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2. Tay-Sachs' retina. Deficiency of acetyl hexosaminidase A. Cotlier E Arch Ophthalmol; 1971 Sep; 86(3):352-6. PubMed ID: 5095559 [No Abstract] [Full Text] [Related]
3. Separation of N-acetyl- -D-hexosaminamidase-isoenzymes from human brain and leukocytes by cellulose acetate paper electrophoresis: a simple procedure for the diagnosis of Tay-Sachs disease. Klibansky C Isr J Med Sci; 1971 Sep; 7(9):1086-9. PubMed ID: 5151274 [No Abstract] [Full Text] [Related]
4. Prenatal diagnosis of Tay-Sachs genotypes. Navon R; Padeh B Br Med J; 1971 Oct; 4(5778):17-20. PubMed ID: 5096878 [TBL] [Abstract][Full Text] [Related]
5. Enzymic differentiation between different types of Tay-Sachs disease of similar clinical appearance. Clausen J; Melchior JC; Paerregaard P Eur Neurol; 1972; 7(1):56-64. PubMed ID: 4336274 [No Abstract] [Full Text] [Related]
6. The diagnosis of Tay-Sachs disease. Ohman R; Ekelund H; Svennerholm L Acta Paediatr Scand; 1971 Jul; 60(4):399-406. PubMed ID: 5556383 [No Abstract] [Full Text] [Related]
9. Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs. Sandhoff K; Andreae U; Jatzkewitz H Pathol Eur; 1968; 3(2):278-85. PubMed ID: 5688464 [No Abstract] [Full Text] [Related]