Search Results - "Santos, Miguel Oliveira"
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Respiratory phenotypes in amyotrophic lateral sclerosis as determined by respiratory questions on the Amyotrophic Lateral Sclerosis Functional Rating Scale–Revised and their relation to respiratory tests
Published in European journal of neurology (01-06-2023)“…© 2023 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology. This is an open access article…”
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2
Gold Coast diagnostic criteria increase sensitivity in amyotrophic lateral sclerosis
Published in Clinical neurophysiology (01-12-2021)“…•New simpler Gold Coast diagnostic criteria for amyotrophic lateral sclerosis were validated.•The Gold Coast criteria have higher sensitivity with preserved…”
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3
Respiratory onset in amyotrophic lateral sclerosis: clinical features and spreading pattern
Published in Amyotrophic lateral sclerosis and frontotemporal degeneration (01-01-2023)“…Objective To describe the clinical features and progression of patients with respiratory onset amyotrophic lateral sclerosis (ALS). Methods: We analyzed the…”
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Impact of diabetes mellitus on the respiratory function of amyotrophic lateral sclerosis patients
Published in European journal of neurology (01-02-2024)“…Background and purpose Respiratory insufficiency and its complications are the main cause of death in amyotrophic lateral sclerosis (ALS). The impact of…”
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Upper motor neuron signs in primary lateral sclerosis and hereditary spastic paraplegia
Published in Muscle & nerve (01-07-2024)“…Introduction/Aims The frequency and distribution of upper motor neuron (UMN) signs in primary lateral sclerosis (PLS) are unknown. We aimed to study the…”
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First Portuguese patient presenting with hereditary sensory and autonomic neuropathy type 1E associated with a novel mutation in DNMT1 gene
Published in Neurological sciences (01-05-2020)Get full text
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Dynamic Bayesian networks for stratification of disease progression in amyotrophic lateral sclerosis
Published in European journal of neurology (01-08-2022)“…© 2022 European Academy of Neurology. Background and purpose Progression rate is quite variable in amyotrophic lateral sclerosis (ALS); thus, tools for…”
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Epilepsy Secondary to Occipital Cobblestone Malformation in an Adult Patient with Merosin-Deficient Congenital Muscular Dystrophy Type 1A
Published in Acta médica portuguesa (04-10-2024)“…N/a…”
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Clinical characteristics in amyotrophic lateral sclerosis with Sub-Saharan Africa ancestry – A Portuguese hospital-based cohort study
Published in Clinical neurology and neurosurgery (01-04-2023)“…•Clinical data of ALS in Sub-Saharan Africa (SA) is scarce.•SAALS is a specific ALS population with a younger onset.•Survival is not dependent on the…”
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10
Acute non-traumatic tetraparesis – Differential diagnosis
Published in Journal of clinical neuroscience (01-05-2021)“…•Acute tetraparesis is a debilitating and sometimes life-threatening condition.•History and examination are essential in establishing the correct diagnosis.•A…”
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Complex sleep-disordered breathing after vagus nerve stimulation: broadening the spectrum of adverse events of special interest
Published in Epileptic disorders (01-12-2020)“…Copyright © 1999-2021 John Wiley & Sons, Inc. All rights reserved. Two young males with refractory epilepsy of unknown aetiology were referred for vagus nerve…”
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Delayed Diagnosis and Diagnostic Pathway of ALS Patients in Portugal: Where Can We Improve?
Published in Frontiers in neurology (27-10-2021)“…Background: Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease with unsatisfactory treatment options. Best management and…”
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Creatine Kinase and Respiratory Decline in Amyotrophic Lateral Sclerosis
Published in Brain sciences (28-06-2024)“…Respiratory dysfunction is an important hallmark of amyotrophic lateral sclerosis (ALS). Elevation of creatine kinase (CK) has been reported in 23-75% of ALS…”
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Sporadic Spinal-Onset Amyotrophic Lateral Sclerosis Associated with Myopathy in Three Unrelated Portuguese Patients
Published in Brain sciences (01-01-2023)“…Amyotrophic lateral sclerosis (ALS) and myopathy have been already described as part of a common genetic syndrome called multisystem proteinopathy. They may…”
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Impact of SARS-CoV-2 Infection Among Non-Invasive Ventilated ALS Patients
Published in Journal of neuromuscular diseases (01-01-2022)“…The impact of SARS-CoV-2 infection among neuromuscular diseases with respiratory involvement, including amyotrophic lateral sclerosis (ALS), is still to be…”
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16
Serum uric acid as a predictor of bipolarity in individuals with a major depressive episode
Published in Bipolar disorders (01-05-2019)“…Objectives There are no well‐established biomarkers to predict the risk of conversion to bipolar disorder (BD) in patients with depression. Given the putative…”
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Profiling tofersen as a treatment of superoxide dismutase 1 amyotrophic lateral sclerosis
Published in Expert review of neurotherapeutics (02-06-2024)“…Amyotrophic lateral sclerosis (ALS) is a rapidly progressive motor neuron disorder with a fatal outcome 3-5 years after disease onset due to respiratory…”
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Neurology of inflammatory bowel disease
Published in Journal of the neurological sciences (15-05-2021)“…Inflammatory bowel diseases (IBD) are chronic inflammatory conditions affecting the digestive system, comprising two main distinctive entities, ulcerative…”
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Teaching Video NeuroImage: Disabling Jaw Clonus in a Patient With Bulbar-Onset Amyotrophic Lateral Sclerosis Successfully Treated With Botulinum Toxin
Published in Neurology (11-10-2022)Get full text
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Results from Portugal's 2022 report card on physical activity for children and youth
Published in Journal of exercise science and fitness (01-07-2023)“…The purpose of this study is to update results of Portuguese's Report Card on Physical activity (PA) for Children and Adolescents. The grades were assigned by…”
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