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Journal Abstract Search

137 related items for PubMed ID: 4785164

  • 1. On the molecular basis of Sandhoff's disease.
    Ropers HH, Schwantes U.
    Humangenetik; 1973; 20(2):167-70. PubMed ID: 4785164
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  • 4. [GM2 gangliosidosis with total beta-N-acetyl-hexosaminidase deficit or Sandhoff's disease].
    Juif JG, Luckel JC, Nussbaum JL, Stoebner R, Kapps R.
    Arch Fr Pediatr; 1973 Jan; 30(1):29-43. PubMed ID: 4721586
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  • 5. [Sandhoff's disease (GM2 gangliosidosis, type 2). Clinical, biochemical and anatomo-clinical study].
    Vidailhet M, Neimann N, Grignon G, Hartemann P, Philippart M, Paysant P, Nabet P, Floquet J.
    Arch Fr Pediatr; 1973 Jan; 30(1):45-60. PubMed ID: 4721587
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  • 6. [Prenatal diagnosis of Sandhoff's disease (GM2-gangliosidosis, type 2)].
    Harzer K, Stengel-Rutkowski S, Gley EO, Albert A, Murken JD, Zahn V, Henkel KP.
    Dtsch Med Wochenschr; 1975 Jan 17; 100(3):106-8. PubMed ID: 234374
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  • 7. Cardiac involvement in Sandhoff's disease. Inborn error of glycosphingolipid metabolism.
    Blieden LC, Desnick RJ, Carter JB, Krivit W, Moller JH, Sharp HL.
    Am J Cardiol; 1974 Jul 17; 34(1):83-8. PubMed ID: 4835758
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  • 9. Studies on human beta-D-N-acetylhexosaminidases. 3. Biochemical genetics of Tay-Sachs and Sandhoff's diseases.
    Srivastava SK, Beutler E.
    J Biol Chem; 1974 Apr 10; 249(7):2054-7. PubMed ID: 4206549
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  • 11. Tay-Sachs and Sandhoff's disease: intergenic complementation after somatic cell hybridization.
    Galjaard H, Hoogeveen A, de Wit-Verbeek HA, Reuser AJ, Keijzer W, Westerveld A, Bootsma D.
    Exp Cell Res; 1974 Aug 10; 87(2):444-8. PubMed ID: 4416048
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  • 16. Sandhoff's disease (GM2gangliosidosis, type 2) in a Scottish family.
    Bain AD, Tateson R, Anderson JM, Cumings JN.
    J Ment Defic Res; 1972 Jun 10; 16(2):119-27. PubMed ID: 4671982
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  • 17. Sandhoff's disease (GM 2 gangliosidosis type 2): clinical, chemical, and enzyme studies in five patients.
    Okada S, McCrea M, O'Brien JS.
    Pediatr Res; 1972 Jul 10; 6(7):606-15. PubMed ID: 5057290
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  • 18. Ceramidase deficiency in Farber's disease (lipogranulomatosis).
    Sugita M, Dulaney JT, Moser HW.
    Science; 1972 Dec 08; 178(4065):1100-2. PubMed ID: 4678225
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