José Fernando da Rocha Barros


AuthID: R-000-8A2

Confirmed Publications: 67



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TITLE: Genetic and molecular study of migraine.
AUTHORS: Castro, MJ; Alonso, I; Maciel, P; Sousa, A; Guimaraes, L ; Fraga, C; Barros, José ; Sequeiros, J ; Peieira Monteiro, J; Silveira, I;
PUBLISHED: 2002, SOURCE: 52nd Annual Meeting of the American-Society-of-Human-Genetics in AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 71, ISSUE: 4
INDEXED IN: WOS
44
TITLE: Trinucleotide repeats in 202 families with ataxia - A small expanded (CAG)(n) allele at the SCA17 locus. A Small Expanded (CAG) n Allele at the SCA17 Locus
AUTHORS: Silveira, I ; Miranda, C; Guimaraes, L ; Moreira, MC; Alonso, I ; Mendonca, P; Ferro, A; Pinto Basto, J; Coelho, J; Ferreirinha, F ; Poirier, J; Parreira, E; Vale, J; Januario, C; Barbot, C ; Tuna, A; Barros, José ; Koide, R; Tsuji, S; Holmes, SE; Margolis, RL; Jardim, L; Pandolfo, M; Coutinho, P ; Sequeiros, J ; ...More
PUBLISHED: 2002, SOURCE: ARCHIVES OF NEUROLOGY, VOLUME: 59, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 126
IN MY: ORCID
45
TITLE: A missense mutation in a calcium-channel gene causes SCA in a four generation family also with hemiplegic migraine.
AUTHORS: Alonso, I; Tuna, A; Coelho, J; Barros, José ; Sequeiros, J ; Silveira, I; Coutinho, P;
PUBLISHED: 2001, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 69, ISSUE: 4
INDEXED IN: WOS
46
TITLE: Homozygosity mapping of portuguese and Japanese forms of ataxia-oculomotor apraxia to 9p13, and evidence for genetic heterogeneity
AUTHORS: Moreira, MD; Barbot, C ; Tachi, N; Kozuka, N; Mendonca, P; Barros, José ; Coutinho, P ; Sequeiros, J ; Koenig, M;
PUBLISHED: 2001, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 68, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef
47
TITLE: Improvement in the molecular diagnosis of Machado-Joseph disease
AUTHORS: Maciel, P ; Costa, MDC; Ferro, A; Rousseau, M; Santos, CS; Gaspar, C; Barros, José ; Rouleau, GA; Coutinho, P ; Sequeiros, J ;
PUBLISHED: 2001, SOURCE: ARCHIVES OF NEUROLOGY, VOLUME: 58, ISSUE: 11
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
48
TITLE: Recessive Ataxia With Ocular Apraxia. Review of 22 Portuguese Patients
AUTHORS: Clara Barbot; Paula Coutinho; Rui Chorão; Carla Ferreira; Barros, José ; Isabel Fineza; Karin Dias; José P Monteiro; António Guimarães; Pedro Mendonça; Maria do Céu Moreira; Jorge Sequeiros;
PUBLISHED: 2001, SOURCE: Arch Neurol - Archives of Neurology, VOLUME: 58, ISSUE: 2
INDEXED IN: CrossRef
IN MY: ORCID
49
TITLE: Recessive ataxia with ocular apraxia - Review of 22 Portuguese patients
AUTHORS: Barbot, C ; Coutinho, P ; Chorao, R; Ferreira, C; Barros, José ; Fineza, I; Dias, K; Monteiro, JP; Guimaraes, A; Mendonca, P; Moreira, MD; Sequeiros, J ;
PUBLISHED: 2001, SOURCE: ARCHIVES OF NEUROLOGY, VOLUME: 58, ISSUE: 2
INDEXED IN: Scopus WOS
50
TITLE: The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin  Full Text
AUTHORS: Moreira, MC; Barbot, C ; Tachi, N; Kozuka, N; Uchida, E; Gibson, T; Mendonca, P; Costa, M; Barros, José ; Yanagisawa, T; Watanabe, M; Ikeda, Y; Aoki, M; Nagata, T; Coutinho, P ; Sequeiros, J ; Koenig, M;
PUBLISHED: 2001, SOURCE: NATURE GENETICS, VOLUME: 29, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 307
IN MY: ORCID
Página 5 de 7. Total de resultados: 67.

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