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Publications by Michelle E. Kruijshaar
Cost-Effectiveness of Enzyme Replacement Therapy With Alglucosidase Alfa in Adult Patients With Pompe Disease
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Related publications
Alglucosidase Alfa: 5 Years of Experience in Late-Onset Pompe Disease
BMC Musculoskeletal Disorders
Rheumatology
Orthopedics
Sports Medicine
Enzyme Replacement Therapy for Late-Onset Pompe Disease
Cochrane Database of Systematic Reviews
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
Immune Modulation Therapy in a CRIM-Positive and IgG Antibody-Positive Infant With Pompe Disease Treated With Alglucosidase Alfa: A Case Report
JIMD Reports
Internal Medicine
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Improvement of Dysphagia in a Child Affected by Pompe Disease Treated With Enzyme Replacement Therapy
Italian Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Cost-Effectiveness of Enzyme Replacement Therapy for Type 1 Gaucher Disease
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Late-Onset Pompe Disease: Preliminary Results of Enzyme Replacement Therapy
Nervno-Myshechnye Bolezni
Neurology
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
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