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Publications by Otto P Van Diggelen
Prenatal Diagnosis of Glycogen Storage Disease Type II: Enzyme Assay or Mutation Analysis?
Pediatric Research
Child Health
Pediatrics
Perinatology
Related publications
Impaired Autophagy Contributes to Muscle Atrophy in Glycogen Storage Disease Type II Patients
Autophagy
Cell Biology
Molecular Biology
Hepatic and Neuromuscular Forms of Glycogen Storage Disease Type IV Caused by Mutations in the Same Glycogen-Branching Enzyme Gene.
Journal of Clinical Investigation
Medicine
Pulmonary Arterial Hypertension in Glycogen Storage Disease Type I
Journal of Inborn Errors of Metabolism and Screening
Child Health
Genetics
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Orthotopic Liver Transplantation in Glycogen Storage Disease Type 1a
Journal of Inborn Errors of Metabolism and Screening
Child Health
Genetics
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Markedly Elevated Serum Transaminases in Glycogen Storage Disease Type III
Journal of Pediatric Gastroenterology and Nutrition
Child Health
Pediatrics
Perinatology
Gastroenterology
Different Strategies in the Laboratory Diagnosis of Autoimmune Disease: Immunofluorescence, Enzyme-Linked Immunosorbent Assay or Both?
Annals of Clinical Biochemistry
Medicine
Clinical Biochemistry
Chimerism After Liver Transplantation for Type IV Glycogen Storage Disease and Type 1 Gaucher's Disease
New England Journal of Medicine
Medicine
Glycogen Storage Disease of Skeletal Muscle
Proceedings of the Association of Clinical Biochemists
Molecular Genetic Analysis and Phenotypic Characteristics of a Consanguineous Family With Glycogen Storage Disease Type Ia
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine