131
TITLE: Familial ATTR amyloidosis: microalbuminuria as a predictor of symptomatic disease and clinical nephropathy
AUTHORS: Lobato, L ; Beirao, I ; Silva, M; Bravo, F; Silvestre, F; Guimaraes, S; Sousa, A ; Noel, LH; Sequeiros, J ;
PUBLISHED: 2003, SOURCE: NEPHROLOGY DIALYSIS TRANSPLANTATION, VOLUME: 18, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 40
IN MY: ORCID
132
TITLE: Genetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patients  Full Text
AUTHORS: Alizadeh, M; Babron, MC; Birebent, B; Matsuda, F; Quelvennec, E; Liblau, R; Cournu Rebeix, I; Momigliano Richiardi, P; Sequeiros, J ; Yaouanq, J; Genin, E; Vasilescu, A; Bougerie, H; Trojano, M; Silva, BM ; Maciel, P ; Clerget Darpoux, F; Clanet, M; Edan, G; Fontaine, B; Semana, G; ...More
PUBLISHED: 2003, SOURCE: ANNALS OF NEUROLOGY, VOLUME: 54, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
133
TITLE: Genetic study of Portuguese patients with Huntington disease-like phenotype
AUTHORS: Costa, MC; Pereira, MC; Magalhaes, P; Matama, MT; Ferreirinha, F; Cerqueira, J; Santos, MM ; Sequeiros, J ; Maciel, P;
PUBLISHED: 2003, SOURCE: Annual Meeting of the American-Society-of-Human-Genetics in AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 73, ISSUE: 5
INDEXED IN: WOS
134
TITLE: Inherited and acquired risk factors and their combined effects in pediatric stroke  Full Text
AUTHORS: Barreirinho, S; Ferro, A; Santos, M; Costa, E ; Pinto Basto, J; Sousa, A ; Sequeiros, J ; Maciel, P ; Barbot, C ; Barbot, J;
PUBLISHED: 2003, SOURCE: PEDIATRIC NEUROLOGY, VOLUME: 28, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 56
IN MY: ORCID
135
TITLE: Iron metabolism in mice with partial frataxin deficiency  Full Text
AUTHORS: Santos, MM ; Miranda, CJ; Levy, JE; Montross, LK; Cossee, M; Sequeiros, J ; Andrews, N; Koenig, M; Pandolfo, M;
PUBLISHED: 2003, SOURCE: CEREBELLUM, VOLUME: 2, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
136
TITLE: MJD haplotypes unequally distributed throughout mainland Portugal
AUTHORS: Martins, S; Gaspar, C; Silveira, I; Calafell, F; Rouleau, G; Coutinho, R; Sequeiros, J ;
PUBLISHED: 2003, SOURCE: Annual Meeting of the American-Society-of-Human-Genetics in AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 73, ISSUE: 5
INDEXED IN: WOS
137
TITLE: Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice
AUTHORS: Costa, MD ; Magalhaes, P; Ferreirinha, F ; Guimaraes, L ; Januario, C; Gaspar, I; Loureiro, L; Vale, J; Garrett, C ; Regateiro, F; Magalhaes, M; Sousa, A ; Maciel, P ; Sequeiros, J ;
PUBLISHED: 2003, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 11, ISSUE: 11
INDEXED IN: Scopus WOS CrossRef: 15 Handle
IN MY: ORCID
138
139
TITLE: Portuguese families with dentatorubropallidoluysian atrophy (DRPLA) share a common haplotype of Asian origin  Full Text
AUTHORS: Martins, S ; Matama, T ; Guimaraes, L ; Vale, J; Guimaraes, J; Ramos, L; Coutinho, P ; Sequeiros, J ; Silveira, I ;
PUBLISHED: 2003, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 11, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef: 26
IN MY: ORCID
140
TITLE: Searching for modulating effects of SCA2, SCA6 and DRPLA CAG tracts on the Machado-Joseph disease (SCA3) phenotype  Full Text
AUTHORS: Jardim, L; Silveira, I ; Pereira, ML; Moreira, MD; Mendonca, P; Sequeiros, J ; Giugliani, R;
PUBLISHED: 2003, SOURCE: ACTA NEUROLOGICA SCANDINAVICA, VOLUME: 107, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
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