Mutations in the Na+/K+-ATPase α3 Gene ATP1A3 Are Associated with Rapid-Onset Dystonia Parkinsonism

Patrícia de Carvalho Aguiar, Kathleen J. Sweadner, John T. Penniston, +10

Neuron

Neurodegenerative DiseasesDegenerative DiseaseMotor DisorderNeurologyNeuroscience +4

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

Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa

Pablo Ibáñez, Suzanne Lesage, Ebba Lohmann, +6

Brain

Effect of subthalamic nucleus stimulation on obsessive—compulsive disorder in a patient with Parkinson disease

Denys Fontaine, Vianney Mattei, Michel Borg, +5

Journal of neurosurgery

Origin of the Mutations in the parkin Gene in Europe: Exon Rearrangements Are Independent Recurrent Events, whereas Point Mutations May Result from Founder Effects

Magali Periquet, Christoph B. Lücking, Jenny Vaughan, +14

The American Journal of Human Genetics

BiologyParkin GeneIndependent Recurrent EventsGenetic DisorderGenetics +9

Anterior pallidal deep brain stimulation for Tourette's syndrome: a randomised, double-blind, controlled trial

Marie‐Laure Welter, Jean‐Luc Houéto, Stéphane Thobois, +112

The Lancet Neurology

Stimulation DeviceNeuropsychologyPsychiatryMedicineMotor Control +9

Disease Severity and Progression in Progressive Supranuclear Palsy and Multiple System Atrophy: Validation of the NNIPPS – PARKINSON PLUS SCALE

C. Payán, François Viallet, G. Bernhard Landwehrmeyer, +10

PLoS ONE

Complex partial status epilepticus revealing anti‐NMDA receptor encephalitis

C. Bayreuther, Véronique Bourg, Jean Dellamonica, +3

Epileptic Disorders

Anti-nmda Receptor EncephalitisNeurological DisorderMedicineAnti-nmda Receptor AntibodiesPathology +9

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

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

Erik Boot, Nancy J. Butcher, Sean Udow, +40

Neurology