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	1.	[Early complications after insertion of pacemaker]. [electronic resource] by Méneret, Aurélie Rohaut, Benjamin Bachmeyer, Claude Producer: 20090619 In: Presse medicale (Paris, France : 1983) vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Chvostek sign, frequently found in healthy subjects, is not a useful clinical sign. [electronic resource] by Méneret, Aurélie Guey, Stéphanie Degos, Bertrand Producer: 20130430 In: Neurology vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Congenital mirror movements caused by a mutation in the DCC gene. [electronic resource] by Meneret, Aurelie Trouillard, Oriane Brochard, Vanessa Roze, Emmanuel Producer: 20150929 In: Developmental medicine and child neurology vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Congenital mirror movements: from piano player to opera singer. [electronic resource] by Méneret, Aurélie Welniarz, Quentin Trouillard, Oriane Roze, Emmanuel Producer: 20150430 In: Neurology vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Congenital mirror movements: no mutation in DNAL4 in 17 index cases. [electronic resource] by Méneret, Aurélie Trouillard, Oriane Vidailhet, Marie Depienne, Christel Roze, Emmanuel Producer: 20150615 In: Journal of neurology vol. 261 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Congenital mirror movements: a clue to understanding bimanual motor control. [electronic resource] by Galléa, Cécile Popa, Traian Billot, Ségolène Méneret, Aurélie Depienne, Christel Roze, Emmanuel Producer: 20120229 In: Journal of neurology vol. 258 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A serine synthesis defect presenting with a Charcot-Marie-Tooth-like polyneuropathy. [electronic resource] by Méneret, Aurélie Wiame, Elsa Marelli, Cecilia Lenglet, Timothée Van Schaftingen, Emile Sedel, Frédéric Producer: 20121119 In: Archives of neurology vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Adult-onset Generalized Dystonia as the Main Manifestation of MEGDEL Syndrome. [electronic resource] by Giron, Camille Roze, Emmanuel Degos, Bertrand Méneret, Aurélie Jardel, Claude Lannuzel, Annie Mochel, Fanny Producer: 20181123 In: Tremor and other hyperkinetic movements (New York, N.Y.) vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	ADCY5-related dyskinesia: Comments on characteristic manifestations and variant-associated severity. [electronic resource] by Raskind, Wendy H Friedman, Jennifer R Roze, Emmanuel Méneret, Aurélie Chen, Dong-Hui Bird, Thomas D Producer: 20180726 In: Movement disorders : official journal of the Movement Disorder Society vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Generalized dystonia, athetosis, and parkinsonism associated with FOXG1 mutation. [electronic resource] by Méneret, Aurélie Mignot, Cyril An, Isabelle Habert, Marie-Odile Jacquette, Aurélia Vidailhet, Marie Bienvenu, Thierry Roze, Emmanuel Producer: 20120521 In: Movement disorders : official journal of the Movement Disorder Society vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	ADCY5 mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesias. [electronic resource] by Friedman, Jennifer R Méneret, Aurélie Chen, Dong-Hui Trouillard, Oriane Vidailhet, Marie Raskind, Wendy H Roze, Emmanuel Producer: 20161021 In: Movement disorders : official journal of the Movement Disorder Society vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Congenital Mirror Movements Due to RAD51: Cosegregation with a Nonsense Mutation in a Norwegian Pedigree and Review of the Literature. [electronic resource] by Trouillard, Oriane Koht, Jeanette Gerstner, Thorsten Moland, Siri Depienne, Christel Dusart, Isabelle Méneret, Aurélie Ruiz, Marta Dubacq, Caroline Roze, Emmanuel Publication details: Tremor and other hyperkinetic movements (New York, N.Y.) 2016 In: Tremor and other hyperkinetic movements (New York, N.Y.) vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	