Cited by

• Biochemistry and genetics of gangliosidoses.

  Sandhoff K, Christomanou H. Sandhoff K, et al. Hum Genet. 1979;50(2):107-43. doi: 10.1007/BF00390234. Hum Genet. 1979. PMID: 116955 Review.
• Generalized gangliosidosis type II (juvenile GM1 gangliosidosis). A pathological, histochemical and ultrastructural study.

  Gilbert EF, Varakis J, Opitz JM, ZuRhein GM, Ware R, Viseskul C, Kaveggia EG, Hartmann HA. Gilbert EF, et al. Z Kinderheilkd. 1975 Sep 11;120(3):151-80. doi: 10.1007/BF00439006. Z Kinderheilkd. 1975. PMID: 126533
• Diagnosis of mucopolysaccharidoses: how to avoid false positives and false negatives.

  Mahalingam K, Janani S, Priya S, Elango EM, Sundari RM. Mahalingam K, et al. Indian J Pediatr. 2004 Jan;71(1):29-32. doi: 10.1007/BF02725652. Indian J Pediatr. 2004. PMID: 14979382
• An electrophoretic variant of beta-galactosidase with altered catalytic properties in a patient with GM1 gangliosidosis.

  Norden AG, O'Brien JS. Norden AG, et al. Proc Natl Acad Sci U S A. 1975 Jan;72(1):240-4. doi: 10.1073/pnas.72.1.240. Proc Natl Acad Sci U S A. 1975. PMID: 804170 Free PMC article.
• Sustained normalization of neurological disease after intracranial gene therapy in a feline model.

  McCurdy VJ, Johnson AK, Gray-Edwards HL, Randle AN, Brunson BL, Morrison NE, Salibi N, Johnson JA, Hwang M, Beyers RJ, Leroy SG, Maitland S, Denney TS, Cox NR, Baker HJ, Sena-Esteves M, Martin DR. McCurdy VJ, et al. Sci Transl Med. 2014 Apr 9;6(231):231ra48. doi: 10.1126/scitranslmed.3007733. Sci Transl Med. 2014. PMID: 24718858 Free PMC article.