Ambroxol for the Treatment of Patients With Parkinson Disease With and Without Glucocerebrosidase Gene Mutations

Author:

Mullin Stephen12,Smith Laura1,Lee Katherine1,D’Souza Gayle3,Woodgate Philip3,Elflein Josh3,Hällqvist Jenny4,Toffoli Marco1,Streeter Adam5,Hosking Joanne5,Heywood Wendy E.4,Khengar Rajeshree3,Campbell Philip1,Hehir Jason6,Cable Sarah1,Mills Kevin4,Zetterberg Henrik78910,Limousin Patricia1,Libri Vincenzo3,Foltynie Tom1,Schapira Anthony H. V.1

Affiliation:

1. Department of Clinical and Movement Neurosciences, University College London Institute of Neurology, London, United Kingdom

2. Institute of Translational and Stratified Medicine, University of Plymouth School of Medicine, Plymouth, United Kingdom

3. NIHR UCLH Clinical Research Facility, University College London Hospitals NHS Foundation Trust, London, United Kingdom

4. Translational Mass Spectrometry Research Group, University College London Institute of Child Health, London, United Kingdom

5. Department of Medical Statistics, University of Plymouth School of Medicine, Plymouth, United Kingdom

6. Neurogenetics Unit, National Hospital for Neurology and Neurosurgery, UCLH NHS Foundation Trust, London, United Kingdom

7. Department of Neurodegenerative Disease, University College London Institute of Neurology, London, United Kingdom

8. UK Dementia Research Institute at University College London, London, United Kingdom

9. Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Molndal, Sweden

10. Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, Sahlgrenska Academy, University of Gothenburg, Molndal, Sweden

Publisher

American Medical Association (AMA)

Subject

Clinical Neurology

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