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José Vale

Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration
2007 · Giovanni Stevanin, Hamid Azzedine, et al. · Brain · 261
Trinucleotide Repeats in 202 Families With Ataxia: A Small Expanded (CAG)nAllele at theSCA17 Locus
2002 · I. Silveira, C. Miranda, et al. · Archives of Neurology · 169
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Risk of Developing Parkinson Disease in Bipolar Disorder: A Systematic Review and Meta-analysis
2019 · Patrícia R. Faustino, Gonçalo S. Duarte, et al. · JAMA Neurology · 90
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Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal
2009 · J. Vale, P. Bugalho, et al. · European Journal of Neurology · 71
Validation of the brief international cognitive assessment for multiple sclerosis (BICAMS) in the Portuguese population with multiple sclerosis
2018 · Cláudia Sousa, Mariana Rigueiro-Neves, et al. · BMC Neurology · 49
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Diagnostic Delay of Multiple Sclerosis in a Portuguese Population
2019 · Ana Aires, Ariana Barros, et al. · Acta Médica Portuguesa · 46
Portuguese families with dentatorubropallidoluysian atrophy (DRPLA) share a common haplotype of Asian origin
2003 · Sandra Martins, Teresa Matamá, et al. · European Journal of Human Genetics · 44
POLG1-related levodopa-responsive parkinsonism
2014 · Rita Miguel, Miguel Fernandes Gago, et al. · Clinical Neurology and Neurosurgery · 38
The electroclinical spectrum, etiologies, treatment and outcome of nonconvulsive status epilepticus in the elderly
2017 · Nuno Canas, Henrique Delgado, et al. · Epilepsy & Behavior · 34
Tetrabenazine in treatment of hyperkinetic movement disorders: an observational study
2016 · Rita Miguel, Marcelo D. Mendonça, et al. · Therapeutic Advances in Neurological Disorders · 29
Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype
2006 · Maria do Carmo Costa, Andreia Teixeira-Castro, et al. · Journal of Human Genetics · 29
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Brief Cognitive Assessment in the Early Stages of Parkinson Disease
2011 · Paulo Bugalho, José Vale · Cognitive and Behavioral Neurology · 28
Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice
2003 · Maria do Carmo Costa, Paula Magalhães, et al. · European Journal of Human Genetics · 26
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Esclerosis múltiple y decisión de la maternidad: estudio observacional en pacientes portuguesas
2014 · Ana Teresa Barbosa de Carvalho, Andreia Veiga, et al. · Revista de Neurología · 24
Symptomatic paroxysmal hemidystonia due to a demyelinating subthalamic lesion
2000 · P. Fontoura, J. Vale, et al. · European Journal of Neurology · 19
Therapeutic inertia in relapsing-remitting multiple sclerosis
2021 · Rita Rodrigues, Raquel Rocha, et al. · Multiple Sclerosis and Related Disorders · 14
Neuromyelitis optica in Portugal (NEMIPORT) – A multicentre study
2015 · Joana Domingos, Luís Isidoro, et al. · Clinical Neurology and Neurosurgery · 13
FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes
2011 · Ana I. Seixas, José Vale, et al. · Behavioral and Brain Functions · 10
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[Post-malaria neurologic syndrome].
2008 · Gonçalo Matias, Nuno Canas, et al. · PubMed · 10
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Natalizumab Treatment Modulates Peroxisome Proliferator-Activated Receptors Expression in Women with Multiple Sclerosis
2016 · Véronique Ferret-Sena, Alexandra Maia e Silva, et al. · PPAR Research · 9
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[Thyrotoxic periodic paralysis: a case report].
2005 · José Vale, Nuno Canas, et al. · PubMed · 9
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Cognitive impairment and markers of optical neurodegeneration in early multiple sclerosis
2022 · Renata Silva, Pedro Coelho, et al. · Neurological Sciences · 8
Acute reversible toxic encephalopathy during capecitabine and oxaliplatin treatment
2017 · João Godinho, Mafalda Casa-Nova, et al. · Journal of Oncology Pharmacy Practice · 8
Defining the prodromal phase of multiple sclerosis based on healthcare access in a Portuguese population - ProdMS study
2021 · André Jorge, Ana André, et al. · Multiple Sclerosis and Related Disorders · 7
Multiple Sclerosis Patient Management During the COVID-19 Pandemic: Practical Recommendations From the Portuguese Multiple Sclerosis Study Group (GEEM)
2021 · João J. Cerqueira, Ana F. Ladeira, et al. · Frontiers in Neurology · 7
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Works count: 43
Citation count: 1,084
H-index: 15
I10-index: 19
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