PRRT2 mutations cause hemiplegic migraine. [electronic resource] by Riant, Florence Roze, Emmanuel Barbance, Cecile Méneret, Aurélie Guyant-Maréchal, Lucie Lucas, Christian Sabouraud, Pascal Trébuchon, Agnes Depienne, Christel Tournier-Lasserve, Elisabeth Producer: 20130118 In: Neurology vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	The multiple faces of the ATP1A3-related dystonic movement disorder. [electronic resource] by Roubergue, Anne Roze, Emmanuel Vuillaumier-Barrot, Sandrine Fontenille, Marie-Joséphine Méneret, Aurélie Vidailhet, Marie Fontaine, Bertrand Doummar, Diane Philibert, Bertrand Riant, Florence Nicole, Sophie Producer: 20140509 In: Movement disorders : official journal of the Movement Disorder Society vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Abnormalities of motor function, transcription and cerebellar structure in mouse models of THAP1 dystonia. [electronic resource] by Ruiz, Marta Perez-Garcia, Georgina Ortiz-Virumbrales, Maitane Méneret, Aurelie Morant, Andrika Kottwitz, Jessica Fuchs, Tania Bonet, Justine Gonzalez-Alegre, Pedro Hof, Patrick R Ozelius, Laurie J Ehrlich, Michelle E Producer: 20160920 In: Human molecular genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midline. [electronic resource] by Welniarz, Quentin Morel, Marie-Pierre Pourchet, Oriane Gallea, Cécile Lamy, Jean-Charles Cincotta, Massimo Doulazmi, Mohamed Belle, Morgane Méneret, Aurélie Trouillard, Oriane Ruiz, Marta Brochard, Vanessa Meunier, Sabine Trembleau, Alain Vidailhet, Marie Chédotal, Alain Dusart, Isabelle Roze, Emmanuel Producer: 20180828 In: Scientific reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Miming neurological syndromes improves medical student's long-term retention and delayed recall of neurology. [electronic resource] by Roze, Emmanuel Worbe, Yulia Louapre, Céline Méneret, Aurélie Delorme, Cécile McGovern, Eavan Ruiz, Marta Capron, Jean Le Bouc, Raphaël Epelbaum, Stéphane Alamowitch, Sonia Duguet, Alexandre Renaud, Marie-Christine Palombi, Olivier Pringsheim, Tamara M Flamand-Roze, Constance Steichen, Olivier Producer: 20190627 In: Journal of the neurological sciences vol. 391 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European population. [electronic resource] by Méneret, Aurélie Grabli, David Depienne, Christel Gaudebout, Cécile Picard, Fabienne Dürr, Alexandra Lagroua, Isabelle Bouteiller, Delphine Mignot, Cyril Doummar, Diane Anheim, Mathieu Tranchant, Christine Burbaud, Pierre Jedynak, Charles Pierre Gras, Domitille Steschenko, Dominique Devos, David Billette de Villemeur, Thierry Vidailhet, Marie Brice, Alexis Roze, Emmanuel Producer: 20121004 In: Neurology vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	RAD51 deficiency disrupts the corticospinal lateralization of motor control. [electronic resource] by Gallea, Cécile Popa, Traian Hubsch, Cécile Valabregue, Romain Brochard, Vanessa Kundu, Prantik Schmitt, Benoît Bardinet, Eric Bertasi, Eric Flamand-Roze, Constance Alexandre, Nicolas Delmaire, Christine Méneret, Aurélie Depienne, Christel Poupon, Cyril Hertz-Pannier, Lucie Cincotta, Massimo Vidailhet, Marie Lehericy, Stéphane Meunier, Sabine Roze, Emmanuel Producer: 20131231 In: Brain : a journal of neurology vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	The pleiotropic movement disorders phenotype of adult ataxia-telangiectasia. [electronic resource] by Méneret, Aurélie Ahmar-Beaugendre, Yara Rieunier, Guillaume Mahlaoui, Nizar Gaymard, Bertrand Apartis, Emmanuelle Tranchant, Christine Rivaud-Péchoux, Sophie Degos, Bertrand Benyahia, Baya Suarez, Felipe Maisonobe, Thierry Koenig, Michel Durr, Alexandra Stern, Marc-Henri Dubois d'Enghien, Catherine Fischer, Alain Vidailhet, Marie Stoppa-Lyonnet, Dominique Grabli, David Anheim, Mathieu Producer: 20141224 In: Neurology vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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