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Frontiers in Neurology|May 5, 2012
Clinico-pathological correlations of the most common neurodegenerative dementiasRicardo Taipa, João Pinho, Manuel Melo-PiresJournal of Alzheimer'S Disease : JAD|May 14, 2016
Does the Interplay Between Aging and Neuroinflammation Modulate Alzheimer's Disease Clinical Phenotypes? A Clinico-Pathological PerspectiveRicardo Taipa, Ana Luísa Sousa, Manuel Melo Pires, et al.Clinical Neuropathology|November 21, 2017
The etiology of spontaneous intracerebralhemorrhage: Insights from a neuropathological seriesLuis Ruano, Mariana Branco, Raquel Samões, et al.Acta Medica Portuguesa|October 1, 2015
Hansen Neuropathy: Still a Possible Diagnosis in the Investigation of a Peripheral NeuropathyAndreia Veiga, Alexandre Costa, Ricardo Taipa, et al.Journal of Magnetic Resonance Imaging : JMRI|March 31, 2011
Acute hemorrhagic leukoencephalitis with severe brainstem and spinal cord involvement: MRI features with neuropathological confirmationPedro S Pinto, Ricardo Taipa, Bruno Moreira, et al.Journal of the Neurological Sciences|December 19, 2012
Multiple cerebral infarcts and intravascular central nervous system lymphoma: a rare but potentially treatable associationCatarina Cruto, Ricardo Taipa, Cecília Monteiro, et al.Movement Disorders Clinical Practice|October 27, 2018
Vascular Pathology Causing Late Onset Generalized Chorea: A Clinico-Pathological Case ReportPaula Salgado, Ricardo Taipa, Joana Domingos, et al.Pediatric Neurology|June 22, 2014
Ryanodine myopathies without central cores--clinical, histopathologic, and genetic description of three casesJoão Rocha, Ricardo Taipa, Manuel Melo Pires, et al.Case Reports in Pediatrics|November 20, 2013
Hereditary neuropathy with liability to pressure palsy: a recurrent and bilateral foot drop case reportFilipa Flor-de-Lima, Liliana Macedo, Ricardo Taipa, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 31, 2021
Adult polyglucosan body disease-an atypical compound heterozygous with a novel GBE1 mutationAndreia Carvalho, Joana Nunes, Ricardo Taipa, et al.Pageof 4