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Publications by Magna Van Der Kraan

Prenatal Diagnosis of Glycogen Storage Disease Type II: Enzyme Assay or Mutation Analysis?

Pediatric Research

English

Related publications

Impaired Autophagy Contributes to Muscle Atrophy in Glycogen Storage Disease Type II Patients

Molecular Biology

English

Hepatic and Neuromuscular Forms of Glycogen Storage Disease Type IV Caused by Mutations in the Same Glycogen-Branching Enzyme Gene.

Journal of Clinical Investigation

English

Pulmonary Arterial Hypertension in Glycogen Storage Disease Type I

Journal of Inborn Errors of Metabolism and Screening

English

Orthotopic Liver Transplantation in Glycogen Storage Disease Type 1a

Journal of Inborn Errors of Metabolism and Screening

English

Markedly Elevated Serum Transaminases in Glycogen Storage Disease Type III

Journal of Pediatric Gastroenterology and Nutrition

Gastroenterology

English

Different Strategies in the Laboratory Diagnosis of Autoimmune Disease: Immunofluorescence, Enzyme-Linked Immunosorbent Assay or Both?

Annals of Clinical Biochemistry

Clinical Biochemistry

English

Chimerism After Liver Transplantation for Type IV Glycogen Storage Disease and Type 1 Gaucher's Disease

New England Journal of Medicine

English

Glycogen Storage Disease of Skeletal Muscle

Proceedings of the Association of Clinical Biochemists

English

Molecular Genetic Analysis and Phenotypic Characteristics of a Consanguineous Family With Glycogen Storage Disease Type Ia

Molecular Medicine Reports

Molecular Biology

Cancer Research

Molecular Medicine

English