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Browse PlansClaudia Senesac
PT, PhD, PCS
Claudia Senesac is a clinical associate professor at University of Florida in the Doctor of Physical Therapy department. Her teaching responsibilities include functional anatomy dissection and pediatrics in physical therapy. She has over 37 years of pediatric clinical experience. She has been the owner and administrator of a pediatric physical therapy private practice since 1984 and is a board certified clinical specialist in pediatrics. Claudia is still providing therapy to children with a variety of conditions. Her research focus has been in Duchenne Muscular Dystrophy (DMD). She is a sub-investigator for a multi-center NIH funded grant investigating Magnetic Resonance Imaging and Biomarkers in boys with Duchenne Muscular Dystrophy. In addition, she has spearheaded investigating the reliability and common errors seen in outcome measures in DMD across research and clinic sites. She is a national educator for Parent Project Muscular Dystrophy, translating research to clinical practice. She has several publications in peer-reviewed journals related to Duchenne Muscular Dystrophy as author and co-author. Most recently, she was the recipient of the International Educator of the Year award for the College of Public Health and Health Professions at UF in 2016, and in 2014 received the Outstanding Pediatric Clinician Award from the Pediatric Section of the APTA.
Courses with Claudia Senesac
Browse Course CatalogDuchenne Muscular Dystrophy Part 1: What We Know Now
Presented by Claudia Senesac, PT, PhD, PCS
Duchenne Muscular Dystrophy Part 1: What We Know Now
Subscribe now, and access clinical education
and patient education—anytime, anywhere—with video instruction from
recognized industry experts.
Duchenne Muscular Dystrophy (DMD) is the most common childhood muscular dystrophy. Much of what we have known about this disease has been based on years of clinical observation, muscle biopsy, and other limited testing. Longitudinal studies and clinical trials are shaping our "new understanding" of this disease. The courses related to DMD will span pathophysiology, research, the development of therapy recommendations, and quality of life issues. Therapy recommendations are based on predictive models of biomarkers and function, helping therapists and families plan for the future. Therapists play a critical role in caring for boys and young men with this disease.
Duchenne Muscular Dystrophy Part 2: Therapy Across the Lifespan
Presented by Claudia Senesac, PT, PhD, PCS
Duchenne Muscular Dystrophy Part 2: Therapy Across the Lifespan
Subscribe now, and access clinical education
and patient education—anytime, anywhere—with video instruction from
recognized industry experts.
Duchenne Muscular Dystrophy (DMD) is the most common childhood muscular dystrophy. Much of what we have known about this disease has been based on years of clinical observation, muscle biopsy, and other limited testing. Longitudinal studies and clinical trials are shaping our "new understanding" of this disease. The courses related to DMD will span pathophysiology, research, the development of therapy recommendations, and quality of life issues. Therapy recommendations are based on predictive models of biomarkers and function helping therapists and families plan for the future. Therapists play a critical role in caring for boys and young men with this disease.
Duchenne Muscular Dystrophy Part 3: Community & Home Environments
Presented by Claudia Senesac, PT, PhD, PCS
Duchenne Muscular Dystrophy Part 3: Community & Home Environments
Subscribe now, and access clinical education
and patient education—anytime, anywhere—with video instruction from
recognized industry experts.
Duchenne Muscular Dystrophy (DMD) is the most common childhood muscular dystrophy. Much of what we have known about this disease has been based on years of clinical observation, muscle biopsy, and other limited testing. Longitudinal studies and clinical trials are shaping our "new understanding" of this disease. The courses related to DMD will span pathophysiology, research, the development of therapy recommendations, and quality of life issues. Therapy recommendations are based on predictive models of biomarkers and function, helping therapists and families plan for the future. Therapists play a critical role in caring for boys and young men with this disease.
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