David A. Wenger, PhD

David A. Wenger, PhD

Contact Dr. Wenger

1020 Locust Street
Room 394
Philadelphia, PA 19107

(215) 955-1666
(215) 955-9554 fax

Most Recent Peer-reviewed Publications

  1. GM2 Gangliosidosis in Shiba Inu Dogs with an In-Frame Deletion in HEXB
  2. Clinical outcomes of children with abnormal newborn screening results for Krabbe disease in New York State
  3. Krabbe disease: One Hundred years from the bedside to the bench to the bedside
  4. Expression of individual mutations and haplotypes in the galactocerebrosidase gene identified by the newborn screening program in New York State and in confirmed cases of Krabbe's disease
  5. A patient with atypical multiple sulfatase deficiency
  6. Long-term improvements in lifespan and pathology in CNS and PNS after BMT plus one intravenous injection of AAVrh10-GALC in twitcher mice
  7. Enzyme replacement therapy of a novel humanized mouse model of globoid cell leukodystrophy
  8. Intravenous injection of AAVrh10-GALC after the neonatal period in twitcher mice results in significant expression in the central and peripheral nervous systems and improvement of clinical features
  9. Preclinical characterization of DUOC-01, a cell therapy product derived from banked umbilical cord blood for use as an adjuvant to umbilical cord blood transplantation for treatment of inherited metabolic diseases
  10. Reprint of: Preclinical characterization of DUOC-01, a cell therapy product derived from banked umbilical cord blood for use as an adjuvant to umbilical cord blood transplantation for treatment of inherited metabolic diseases
  11. Krabbe Disease: Globoid Cell Leukodystrophy
  12. Krabbe disease: Are certain mutations disease-causing only when specific polymorphisms are present or when inherited in trans with specific second mutations?
  13. Iminosugar-based galactoside mimics as inhibitors of galactocerebrosidase: SAR studies and comparison with other lysosomal galactosidases
  14. Lysosomal storage diseases: Heterogeneous group of disorders
  15. Sixteen novel mutations in the arylsulfatase A gene causing metachromatic leukodystrophy
  16. Sphingomyelin lipidosis (Niemann-Pick Disease) in a juvenile raccoon (Procyon lotor)
  17. GM2 Gangliosidosis (B Variant) in Two Japanese Chins: Clinical, Magnetic Resonance Imaging and Pathological Characteristics
  18. Determination of psychosine concentration in dried blood spots from newborns that were identified via newborn screening to be at risk for Krabbe disease
  19. GM2 gangliosidosis associated with a HEXA missense mutation in Japanese Chin dogs: A potential model for Tay Sachs disease
  20. Metachromatic Leukodystrophy and Globoid Cell Leukodystrophy