J. Deol

Relationships of thigh muscle contractile and non-contractile tissue with function, strength, and age in boys with Duchenne muscular dystrophy

C. Senesac, H. Akima, D. Lott, 2012, Neuromuscular Disorders.

Title: A novel time-based surface EMG measure for quantifying hypertonia in paretic arm muscles

J. Dewald, M. H. Sohn, J. Deol, 2022 .

Magnetic Resonance Assessment of Hypertrophic and Pseudo-Hypertrophic Changes in Lower Leg Muscles of Boys with Duchenne Muscular Dystrophy and Their Relationship to Functional Measurements

C. Senesac, H. Sweeney, D. Lott, 2015, PloS one.

T2 mapping provides multiple approaches for the characterization of muscle involvement in neuromuscular diseases: a cross‐sectional study of lower leg muscles in 5–15‐year‐old boys with Duchenne muscular dystrophy

W. Triplett, C. Senesac, H. Sweeney, 2013, NMR in biomedicine.

Multi-slice MRI reveals heterogeneity in disease distribution along the length of muscle in Duchenne muscular dystrophy.

C. Senesac, D. Lott, R. Willcocks, 2017, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.

A Method for Quantifying Trunk Motor Control During Reaching in Individuals Post Hemiparetic Stroke*

Ana Maria Acosta, Julius P.A. Dewald, A. M. Acosta, 2020, 2020 42nd Annual International Conference of the IEEE Engineering in Medicine & Biology Society (EMBC).

Longitudinal measurements of MRI-T2 in boys with Duchenne muscular dystrophy: Effects of age and disease progression

W. Triplett, C. Senesac, D. Lott, 2014, Neuromuscular Disorders.

Two-Year Longitudinal Changes in Lower Limb Strength and Its Relation to Loss in Function in a Large Cohort of Patients With Duchenne Muscular Dystrophy

R. Finkel, B. Byrne, W. Rooney, 2018, American journal of physical medicine & rehabilitation.

Optimism persists when walking in unpredictable environments

E. Perreault, K. Gordon, Geoffrey L. Brown, 2023, Scientific reports.