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Appendectomy may delay Parkinson's disease Onset.
- Published in:
- Movement Disorders, 2015, v. 30, n. 10, p. 1404, doi. 10.1002/mds.26311
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- Publication type:
- Article
Adult-onset dystonia in Aicardi-Goutières syndrome.
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- Movement Disorders, 2010, v. 25, n. 6, p. 791, doi. 10.1002/mds.23013
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- Publication type:
- Article
Kalirin: a novel genetic risk factor for ischemic stroke.
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- Human Genetics, 2010, v. 127, n. 5, p. 513, doi. 10.1007/s00439-010-0790-y
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- Publication type:
- Article
New splicing mutation in the choline kinase beta (CHKB) gene causing a muscular dystrophy detected by whole-exome sequencing.
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- Journal of Human Genetics, 2015, v. 60, n. 6, p. 305, doi. 10.1038/jhg.2015.20
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- Publication type:
- Article
α-Synuclein triggers cofilin pathology and dendritic spine impairment via a PrP<sup>C</sup>-CCR5 dependent pathway.
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- Cell Death & Disease, 2024, v. 15, n. 4, p. 1, doi. 10.1038/s41419-024-06630-9
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- Publication type:
- Article
Neurological Involvement in a Portuguese Cohort of IgG4-Related Disease.
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- Acta Médica Portuguesa, 2024, v. 37, n. 6, p. 429, doi. 10.20344/amp.20767
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- Publication type:
- Article
Novel TTC19 mutation in a family with severe psychiatric manifestations and complex III deficiency.
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- Neurogenetics, 2013, v. 14, n. 2, p. 153, doi. 10.1007/s10048-013-0361-1
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- Publication type:
- Article
Acute hemorrhagic leukoencephalitis with severe brainstem and spinal cord involvement: MRI features with neuropathological confirmation.
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- Journal of Magnetic Resonance Imaging, 2011, v. 33, n. 4, p. 957, doi. 10.1002/jmri.22505
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- Publication type:
- Article
Structural and molecular correlates of cognitive aging in the rat.
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- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-39645-w
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- Publication type:
- Article
Specific Configuration of Dendritic Degeneration in Pyramidal Neurons of the Medial Prefrontal Cortex Induced by Differing Corticosteroid Regimens.
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- Cerebral Cortex, 2007, v. 17, n. 9, p. 1998, doi. 10.1093/cercor/bhl108
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- Publication type:
- Article
Clinico-pathological correlations of the most common neurodegenerative dementias.
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- Frontiers in Neurology, 2012, v. 3, p. 1, doi. 10.3389/fneur.2012.00068
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- Publication type:
- Article
Expanding the MTM1 mutational spectrum: novel variants including the first multi-exonic duplication and development of a locus-specific database.
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- European Journal of Human Genetics, 2013, v. 21, n. 5, p. 540, doi. 10.1038/ejhg.2012.201
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- Publication type:
- Article
Peripheral neuropathy in Parkinson's disease: prevalence and functional impact on gait and balance.
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- Brain: A Journal of Neurology, 2023, v. 146, n. 1, p. 225, doi. 10.1093/brain/awac026
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- Publication type:
- Article
PD-L1 tumor expression is associated with poor prognosis and systemic immunosuppression in glioblastoma.
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- Journal of Neuro-Oncology, 2022, v. 156, n. 3, p. 453, doi. 10.1007/s11060-021-03907-3
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- Publication type:
- Article
Neuropathology of central nervous system involvement in TTR amyloidosis.
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- Acta Neuropathologica, 2023, v. 145, n. 1, p. 113, doi. 10.1007/s00401-022-02501-9
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- Publication type:
- Article
Evidence of amyloid-β cerebral amyloid angiopathy transmission through neurosurgery.
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- Acta Neuropathologica, 2018, v. 135, n. 5, p. 671, doi. 10.1007/s00401-018-1822-2
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- Publication type:
- Article
Rapidly Progressive Corticobasal Degeneration Mimicking Brainstem Encephalitis.
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- Movement Disorders Clinical Practice, 2023, v. 10, n. 2, p. 300, doi. 10.1002/mdc3.13633
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- Publication type:
- Article
Diagnosis of Aicardi‐Goutières Syndrome in Adults: A Case Series.
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- Movement Disorders Clinical Practice, 2020, v. 7, n. 3, p. 303, doi. 10.1002/mdc3.12903
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- Publication type:
- Article
Late‐onset Levodopa Responsive Parkinsonism Due to Polymerase γ 1 Mutations.
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- Movement Disorders Clinical Practice, 2018, v. 5, n. 6, p. 645, doi. 10.1002/mdc3.12668
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- Publication type:
- Article
Vascular Pathology Causing Late Onset Generalized Chorea: A Clinico-Pathological Case Report.
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- Movement Disorders Clinical Practice, 2017, v. 4, n. 6, p. 819, doi. 10.1002/mdc3.12528
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- Publication type:
- Article
MCARDLE'S DISEASE: DIAGNOSTIC APPROACH AFTER CLINICAL SYMPTOMS OF VIGOROUS EXERCISE INTOLERANCE IN A SNOWBOARDER IN ALPES.
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- Acta Reumatológica Portuguesa, 2019, p. 139
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- Publication type:
- Article
Patterns of Microglial Cell Activation in Alzheimer Disease and Frontotemporal Lobar Degeneration.
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- Neurodegenerative Diseases, 2017, v. 17, n. 4/5, p. 145, doi. 10.1159/000457127
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- Publication type:
- Article
Brain biopsy in suspected non-neoplastic neurological disease.
