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27 in total

Review 1. New biotechnological and nanomedicine strategies for treatment of lysosomal storage disorders.

Authors: Silvia Muro
Journal: Wiley Interdiscip Rev Nanomed Nanobiotechnol Date: 2010 Mar-Apr

Review 2. Enzyme-replacement therapy: problems and prospects.

Authors: B Rademaker; J Raber
Journal: Pharm Weekbl Sci Date: 1989-10-20

3. Strategies for delivery of therapeutics into the central nervous system for treatment of lysosomal storage disorders.

Authors: Silvia Muro
Journal: Drug Deliv Transl Res Date: 2012-06-01 Impact factor: 4.617

4. The mucopolysaccharidoses.

Authors: C A Pennock; I C Barnes
Journal: J Med Genet Date: 1976-06 Impact factor: 6.318

5. Regional assignment of the structural gene for human alpha-L-iduronidase.

Authors: E H Schuchman; K H Astrin; P Aula; R J Desnick
Journal: Proc Natl Acad Sci U S A Date: 1984-02 Impact factor: 11.205

6. Enzyme replacement in a canine model of Hurler syndrome.

Authors: R M Shull; E D Kakkis; M F McEntee; S A Kania; A J Jonas; E F Neufeld
Journal: Proc Natl Acad Sci U S A Date: 1994-12-20 Impact factor: 11.205

7. The disorder of hyaluronic acid metabolism in cultured skin fibroblasts derived from a patient with the Hurler syndrome.

Authors: R J Germinario; A Kahlenberg; L Pinsky
Journal: Biochem J Date: 1973-03 Impact factor: 3.857

8. The mucopolysaccharidoses: inborn errors of glycosaminoglycan catabolism.

Authors: M Cantz; J Gehler
Journal: Hum Genet Date: 1976-06-29 Impact factor: 4.132

9. Biochemical studies on the sulphated glycosaminoglycan fraction of skin fibroblasts cultured from a patient with the Hurler syndrome.

Authors: R J Germinario; A Kahlenberg; L Pinsky
Journal: Biochem J Date: 1973-03 Impact factor: 3.857

10. The defect in the Hurler and Scheie syndromes: deficiency of -L-iduronidase.

Authors: G Bach; R Friedman; B Weissmann; E F Neufeld
Journal: Proc Natl Acad Sci U S A Date: 1972-08 Impact factor: 11.205