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Publications by Amie E. Vaisnins

Baseline Urinary Glucose Tetrasaccharide Concentrations in Patients With Infantile- And Late-Onset Pompe Disease Identified by Newborn Screening

Internal Medicine

Molecular Biology

English

Related publications

Swallow Prognosis and Follow-Up Protocol in Infantile Onset Pompe Disease

Internal Medicine

Molecular Biology

English

Newborn Screening for Pompe Disease in Illinois: Experience With 684,290 Infants

International Journal of Neonatal Screening

English

Enzyme Replacement Therapy for Late-Onset Pompe Disease

Cochrane Database of Systematic Reviews

English

Dynamic Respiratory Muscle Function in Late-Onset Pompe Disease

Scientific Reports

Multidisciplinary

English

Lessons Learned From Pompe Disease Newborn Screening and Follow-Up

International Journal of Neonatal Screening

English

Alglucosidase Alfa: 5 Years of Experience in Late-Onset Pompe Disease

BMC Musculoskeletal Disorders

Sports Medicine

English

Late-Onset Pompe Disease: Preliminary Results of Enzyme Replacement Therapy

Nervno-Myshechnye Bolezni

English

Hypertrophic Cardiomyopathy in Pompe Disease Is Not Limited to the Classic Infantile-Onset Phenotype

Internal Medicine

Molecular Biology

English

212. Disease Modeling of Late-Onset Pompe Disease-Specific Induced Pluripotent Stem Cells

Molecular Therapy

Molecular Medicine

Molecular Biology

English