Vítor Pedro Tedim Ramos Cruz


AuthID: R-001-Y9G

Confirmed Publications: 129



101
TITLE: Autosomal recessive spastic ataxias - Clinical review of 19 Portuguese families  Full Text
AUTHORS: Oliveira, A; Cruz, V ; Loureiro, J; Ribeiro, P; Coutinho, P;
PUBLISHED: 2009, SOURCE: 19th Meeting of the European-Neurological-Society in JOURNAL OF NEUROLOGY, VOLUME: 256
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
102
TITLE: Novel SPG3A and SPG4 mutations in dominant spastic paraplegia families  Full Text
AUTHORS: Loureiro, JL ; Miller Fleming, L; Thieleke Matos, C; Magalhaes, P; Cruz, VT ; Coutinho, P ; Sequeiros, J ; Silveira, I ;
PUBLISHED: 2009, SOURCE: ACTA NEUROLOGICA SCANDINAVICA, VOLUME: 119, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 14
IN MY: ORCID | CIÊNCIAVITAE
103
TITLE: PORTYSTROKE: Screening Genetic Conditions in Portuguese Young Stroke Patients
AUTHORS: Miguel Viana Baptista; Susana Ferreira; Teresa Pinho e Melo; Marta Carvalho; Vitor Tedim Cruz ; Catia Carmona; Fernando Silva; Assuncao Tuna; Miguel Rodrigues; Carla Ferreira; Ana Amelia N Nogueira Pinto; Andre Leitao; Joao Paulo Gabriel; Sofia Calado; Oliveira, JP ; Ferro, JM;
PUBLISHED: 2009, SOURCE: 9th Annual European Round Table Meeting on Fabry Disease in CLINICAL THERAPEUTICS, VOLUME: 31
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
104
TITLE: PORTYSTROKE: Screening genetic conditions in portuguese young stroke patients  Full Text
AUTHORS: Miguel Viana-Baptista; Susana Ferreira; Teresa Pinho-e-Melo; Marta Carvalho; Vítor Tedim Cruz ; Cátia Carmona; Fernando Silva; Assunção Tuna; Miguel Rodrigues; Carla Ferreira; Ana Amélia Nogueira Pinto; André Leitão; Joao Paulo Gabriel; Sofia Calado; Oliveira, JP ; J.M Ferro;
PUBLISHED: 2009, SOURCE: Clinical Therapeutics, VOLUME: 31
INDEXED IN: CrossRef
IN MY: ORCID | CIÊNCIAVITAE
105
TITLE: Autosomal recessive spastic ataxias: clinical review of 19 Portuguese families  Full Text
AUTHORS: Oliveira, AC; Loureiro, JL; Cruz, VT ; Tuna, A; Ribeiro, P; Coutinho, P;
PUBLISHED: 2008, SOURCE: 12th Congress of the European-Federation-of-Neurological-Societies in EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 15
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
106
TITLE: Huntington's disease and Huntington-like phenotype: 10 years of local molecular diagnostic experience
AUTHORS: Santos, C; Cerqueira, J; Magalhaes, P; Costa, MC; Jardim, L; Costa, C; Cruz, V ; Coutinho, P; Maciel, P; Sequeiros, J ;
PUBLISHED: 2008, SOURCE: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, VOLUME: 79
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
107
TITLE: Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration  Full Text
AUTHORS: Giovanni Stevanin; Hamid Azzedine; Paola Denora; Amir Boukhris; Meriem Tazir; Alexander Lossos; Alberto Luis Rosa; Israela Lerer; Abdelmadjid Hamri; Paulo Alegria; Jose Loureiro ; Masayoshi Tada; Didier Hannequin; Mathieu Anheim; Cyril Goizet; Victoria Gonzalez Martinez; Isabelle Le Ber; Sylvie Forlani; Kiyoshi Iwabuchi; Vardiela Meiner; Goekhan Uyanik; Anne Kjersti Erichsen; Imed Feki; Florence Pasquier; Soreya Belarbi; Vitor T Cruz ; Christel Depienne; Jeremy Truchetto; Guillaume Garrigues; Chantal Tallaksen; Christine Tranchant; Masatoyo Nishizawa; Jose Vale; Paula Coutinho ; Filippo M Santorelli; Chokri Mhiri; Alexis Brice; Alexandra Durr; ...More
PUBLISHED: 2008, SOURCE: BRAIN, VOLUME: 131, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 180
IN MY: ORCID | CIÊNCIAVITAE
108
TITLE: PORTYSTROKE: SCREENING GENETIC CONDITIONS IN PORTUGUESE YOUNG STROKE PATIENTS
AUTHORS: Viana Baptista, M; Ferreira, S; Melo, TP; Carvalho, M; Cruz, VT ; Carmona, C; Tuna, A; Rodrigues, M; Ferreira, C; Pinto, AN; Silva, FA; Leitao, A; Gabriel, JP; Calado, S; Oliveira, JP ; Ferro, JM;
PUBLISHED: 2008, SOURCE: 5th Symposium on Lysosomal Storage Disorders in CLINICAL THERAPEUTICS, VOLUME: 30
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
109
TITLE: Seizures, subacute dementia and ear inflammation  Full Text
AUTHORS: Oliveira, A; Cruz, V ; Coutinho, P;
PUBLISHED: 2008, SOURCE: 18th Meeting of the European-Neurological-Society in JOURNAL OF NEUROLOGY, VOLUME: 255
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
110
TITLE: A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21
AUTHORS: Stevanin, G; Paternotte, C; Coutinho, P ; Klebe, S; Elleuch, N; Loureiro, JL ; Denis, E; Cruz, VT ; Durr, A; Prud'homme, JF; Weissenbach, J; Brice, A; Hazan, J;
PUBLISHED: 2007, SOURCE: NEUROLOGY, VOLUME: 68, ISSUE: 21
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID | CIÊNCIAVITAE
Page 11 of 13. Total results: 129.

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