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Publications by D. A. Wenger
Immunological Evidence for Deficiency in an Activator Protein for Sulfatide Sulfatase in a Variant Form of Metachromatic Leukodystrophy.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Related publications
Metachromatic Leukodystrophy
Classical Case of Late-Infantile Form of Metachromatic Leukodystrophy
Journal of Neurosciences in Rural Practice
Neuroscience
Neurology
Metachromatic Leukodystrophy: Two Sides of a Coin.
BMJ
Molecular Bases of Metachromatic Leukodystrophy in Polish Patients
Journal of Human Genetics
Genetics
Deficiency of the Hexosaminidase a Activator Protein in a Case of GM2 Gangliosidosis; Variant AB
Pediatric Research
Child Health
Pediatrics
Perinatology
A Novel Mutation of the Arylsulfatase a Gene in Late-Onset Metachromatic Leukodystrophy
Journal of Clinical Psychiatry
Medicine
Psychiatry
Mental Health
Synthetic Sulfogalactosylceramide (Sulfatide) and Its Use for the Mass Spectrometric Quantitative Urinary Determination in Metachromatic Leukodystrophies
Glycoconjugate Journal
Biochemistry
Cell Biology
Molecular Biology
Induction of Tolerance to Human Arylsulfatase a in a Mouse Model of Metachromatic Leukodystrophy
Molecular Medicine
Molecular Medicine
Genetics
Molecular Biology
880. Hematopoietic Stem Cell Gene Therapy for the Treatment of Metachromatic Leukodystrophy: Clinical Trial Design
Molecular Therapy
Molecular Medicine
Molecular Biology
Pharmacology
Medicine
Genetics
Drug Discovery
