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5. [Peripheral nerve involvement in congenital metabolic disorders (author's transl)]. Nonaka I No To Shinkei; 1979 May; 31(5):445-54. PubMed ID: 90516 [No Abstract] [Full Text] [Related]
6. Genetic disorders of lysosomes. Hirschhorn R; Weissmann G Prog Med Genet; 1976; 1():49-101. PubMed ID: 180565 [No Abstract] [Full Text] [Related]
7. Inherited lipid storage diseases of the central nervous system. Percy AK; Shapiro LJ; Kaback MM Curr Probl Pediatr; 1979 Sep; 9(11):1-51. PubMed ID: 117977 [No Abstract] [Full Text] [Related]
8. [Diagnosis of lysosomal storage diseases using ultrastructural studies and biopsies of the conjunctiva]. Libert J; Danis P Bull Mem Soc Fr Ophtalmol; 1981; 93():144-50. PubMed ID: 6809088 [No Abstract] [Full Text] [Related]
9. The liver in lipid storage disease: biochemical basis of pathogenesis and clinical features. Brady RO; James SP; Barranger JA Prog Liver Dis; 1982; 7():331-46. PubMed ID: 6810410 [No Abstract] [Full Text] [Related]
10. [Models of enzymopathies and their role in elaborating methods of enzyme therapy (review)]. Rozenfel'd EL Vopr Med Khim; 1981; 27(1):7-18. PubMed ID: 6110281 [No Abstract] [Full Text] [Related]
11. [Pulmonary manifestations of inborn errors of metabolism]. Kamoshita S Nihon Rinsho; 1990 Mar; 48(3):608-11. PubMed ID: 2113111 [No Abstract] [Full Text] [Related]
15. 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]