Cargando…

A rehabilitation program to increase balance and mobility in ataxia of Charlevoix-Saguenay: An exploratory study

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is characterized by balance impairment and mobility limitations, which both increase the risk of falling. The objective of this study was to explore the effects of a rehabilitation program aimed at increasing trunk and lower limb mot...

Descripción completa

Detalles Bibliográficos
Autores principales:	Lessard, Isabelle, Masterman, Viviane, Côté, Isabelle, Gagnon, Cynthia, Duchesne, Elise
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2022
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9797069/ https://www.ncbi.nlm.nih.gov/pubmed/36576926 http://dx.doi.org/10.1371/journal.pone.0279406

Ejemplares similares

Functional mobility in walking adult population with ataxia of Charlevoix-Saguenay
por: Lessard, Isabelle, et al.
Publicado: (2021)

Participation and Functional Independence in Adults With Recessive Spastic Ataxia of Charlevoix-Saguenay
por: Muslemani, Samar, et al.
Publicado: (2022)

From motor performance to participation: a quantitative descriptive study in adults with autosomal recessive spastic ataxia of Charlevoix-Saguenay
por: Gagnon, Cynthia, et al.
Publicado: (2018)

Documenting manifestations and impacts of autosomal recessive spastic ataxia of Charlevoix–Saguenay to develop patient-reported outcome
por: Tremblay, Marjolaine, et al.
Publicado: (2022)

Retinal nerve fiber hypertrophy in ataxia of Charlevoix-Saguenay patients
por: Pablo, Luis E, et al.
Publicado: (2011)

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay without Spasticity
por: Aida, Izumi, et al.
Publicado: (2021)

Inner Retinal Dysfunction in the Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
por: Borruat, François-Xavier, et al.
Publicado: (2017)

Autosomal-Recessive Spastic Ataxia of Charlevoix-Saguenay: A Turkish Child
por: Incecik, Faruk, et al.
Publicado: (2018)

Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
por: Bagaria, Jaya, et al.
Publicado: (2022)

Autosomal Recessive Spastic Ataxia of Charlevoix–Saguenay due to Novel Mutations in the SACS Gene
por: Sharma, Rohan, et al.
Publicado: (2022)

Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum
por: Synofzik, Matthis, et al.
Publicado: (2013)

SACS Mutation-Positive Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay (ARSACS) from Kerala
por: Sheetal, S, et al.
Publicado: (2020)

Development of Nanostructured Lipid Carriers for the Delivery of Idebenone in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
por: Martinelli, Chiara, et al.
Publicado: (2020)

Case Report: Expanding the Genetic and Phenotypic Spectrum of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
por: Habibzadeh, Parham, et al.
Publicado: (2020)

Optical Coherence Tomography Findings Facilitate the Diagnosis of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
por: Cho, Hyuna, et al.
Publicado: (2021)

Autosomal recessive spastic ataxia of charlevoix-saguenay: Findings from MRI in two adult Italian siblings
por: Pensabene, Maria Claudia, et al.
Publicado: (2020)

Molecular Identity and Location Influence Purkinje Cell Vulnerability in Autosomal-Recessive Spastic Ataxia of Charlevoix-Saguenay Mice
por: Toscano Márquez, Brenda, et al.
Publicado: (2021)

A reduction in Drp1-mediated fission compromises mitochondrial health in autosomal recessive spastic ataxia of Charlevoix Saguenay
por: Bradshaw, Teisha Y., et al.
Publicado: (2016)

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Case Report of a Novel Nonsense Mutation in the SACS Gene
por: Agarwal, Ayush, et al.
Publicado: (2020)

Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
por: Tzoulis, Charalampos, et al.
Publicado: (2013)

Purkinje Cell Degeneration and Motor Coordination Deficits in a New Mouse Model of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
por: Ding, Man, et al.
Publicado: (2017)

Novel Variants in MPV17, PRX, GJB1, and SACS Cause Charcot–Marie–Tooth and Spastic Ataxia of Charlevoix–Saguenay Type Diseases
por: Zaman, Qaiser, et al.
Publicado: (2023)

Novel compound heterozygous mutation in SACS gene leads to a milder autosomal recessive spastic ataxia of Charlevoix‐Saguenay, ARSACS, in a Finnish family
por: Palmio, Johanna, et al.
Publicado: (2016)

Novel frameshift mutation in the SACS gene causing spastic ataxia of charlevoix-saguenay in a consanguineous family from the Arabian Peninsula: A case report and review of literature
por: Al-Ajmi, Abdullah, et al.
Publicado: (2020)

In Vitro Characterization of Motor Neurons and Purkinje Cells Differentiated from Induced Pluripotent Stem Cells Generated from Patients with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
por: Louit, Aurélie, et al.
Publicado: (2023)

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) in a Thai Patient: The Classic Clinical Manifestations, Funduscopic Feature, and Brain Imaging Findings with a Novel Mutation in the SACS Gene
por: Srikajon, Jindapa, et al.
Publicado: (2020)

Physical and Functional Clinical Profile of Older Adults in Specialized Geriatric Rehabilitation Care Services in Saguenay-Québec: A Retrospective Study at La Baie Hospital
por: de Lima, Maria do Carmo Correia, et al.
Publicado: (2022)

Accomplishment of instrumental activities of daily living and its relationship with cognitive functions in adults with myotonic dystrophy type 1 childhood phenotype: an exploratory study
por: Tremblay, Marjolaine, et al.
Publicado: (2021)

Rehabilitation in patients with cerebellar ataxias
por: Chien, Hsin Fen, et al.
Publicado: (2022)

Parents’ and adolescents’ willingness to be vaccinated against serogroup B meningococcal disease during a mass vaccination in Saguenay–Lac-St-Jean (Quebec)
por: Dubé, Eve, et al.
Publicado: (2015)

Evaluation of a Road Safety Awareness Campaign Deployed along the Roadside in Saguenay (Québec, Canada)
por: Desjardins, France, et al.
Publicado: (2023)

Ideal timing to transfer from an acute care hospital to an interdisciplinary inpatient rehabilitation program following a stroke: an exploratory study
por: Gagnon, Dany, et al.
Publicado: (2006)

What is known about the effects of exercise or training to reduce skeletal muscle impairments of patients with myotonic dystrophy type 1? A scoping review
por: Roussel, Marie-Pier, et al.
Publicado: (2019)

Correction to: What is known about the effects of exercise or training to reduce skeletal muscle impairments of patients with myotonic dystrophy type 1? A scoping review
por: Roussel, Marie-Pier, et al.
Publicado: (2019)

Training program-induced skeletal muscle adaptations in two men with myotonic dystrophy type 1
por: Roussel, Marie-Pier, et al.
Publicado: (2019)

Saguenay Youth Study: A multi-generational approach to studying virtual trajectories of the brain and cardio-metabolic health
por: Paus, T., et al.
Publicado: (2014)

Inventory and perspectives of chronic disease management programs in Switzerland: an exploratory survey
por: Peytremann-Bridevaux, Isabelle, et al.
Publicado: (2009)

Targeted ballet program mitigates ataxia and improves balance in females with mild-to-moderate multiple sclerosis
por: Scheidler, Andrew M., et al.
Publicado: (2018)

Effectiveness of rehabilitation intervention in persons with Friedreich ataxia
por: Paparella, Gabriella, et al.
Publicado: (2023)

Utility of a Three-Dimensional Interactive Augmented Reality Program for Balance and Mobility Rehabilitation in the Elderly: A Feasibility Study
por: Im, Dal Jae, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_sbhgopc9cd1o7fa9177cjemprh