H
Harrison N. Jones
Researcher at Duke University
Publications - 42
Citations - 955
Harrison N. Jones is an academic researcher from Duke University. The author has contributed to research in topics: Dysphagia & Alglucosidase alfa. The author has an hindex of 15, co-authored 35 publications receiving 771 citations. Previous affiliations of Harrison N. Jones include University of Florida & Durham University.
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Journal ArticleDOI
The emerging phenotype of long-term survivors with infantile Pompe disease
Sean N. Prater,Suhrad G. Banugaria,Stephanie DeArmey,Eleanor G. Botha,Erin M. Stege,Laura E. Case,Harrison N. Jones,Chanika Phornphutkul,Raymond Y. Wang,Sarah P. Young,Priya S. Kishnani +10 more
TL;DR: Enzyme replacement therapy with alglucosidase alfa for infantile Pompe disease has improved survival creating new management challenges, and an emerging phenotype is described in a retrospective review of long-term survivors.
Journal ArticleDOI
The emerging phenotype of late-onset Pompe disease: A systematic literature review.
Justin M. Chan,Ankit K. Desai,Zoheb B. Kazi,Kaitlyn Corey,Stephanie Austin,Lisa D. Hobson-Webb,Laura E. Case,Harrison N. Jones,Priya S. Kishnani +8 more
TL;DR: The condition once primarily conceptualized as a limb-girdle muscle disease with prominent respiratory involvement is increasingly recognized to be a condition that results in signs and symptoms across body systems and structures.
Journal ArticleDOI
Oropharyngeal dysphagia in infants and children with infantile Pompe disease.
Harrison N. Jones,Carolyn W. Muller,Min Lin,Suhrad G. Banugaria,Laura E. Case,Jennifer S. Li,Gwendolyn O'Grady,James H. Heller,Priya S. Kishnani +8 more
TL;DR: Dysphagia was present in all 13 subjects, even in a participant only 15 days old, and no relationship in the relative involvement of swallowing, gross motor function, and cardiac disease appeared to be present.
Journal ArticleDOI
Expanding the phenotype of late‐onset pompe disease: Tongue weakness: A new clinical observation
TL;DR: Lingual weakness may be present as an axial sign of LOPD, even relatively early in the disease course, and may contribute to the differential diagnosis of this now treatable condition.
Journal ArticleDOI
Oropharyngeal dysphagia may occur in late-onset Pompe disease, implicating bulbar muscle involvement
TL;DR: A retrospective review of patients evaluated in the neuromuscular clinic at Duke University Medical Center from 1999-2010 found oropharyngeal dysphagia may occur in patients with late-onset Pompe disease, implicating bulbar muscle involvement.