Necesidad de una evaluación e intervención en esclerosis lateral amiotrófica

ABS Sánchez, EMP del Pozo - Revista de Logopedia, Foniatría y …, 2018 - Elsevier
Antecedentes La esclerosis lateral amiotrófica es una enfermedad neurodegenerativa rara y
de rápido progreso que causa un deterioro en las motoneuronas de la corteza cerebral …

[PDF][PDF] Evaluation of overloading on caregivers of people with Amyotrophic Lateral Sclerosis (ALS) 1

LMS de Almeida, IV Falcão… - Cadernos de Terapia …, 2017 - docs.bvsalud.org
Introduction: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder that results
in the selective death of motor neurons, with weakness and generalized muscle atrophy as …

[PDF][PDF] Adapting to progressive paralysis: A tongue-brain hybrid robot interface for individuals with amyotrophic lateral sclerosis

RL Kæseler - 2023 - vbn.aau.dk
Abstract Amyotrophic Lateral Sclerosis (ALS) is a motor neuron disease that causes
progressive paralysis of all motor functions. Individuals with ALS will therefore have an …

Amyotrophic lateral sclerosis in Belo Horizont, Brazil between 2010 and 2020: a clinical epidemiological study

M Harriman, LC Morais, BP Pessoa, JC Polese - Acta Fisiátrica, 2022 - revistas.usp.br
Objective: To describe the clinical profile of individuals with Amyotrophic Lateral Sclerosis
(ALS) from a reference hospital in the city of Belo Horizonte, Brazil. Method: This is a …

SPTLC1 variants associated with childhood onset amyotrophic lateral sclerosis produce distinct sphingolipid signatures through impaired interaction with ORMDL …

MA Lone, MJ Aaltonen, A Zidell, HF Pedro… - bioRxiv, 2022 - biorxiv.org
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease affecting
motor neurons. Mutations in the SPTLC1 subunit of serine-palmitoyltransferase (SPT), which …

Tear-based vibrational spectroscopy for non-invasive biomarker discovery in Amyotrophic Lateral Sclerosis

A Duse, F Ambrosio, D Ami, A Borghesi… - IL NUOVO CIMENTO …, 2023 - boa.unimib.it
In recent literature, tear's biomarkers analysis through spectroscopic techniques is emerging
as a reliable tool to identify neurodegenerative diseases such as Alzheimer's and …

Ventilatory support and respiratory infection in patients with Amyotrophic Lateral Sclerosis

FC Cezar, KV Cantarini, HA Gaspar… - Medical Research …, 2023 - esmed.org
Methods This observational retrospective cohort study analyzed the electronic medical
records of patients treated between January and December 2022. Results A total of 91 …

[PDF][PDF] Cognitive Performance of Patients with Adult 5q-Spinal Muscular Atrophy and with Amyotrophic Lateral Sclerosis. Brain Sci. 2021, 11, 8

A Osmanovic, G Wieselmann, L Mix, HA Siegler… - 2020 - pdfs.semanticscholar.org
Motor neuron diseases, such as spinal muscular atrophy (SMA) and amyotrophic lateral
sclerosis (ALS), share several clinical similarities while differing substantially in etiology …

Voltage-gated potassium channel antibodies in slow-progression motor neuron disease

M Godani, M Zoccarato, A Beronio, L Zuliani… - Neurodegenerative …, 2016 - karger.com
Background: The spectrum of autoimmune neurological diseases associated with voltage-
gated potassium channel (VGKC)-complex antibodies (Abs) ranges from peripheral nerve …

[PDF][PDF] Results: Cross-sectional analysis demonstrated individually variable states of cortical thinning, which was most pronounced in the ventral section of the …

AM Wirth, A Khomenko, D Baldaranov, I Kobor… - academia.edu
Objective: Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative process
affecting upper and lower motor neurons as well as non-motor systems. In this study …