List of works - Aurélie Méneret

'The Move', an innovative simulation-based medical education program using roleplay to teach neurological semiology: Students' and teachers' perceptions

scientific article published on 6 April 2016

A randomized, controlled, double-blind, crossover trial of triheptanoin in alternating hemiplegia of childhood

scientific article published on 2 October 2017

A randomized, controlled, double-blind, crossover trial of zonisamide in myoclonus-dystonia

scientific article published on 6 April 2016

A recent dyspnea on exertion

scientific article published on 9 June 2008

A serine synthesis defect presenting with a Charcot-Marie-Tooth-like polyneuropathy

scientific article published in July 2012

ADCY5 mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesias

scientific article

ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations.

scientific article

ADCY5-related dyskinesia: Comments on characteristic manifestations and variant-associated severity.

scientific article

Abnormalities of motor function, transcription and cerebellar structure in mouse models of THAP1 dystonia.

scientific article published on 16 September 2015

Adult-onset Generalized Dystonia as the Main Manifestation of MEGDEL Syndrome.

scientific article published on 18 April 2018

Chvostek sign, frequently found in healthy subjects, is not a useful clinical sign.

scientific article

Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein

scientific article published on 10 November 2017

Congenital Mirror Movements

scientific article

Congenital Mirror Movements Due to RAD51: Cosegregation with a Nonsense Mutation in a Norwegian Pedigree and Review of the Literature

scientific article

Congenital mirror movements caused by a mutation in the DCC gene.

scientific article

Congenital mirror movements: a clue to understanding bimanual motor control

scientific article published on 03 June 2011

Congenital mirror movements: from piano player to opera singer.

scientific article

Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases

scientific article published on 7 May 2014

Congenital mirror movements: no mutation in DNAL4 in 17 index cases

scientific article published on 19 September 2014

DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.

scientific article

First European case of Creutzfeldt-Jakob disease with a PRNP G114V mutation

scientific article published on 01 September 2018

GLUT1 deficiency syndrome: an update

scientific article

Generalized dystonia, athetosis, and parkinsonism associated with FOXG1 mutation ⬇️

scientific article published on September 23, 2011

Miming neurological syndromes improves medical student's long-term retention and delayed recall of neurology

scientific article published on 07 June 2018

Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance

scientific article

Mutations in the netrin-1 gene cause congenital mirror movements

scientific article

Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midline. ⬇️

scientific article

PRRT2 mutations and paroxysmal disorders.

scientific article published on 09 February 2013

PRRT2 mutations cause hemiplegic migraine

scientific article published on 17 October 2012

PRRT2 mutations: A major cause of paroxysmal kinesigenic dyskinesia in the European population

scientific article published on 27 June 2012

Paroxysmal movement disorders: An update.

scientific article

RAD51 deficiency disrupts the corticospinal lateralization of motor control

scientific article published on 20 September 2013

RAD51 haploinsufficiency causes congenital mirror movements in humans

scientific article published on 2 February 2012

Systematic review of movement disorders and oculomotor abnormalities in Whipple's disease

article

The multiple faces of the ATP1A3-related dystonic movement disorder.

scientific article

The pleiotropic movement disorders phenotype of adult ataxia-telangiectasia

scientific article published on 13 August 2014

[A recurrent diarrhea]

scientific article published on 24 June 2008

[Early complications after insertion of pacemaker].

scientific article published on 25 December 2008

List of works by Aurélie Méneret

'The Move', an innovative simulation-based medical education program using roleplay to teach neurological semiology: Students' and teachers' perceptions

A randomized, controlled, double-blind, crossover trial of triheptanoin in alternating hemiplegia of childhood

A randomized, controlled, double-blind, crossover trial of zonisamide in myoclonus-dystonia

A recent dyspnea on exertion

A serine synthesis defect presenting with a Charcot-Marie-Tooth-like polyneuropathy

ADCY5 mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesias

ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations.

ADCY5-related dyskinesia: Comments on characteristic manifestations and variant-associated severity.

Abnormalities of motor function, transcription and cerebellar structure in mouse models of THAP1 dystonia.

Adult-onset Generalized Dystonia as the Main Manifestation of MEGDEL Syndrome.

Chvostek sign, frequently found in healthy subjects, is not a useful clinical sign.

Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein

Congenital Mirror Movements

Congenital Mirror Movements Due to RAD51: Cosegregation with a Nonsense Mutation in a Norwegian Pedigree and Review of the Literature

Congenital mirror movements caused by a mutation in the DCC gene.

Congenital mirror movements: a clue to understanding bimanual motor control

Congenital mirror movements: from piano player to opera singer.

Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases

Congenital mirror movements: no mutation in DNAL4 in 17 index cases

DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.

First European case of Creutzfeldt-Jakob disease with a PRNP G114V mutation

GLUT1 deficiency syndrome: an update

Generalized dystonia, athetosis, and parkinsonism associated with FOXG1 mutation ⬇️

Miming neurological syndromes improves medical student's long-term retention and delayed recall of neurology

Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance

Mutations in the netrin-1 gene cause congenital mirror movements

Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midline. ⬇️

PRRT2 mutations and paroxysmal disorders.

PRRT2 mutations cause hemiplegic migraine

PRRT2 mutations: A major cause of paroxysmal kinesigenic dyskinesia in the European population

Paroxysmal movement disorders: An update.

RAD51 deficiency disrupts the corticospinal lateralization of motor control

RAD51 haploinsufficiency causes congenital mirror movements in humans

Systematic review of movement disorders and oculomotor abnormalities in Whipple's disease

The multiple faces of the ATP1A3-related dystonic movement disorder.

The pleiotropic movement disorders phenotype of adult ataxia-telangiectasia

[A recurrent diarrhea]

[Early complications after insertion of pacemaker].