Prediction of Survival With Long‐Term Disease Progression in Most Common Spinocerebellar Ataxia-Reference-Cited by-同舟云学术

Prediction of Survival With Long‐Term Disease Progression in Most Common Spinocerebellar Ataxia

Published:2019-06-18 Issue:8 Volume:34 Page:1220-1227
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord

Author:

Diallo Alhassane¹,Jacobi Heike²,Cook Arron³^ORCID,Giunti Paola³,Parkinson Michael H.³,Labrum Robyn⁴,Durr Alexandra⁵,Brice Alexis⁵,Charles Perrine⁶,Marelli Cecilia⁷,Mariotti Caterina⁸,Nanetti Lorenzo⁸,Panzeri Marta⁸,Castaldo Anna⁸,Rakowicz Maria⁹,Rola Rafal¹⁰,Sulek Anna¹¹,Schmitz‐Hübsch Tanja²¹²,Schöls Ludger¹³¹⁴,Hengel Holger¹³¹⁴,Baliko Laszlo¹⁵,Melegh Bela¹⁵¹⁶,Filla Alessandro¹⁷,Antenora Antonella¹⁷,Infante Jon¹⁸,Berciano José¹⁸,Warrenburg Bart P.¹⁹,Timmann Dagmar²⁰,Boesch Sylvia²¹,Nachbauer Wolfgang²¹,Pandolfo Massimo²²,Schulz Jörg B.²³,Bauer Peter²⁴,Jun‐Suk Kang¹⁴,Klockgether Thomas²²⁵,Tezenas du Montcel Sophie¹²⁶^ORCID

Affiliation:

1. INSERM U 1136, Sorbonne Universités, Institut Pierre Louis d'Epidémiologie et de Santé Publique, IPLESP Paris France

2. Department of NeurologyUniversity Hospital of Heidelberg, Heidelberg, and German Center for Neurodegenerative Diseases (DZNE) Bonn Germany

3. Department of Molecular NeuroscienceUCL, Institute of Neurology London United Kingdom

4. Neurogenetics LaboratoryNational Hospital of Neurology and Neurosurgery, UCLH London United Kingdom

5. Sorbonne Université, Institut du Cerveau et de la Moelle épinière (ICM), AP‐HP, Inserm, CNRS, University Hospital Pitié‐Salpêtrière Paris France

6. Service de Neurologie–CMRRCHRU Gui de Chauliac Montpellier France

7. APHP, Genetics DepartmentPitié‐Salpêtrière University Hospital Paris Paris France

8. Unit of Medical Genetics and Neurogenetics (department)Fondazione IRCCS Istituto Neurologico Carlo Besta Milan Italy

9. First Department of NeurologyInstitute of Psychiatry and Neurology Warsaw Poland

10. Department of NeurologyMilitary Institute of Aviation Medicine Warsaw Poland

11. Department of GeneticsInstitute of Psychiatry and Neurology Warsaw Poland

12. Charité‐Universitätsmedizin Berlin, NeuroCure Clinical Research CenterClinical Neuroimmunology Group Berlin Germany

13. Department of Neurodegeneration and Hertie‐Institute for Clinical Brain ResearchUniversity of Tübingen and Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE) Tübingen Germany

14. Department of NeurologyUniversity of Frankfurt Frankfurt Germany

15. Department of Medical Genetics, and Szentagothai Research CenterUniversity of Pécs Pécs Hungary

16. Department of NeurologyZala County Hospital Zalaegerszeg Hungary

17. Department of Neuroscience, and Reproductive and Odontostomatological SciencesFederico II University Naples Naples Italy

18. Service of NeurologyUniversity Hospital Marqués de Valdecilla (IDIVAL), University of Cantabria (UC) and Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED) Santander Spain

19. Department of NeurologyDonders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center Nijmegen The Netherlands

20. Department of NeurologyEssen University Hospital, University of Duisburg‐Essen Essen Germany

21. Department of NeurologyMedical University Innsbruck, Innsbruck Austria

22. Université Libre de Bruxelles (ULB)Neurology Service–ULB Hôpital Erasme, ULB Laboratory of Experimental Neurology Brussels Belgium

23. Department of NeurologyRWTH Aachen University, Aachen, Germany; JARA–Translational Brain Medicine Aachen‐Jülich Germany

24. Institute of Medical Genetics and Applied Genomics, University of Tübingen Tübingen Germany

25. Department of NeurologyUniversity Hospital of Bonn Bonn Germany

26. Assistance Publique–Hôpitaux de Paris AP‐HPHôpitaux Universitaires Pitié‐Salpêtrière–Charles Foix Paris France

Funder

Fondation pour la Recherche Médicale

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.27739

Reference23 articles.

1. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond

2. Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study

3. Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort study

4. Scale for the assessment and rating of ataxia: Development of a new clinical scale

5. Spinocerebellar ataxia types 1, 2, 3, and 6: Disease severity and nonataxia symptoms

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