José Vale

Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration

Giovanni Stévanin, Hamid Azzedine, Paola S. Denora et al. · Brain · 2007 · 253 citations

Life Sciences, Genetics, Neurology +17

Trinucleotide Repeats in 202 Families With Ataxia

Isabel Silveira, Carlos J. Miranda, Laura Guimarães et al. · Archives of Neurology · 2002 · 166 citations

Life Sciences, Genetics, Molecular Genetics +17

Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal

José Vale, Paulo Bugalho, Isabel Silveira et al. · European Journal of Neurology · 2009 · 68 citations

Life Sciences, Genetics, Neurology +17

Portuguese families with dentatorubropallidoluysian atrophy (DRPLA) share a common haplotype of Asian origin

Sandra Martins, Teresa Matamá, Laura Guimarães et al. · European Journal of Human Genetics · 2003 · 45 citations

Life Sciences, Genetics, Human Genetics +7

Validation of the brief international cognitive assessment for multiple sclerosis (BICAMS) in the Portuguese population with multiple sclerosis

Cláudia Sousa, Mariana Rigueiro-Neves, Telma Miranda et al. · BMC Neurology · 2018 · 44 citations · Full text

Medicine, Neurology, Cognitive Neurology +16