The relationships between the Expanded Hammersmith Functional Motor Scale (HFMSE) and genotype and motor and respiratory outcomes were examined in patients with spinal muscular atrophy types II and III (n 70). The correlation between the HFMSE and Gross Motor Function Measure was r 0.98. Correlations between HFMSE and forced vital capacity (percentage of predicted normal) (n 56) and a functional rating (n 57) were r 0.87 and r 0.92, respectively. Correlations with strength were as follows: knee extension, r 0.74 (n 60); elbow flexion, r 0.77 (n 61); and knee flexion, r 0.74 (n 58). The HFMSE differentiated patients by SMN2 copy number (P .0007); bi-level positive airway pressure use, <8 versus 8 hours/day (P <.0001); ambul...
PURPOSE: To quantitatively describe passive lower extremity range of motion in participants with sp...
Recent translational research developments in Spinal Muscular Atrophy (SMA), outcome measure design ...
OBJECTIVE: To characterize the natural history of spinal muscular atrophy (SMA) over 24 months using...
Background: Reports on the clinical meaningfulness of outcome measures in spinal muscular atrophy (S...
Introduction: The Hammersmith Functional Motor Scale Expanded (HFMSE) and the Revised Upper Limb Mod...
Danielle Ramsey, Mariacristina Scoto, Anna Mayhew, Marion Main, Elena Mazzone, Jacqueline Montes, Sa...
Background and purpose: Natural history studies in spinal muscular atrophy (SMA) have primarily focu...
Recent translational research developments in Spinal Muscular Atrophy (SMA), outcome measure design ...
Objective: We report natural history data in a large cohort of 199 patients with spinal muscular atr...
The aim of this study was to validate the Hammersmith functional motor scale for children with spina...
Abstract The aim of this study was to validate the Hammersmith functional motor scale for childre...
Spinal muscular atrophy is one of the most devastating neurological diseases of childhood. Affected ...
Objective. To describe the respiratory trajectories and their correlation with motor function in an ...
A recent Rasch analysis performed on the Hammersmith Functional Motor Scale-Expanded (HFMSE) in pati...
Thigh muscle volume was assessed using magnetic resonance imaging in 16 subjects with spinal muscula...
PURPOSE: To quantitatively describe passive lower extremity range of motion in participants with sp...
Recent translational research developments in Spinal Muscular Atrophy (SMA), outcome measure design ...
OBJECTIVE: To characterize the natural history of spinal muscular atrophy (SMA) over 24 months using...
Background: Reports on the clinical meaningfulness of outcome measures in spinal muscular atrophy (S...
Introduction: The Hammersmith Functional Motor Scale Expanded (HFMSE) and the Revised Upper Limb Mod...
Danielle Ramsey, Mariacristina Scoto, Anna Mayhew, Marion Main, Elena Mazzone, Jacqueline Montes, Sa...
Background and purpose: Natural history studies in spinal muscular atrophy (SMA) have primarily focu...
Recent translational research developments in Spinal Muscular Atrophy (SMA), outcome measure design ...
Objective: We report natural history data in a large cohort of 199 patients with spinal muscular atr...
The aim of this study was to validate the Hammersmith functional motor scale for children with spina...
Abstract The aim of this study was to validate the Hammersmith functional motor scale for childre...
Spinal muscular atrophy is one of the most devastating neurological diseases of childhood. Affected ...
Objective. To describe the respiratory trajectories and their correlation with motor function in an ...
A recent Rasch analysis performed on the Hammersmith Functional Motor Scale-Expanded (HFMSE) in pati...
Thigh muscle volume was assessed using magnetic resonance imaging in 16 subjects with spinal muscula...
PURPOSE: To quantitatively describe passive lower extremity range of motion in participants with sp...
Recent translational research developments in Spinal Muscular Atrophy (SMA), outcome measure design ...
OBJECTIVE: To characterize the natural history of spinal muscular atrophy (SMA) over 24 months using...