Publications by authors named "Michel Borg"

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Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2.
Erik Boot, Nancy J Butcher, Sean Udow, Connie Marras, Kin Y Mok, Michel Borg

Neurology· June 2018

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Anterior pallidal deep brain stimulation for Tourette's syndrome: a randomised, double-blind, controlled trial.
Marie-Laure Welter, Jean-Luc Houeto, Stéphane Thobois, Benoit Bataille, Marc Guenot, Michel Borg

Lancet Neurol· August 2017

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Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders.
Katell Peoc'h, Etienne Levavasseur, Emilien Delmont, Alfonso De Simone, Isabelle Laffont-Proust, Michel Borg

Hum Mol Genet· December 2012

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Disease severity and progression in progressive supranuclear palsy and multiple system atrophy: validation of the NNIPPS--Parkinson Plus Scale.
Christine A M Payan, François Viallet, Bernhard G Landwehrmeyer, Anne-Marie Bonnet, Michel Borg

PLoS One· December 2011

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Singular DYT6 phenotypes in association with new THAP1 frameshift mutations.
Arnaud Blanchard, Agathe Roubertie, Marion Simonetta-Moreau, Vuthy Ea, Coline Coquart, Michel Borg

Mov Disord· August 2011

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Deep brain stimulation of the ventral intermediate thalamic nucleus for severe tremor in anti-MAG neuropathy.
Caroline Bayreuther, Emilien Delmont, Michel Borg, Denys Fontaine

Mov Disord· October 2009

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Complex partial status epilepticus revealing anti-NMDA receptor encephalitis.
Caroline Bayreuther, Véronique Bourg, Jean Dellamonica, Michel Borg, Gilles Bernardin

Epileptic Disord· September 2009

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Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease.
Suzanne Lesage, Laurence Leclere, Ebba Lohmann, Michel Borg, Merle Ruberg

Neurodegener Dis· October 2007

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The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene.
Allison Brashear, William B Dobyns, Patricia de Carvalho Aguiar, Michel Borg, C J M Frijns

Brain· March 2007

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LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans.
Suzanne Lesage, Sabine Janin, Ebba Lohmann, Anne-Louise Leutenegger, Laurence Leclere, Michel Borg

Arch Neurol· March 2007

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Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa.
Pablo Ibáñez, Suzanne Lesage, Ebba Lohmann, Stéphane Thobois, Giuseppe De Michele, Michel Borg

Brain· March 2006

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Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism.
Patricia de Carvalho Aguiar, Kathleen J Sweadner, John T Penniston, Jacek Zaremba, Liu Liu, Michel Borg

Neuron· July 2004

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Effect of subthalamic nucleus stimulation on obsessive-compulsive disorder in a patient with Parkinson disease. Case report.
Denys Fontaine, Vianney Mattei, Michel Borg, Daniel von Langsdorff, Marie-Noelle Magnie

J Neurosurg· June 2004

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