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8. Enzyme replacement for lysosomal diseases. Brady RO Annu Rev Med; 2006; 57():283-96. PubMed ID: 16409150 [TBL] [Abstract][Full Text] [Related]
9. Enzyme replacement in Pompe disease with an alpha-glucosidase-low density lipoprotein complex. Williams JC; Murray AK Birth Defects Orig Artic Ser; 1980; 16(1):415-23. PubMed ID: 7004520 [No Abstract] [Full Text] [Related]
10. [Macula findings in thesaurismoses]. François J Ber Zusammenkunft Dtsch Ophthalmol Ges; 1975; (73):223-65. PubMed ID: 54161 [No Abstract] [Full Text] [Related]
11. Common antigenicity for two glycosidases. Kakavanos R; Lehn P; Callebaut I; Meikle PJ; Parkinson-Lawrence EJ; Hopwood JJ; Brooks DA FEBS Lett; 2006 Jan; 580(1):87-92. PubMed ID: 16359666 [TBL] [Abstract][Full Text] [Related]
12. Human trials: direct enzyme replacement--summary and discussion. Nadler HL Birth Defects Orig Artic Ser; 1980; 16(1):425-6. PubMed ID: 7004521 [No Abstract] [Full Text] [Related]
13. [Use of the electron microscope in the diagnosis of various metabolic storage diseases]. Porfiri B; Ricci R; Riccardi A; Segni G Minerva Pediatr; 1982 Feb; 34(4):139-50. PubMed ID: 6806599 [No Abstract] [Full Text] [Related]
14. Genetic disorders of lysosomes. Hirschhorn R; Weissmann G Prog Med Genet; 1976; 1():49-101. PubMed ID: 180565 [No Abstract] [Full Text] [Related]
15. Current status of treatment in storage disorders. Nadler HL Birth Defects Orig Artic Ser; 1976; 12(6):177-88. PubMed ID: 10023 [No Abstract] [Full Text] [Related]
16. [Characteristics of biochemical disorders in hereditary enzymopathies in humans and animals]. Rozenfel'd EL Vopr Med Khim; 1982; 28(3):2-7. PubMed ID: 6125053 [No Abstract] [Full Text] [Related]