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Publications by Stephanie DeArmey
Ocular and Histologic Findings in a Series of Children With Infantile Pompe Disease Treated With Enzyme Replacement Therapy
Journal of Pediatric Ophthalmology and Strabismus
Medicine
Child Health
Ophthalmology
Pediatrics
Perinatology
Related publications
Improvement of Dysphagia in a Child Affected by Pompe Disease Treated With Enzyme Replacement Therapy
Italian Journal of Pediatrics
Child Health
Pediatrics
Perinatology
High Sustained Antibody Titers in Patients With Classic Infantile Pompe Disease Following Immunomodulation at Start of Enzyme Replacement Therapy
Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Enzyme Replacement Therapy for Late-Onset Pompe Disease
Cochrane Database of Systematic Reviews
Cost-Effectiveness of Enzyme Replacement Therapy With Alglucosidase Alfa in Adult Patients With Pompe Disease
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Survival and Associated Factors in 268 Adults With Pompe Disease Prior to Treatment With Enzyme Replacement Therapy
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Late-Onset Pompe Disease: Preliminary Results of Enzyme Replacement Therapy
Nervno-Myshechnye Bolezni
Neurology
Observational Clinical Study of 22 Adult-Onset Pompe Disease Patients Undergoing Enzyme Replacement Therapy Over 5years
Molecular Genetics and Metabolism
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Effects of Enzyme Replacement Therapy and Antidrug Antibodies in Patients With Fabry Disease
Journal of the American Society of Nephrology : JASN
Medicine
Nephrology
Post-Mortem Findings in Critically Ill Patients Treated With Continuous Renal Replacement Therapy
Intensive Care Medicine Experimental
Critical Care
Intensive Care Medicine