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Harrison N Jones

Showing results (31-40 of 47) with videos related to

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Journal of Autism and Developmental Disorders|January 23, 2026
Association of the Observer-Reported Communication Ability (ORCA) Measure with Established Communication Measures: Insights From the Angelman Syndrome Natural History StudyAbigail Rader, Li Lin, Harrison N Jones, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research|February 25, 2026
Caregiver Meaningful Score Differences and Meaningful Score Regions for the Observer-Reported Communication Ability (ORCA) Measure for Individuals with Angelman SyndromeAbigail Rader, Li Lin, Anjali Sadhwani, et al.
Molecular Genetics and Metabolism|October 16, 2012
Bulbar muscle weakness and fatty lingual infiltration in glycogen storage disorder type IIIaJeffrey J Horvath, Stephanie L Austin, Harrison N Jones, et al.
American Journal on Intellectual and Developmental Disabilities|April 27, 2023
Validation of the Observer-Reported Communication Ability (ORCA) Measure for Individuals With Angelman SyndromeChristina K Zigler, Li Lin, Molly McFatrich, et al.
Muscle & Nerve|August 27, 2014
Correlation between quantitative whole-body muscle magnetic resonance imaging and clinical muscle weakness in Pompe diseaseJeffrey J Horvath, Stephanie L Austin, Laura E Case, et al.
Molecular Genetics and Metabolism|May 31, 2021
Tongue weakness and atrophy differentiates late-onset Pompe disease from other forms of acquired/hereditary myopathyHarrison N Jones, Lisa D Hobson-Webb, Maragatha Kuchibhatla, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|February 26, 2025
Eating and swallowing care disparities in persons with dementia: A conceptual frameworkRaele Donetha Loy, Nicole Rogus-Pulia, Fred Ketchum, et al.
Molecular Genetics and Metabolism|April 5, 2026
Early enzyme replacement therapy in late-onset Pompe disease diagnosed by newborn screeningLaura E Case, Erin Huggins, Harrison N Jones, et al.
Molecular Genetics and Metabolism|February 11, 2017
The emerging phenotype of late-onset Pompe disease: A systematic literature reviewJustin Chan, Ankit K Desai, Zoheb B Kazi, et al.
Dysphagia|September 19, 2009
Oropharyngeal dysphagia in infants and children with infantile Pompe diseaseHarrison N Jones, Carolyn W Muller, Min Lin, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Journal of Autism and Developmental Disorders|January 23, 2026
Association of the Observer-Reported Communication Ability (ORCA) Measure with Established Communication Measures: Insights From the Angelman Syndrome Natural History StudyAbigail Rader, Li Lin, Harrison N Jones, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research|February 25, 2026
Caregiver Meaningful Score Differences and Meaningful Score Regions for the Observer-Reported Communication Ability (ORCA) Measure for Individuals with Angelman SyndromeAbigail Rader, Li Lin, Anjali Sadhwani, et al.
Molecular Genetics and Metabolism|October 16, 2012
Bulbar muscle weakness and fatty lingual infiltration in glycogen storage disorder type IIIaJeffrey J Horvath, Stephanie L Austin, Harrison N Jones, et al.
American Journal on Intellectual and Developmental Disabilities|April 27, 2023
Validation of the Observer-Reported Communication Ability (ORCA) Measure for Individuals With Angelman SyndromeChristina K Zigler, Li Lin, Molly McFatrich, et al.
Muscle & Nerve|August 27, 2014
Correlation between quantitative whole-body muscle magnetic resonance imaging and clinical muscle weakness in Pompe diseaseJeffrey J Horvath, Stephanie L Austin, Laura E Case, et al.
Molecular Genetics and Metabolism|May 31, 2021
Tongue weakness and atrophy differentiates late-onset Pompe disease from other forms of acquired/hereditary myopathyHarrison N Jones, Lisa D Hobson-Webb, Maragatha Kuchibhatla, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|February 26, 2025
Eating and swallowing care disparities in persons with dementia: A conceptual frameworkRaele Donetha Loy, Nicole Rogus-Pulia, Fred Ketchum, et al.
Molecular Genetics and Metabolism|April 5, 2026
Early enzyme replacement therapy in late-onset Pompe disease diagnosed by newborn screeningLaura E Case, Erin Huggins, Harrison N Jones, et al.
Molecular Genetics and Metabolism|February 11, 2017
The emerging phenotype of late-onset Pompe disease: A systematic literature reviewJustin Chan, Ankit K Desai, Zoheb B Kazi, et al.
Dysphagia|September 19, 2009
Oropharyngeal dysphagia in infants and children with infantile Pompe diseaseHarrison N Jones, Carolyn W Muller, Min Lin, et al.
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