Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease

M Scarpa; Z Almassy; M Beck; OA Bodamer; IA Bruce; L de Meirleir; N Guffon; E Guillen-Navarro; P Hensman; S Jones; W Kamin; C Kampmann; C Lampe; CA Lavery; E Leao Teles; BK Link; AM Lund; G Malm; S Pitz; M Rothera; C Stewart; A Tylki-Szmanska; Ans van der Ploeg; R walker; J Zeman; JE Wraith

doi:10.1186/1750-1172-6-72

Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease

M Scarpa, Z Almassy, M Beck, OA Bodamer, IA Bruce, L de Meirleir, N Guffon, E Guillen-Navarro, P Hensman, S Jones, W Kamin, C Kampmann, C Lampe, CA Lavery, E Leao Teles, BK Link, AM Lund, G Malm, S Pitz, M RotheraC Stewart, A Tylki-Szmanska, Ans van der Ploeg, R walker, J Zeman, JE Wraith

Pediatrics

Research output: Contribution to journal › Article › Academic › peer-review

149 Citations (Scopus)

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Original language	Undefined/Unknown
Number of pages	18
Journal	Orphanet Journal of Rare Diseases
Volume	6
Issue number	72
DOIs	https://doi.org/10.1186/1750-1172-6-72
Publication status	Published - 2011

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10.1186/1750-1172-6-72

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http://hdl.handle.net/1765/34566

Cite this

Scarpa, M., Almassy, Z., Beck, M., Bodamer, OA., Bruce, IA., de Meirleir, L., Guffon, N., Guillen-Navarro, E., Hensman, P., Jones, S., Kamin, W., Kampmann, C., Lampe, C., Lavery, CA., Leao Teles, E., Link, BK., Lund, AM., Malm, G., Pitz, S., ... Wraith, JE. (2011). Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease. Orphanet Journal of Rare Diseases, 6(72). https://doi.org/10.1186/1750-1172-6-72

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Scarpa, M, Almassy, Z, Beck, M, Bodamer, OA, Bruce, IA, de Meirleir, L, Guffon, N, Guillen-Navarro, E, Hensman, P, Jones, S, Kamin, W, Kampmann, C, Lampe, C, Lavery, CA, Leao Teles, E, Link, BK, Lund, AM, Malm, G, Pitz, S, Rothera, M, Stewart, C, Tylki-Szmanska, A, van der Ploeg, A, walker, R, Zeman, J & Wraith, JE 2011, 'Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease', Orphanet Journal of Rare Diseases, vol. 6, no. 72. https://doi.org/10.1186/1750-1172-6-72

TY - JOUR

T1 - Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease

AU - Scarpa, M

AU - Almassy, Z

AU - Beck, M

AU - Bodamer, OA

AU - Bruce, IA

AU - de Meirleir, L

AU - Guffon, N

AU - Guillen-Navarro, E

AU - Hensman, P

AU - Jones, S

AU - Kamin, W

AU - Kampmann, C

AU - Lampe, C

AU - Lavery, CA

AU - Leao Teles, E

AU - Link, BK

AU - Lund, AM

AU - Malm, G

AU - Pitz, S

AU - Rothera, M

AU - Stewart, C

AU - Tylki-Szmanska, A

AU - van der Ploeg, Ans

AU - walker, R

AU - Zeman, J

AU - Wraith, JE

PY - 2011

Y1 - 2011

U2 - 10.1186/1750-1172-6-72

DO - 10.1186/1750-1172-6-72

M3 - Article

VL - 6

JO - Orphanet Journal of Rare Diseases

JF - Orphanet Journal of Rare Diseases

SN - 1750-1172

IS - 72

ER -