A Randomized Trial of Deep-Brain Stimulation for Parkinson's Disease

Günther Deuschl, Carmen Schade‐Brittinger, Paul Krack, +35

New England Journal of Medicine

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

Suzanne Lesage, Valérie Drouet, Elisa Majounie, +212

The American Journal of Human Genetics

Cell AutophagyMitophagyMitochondrial FunctionGeneticsAutophagy +5

Dermal phospho-alpha-synuclein deposits confirm REM sleep behaviour disorder as prodromal Parkinson’s disease

Kathrin Doppler, Hanna-Maria Jentschke, Lena Schulmeyer, +13

Acta Neuropathologica

Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers

Niccolò E. Mencacci, Ioannis U. Isaias, Martin M. Reich, +42

Brain

Distinctive distribution of phospho‐alpha‐synuclein in dermal nerves in multiple system atrophy

Kathrin Doppler, Jessica Weis, Katharina Karl, +6

Movement Disorders

Force overflow and levodopa‐induced dyskinesias in Parkinson’s disease

Roland Wenzelburger, Baorong Zhang, S. Pohle, +6

Brain

High nigral iron deposition in LRRK2 and Parkin mutation carriers using R2* relaxometry

Nadya Pyatigorskaya, Michael Sharman, Jean‐Christophe Corvol, +9

Movement Disorders

Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1

Alleene V. Strickland, Maria Schabhüttl, H. Offenbacher, +17

Journal of Neurology

Genome InstabilityEngineeringSomatic VariantGenetic DisorderMedicine +6

Identification of <i>VPS35</i> mutations replicated in French families with Parkinson disease

Suzanne Lesage, Christel Condroyer, Sonja Klebe, +28

Neurology

GeneticsMolecular BiologyDisease Gene IdentificationGenetic DisordersGenetic Medicine +19

<i>LINGO1</i> polymorphisms are associated with essential tremor in Europeans

Sandra Thier, Delia Lorenz, Michael Nothnagel, +7

Movement Disorders