about
Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients.Primary antiphospholipid antibody syndrome presenting with encephalopathy, psychosis and seizures.Sporadic hemiplegic migraine with normal imaging as the initial manifestation of CADASIL.Acute ischemic stroke secondary to glioblastoma. A case reportGenetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R gene.Patterns of Microglial Cell Activation in Alzheimer Disease and Frontotemporal Lobar Degeneration.Clinico-pathological correlations of the most common neurodegenerative dementias.TTC7B emerges as a novel risk factor for ischemic stroke through the convergence of several genome-wide approaches.Post-mortem assessment in vascular dementia: advances and aspirations.Expanding the MTM1 mutational spectrum: novel variants including the first multi-exonic duplication and development of a locus-specific database.Hansen Neuropathy: Still a Possible Diagnosis in the Investigation of a Peripheral Neuropathy.RYR1-Related Myopathies: Clinical, Histopathologic and Genetic Heterogeneity Among 17 Patients from a Portuguese Tertiary Centre.Does the Interplay Between Aging and Neuroinflammation Modulate Alzheimer's Disease Clinical Phenotypes? A Clinico-Pathological Perspective.Inflammatory myopathy associated with myasthenia gravis with and without thymic pathology: Report of four cases and literature review.Acute hemorrhagic leukoencephalitis with severe brainstem and spinal cord involvement: MRI features with neuropathological confirmation.Nonprimary Cytomegalovirus Fetal Infection.New splicing mutation in the choline kinase beta (CHKB) gene causing a muscular dystrophy detected by whole-exome sequencing.Hereditary neuropathy with liability to pressure palsy: a recurrent and bilateral foot drop case report.Specific configuration of dendritic degeneration in pyramidal neurons of the medial prefrontal cortex induced by differing corticosteroid regimens.Exonization of an Intronic LINE-1 Element Causing Becker Muscular Dystrophy as a Novel Mutational Mechanism in Dystrophin Gene.Streptococcus suis meningitis: first case report from Portugal.Multiple cerebral infarcts and intravascular central nervous system lymphoma: a rare but potentially treatable association.Recurrent Focal myositis: a rare inflammatory myopathy.Task-specific contribution of the human striatum to perceptual-motor skill learning.CNS involvement in V30M transthyretin amyloidosis: clinical, neuropathological and biochemical findings.Morphological correlates of corticosteroid-induced changes in prefrontal cortex-dependent behaviors.Amyloid detection in the transverse carpal ligament of patients with hereditary ATTR V30M amyloidosis and carpal tunnel syndrome.The etiology of spontaneous intracerebralhemorrhage: Insights from a neuropathological series.Inflammatory pathology markers (activated microglia and reactive astrocytes) in early and late onset Alzheimer disease: a post mortem study.Supratentorial hemangioblastomas in von Hippel-Lindau wild-type patients - case series and literature review.Clinical, biochemical, molecular, and histological features of 65 Portuguese patients with mitochondrial disorders.Letter: Transient peripheral facial nerve paralysis after local anesthetic procedure.Frontotemporal lobar degeneration-TDP with 'multiple system atrophy phenocopy syndrome'.Kalirin: a novel genetic risk factor for ischemic stroke.Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS): postmortem findings.Clinical, neuropathological, and genetic characteristics of the novel IVS9+1delG GRN mutation in a patient with frontotemporal dementia.Freezing of gait--first motor manifestation in late infantile variant neuronal ceroid lipofuscinosis.Evidence of amyloid-β cerebral amyloid angiopathy transmission through neurosurgery.New massive parallel sequencing approach improves the genetic characterization of congenital myopathies.CADASIL: MRI may be normal in the fourth decade of life - a case report.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Ricardo Taipa
@ast
Ricardo Taipa
@en
Ricardo Taipa
@es
Ricardo Taipa
@pt
Ricardo Taipa
@sl
type
label
Ricardo Taipa
@ast
Ricardo Taipa
@en
Ricardo Taipa
@es
Ricardo Taipa
@pt
Ricardo Taipa
@sl
prefLabel
Ricardo Taipa
@ast
Ricardo Taipa
@en
Ricardo Taipa
@es
Ricardo Taipa
@pt
Ricardo Taipa
@sl
P1053
R-7472-2017
P106
P21
P2798
P31
P3829
P496
0000-0002-9260-0227