Early initiation of enzyme replacement therapy improves metabolic correction in the brain tissue of aspartylglycosaminuria mice

Author:

Dunder Ulla,Valtonen Pirjo,Kelo Eira,Mononen Ilkka

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference43 articles.

1. Arvio M, Autio S, Mononen T (1997) Clinical manifestations of aspartylglycosaminuria. In: Mononen I, Aronson NN (eds) Lysosomal storage disease: aspartylglycosaminuria. R.G.Landes/Springer, Austin, pp 19–28

2. Aula P, Jalanko A, Peltonen L (2001) Aspartylglucosaminuria. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular bases of inherited disease I–VII. McGraw-Hill, New York, pp 3535–3550

3. Barton NW, Brady RO, Dambrosia JM et al (1991) Replacement therapy for inherited enzyme deficiency–macrophage-targeted glucocerebrosidase for Gaucher's disease. N Engl J Med 324:1464–1470

4. Bielicki J, Crawley AC, Davey RC, Varnai JC, Hopwood JJ (1999) Advantages of using same species enzyme for replacement therapy in a feline model of mucopolysaccharidosis type VI. J Biol Chem 274:36335–36343

5. Bijvoet AG, Van HH, Kroos MA et al (1999) Human acid alpha-glucosidase from rabbit milk has therapeutic effect in mice with glycogen storage disease type II. Hum Mol Genet 8:2145–2153

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