Search filters

List of works by Cynthia Gagnon

222nd ENMC International Workshop:

scientific article published on 12 February 2018

A 9-year follow-up study of quantitative muscle strength changes in myotonic dystrophy type 1

A 9-year follow-up study of the natural progression of upper limb performance in myotonic dystrophy type 1: A similar decline for phenotypes but not for gender

scientific article published on 02 May 2017

An exploratory natural history of ataxia of Charlevoix-Saguenay: A 2-year follow-up

Assessing mobility and balance in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay population: Validity and reliability of four outcome measures

article

Assessing upper extremity capacity as a potential indicator of needs related to household activities for rehabilitation services in people with myotonic dystrophy type 1.

scientific article published on 9 April 2015

Autosomal recessive spastic ataxia of Charlevoix-Saguenay: upper extremity aptitudes, functional independence and social participation

scientific article

Clinical, psychosocial, and central correlates of quality of life in myotonic dystrophy type 1 patients

scientific article published on 19 October 2013

Cognitive Deficits Associated with Sleep Apnea in Myotonic Dystrophy Type 1.

scientific article published in January 2014

Cognitive decline over time in adults with myotonic dystrophy type 1: A 9-year longitudinal study

scientific article published on 14 October 2016

Computer-based assessment of upper-limb incoordination in autosomal recessive spastic ataxia of Charlevoix-Saguenay patients: A pilot study

scientific article published on 9 July 2017

Consensus-based care recommendations for adults with myotonic dystrophy type 1

Coordination and timing deficits in speech and swallowing in autosomal recessive spastic ataxia of Charlevoix–Saguenay (ARSACS)

CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy

scientific article published on March 2017

Daytime sleepiness and myotonic dystrophy

scientific article published on April 2013

Expanding the clinical description of autosomal recessive spastic ataxia of Charlevoix-Saguenay

scientific article published on 12 March 2019

Fatigue and daytime sleepiness rating scales in myotonic dystrophy: a study of reliability

scientific article

French Translation and Cross-cultural Adaptation of the Scale for the Assessment and Rating of Ataxia

scientific article published in 2022

French translation and cross-cultural adaptation of The Myotonic Dystrophy Health Index

scientific article

From motor performance to participation: a quantitative descriptive study in adults with autosomal recessive spastic ataxia of Charlevoix-Saguenay

Further evidence for the reliability and validity of the Fatigue and Daytime Sleepiness Scale

article

Health supervision and anticipatory guidance in adult myotonic dystrophy type 1.

scientific article published on 29 September 2010

Is one trial enough for repeated testing? Same-day assessments of walking, mobility and fine hand use in people with myotonic dystrophy type 1.

scientific article published on 5 December 2016

Lower limb muscle impairment in myotonic dystrophy type 1: the need for better guidelines

scientific article published on 25 February 2015

Lower limb muscle strength impairment in late-onset and adult myotonic dystrophy type 1 phenotypes

scientific article published on 26 October 2016

Measurement properties of a new wireless electrogoniometer for quantifying spasticity during the pendulum test in ARSACS patients

scientific article

Measurement properties of wheelchair use assessment tools in adults with autosomal recessive spastic ataxia of Charlevoix-Saguenay

scientific article published on 26 September 2020

Participation restriction in childhood phenotype of myotonic dystrophy type 1: a systematic retrospective chart review

scientific article published on 27 September 2016

Predictors of disrupted social participation in myotonic dystrophy type 1.

scientific article published in July 2008

Predictors of participation restriction over a 9-year period in adults with myotonic dystrophy type 1

scientific article published on 02 November 2020

Preparing for the Clinical Stage : Lab Development and Testing of Socially Assistive Robot for Physical Health Assessments

scientific article published on 07 August 2024

Prevalence and correlates of apathy in myotonic dystrophy type 1

scientific article published on 22 August 2015

Prevalence of lifestyle risk factors in myotonic dystrophy type 1.

scientific article

Progressive Decline in Daily and Social Activities: A 9-year Longitudinal Study of Participation in Myotonic Dystrophy Type 1

scientific article published on 02 March 2019

Psychological characteristics of patients with myotonic dystrophy type 1.

scientific article published on 11 December 2014

Reliability of the Apathy Evaluation Scale in Myotonic Dystrophy Type 1.

scientific article published on 20 December 2017

Report of the first Outcome Measures in Myotonic Dystrophy type 1 (OMMYD-1) international workshop: Clearwater, Florida, November 30, 2011.

scientific article published on 5 September 2013

Report of the second Outcome Measures in Myotonic Dystrophy type 1 (OMMYD-2) international workshop San Sebastian, Spain, October 16, 2013.

scientific article published on 27 January 2015

Stanford Chronic Disease Self-Management Program in myotonic dystrophy: New opportunities for occupational therapists: Stanford Chronic Disease Self-Management Program dans la dystrophie myotonique : De nouvelles opportunités pour les ergothérapeute

scientific article

The Virtual Peg Insertion Test as an assessment of upper limb coordination in ARSACS patients: a pilot study.

scientific article

The potential of disease management for neuromuscular hereditary disorders

scientific article published on May 2009

Towards an integrative approach to the management of myotonic dystrophy type 1

scientific article

Traduction française de l'échelle Charcot-Marie-Tooth Disease Pediatric Scale.

scientific article published on 17 August 2017

Understanding factors hampering activities of daily living performance in childhood-onset myotonic dystrophy phenotypes

scientific article published on 16 December 2019

Validity and reliability of outcome measures assessing dexterity, coordination, and upper limb strength in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

scientific article published on 17 February 2018

Validity and reliability of the LEMOCOT in the adult ARSACS population: A measure of lower limb coordination

Wheelchair mobility, motor performance and participation of adult wheelchair users with ARSACS: a cross-sectional study

scientific article published on 12 December 2020

Évaluation de l’usage à risque des benzodiazépines chez les personnes âgées : facteurs de risque et impacts

journal article from 'Santé mentale au Québec' published in 2011