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IDGIVP+WarnockPro-Bold Type 1C WinAnsi yes yes yes 105 0 MyriadPro-SemiboldIt Type 1C Custom yes no yes 147 0 Jhove (Rel. 1.28.0, 2023-05-18) Date: 2025-02-17 17:02:16 CET RepresentationInformation: pmc_10367320.pdf ReportingModule: PDF-hul, Rel. 1.12.4 (2023-03-16) LastModified: 2025-02-13 02:31:51 CET Size: 1185114 Format: PDF Version: 1.4 Status: Well-Formed and valid SignatureMatches: PDF-hul MIMEtype: application/pdf PDFMetadata: Objects: 401 FreeObjects: 1 IncrementalUpdates: 0 DocumentCatalog: ViewerPreferences: HideToolbar: false HideMenubar: false HideWindowUI: false FitWindow: false CenterWindow: false DisplayDocTitle: false NonFullScreenPageMode: UseNone Direction: L2R ViewArea: CropBox ViewClip: CropBox PrintArea: CropBox PageClip: CropBox PageLayout: SinglePage PageMode: UseOutlines Language: en-US Outlines: Item: Title: Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participation Children: Item: Title: Abstract Children: Item: Title: Background Item: Title: Methods Item: Title: Results Item: Title: Conclusions Item: Title: Introduction Item: Title: Methods Children: Item: Title: EUROMAC registry Item: Title: Participants and data entry Item: Title: Customized questions Item: Title: Questionnaires Item: Title: Data analysis Item: Title: Results Children: Item: Title: Participants Item: Title: Work participation Item: Title: Previous and ongoing treatments Item: Title: Health care and rehabilitation Item: Title: Validated questionnaires Children: Item: Title: Quality of life Item: Title: Physical activity Item: Title: Discussion Item: Title: Conclusions Item: Title: Acknowledgements Item: Title: References Info: Title: Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participation Author: Walaa Karazi Subject: Orphanet Journal of Rare Diseases, https://doi.org/10.1186/s13023-023-02825-z Keywords: McArdle disease;Glycogen storage disease 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Scalco Mads G. Stemmerik Nicoline Løkken Alejandro Lucia Alfredo Santalla Andrea Martinuzzi Marinela Vavla Gianluigi Reni Antonio Toscano Olimpia Musumeci Carlyn V. Kouwenberg Pascal Laforêt Beatriz San Millán Irene Vieitez Gabriele Siciliano Enrico Kühnle Rebecca Trost Sabrina Sacconi Hacer Durmus Biruta Kierdaszuk Andrew Wakelin Antoni L. Andreu Tomàs Pinós Ramon Marti Ros Quinlivan John Vissing Nicol C. Voermans 10.1186/s13023-023-02825-z 2010-04-23 true springer.com springerlink.com https://doi.org/10.1186/s13023-023-02825-z 10.1186/s13023-023-02825-z 1750-1172 journal Orphanet Journal of Rare Diseases The Author(s) 2010-04-23 true 10.1186/s13023-023-02825-z noindex springer.com springerlink.com uuid:6e270392-89da-4923-9181-8930f701f47e uuid:a43f7c21-c5d6-4920-a6c1-3553c7527546 default 1 converted uuid:6e270392-89da-4923-9181-8930f701f47e converted to PDF/A-2b pdfToolbox 2023-07-25T02:15:34Z 2 B Nicol C. 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