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Pain assessment and treatment in patients with mucopolysaccharidoses: a French multicentric pediatric study.

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Title: Pain assessment and treatment in patients with mucopolysaccharidoses: a French multicentric pediatric study.
Authors: Blin M; Centre de Référence Maladies Héréditaires du Métabolisme ToTeM, CHRU Tours, Tours, France., Tardieu M; Centre de Référence Maladies Héréditaires du Métabolisme ToTeM, CHRU Tours, Tours, France., Lacombe D; Inserm U1211, Université de Bordeaux, Centre de Compétences Maladies Héréditaires du Métabolisme, CHU de Bordeaux, Bordeaux, France., Gorce M; Centre de Référence Maladies Héréditaires du Métabolisme, CHU Toulouse, Toulouse, France., Damaj L; Centre de Compétences Maladies Héréditaires du Métabolisme, CHU Rennes, Rennes, France., Barth M; Centre de Compétences Maladies Héréditaires du Métabolisme, CHU Angers, Angers, France., Genevaz D; Vaincre les Maladies Lysosomales (VML), Massy, France., Vibet S; Centre d'Évaluation et de Traitement de la Douleur, CHRU Tours, Tours, France., Labarthe F; Centre de Référence Maladies Héréditaires du Métabolisme ToTeM, CHRU Tours, Tours, France. labarthe@univ-tours.fr.; N2C, Inserm U1069, Université François Rabelais de Tours, Tours, France. labarthe@univ-tours.fr.
Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2025 Nov 12; Vol. 20 (1), pp. 581. Date of Electronic Publication: 2025 Nov 12.
Publication Type: Journal Article; Multicenter Study
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Pain assessment and treatment in patients with mucopolysaccharidoses: a French multicentric pediatric study.
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  Data: <searchLink fieldCode="AU" term="%22Blin+M%22">Blin M</searchLink>; Centre de Référence Maladies Héréditaires du Métabolisme ToTeM, CHRU Tours, Tours, France.<br /><searchLink fieldCode="AU" term="%22Tardieu+M%22">Tardieu M</searchLink>; Centre de Référence Maladies Héréditaires du Métabolisme ToTeM, CHRU Tours, Tours, France.<br /><searchLink fieldCode="AU" term="%22Lacombe+D%22">Lacombe D</searchLink>; Inserm U1211, Université de Bordeaux, Centre de Compétences Maladies Héréditaires du Métabolisme, CHU de Bordeaux, Bordeaux, France.<br /><searchLink fieldCode="AU" term="%22Gorce+M%22">Gorce M</searchLink>; Centre de Référence Maladies Héréditaires du Métabolisme, CHU Toulouse, Toulouse, France.<br /><searchLink fieldCode="AU" term="%22Damaj+L%22">Damaj L</searchLink>; Centre de Compétences Maladies Héréditaires du Métabolisme, CHU Rennes, Rennes, France.<br /><searchLink fieldCode="AU" term="%22Barth+M%22">Barth M</searchLink>; Centre de Compétences Maladies Héréditaires du Métabolisme, CHU Angers, Angers, France.<br /><searchLink fieldCode="AU" term="%22Genevaz+D%22">Genevaz D</searchLink>; Vaincre les Maladies Lysosomales (VML), Massy, France.<br /><searchLink fieldCode="AU" term="%22Vibet+S%22">Vibet S</searchLink>; Centre d'Évaluation et de Traitement de la Douleur, CHRU Tours, Tours, France.<br /><searchLink fieldCode="AU" term="%22Labarthe+F%22">Labarthe F</searchLink>; Centre de Référence Maladies Héréditaires du Métabolisme ToTeM, CHRU Tours, Tours, France. labarthe@univ-tours.fr.; N2C, Inserm U1069, Université François Rabelais de Tours, Tours, France. labarthe@univ-tours.fr.
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  Data: <searchLink fieldCode="JN" term="%22101266602%22">Orphanet journal of rare diseases</searchLink> [Orphanet J Rare Dis] 2025 Nov 12; Vol. 20 (1), pp. 581. <i>Date of Electronic Publication: </i>2025 Nov 12.
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  Data: Journal Article; Multicenter Study
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101266602 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1750-1172 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217501172%22">17501172 </searchLink><i>NLM ISO Abbreviation: </i>Orphanet J Rare Dis <i>Subsets: </i>MEDLINE
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        Value: 10.1186/s13023-025-04065-9
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              Text: 2025 Nov 12
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