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Mukopolysaccharidosen

Published:2007-12-22 Issue:1 Volume:37 Page:24-30
ISSN:0085-4530
Container-title:Der Orthopäde
language:de
Short-container-title:Orthopäde

Author:

Link B.,Miebach E.,Vetter T.,Schmitt D.,Beck M.,Meurer A.

Publisher

Springer Science and Business Media LLC

Subject

Orthopedics and Sports Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00132-007-1178-0.pdf

Reference30 articles.

1. Auclair D, Hein LK, Hopwood JJ, Byers S (2006) Intra-articular enzyme administration for joint disease in feline mucopolysaccharidosis VI: enzyme dose and interval. Pediatr Res 59: 538–543

2. Crawley AC, Niedzielski KH, Isaac EL et al. (1997) Enzyme replacement therapy from birth in feline model of mucopolysaccharidosis type VI. J Clin Invest 99: 651–662

3. Field RE, Buchanan JAF, Copplemans MJ, Aichroth PM (1994) Bone marrow transplantation in Hurler’s syndrome. J Bone Joint Surg Br 76: 975–981

4. Harmatz P, Giugliani R, Schwartz I et al. (2006) Enzyme replacement therapy for mucopolysaccharidosis VI: a phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, open-label extension study. J Pediatr 148: 33–539

5. Heisel J, Hesselschwerdt HJ (1996) Endoprothetic joint replacement in Morquio-Brailsford syndrome. Z Orthop Ihre Grenzgeb 134: 189–194

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3. Hereditary diseases;Pediatric Orthopedics in Practice;2015

4. Hereditäre Erkrankungen;Kinderorthopädie in der Praxis;2014

5. Skelettsystemerkrankungen;Orthopädie und Unfallchirurgie;2011

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