Mucopolysaccharidosis type II (Hunter syndrome): a : clinical review and recommendations for treatment in the era of enzyme replacement therapy
- Author
- WRAITH, J. Edmond1 ; SCARPA, Maurizio2 ; BECK, Michael3 ; BODAMER, Olaf A4 ; MEIRLEIR, Linda De5 ; GUFFON, Nathalie6 ; MELDGAARD LUND, Allan7 ; MALM, Gunilla8 ; VAN DER PLOEG, Ans T9 ; ZEMAN, Jiri10
[1] Willink Biochemical Genetics Unit, Royal Manchester Children's Hospital, Hospital Road, Manchester M27 4HA, United Kingdom
[2] Centre for Rare Diseases, University of Padua, Padua, Italy
[3] Universitäts Kinderklinik, Mainz, Germany
[4] Universitäts Klinik für Kinder-und Jugendheilkunde, Vienna, Austria
[5] University Hospital VUB, Brussels, Belgium
[6] Edouard Herriott Hospital, Lyon, France
[7] Rigshospitalet, Copenhagen, Denmark
[8] Karolinska Hospital, Huddinge, Sweden
[9] Erasmus Medical Centre, Rotterdam, Netherlands
[10] Charles University, Prague, Czech Republic - Source
European journal of pediatrics. 2008, Vol 167, Num 3, pp 267-277, 11 p ; ref : 40 ref
- CODEN
- EJPEDT
- ISSN
- 0340-6199
- Scientific domain
- Genetics; Pediatrics
- Publisher
- Springer, Berlin
/
Springer, Heidelberg
- Publication country
- Germany
- Document type
- Article
- Language
- English
- Author keyword
- Hunter syndrome, Enzyme replacement therapy Idursulfase, Treatment recommendations Mucopolysaccharidosis type II
- Keyword (fr)
- Article synthèse Chimiothérapie Enzyme Enzymopathie Glucide Mucopolysaccharidose de Hunter Pédiatrie Recommandation Revue bibliographique Traitement substitutif Maladie héréditaire Maladie métabolique Pathologie du système ostéoarticulaire Traitement
- Keyword (en)
- Review Chemotherapy Enzyme Enzymopathy Carbohydrate Hunter's syndrome Pediatrics Recommendation Bibliographic review Replacement therapy Genetic disease Metabolic diseases Diseases of the osteoarticular system Treatment
- Keyword (es)
- Artículo síntesis Quimioterapia Enzima Enzimopatía Glúcido Mucopolisacaridosis Hunter Pediatría Recomendación Revista bibliográfica Tratamiento sustitutivo Enfermedad hereditaria Metabolismo patología Sistema osteoarticular patología Tratamiento
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22D Errors of metabolism / 002B22D03 Carbohydrates (enzymatic deficiencies). Glycogenosis
- Discipline
- Generalities in medical sciences Metabolic diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 20085358
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1007/s00431-007-0635-4 
https://dx.doi.org/10.1007/s00431-007-0635-4
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