G
Glenda Sobey
Researcher at Boston Children's Hospital
Publications - 26
Citations - 1548
Glenda Sobey is an academic researcher from Boston Children's Hospital. The author has contributed to research in topics: Ehlers–Danlos syndrome & Joint hypermobility. The author has an hindex of 11, co-authored 21 publications receiving 1001 citations. Previous affiliations of Glenda Sobey include National Health Service & University of Sheffield.
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Journal ArticleDOI
The 2017 international classification of the Ehlers-Danlos syndromes
Fransiska Malfait,Clair A. Francomano,Peter H. Byers,John W. Belmont,Britta Berglund,James H. Black,Lara Bloom,Jessica M Bowen,Angela F. Brady,Nigel Burrows,Marco Castori,Helen Cohen,Marina Colombi,Serwet Demirdas,Julie De Backer,Anne De Paepe,Sylvie Fournel-Gigleux,Michael Frank,Neeti Ghali,Cecilia Giunta,Rodney Grahame,Alan Hakim,Xavier Jeunemaitre,Diana Johnson,Birgit Juul-Kristensen,Ines Kapferer-Seebacher,Hanadi Kazkaz,Tomoki Kosho,Mark E. Lavallee,Howard P. Levy,Roberto Mendoza-Londono,Melanie Pepin,F. Michael Pope,Eyal Reinstein,Leema Robert,Marianne Rohrbach,Lynn Sanders,Glenda Sobey,Tim Van Damme,Anthony Vandersteen,Caroline van Mourik,Nicol C. Voermans,Nigel Wheeldon,Johannes Zschocke,Brad T. Tinkle +44 more
TL;DR: The International EDS Consortium proposes a revised EDS classification, which recognizes 13 subtypes, and revised the clinical criteria for hypermobile EDS in order to allow for a better distinction from other joint hypermobility disorders.
Journal ArticleDOI
Ehlers-Danlos syndrome, classical type.
Jessica M Bowen,Glenda Sobey,Nigel Burrows,Marina Colombi,Mark E. Lavallee,Fransiska Malfait,Clair A. Francomano +6 more
TL;DR: The aim of this literature review is to summarize the current knowledge and highlight areas for future research in classical EDS.
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Ehlers–Danlos syndrome: how to diagnose and when to perform genetic tests
TL;DR: The genetic basis of many subtypes of Ehlers–Danlos syndrome has been elucidated, confirming heterogeneity and allowing targeted management, family screening and prenatal diagnosis.
Journal ArticleDOI
De Barsy syndrome: a review of the phenotype.
TL;DR: A female infant, the second child of first-cousin parents from a multiply consanguineous family of Pakistani origin, presented at birth with growth retardation, cutis laxa and a progeria-like appearance and has failed to thrive and has marked developmental delay and abnormal athetoid movements.
Journal ArticleDOI
Ehlers-Danlos syndromes
TL;DR: The features of the different types of EDS are discussed and how clinicians can expect their patients to be managed in secondary care are explained.