Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2
In: Neurology 2018; 90(23):e2059-e2067, 2018
academicJournal
Zugriff:
Fil: Boot, Erik. From The Dalglish Family 22q Clinic for Adults and Department of Psychiatry; Canada. ; Fil: Butcher, Nancy J. Academic Medical Center, Amsterdam, the Netherlands; Clinical Genetics Research Program and Campbell Family Mental Health Research Institute; Canada. ; Fil: Udow, Sean. University of Toronto; Deer Lodge Movement Disorders Centre; Canada. ; Fil: Marras, Connie. Division of Neurology, Department of Medicine; Canada. ; Fil: Mok, Kin Y. Toronto Western Hospital and University of Toronto, Canada; Department of Molecular Neuroscience; Canada. ; Fil: Kaneko, Satoshi. Institute of Neurology, London, UK; Department of Neurology; Reino Unido. ; Fil: Barrett, Matthew J. Kansai Medical University, Osaka, Japan; Department of Neurology; Japón. ; Fil: Prontera, Paolo. University of Virginia School of Medicine, Charlottesville; Medical Genetics Unit; Estados Unidos. ; Fil: Berman, Brian D. Perugia University Hospital, Italy; Department of Neurology; Italia. ; Fil: Masellis, Mario. Division of Neurology, Department of Medicine; Canada. ; Fil: Dufournet, Boris. Sunnybrook Health Sciences Centre, Toronto, Canada; Departments of Clinical Neurosciences (Movement Disorders); Canada. ; Fil: Nguyen, Karine. Timone University Hospital (AP-HM), Provence-Alpes-Côte d'Azur; Aix-Marseille University ; Francia. ; Fil: Charles, Perrine. Marseille; Department of Genetics (Neurogenetics); Francia. ; Fil: Mutez, Eugénie. Pitié-Salpêtrière University Hospital; Sorbonne University (P.C., A.J.), Paris; Department of Neurosciences (Movement Disorders); Francia. ; Fil: Danaila, Teodor. Department of Neurology (Movement Disorders); Canada. ; Fil: Jacquette, Aurélia. Marseille; Department of Genetics (Neurogenetics); Francia. ; Fil: Colin, Olivier. Lyon-1 University; Department of Neurology (Movement Disorders) and Clinical Investigation Center (Clinical and Experimental Neurosciences); Francia. ; Fil: Drapier, Sophie. Poitiers University Hospital; Department of Neurology (Movement Disorders); Francia. ; Fil: Borg, Michel. ...
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Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2
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Autor/in / Beteiligte Person: | 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 |
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Zeitschrift: | Neurology 2018; 90(23):e2059-e2067, 2018 |
Veröffentlichung: | Lippincott, Williams & Wilkins, 2018 |
Medientyp: | academicJournal |
DOI: | 10.1212/WNL.0000000000005660 |
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