Ricardo Taipa
Ricardo Taipa
Neuropathology Unit, Centro Hospitalar do Porto
Verified email at chporto.min-saude.pt - 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
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
Post-mortem assessment in vascular dementia: advances and aspirations
KE McAleese, I Alafuzoff, A Charidimou, J De Reuck, LT Grinberg, ...
BMC medicine 14 (1), 1-16, 2016
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
Clinico-pathological correlations of the most common neurodegenerative dementias
R Taipa, J Pinho, M Melo-Pires
Frontiers in neurology 3, 68, 2012
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
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 (5), 513-523, 2010
Evidence of amyloid-β cerebral amyloid angiopathy transmission through neurosurgery
Z Jaunmuktane, A Quaegebeur, R Taipa, M Viana-Baptista, R Barbosa, ...
Acta neuropathologica 135 (5), 671-679, 2018
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), 1-10, 2008
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
Inferior vermian hypoplasia–preconception, misconception
AJ Robinson
Ultrasound in Obstetrics & Gynecology 43 (2), 123-136, 2014
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
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 (2), 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
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
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
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
Expanding the MTM1 mutational spectrum: novel variants including the first multi-exonic duplication and development of a locus-specific database
J Oliveira, ME Oliveira, W Kress, R Taipa, MM Pires, P Hilbert, P Baxter, ...
European Journal of Human Genetics 21 (5), 540-549, 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
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