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Original Article

Gangliosidosis AB

Pages 65-68 | Accepted 04 Nov 1983, Published online: 08 Jul 2009

References

  • De Baecque C. M., Suzuki K, Rapin I, et al. GM2-Gangliosidosis. AB variant: Clinico-pathological study of a case. Acta neuropath. 1975; JJ: 207–226
  • Cogan D G, Kuwabara T, Kolodny E H. A variant of Tay-Sachs disease. 22nd Concilium Ophthalmologicum. Masson, Paris 1974; Vol. 1: 700–701
  • Conzelmann E, Sandhoff K. AB variant of infantile GM2, gangliosidosis: deficiency of a factor necessary for stimulation of hexosaminidase A-catalyzed degradation of ganglioside GM2, and glycolipid GA2. Proc. nat. Acad. Sci. 1975; 75: 3979–3983
  • Goldman E, Yamanaka T, Rapin I, Adachi M, et al. AB-variant of GM2-gangliosidosis. Acta neuropath. 1980; 52: 189–202
  • Gordon B A., Pozanyi J, Geerling S, Kaufman J E, Haust M D. An unusual variant of Tay-Sachs disease. Clin. Res. 1975; 22: 740A
  • Harrell L S. Tay-Sachs disease (amaurotic familial idiocy) in a non-Jewish male: A case report. J. Amer. osteopath. Assoc. 1966; 66: 303–307
  • Hechtman P, Gordon B A, Ng Ying Kin. N. M. Deficiency of the hexosaminidase A activator protein in a case of GM2, gangliosidosis; variant AB. Pediat. Res. 1982; 76: 217–222
  • Hirabayashi Y, Li Y T, Li S. C. The protein activator specific for the enzymic hydrolysis of GM2 ganglioside in normal human brain and brains of three types of GM2, gangliosidosis. J. Neurochem. 1983; 40: 168–175
  • Kolodny E H., Wald L, Moser H W, Cogan D G, Kuwabara T. GM,-gangliosidosis without deficiency in the artificial substrate cleaving activity of hexosaminidases A and B. Abstract Amer. Acad. Neurol. Program 4/28/73. Neurology 1973; 23: 421
  • Li S C., Hirabayashi Y, Li Y T. A new variant of type-AB GM2, gangliosidosis. Biochem. Biophvs. Res. Commun. 1981; 101: 419–485
  • Lods F, Kermarec J., Duplay H, Manassero J, et al. Etude ultrastructurale de la retine dans un casdegangliosidose à GM2 sans déficit en hexosaminidase A et B. 22nd Concilium Ophihalmologicum. Masson, Paris 1974; Vol. 1: 676–680
  • O'Brien J. S. The gangliosidoses. The Metabolic Basis of Inherited Disease, J. B. Stanbury, J. B. Wyngaarden, D. S. Fredrickson, L. J. Goldstein, M. S. Brown. McGraw-Hill. 1983; 945–969, Chapt. 45
  • Pilz H, Heipertz R, Seidel D. Basic findings and current developments in sphingolipidoses. Hum. Genet. 1979; 47: 113–134
  • Sandhoff K. Variation of beta-N acetylhexosaminidase pattern in Tay-Sachs disease. FEES Letters 1969; 4: 351–354
  • Sandhoff K, Harzer K, Wässle W., Jatzkewitz H. Enzyme alterations and lipid storage in three variants of Tay-Sachs disease. J. Neurochem. 1971; 18: 2469–2489
  • Volk B W., Adachi M, Schneck L. The gangliosidoses. Human. Path. 1975; 6: 555–569

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