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4. The biochemistry of sphingolipid storage diseases. Sandhoff K. Angew Chem Int Ed Engl; 1977 May; 16(5):273-85. PubMed ID: 406814 [No Abstract] [Full Text] [Related]
7. The liver in lipid storage disease: biochemical basis of pathogenesis and clinical features. Brady RO, James SP, Barranger JA. Prog Liver Dis; 1982 May; 7():331-46. PubMed ID: 6810410 [No Abstract] [Full Text] [Related]
8. Basic findings and current developments in sphingolipidoses. Pilz H, Heipertz R, Seidel D. Hum Genet; 1979 Mar 12; 47(2):113-34. PubMed ID: 108196 [Abstract] [Full Text] [Related]
9. [Diagnosis of lysosomal storage diseases using ultrastructural studies and biopsies of the conjunctiva]. Libert J, Danis P. Bull Mem Soc Fr Ophtalmol; 1981 Mar 12; 93():144-50. PubMed ID: 6809088 [No Abstract] [Full Text] [Related]
10. [Enzymes of glycolipid metabolism and their role in the development of glycolipidoses]. Mkheian EE. Vestn Akad Med Nauk SSSR; 1983 Mar 12; (4):71-7. PubMed ID: 6306946 [No Abstract] [Full Text] [Related]
11. Patterns of complex carbohydrate storage in four lysosomal storage diseases: fucosidosis, GM1-gangliosidosis, GM2-gangliosidosis (Sandhoff variant) and mannosidosis. Dawson G, Chen Tsay G. Biochem Exp Biol; 1977 Mar 12; 13(1):15-25. PubMed ID: 418790 [No Abstract] [Full Text] [Related]