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Tracy Boggs
Institution:
Duke University Health System
Observed institutions:
Duke University,
Duke Medical Center,
Duke University Health System,
Duke University Hospital
OpenAlex ID:
A5032609641
A retrospective longitudinal study and comprehensive review of adult patients with glycogen storage disease type III
2021
·
Ghada Hijazi
, Anna Paschall
, et al.
·
Molecular Genetics and Metabolism Reports
·
23
PDF
Whole‐body magnetic resonance imaging in late‐onset Pompe disease: Clinical utility and correlation with functional measures
2019
·
Aleena A. Khan
, Tracy Boggs
, et al.
·
Journal of Inherited Metabolic Disease
·
23
Real-world outcomes from a series of patients with late onset Pompe disease who switched from alglucosidase alfa to avalglucosidase alfa
2024
·
Chris Carter
, Tracy Boggs
, et al.
·
Frontiers in Genetics
·
16
Development of high sustained anti-drug antibody titers and corresponding clinical decline in a late-onset Pompe disease patient after 11+ years on enzyme replacement therapy
2023
·
Katherine H. Kim
, Ankit K. Desai
, et al.
·
Molecular Genetics and Metabolism Reports
·
8
Physical therapy assessment and whole-body magnetic resonance imaging findings in children with glycogen storage disease type IIIa: A clinical study and review of the literature
2021
·
Anna Paschall
, Aleena A. Khan
, et al.
·
Molecular Genetics and Metabolism
·
7
Quantitative whole‐body magnetic resonance imaging in children with Pompe disease: Clinical tools to evaluate severity of muscle disease
2020
·
Samuela A. Fernandes
, Aleena A. Khan
, et al.
·
JIMD Reports
·
6
PDF
Infantile-onset Pompe disease entering adulthood: Insights from 2 decades of enzyme replacement therapy experience
2025
·
Neha Regmi
, Daniel Kenney-Jung
, et al.
·
Genetics in Medicine
·
5
A Retrospective Longitudinal Study and Comprehensive Review of Adult Patients With Glycogen Storage Disease Type Iii
2022
·
Ghada Hijazi
, Anna Paschall
, et al.
·
Molecular Genetics and Metabolism
·
4
Lessons from late-onset Pompe disease identified by Newborn screening: A systematic review
2026
·
Myriam Boueri
, Jessica Doxey
, et al.
·
Molecular Genetics and Metabolism
·
3
Quantitative muscle ultrasound as a window into disease progression in infantile-onset Pompe disease
2025
·
Neelam Makhijani
, Myriam Boueri
, et al.
·
Molecular Genetics and Metabolism
·
1
Whole-body MRI in late-onset Pompe disease: Clinical utility and correlation with functional measures
2020
·
Aleena A. Khan
, Tracy Boggs
, et al.
·
Molecular Genetics and Metabolism
·
1
Real-world outcomes after switching to cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a case series
2026
·
Myriam Boueri
, Tracy Boggs
, et al.
·
Orphanet Journal of Rare Diseases
P153: Quantitative muscle ultrasound as a window into disease progression in infantile-onset Pompe disease*
2025
·
Neelam Makhijani
, Myriam Boueri
, et al.
·
Genetics in Medicine Open
PDF
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Works count:
13
Citation count:
97
H-index:
6
I10-index:
3
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