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Glycogen storage diseases
William B Hannah
*
, Terry G J Derks
, Mitchell L Drumm
, Sarah C GrĂ¼nert
, Priya S Kishnani
,
John Vissing
*
Corresponding author for this work
Department of Neurology
88
Citations (Scopus)
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Keyphrases
Glycogen Storage Disease
100%
Diagnosis Management
28%
Hepatic Glycogen Storage Disease
28%
Novel Therapeutics
14%
Quality of Life
14%
Epidemiology
14%
Histology
14%
Disease Diagnosis
14%
Clinical Trials
14%
Clinical Features
14%
Quality Management
14%
Disease Mechanisms
14%
Natural History
14%
Monogenic
14%
Genetic Testing
14%
Neutropenia
14%
Phenotypic Characterization
14%
Enzyme Analysis
14%
Glycogen
14%
Muscle Glycogen
14%
Natural Course
14%
Diagnostic Considerations
14%
Imaging Genetics
14%
Patient-centered Outcomes
14%
Enzyme Replacement Therapy
14%
Enzyme Deficiency
14%
Definitive Therapy
14%
Multi-organ
14%
Pompe Disease
14%
Sodium-glucose Cotransporter 2 Inhibitors (SGLT2i)
14%
Biomarker Imaging
14%
Neutrophil Dysfunction
14%
Therapeutic Interventions
14%
Exercise Dose
14%
Patient Quality of Life
14%
Disease Sequelae
14%
Medicine and Dentistry
Glycogen Storage Disease
100%
Quality of Life
22%
Diseases
22%
Biological Marker
11%
Clinical Trial
11%
Cohort Effect
11%
Clinical Feature
11%
Genetic Screening
11%
Neutropenia
11%
Sequela
11%
Enzyme Activity
11%
Morbidity
11%
Enzyme Replacement Therapy
11%
Enzyme Deficiency
11%
Glycogen Storage Disease Type II
11%
Sodium Glucose Cotransporter 2 Inhibitor
11%
Monogenic Disorder
11%
Glycogen
11%
Neutrophil
11%
Histology
11%