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26. A case of G M2 gangliosidosis of late onset. Buxton P; Cumings JN; Ellis RB; Lake BD; Mair WG; Roberts JR; Young EP J Neurol Neurosurg Psychiatry; 1972 Oct; 35(5):685-92. PubMed ID: 5084137 [TBL] [Abstract][Full Text] [Related]
28. Characterisation of human N-acetyl-beta-hexosaminidase C. Braidman I; Carroll M; Dance N; Robinson D; Poenaru L; Weber A; Dreyfus JC; Overdijk B; Hooghwinkel GJ FEBS Lett; 1974 May; 41(2):181-4. PubMed ID: 4859245 [No Abstract] [Full Text] [Related]
29. Absence of -N-acetyl-D-hexosaminidase A activity in a healthy woman. Vidgoff J; Buist NR; O'Brien JS Am J Hum Genet; 1973 Jul; 25(4):372-81. PubMed ID: 4716656 [No Abstract] [Full Text] [Related]
30. Studies on isolation and characterization of ceramide trihexosidase. Sweeley CC; Mapes CA Birth Defects Orig Artic Ser; 1973 Mar; 9(2):206-13. PubMed ID: 4373101 [No Abstract] [Full Text] [Related]
31. The N-acetyl- -D-hexosaminidases of calf and human brain. Robinson D; Jordan TW; Horsburgh T J Neurochem; 1972 Aug; 19(8):1975-85. PubMed ID: 5047858 [No Abstract] [Full Text] [Related]
32. Electrophoretic separation of -N-acetylhexosaminidases of human and bovine brain and liver and of Tay-Sachs brain tissue. Hooghwinkel GJ; Veltkamp WA; Overdijk B; Lisman JJ Hoppe Seylers Z Physiol Chem; 1972 May; 353(5):839-41. PubMed ID: 5069351 [No Abstract] [Full Text] [Related]
33. The cerebral sphingolipidoses (metachromatic leucodystrophy and infantile amaurotic idiocy) as human inborn errors of metabolism. Jatzkewitz H Biochem J; 1972 Jun; 128(1):6P. PubMed ID: 5085660 [No Abstract] [Full Text] [Related]