Objective: To quantify longitudinal changes in gait in Friedreich’s Ataxia (FA) patients compared to controls during a 24-month period using the GAITRite Walkway System. Background: FA is a devastating neurodegenerative disease. Measures to accurately quantify small changes in neurological function in FA patients are needed to facilitate therapeutic clinical trials. Design/Methods: This was a prospective, longitudinal study that assessed ambulatory FA patients compared to age- and gender-matched controls. FA patients were examined at baseline and at 6, 12, and 24 months, using the GAITRite Walkway system, a portable instrument used to assess gait parameters, and the Friedreich’s Ataxia Rating Scale (FARS). Controls were evaluated at baselin...
Instrumental gait analysis is increasingly recognized as a useful tool for the evaluation of movemen...
The evident ataxic characteristics of gait in patients with cerebellar damage suggest that the cereb...
Background Spinocerebellar ataxia type 6 (SCA6) is an inherited ataxia with no established treatmen...
Objective: To quantify longitudinal changes in gait in Friedreich’s Ataxia (FA) patients compared to...
Objective: To test the validity of the GAITRite Walkway System and Biodex Balance System for measuri...
Friedreich\u27s Ataxia (FA) is an autosomal-recessive, neurodegenerative disease characterized by pr...
International audienceTo date, it has been challenging for clinicians and researchers alike to use t...
Friedreich Ataxia (FA) is a debilitating autosomal-recessive neurodegenerative disorder which is cha...
Friedreich's ataxia is the most common autosomal recessive form of neurodegenerative ataxia. We pres...
Hypothesis: Friedreich’s ataxia (FA) is an inherited disease characterized by progressive motor weak...
OBJECTIVES: With disease-modifying drugs on the horizon for degenerative ataxias, ecologically valid...
Purpose/Hypothesis: Balance deficits are common sequelae of Friedreich’s Ataxia (FA), yet, there are...
In the present study, the progression of gait impairment in a group of patients with primary degener...
Objective Friedreich ataxia (FRDA) is a progressive neurodegenerative disorder of adults and childre...
Objective: To investigate changes in gait quality, balance and mobility associated with treadmill tr...
Instrumental gait analysis is increasingly recognized as a useful tool for the evaluation of movemen...
The evident ataxic characteristics of gait in patients with cerebellar damage suggest that the cereb...
Background Spinocerebellar ataxia type 6 (SCA6) is an inherited ataxia with no established treatmen...
Objective: To quantify longitudinal changes in gait in Friedreich’s Ataxia (FA) patients compared to...
Objective: To test the validity of the GAITRite Walkway System and Biodex Balance System for measuri...
Friedreich\u27s Ataxia (FA) is an autosomal-recessive, neurodegenerative disease characterized by pr...
International audienceTo date, it has been challenging for clinicians and researchers alike to use t...
Friedreich Ataxia (FA) is a debilitating autosomal-recessive neurodegenerative disorder which is cha...
Friedreich's ataxia is the most common autosomal recessive form of neurodegenerative ataxia. We pres...
Hypothesis: Friedreich’s ataxia (FA) is an inherited disease characterized by progressive motor weak...
OBJECTIVES: With disease-modifying drugs on the horizon for degenerative ataxias, ecologically valid...
Purpose/Hypothesis: Balance deficits are common sequelae of Friedreich’s Ataxia (FA), yet, there are...
In the present study, the progression of gait impairment in a group of patients with primary degener...
Objective Friedreich ataxia (FRDA) is a progressive neurodegenerative disorder of adults and childre...
Objective: To investigate changes in gait quality, balance and mobility associated with treadmill tr...
Instrumental gait analysis is increasingly recognized as a useful tool for the evaluation of movemen...
The evident ataxic characteristics of gait in patients with cerebellar damage suggest that the cereb...
Background Spinocerebellar ataxia type 6 (SCA6) is an inherited ataxia with no established treatmen...