Convergence of patient- and physician-reported outcomes in the French National Registry of Facioscapulohumeral Dystrophy.
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| Title: | Convergence of patient- and physician-reported outcomes in the French National Registry of Facioscapulohumeral Dystrophy. |
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| Authors: | Sanson, Benoît1 (AUTHOR) sanson.b@chu-nice.fr, Stalens, Caroline2 (AUTHOR), Guien, Céline3 (AUTHOR), Villa, Luisa1 (AUTHOR), Eng, Catherine2 (AUTHOR), Rabarimeriarijaona, Sitraka4 (AUTHOR), Bernard, Rafaëlle4 (AUTHOR), Cintas, Pascal5 (AUTHOR), Solé, Guilhem6 (AUTHOR), Tiffreau, Vincent7 (AUTHOR), Echaniz-Laguna, Andoni8,9,10 (AUTHOR), Magot, Armelle11 (AUTHOR), Juntas Morales, Raul12 (AUTHOR), Boyer, François Constant13 (AUTHOR), Nadaj-Pakleza, Aleksandra14,15 (AUTHOR), Jacquin-Piques, Agnès16 (AUTHOR), Béroud, Christophe3,4 (AUTHOR), Sacconi, Sabrina1,17 (AUTHOR), The French FSHD registry collaboration group (AUTHOR), Acket, Blandine (AUTHOR) |
| Source: | Orphanet Journal of Rare Diseases. 3/2/2022, Vol. 17 Issue 1, p1-12. 12p. |
| Database: | Academic Search Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 155548780 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=155548780 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-021-01793-6 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 12 StartPage: 1 Titles: – TitleFull: Convergence of patient- and physician-reported outcomes in the French National Registry of Facioscapulohumeral Dystrophy. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Sanson, Benoît – PersonEntity: Name: NameFull: Stalens, Caroline – PersonEntity: Name: NameFull: Guien, Céline – PersonEntity: Name: NameFull: Villa, Luisa – PersonEntity: Name: NameFull: Eng, Catherine – PersonEntity: Name: NameFull: Rabarimeriarijaona, Sitraka – PersonEntity: Name: NameFull: Bernard, Rafaëlle – PersonEntity: Name: NameFull: Cintas, Pascal – PersonEntity: Name: NameFull: Solé, Guilhem – PersonEntity: Name: NameFull: Tiffreau, Vincent – PersonEntity: Name: NameFull: Echaniz-Laguna, Andoni – PersonEntity: Name: NameFull: Magot, Armelle – PersonEntity: Name: NameFull: Juntas Morales, Raul – PersonEntity: Name: NameFull: Boyer, François Constant – PersonEntity: Name: NameFull: Nadaj-Pakleza, Aleksandra – PersonEntity: Name: NameFull: Jacquin-Piques, Agnès – PersonEntity: Name: NameFull: Béroud, Christophe – PersonEntity: Name: NameFull: Sacconi, Sabrina – PersonEntity: Name: NameFull: The French FSHD registry collaboration group – PersonEntity: Name: NameFull: Acket, Blandine IsPartOfRelationships: – BibEntity: Dates: – D: 02 M: 03 Text: 3/2/2022 Type: published Y: 2022 Identifiers: – Type: issn-print Value: 17501172 Numbering: – Type: volume Value: 17 – Type: issue Value: 1 Titles: – TitleFull: Orphanet Journal of Rare Diseases Type: main |
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