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Genomic and Epigenetic Advances in Focal Cortical Dysplasia Types I and II: A Scoping Review

Frontiers in neuroscience, 2021-01, Vol.14, p.580357-580357

2021

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Management and Outcome of Solitary Spinal Amyloidoma—A Systematic Literature Review

World neurosurgery, 2020-08, Vol.140, p.325-331

2020

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The landscape of common genetic drivers and DNA methylation in low‐grade (epilepsy‐associated) neuroepithelial tumors: A review

Neuropathology, 2022-12, Vol.42 (6), p.467-482

2022

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Resective Epilepsy Surgery and Respective Histopathological Diagnoses: A Retrospective Cohort Study

Acta medica portuguesa, 2023-04, Vol.36 (4), p.229

2023

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Amplified and homozygously deleted genes in glioblastoma: impact on gene expression levels

PloS one, 2012-09, Vol.7 (9), p.e46088

2012

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Phenotyping GABA transaminase deficiency: a case description and literature review

Journal of inherited metabolic disease, 2016-09, Vol.39 (5), p.743-747

2016

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The Expression of Connexins and SOX2 Reflects the Plasticity of Glioma Stem-Like Cells

Translational oncology, 2017-08, Vol.10 (4), p.555-569

2017

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Chordoid Glioma of the Third Ventricle, a Rare Tumor with an Unexpected Outcome

Arquivos brasileiros de neurocirurgia, 2017-03, Vol.36 (1), p.32-37

2017

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Novel progranulin mutation: Screening for PGRN mutations in a Portuguese series of FTD/CBS cases

Movement disorders, 2008-07, Vol.23 (9), p.1269-1273

2008

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HGG-55. An adolescent with a High-Grade Glioma: persuing a specific diagnosis

Neuro-oncology (Charlottesville, Va.), 2022-06, Vol.24 (Supplement_1), p.i74-i74

2022

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Pediatric Mitochondrial Respiratory Chain Disorders in the Centro Region of Portugal

Pediatric neurology, 2009-05, Vol.40 (5), p.351-356

2009

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Null mutations and lethal congenital form of glycogen storage disease type IV

Biochemical and biophysical research communications, 2007-09, Vol.361 (2), p.445-450

2007

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Immune-Mediated Necrotizing Myopathy: An Often Misdiagnosed Entity

European journal of case reports in internal medicine, 2015-01, Vol.2 (1)

2015

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Neuro-Behçet’s Disease Mimicking Adult-Type Diffuse Glioma

Sinapse, 2024-01, Vol.23 (4), p.227-229

2024

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DOK7-Associated Congenital Myasthenic Syndrome: A Differential Diagnosis of Core Myopathies?

Sinapse, 2024-01, Vol.23 (4), p.230-231

2024

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World Health Organization Grade III Meningiomas: A Retrospective Study at an Academic Medical Center

World neurosurgery, 2021-05, Vol.149, p.e877-e893

2021

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OTHR-14. AN ADOLESCENT WITH A RARE SCHWANNOMA LOCALIZATION AND THE IMPORTANCE OF METHYLATION STUDIES

Neuro-oncology (Charlottesville, Va.), 2024-06, Vol.26 (Suppl 4), p.0-0

2024

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Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course

Acta neuropathologica, 2020-01, Vol.139 (1), p.193-209

2020

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PNR-20PRIMARY METASTATIC LEIOMYOSARCOMA OF THE SKULL

Neuro-oncology (Charlottesville, Va.), 2016-06, Vol.18 (suppl 3), p.iii10.4-iii10

2016

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MiR-200c-based metabolic modulation in glioblastoma cells as a strategy to overcome tumor chemoresistance

Human molecular genetics, 2021-11, Vol.30 (23), p.2315-2331

2021

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Limb-girdle muscular dystrophy type 2L - A case series from a tertiary center (P5.449)

Neurology, 2018-04, Vol.90 (15_supplement)

2018

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Clinical, pathological and molecular characterization of a Limb-girdle muscular dystrophy type 2I(LGMD-2I) cohort (P5.452)

Neurology, 2018-04, Vol.90 (15_supplement)

2018

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Hiperintensidade Bilateral do Pulvinar e Núcleo Dorso-medial do Tálamo na Forma Esporádica da Doença de Creutzfeldt-Jakob

Acta médica portuguesa, 2012-11, Vol.25, p.41-44

2012

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Inclusion body myositis and muscular granulomas - a rare finding

Rheumatology (Oxford, England), 2021-02, Vol.60 (2), p.989-990

2021

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Neurological impact of eosinophilic granulomatosis with polyangiitis

Acta neurologica Belgica, 2022-02, Vol.122 (1), p.123-128

2022

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Genomic and Epigenetic Advances in Focal Cortical Dysplasia Types I and II: A Scoping Review

Management and Outcome of Solitary Spinal Amyloidoma—A Systematic Literature Review

The landscape of common genetic drivers and DNA methylation in low‐grade (epilepsy‐associated) neuroepithelial tumors: A review

Resective Epilepsy Surgery and Respective Histopathological Diagnoses: A Retrospective Cohort Study

Amplified and homozygously deleted genes in glioblastoma: impact on gene expression levels

Phenotyping GABA transaminase deficiency: a case description and literature review

The Expression of Connexins and SOX2 Reflects the Plasticity of Glioma Stem-Like Cells

Chordoid Glioma of the Third Ventricle, a Rare Tumor with an Unexpected Outcome

Novel progranulin mutation: Screening for PGRN mutations in a Portuguese series of FTD/CBS cases

HGG-55. An adolescent with a High-Grade Glioma: persuing a specific diagnosis

Pediatric Mitochondrial Respiratory Chain Disorders in the Centro Region of Portugal

Null mutations and lethal congenital form of glycogen storage disease type IV

Immune-Mediated Necrotizing Myopathy: An Often Misdiagnosed Entity

Neuro-Behçet’s Disease Mimicking Adult-Type Diffuse Glioma

DOK7-Associated Congenital Myasthenic Syndrome: A Differential Diagnosis of Core Myopathies?

World Health Organization Grade III Meningiomas: A Retrospective Study at an Academic Medical Center

OTHR-14. AN ADOLESCENT WITH A RARE SCHWANNOMA LOCALIZATION AND THE IMPORTANCE OF METHYLATION STUDIES

Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course

PNR-20PRIMARY METASTATIC LEIOMYOSARCOMA OF THE SKULL

MiR-200c-based metabolic modulation in glioblastoma cells as a strategy to overcome tumor chemoresistance

Limb-girdle muscular dystrophy type 2L - A case series from a tertiary center (P5.449)

Clinical, pathological and molecular characterization of a Limb-girdle muscular dystrophy type 2I(LGMD-2I) cohort (P5.452)

Hiperintensidade Bilateral do Pulvinar e Núcleo Dorso-medial do Tálamo na Forma Esporádica da Doença de Creutzfeldt-Jakob

Inclusion body myositis and muscular granulomas - a rare finding

Neurological impact of eosinophilic granulomatosis with polyangiitis

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