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- Acta Neurochirurgica, 2019, v. 161, n. 6, p. 1139, doi. 10.1007/s00701-019-03910-8
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- Publication type:
- Article
Exonization of an Intronic LINE-1 Element Causing Becker Muscular Dystrophy as a Novel Mutational Mechanism in Dystrophin Gene.
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- Genes, 2017, v. 8, n. 10, p. 253, doi. 10.3390/genes8100253
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- Publication type:
- Article
Cadherin-3 is a novel oncogenic biomarker with prognostic value in glioblastoma.
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- Molecular Oncology, 2022, v. 16, n. 14, p. 2611, doi. 10.1002/1878-0261.13162
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- Publication type:
- Article
Leprosy presenting as remitting seronegative symmetrical synovitis with pitting oedema syndrome - a case report.
- Published in:
- 2019
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- Publication type:
- journal article
Adult polyglucosan body disease—an atypical compound heterozygous with a novel GBE1 mutation.
- Published in:
- Neurological Sciences, 2021, v. 42, n. 7, p. 2955, doi. 10.1007/s10072-021-05096-3
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- Publication type:
- Article
Clinical features of hypertrophic pachymeningitis in a center survey.
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- 2019
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- Publication type:
- journal article
PARK2 presenting as a disabling peripheral axonal neuropathy.
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- 2015
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- Publication type:
- Letter
Medulloblastoma and gliomatosis cerebri: rare brain tumors in multiple sclerosis patients.
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- Neurological Sciences, 2011, v. 32, n. 5, p. 893, doi. 10.1007/s10072-010-0468-1
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- Publication type:
- Article
Acute Ischemic Stroke Secondary to Glioblastoma: A Case Report.
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- Neuroradiology Journal, 2014, v. 27, n. 1, p. 85, doi. 10.15274/NRJ-2014-10009
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- Publication type:
- Article
Consenso Português para o Diagnóstico e Gestão Clínica da Demência com Corpos de Lewy (PORTUCALE).
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- Acta Médica Portuguesa, 2020, v. 33, n. 12, p. 844, doi. 10.20344/amp.13696
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- Publication type:
- Article
Neuropatia da Doença de Hansen: Um Diagnóstico a Considerar na Investigação da Neuropatia Periférica.
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- Acta Médica Portuguesa, 2015, v. 28, n. 3, p. 329, doi. 10.20344/amp.5876
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- Publication type:
- Article
Lesão Renal Aguda e Rabdomiólise como Apresentação da Doença de Mcardle.
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- 2013
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- Publication type:
- Case Study
Post-mortem assessment in vascular dementia: advances and aspirations.
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- 2016
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- Publication type:
- journal article
Hereditary Neuropathy with Liability to Pressure Palsy: A Recurrent and Bilateral Foot Drop Case Report.
- Published in:
- Case Reports in Pediatrics, 2013, p. 1, doi. 10.1155/2013/230541
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- Publication type:
- Article
Association Between Iron-Related Protein Lipocalin 2 and Cognitive Impairment in Cerebrospinal Fluid and Serum.
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- Frontiers in Aging Neuroscience, 2021, v. 13, p. 1, doi. 10.3389/fnagi.2021.663837
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- Publication type:
- Article
Morphological Correlates of Corticosteroid-Induced Changes in Prefrontal Cortex-Dependent Behaviors.
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- Journal of Neuroscience, 2005, v. 25, n. 34, p. 7792, doi. 10.1523/JNEUROSCI.1598-05.2005
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- Publication type:
- Article
Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-57
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- Publication type:
- Article
Cadherin Expression and EMT: A Focus on Gliomas.
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- Biomedicines, 2021, v. 9, n. 10, p. 1328, doi. 10.3390/biomedicines9101328
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- Publication type:
- Article
Cadherin Expression Profiles Define Glioblastoma Differentiation and Patient Prognosis.
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- Cancers, 2024, v. 16, n. 13, p. 2298, doi. 10.3390/cancers16132298
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- Publication type:
- Article
DJ-1 linked parkinsonism (PARK7) is associated with Lewy body pathology.
- Published in:
- 2016
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- Publication type:
- journal article
Letter to the Editor on "Copathology in Progressive Supranuclear Palsy: Does It Matter?".
- Published in:
- 2020
- By:
- Publication type:
- letter
LAMA2 gene mutation update: Toward a more comprehensive picture of the laminin‐α2 variome and its related phenotypes.
- Published in:
- Human Mutation, 2018, v. 39, n. 10, p. 1314, doi. 10.1002/humu.23599
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- Publication type:
- Article
Clinical, biochemical, molecular, and histological features of 65 Portuguese patients with mitochondrial disorders.
- Published in:
- 2017
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- Publication type:
- journal article
Reply.
- Published in:
- 2017
- By:
- Publication type:
- letter
Immune-mediated necrotizing myopathy associated with antibodies to the signal recognition particle: A rare cause of hyperCKaemia.
- Published in:
- European Journal of Rheumatology, 2021, v. 8, n. 2, p. 143, doi. 10.5152/eurjrheum.2019.19162
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- Publication type:
- Article
Genetic Analysis of Inherited Leukodystrophies Genotype-Phenotype Correlations in the CSF1R Gene.
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- JAMA Neurology, 2013, v. 70, n. 7, p. 875, doi. 10.1001/jamaneurol.2013.698
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- Publication type:
- Article
CADASIL: MRI may be normal in the fourth decade of life - a case report.
- Published in:
- 2016
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- Publication type:
- journal article
Sporadic hemiplegic migraine with normal imaging as the initial manifestation of CADASIL.
- Published in:
- Cephalalgia, 2012, v. 32, n. 3, p. 255, doi. 10.1177/0333102411434809
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- Publication type:
- Article