P; Maciel, P;
PUBLISHED: 2005, SOURCE: Human Heredity - Hum Hered, VOLUME: 60, ISSUE: 3
INDEXED IN: CrossRef
IN MY: ORCID
28
TITLE: Atlastin1 Mutations Are Frequent in Young-Onset Autosomal Dominant Spastic Paraplegia
AUTHORS: Alexandra Dürr; Agnès Camuzat; Emilie Colin; Chantal Tallaksen; Didier Hannequin; Paula Coutinho; Bertrand Fontaine; Annick Rossi; Roger Gil; Christophe Rousselle; Merle Ruberg; Giovanni Stevanin; Alexis Brice;
PUBLISHED: 2004, SOURCE: Arch Neurol - Archives of Neurology, VOLUME: 61, ISSUE: 12
INDEXED IN: CrossRef
IN MY: ORCID
29
TITLE: Ocular apraxia in recessive ataxia - Reply
AUTHORS: Coutinho, P; Barbot, C;
PUBLISHED: 2002, SOURCE: ARCHIVES OF NEUROLOGY, VOLUME: 59, ISSUE: 5
INDEXED IN: WOS
30
TITLE: NATURAL SELECTION AT THE MJD LOCUS: PHENOTYPIC DIVERSITY, SURVIVAL AND FERTILITY AMONG MACHADO-JOSEPH DISEASE PATIENTS FROM THE AZORES
AUTHORS: LIMA, M; SMITH, M; SILVA, C; ABADE, A; MAYER, F; COUTINHO, P;
PUBLISHED: 2001, SOURCE: J. Biosoc. Sci - Journal of Biosocial Science, VOLUME: 33, ISSUE: 3
INDEXED IN: CrossRef
IN MY: ORCID
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