Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2

OBJECTIVE: To delineate the natural history, diagnosis, and treatment response of Parkinson disease (PD) in individuals with 22q11.2 deletion syndrome (22q11.2DS), and to determine if these patients differ from those with idiopathic PD. METHODS: In this international observational study, we characte...

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Detalhes bibliográficos
Publicado no:Neurology
Main Authors: Boot, Erik, Butcher, Nancy J., Udow, Sean, Marras, Connie, Mok, Kin Y., Kaneko, Satoshi, Barrett, Matthew J., Prontera, Paolo, Berman, Brian D., Masellis, Mario, Dufournet, Boris, Nguyen, Karine, Charles, Perrine, Mutez, Eugénie, Danaila, Teodor, Jacquette, Aurélia, Colin, Olivier, Drapier, Sophie, Borg, Michel, Fiksinski, Ania M., Vergaelen, Elfi, Swillen, Ann, Vogels, Annick, Plate, Annika, Perandones, Claudia, Gasser, Thomas, Clerinx, Kristien, Bourdain, Frédéric, Mills, Kelly, Williams, Nigel M., Wood, Nicholas W., Booij, Jan, Lang, Anthony E., Bassett, Anne S.
Formato: Artigo
Idioma:Inglês
Publicado em: Lippincott Williams & Wilkins 2018
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5993183/
https://ncbi.nlm.nih.gov/pubmed/29752303
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000005660
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