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11. Gm-gangliosidosis type I: in utero detection and fetal manifestations. Kaback MM, Sloan HR, Sonneborn M, Herndon RM, Percy AK. J Pediatr; 1973 Jun; 82(6):1037-41. PubMed ID: 4702895 [No Abstract] [Full Text] [Related]
12. Hexosaminidase activities in a case of systemic GM2 gangliosidosis of late infantile type. Schneck L, Friedland J, Pourfar M, Saifer A, Volk BW. Proc Soc Exp Biol Med; 1970 Mar; 133(3):997-8. PubMed ID: 5435594 [No Abstract] [Full Text] [Related]
14. Gm1-gangliosidosis and juvenile cerebral lipidosis. Clinical, histochemical, and chemical study. Patton VM, Dekaban AS. Arch Neurol; 1971 Jun; 24(6):529-37. PubMed ID: 5089899 [No Abstract] [Full Text] [Related]
15. GM1 gangliosidosis in skin fibroblast culture: enzymatic differences between types 1 and 2 and observations on a third variant. Pinsky L, Miller J, Shanfield B, Watters G, Wolfe LS. Am J Hum Genet; 1974 Sep; 26(5):563-77. PubMed ID: 4420522 [No Abstract] [Full Text] [Related]
17. Gm2-gangliosidosis with total hexosaminidase deficiency. Suzuki Y, Jacob JC, Suzuki K, Kutty KM, Suzuki K. Neurology; 1971 Apr; 21(4):313-28. PubMed ID: 4251893 [No Abstract] [Full Text] [Related]
18. Morphological, histochemical and biochemical studies on a case of systemic late infantile lipidosis (generalized gangliosidosis). Suzuki K, Chen GC. J Neuropathol Exp Neurol; 1968 Jan; 27(1):15-38. PubMed ID: 5656575 [No Abstract] [Full Text] [Related]