Christian Wider

Lausanne, VD, Switzerland

Last Updated: 09/26/2026

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Found 22 publications

Tuberous sclerosis: a survey in the canton of Vaud, Switzerland.

Tuberous sclerosis: a survey in the canton of Vaud, Switzerland.

Journal: Frontiers in medicine
Published: October 18, 2024

Neurology

Neurology

Journal: Revue medicale suisse
Published: March 08, 2016

Rare genetic variants support mitochondrial dysfunction in Lewy body disorders.

Rare genetic variants support mitochondrial dysfunction in Lewy body disorders.

Journal: Neurology
Published: November 13, 2015

Trajectory of a patient with deep brain stimulation (DBS)

Trajectory of a patient with deep brain stimulation (DBS)

Journal: Revue medicale suisse
Published: June 12, 2015

News in neurology 2014

News in neurology 2014

Journal: Revue medicale suisse
Published: March 25, 2015

Clinically meaningful parameters of progression and long-term outcome of Parkinson disease: An international consensus statement.

Clinically meaningful parameters of progression and long-term outcome of Parkinson disease: An international consensus statement.

Journal: Parkinsonism & related disorders
Published: December 15, 2014

p.L1612P, a novel voltage-gated sodium channel Nav1.7 mutation inducing a cold sensitive paroxysmal extreme pain disorder.

p.L1612P, a novel voltage-gated sodium channel Nav1.7 mutation inducing a cold sensitive paroxysmal extreme pain disorder.

Journal: Anesthesiology
Published: October 07, 2014

PTPN11 mutation manifesting as LEOPARD syndrome associated with hypertrophic plexi and neuropathic pain.

PTPN11 mutation manifesting as LEOPARD syndrome associated with hypertrophic plexi and neuropathic pain.

Journal: BMC neurology
Published: July 26, 2014

Hereditary diffuse leukoencephalopathy with axonal spheroids: more than just a rare disease.

Hereditary diffuse leukoencephalopathy with axonal spheroids: more than just a rare disease.

Journal: Neurology
Published: December 17, 2013

Genetics of Parkinson's disease: the yield.

Genetics of Parkinson's disease: the yield.

Journal: Parkinsonism & related disorders
Published: November 23, 2013

GNAL deletion as a probable cause of dystonia in a patient with the 18p- syndrome.

GNAL deletion as a probable cause of dystonia in a patient with the 18p- syndrome.

Journal: Parkinsonism & related disorders
Published: August 28, 2013

CSF1R mutations link POLD and HDLS as a single disease entity.

CSF1R mutations link POLD and HDLS as a single disease entity.

Journal: Neurology
Published: February 15, 2013
Showing 1-12 of 22

Last Updated: 09/26/2026