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Inflammatory pathology markers (activated microglia and reactive astrocytes) in early and late onset Alzheimer disease: a post mortem study

Neuropathology and applied neurobiology, 2018-04, Vol.44 (3), p.298-313

2018

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Frontotemporal lobar degeneration‐TDP with ‘multiple system atrophy phenocopy syndrome’

Neuropathology and applied neurobiology, 2017-10, Vol.43 (6), p.533-536

2017

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Primary antiphospholipid antibody syndrome presenting with encephalopathy, psychosis and seizures

Lupus, 2011-11, Vol.20 (13), p.1433-1435

2011

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Ryanodine-related myopathies: Clinical, histopathologic and genetic heterogeneity among 16 patients from a Portuguese tertiary centre

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S135-S136

2016

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Duchenne muscular dystrophy: Clinical, genetic and pathological changes in preclinical and early stages

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S124-S124

2016

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The expanding phenotype of LAMA2-related muscular dystrophies: Four additional cases diagnosed during adulthood

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S190-S190

2016

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Regulation of WNT6 by HOXA9 in glioblastoma: functional and clinical relevance

European journal of cancer (1990), 2016-07, Vol.61, p.S45-S46

2016

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Isolated psychosis with an organic etiology: A diagnostic challenge

Journal of the neurological sciences, 2013-10, Vol.333, p.e681-e681

2013

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Cerebral amyloid angiopathy presenting as a diffuse leukoencephalopathy

Journal of the neurological sciences, 2013-10, Vol.333, p.e343-e343

2013

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Freezing of gait – First motor manifestation in late infantile variant neuronal ceroid lipofuscinosis

Parkinsonism & related disorders, 2014-02, Vol.20 (2), p.243-244

2014

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Neuropathology of central nervous system involvement in TTR amyloidosis

Acta neuropathologica, 2023-01, Vol.145 (1), p.113-126

2023

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PO-473 WNT6 expression in glioblastoma: mechanistic, functional and clinical implications

ESMO open, 2018-07, Vol.3 (Suppl 2), p.A416-A416

2018

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CNS involvement in V30M transthyretin amyloidosis: clinical, neuropathological and biochemical findings

Journal of neurology, neurosurgery and psychiatry, 2015-02, Vol.86 (2), p.159-167

2015

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Post-mortem assessment in vascular dementia: advances and aspirations

BMC medicine, 2016-08, Vol.14 (1), p.129-129, Article 129

2016

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LAMA2 gene mutation update: Toward a more comprehensive picture of the laminin‐α2 variome and its related phenotypes

Human mutation, 2018-10, Vol.39 (10), p.1314-1337

2018

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Cadherin Expression and EMT: A Focus on Gliomas

Biomedicines, 2021-10, Vol.9 (10), p.1328

2021

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317VP Overview of a cohort of 35 manifesting dystrophinopathy females – and addressing the forthcoming challenges

Neuromuscular disorders : NMD, 2024-10, Vol.43, p.104441, Article 104441.512

2024

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VP.79 Challenges in genetic diagnosis of LAMA2-MD - when the pieces do not fit

Neuromuscular disorders : NMD, 2022-10, Vol.32, p.S124

2022

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Recurrent Focal myositis: a rare inflammatory myopathy

Acta reumatológica portuguesa, 2014-04, Vol.39 (2), p.172

2014

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Progressive proximal muscle weakness with subacute onset in an elderly patient: a case report

Revista de neurologiá, 2023-01, Vol.76 (1), p.31-34

2023

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Association Between Iron-Related Protein Lipocalin 2 and Cognitive Impairment in Cerebrospinal Fluid and Serum

Frontiers in aging neuroscience, 2021-06, Vol.13, p.663837-663837

2021

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Late-onset limb-girdle myopathy with oculobulbar signs and rimmed vacuoles associated with a novel Pompe disease mutation

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S163

2017

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P.226 - Late-onset limb-girdle myopathy with oculobulbar signs and rimmed vacuoles associated with a novel Pompe disease mutation

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S163-S163

2017

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POSB188 Burden of Disease and Cost of Illness of Alzheimer’S Disease in Portugal

Value in health, 2022-01, Vol.25 (1), p.S131-S131

2022

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Morphological Correlates of Corticosteroid-Induced Changes in Prefrontal Cortex-Dependent Behaviors

The Journal of neuroscience, 2005-08, Vol.25 (34), p.7792-7800

2005

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Inflammatory pathology markers (activated microglia and reactive astrocytes) in early and late onset Alzheimer disease: a post mortem study

Frontotemporal lobar degeneration‐TDP with ‘multiple system atrophy phenocopy syndrome’

Primary antiphospholipid antibody syndrome presenting with encephalopathy, psychosis and seizures

Ryanodine-related myopathies: Clinical, histopathologic and genetic heterogeneity among 16 patients from a Portuguese tertiary centre

Duchenne muscular dystrophy: Clinical, genetic and pathological changes in preclinical and early stages

The expanding phenotype of LAMA2-related muscular dystrophies: Four additional cases diagnosed during adulthood

Regulation of WNT6 by HOXA9 in glioblastoma: functional and clinical relevance

Isolated psychosis with an organic etiology: A diagnostic challenge

Cerebral amyloid angiopathy presenting as a diffuse leukoencephalopathy

Freezing of gait – First motor manifestation in late infantile variant neuronal ceroid lipofuscinosis

Neuropathology of central nervous system involvement in TTR amyloidosis

PO-473 WNT6 expression in glioblastoma: mechanistic, functional and clinical implications

CNS involvement in V30M transthyretin amyloidosis: clinical, neuropathological and biochemical findings

Post-mortem assessment in vascular dementia: advances and aspirations

LAMA2 gene mutation update: Toward a more comprehensive picture of the laminin‐α2 variome and its related phenotypes

Cadherin Expression and EMT: A Focus on Gliomas

317VP Overview of a cohort of 35 manifesting dystrophinopathy females – and addressing the forthcoming challenges

VP.79 Challenges in genetic diagnosis of LAMA2-MD - when the pieces do not fit

Recurrent Focal myositis: a rare inflammatory myopathy

Progressive proximal muscle weakness with subacute onset in an elderly patient: a case report

Association Between Iron-Related Protein Lipocalin 2 and Cognitive Impairment in Cerebrospinal Fluid and Serum

Late-onset limb-girdle myopathy with oculobulbar signs and rimmed vacuoles associated with a novel Pompe disease mutation

P.226 - Late-onset limb-girdle myopathy with oculobulbar signs and rimmed vacuoles associated with a novel Pompe disease mutation

POSB188 Burden of Disease and Cost of Illness of Alzheimer’S Disease in Portugal

Morphological Correlates of Corticosteroid-Induced Changes in Prefrontal Cortex-Dependent Behaviors

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