Ricardo Taipa
Ricardo Taipa
Neuropathology Department and Portuguese Brain Bank, CHUdSA, Porto
Verified email at - Homepage
Cited by
Cited by
Morphological correlates of corticosteroid-induced changes in prefrontal cortex-dependent behaviors
JJ Cerqueira, JM Pêgo, R Taipa, JM Bessa, OFX Almeida, N Sousa
Journal of Neuroscience 25 (34), 7792-7800, 2005
Specific configuration of dendritic degeneration in pyramidal neurons of the medial prefrontal cortex induced by differing corticosteroid regimens
JJ Cerqueira, R Taipa, HBM Uylings, OFX Almeida, N Sousa
Cerebral cortex 17 (9), 1998-2006, 2007
Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study
EL van der Ende, LH Meeter, JM Poos, JL Panman, LC Jiskoot, ...
The Lancet Neurology 18 (12), 1103-1111, 2019
Proinflammatory and anti-inflammatory cytokines in the CSF of patients with Alzheimer's disease and their correlation with cognitive decline
R Taipa, SP das Neves, AL Sousa, J Fernandes, C Pinto, AP Correia, ...
Neurobiology of aging 76, 125-132, 2019
Post-mortem assessment in vascular dementia: advances and aspirations
KE McAleese, I Alafuzoff, A Charidimou, J De Reuck, LT Grinberg, ...
BMC medicine 14, 1-16, 2016
CNS involvement in V30M transthyretin amyloidosis: clinical, neuropathological and biochemical findings
LF Maia, R Magalhães, J Freitas, R Taipa, MM Pires, H Osório, D Dias, ...
Journal of Neurology, Neurosurgery & Psychiatry 86 (2), 159-167, 2015
DJ-1 linked parkinsonism (PARK7) is associated with Lewy body pathology
R Taipa, C Pereira, I Reis, I Alonso, A Bastos-Lima, M Melo-Pires, ...
Brain 139 (6), 1680-1687, 2016
Evidence of amyloid-β cerebral amyloid angiopathy transmission through neurosurgery
Z Jaunmuktane, A Quaegebeur, R Taipa, M Viana-Baptista, R Barbosa, ...
Acta neuropathologica 135, 671-679, 2018
TTC7B Emerges as a Novel Risk Factor for Ischemic Stroke Through the Convergence of Several Genome-Wide Approaches
T Krug, JP Gabriel, R Taipa, BV Fonseca, S Domingues-Montanari, ...
Journal of Cerebral Blood Flow & Metabolism 32 (6), 1061-1072, 2012
Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R gene
R Guerreiro, E Kara, I Le Ber, J Bras, JD Rohrer, R Taipa, T Lashley, ...
JAMA neurology 70 (7), 875-882, 2013
LAMA2 gene mutation update: Toward a more comprehensive picture of the laminin‐α2 variome and its related phenotypes
J Oliveira, A Gruber, M Cardoso, R Taipa, I Fineza, A Gonçalves, A Laner, ...
Human mutation 39 (10), 1314-1337, 2018
Clinico-pathological correlations of the most common neurodegenerative dementias
R Taipa, J Pinho, M Melo-Pires
Frontiers in neurology 3, 23559, 2012
Inflammatory pathology markers (activated microglia and reactive astrocytes) in early and late onset Alzheimer disease: a post mortem study
R Taipa, V Ferreira, P Brochado, A Robinson, I Reis, F Marques, ...
Neuropathology and Applied Neurobiology 44 (3), 298-313, 2018
Kalirin: a novel genetic risk factor for ischemic stroke
T Krug, H Manso, L Gouveia, J Sobral, JM Xavier, I Albergaria, G Gaspar, ...
Human genetics 127, 513-523, 2010
Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients
A Rosa, BV Fonseca, T Krug, H Manso, L Gouveia, I Albergaria, G Gaspar, ...
BMC Medical Genetics 9, 1-10, 2008
Novel TTC19 mutation in a family with severe psychiatric manifestations and complex III deficiency
C Nogueira, J Barros, MJ Sá, L Azevedo, R Taipa, A Torraco, ...
Neurogenetics 14, 153-160, 2013
Appendectomy may delay P arkinson's disease Onset
A Mendes, A Gonçalves, N Vila‐Chã, I Moreira, J Fernandes, J Damásio, ...
Movement Disorders 30 (10), 1404-1407, 2015
Functional network resilience to pathology in presymptomatic genetic frontotemporal dementia
T Rittman, R Borchert, S Jones, J van Swieten, B Borroni, D Galimberti, ...
Neurobiology of Aging 77, 169-177, 2019
Progression of behavioral disturbances and neuropsychiatric symptoms in patients with genetic frontotemporal dementia
A Benussi, E Premi, S Gazzina, C Brattini, E Bonomi, A Alberici, L Jiskoot, ...
JAMA Network open 4 (1), e2030194-e2030194, 2021
New splicing mutation in the choline kinase beta (CHKB) gene causing a muscular dystrophy detected by whole-exome sequencing
J Oliveira, L Negrão, I Fineza, R Taipa, M Melo-Pires, AM Fortuna, ...
Journal of human genetics 60 (6), 305-312, 2015
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