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	1.	Psychosis, short stature in benign hereditary chorea: a novel thyroid transcription factor-1 mutation. [electronic resource] by Glik, Amir Vuillaume, Isabelle Devos, David Inzelberg, Rivka Producer: 20090408 In: Movement disorders : official journal of the Movement Disorder Society vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Mutation analysis and association studies of the ubiquitin carboxy-terminal hydrolase L1 gene in Huntington's disease. [electronic resource] by Nazé, Peggy Vuillaume, Isabelle Destée, Alain Pasquier, Florence Sablonnière, Bernard Producer: 20021028 In: Neuroscience letters vol. 328 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Quintuplets after a transfer of two embryos following in vitro fertilization: a proved superfecundation. [electronic resource] by Peigné, Maëliss Andrieux, Joris Deruelle, Philippe Vuillaume, Isabelle Leroy, Maryse Producer: 20110621 In: Fertility and sterility vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation. [electronic resource] by Devos, David Tchofo, P Jissendi Vuillaume, Isabelle Destée, Alain Batey, Stephanie Burn, John Chinnery, Patrick F Producer: 20090630 In: Brain : a journal of neurology vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Pneumatic transport is critical for leukaemic patients with major leukocytosis: what precautions to measure lactate dehydrogenase, potassium and aspartate aminotransferase? [electronic resource] by Guiheneuf, Raphael Vuillaume, Isabelle Mangalaboyi, Jacques Launay, David Berthon, Céline Maury, J-Claude Maboudou, Patrice Rousseaux, Jean Producer: 20100305 In: Annals of clinical biochemistry vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Thickening of peripapillar retinal fibers for the diagnosis of autosomal recessive spastic ataxia of Charlevoix-Saguenay. [electronic resource] by Desserre, Jeremy Devos, David Sautière, Bruno Georges Debruyne, Philippe Santorelli, Filippo M Vuillaume, Isabelle Defoort-Dhellemmes, Sabine Producer: 20120813 In: Cerebellum (London, England) vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Attenuated presentation of ataxia-telangiectasia with familial cancer history. [electronic resource] by Simonin, Clémence Devos, David Vuillaume, Isabelle de Martinville, Bérengère Sablonnière, Bernard Destée, Alain Stoppa-Lyonnet, Dominique Defebvre, Luc Producer: 20090414 In: Journal of neurology vol. 255 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Spinocerebellar ataxia: a rational approach to aetiological diagnosis. [electronic resource] by Degardin, Adrian Dobbelaere, Dries Vuillaume, Isabelle Defoort-Dhellemmes, Sabine Hurtevent, Jean-François Sablonnière, Bernard Destée, Alain Defebvre, Luc Devos, David Producer: 20121204 In: Cerebellum (London, England) vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	[Hemolysis interferences on frequently required stat analysis: a French multicentric study]. [electronic resource] by Poupon, Carole Lefèvre, Guillaume Ngo-François, Sandrine Alibeu, Catherine Barbé, Françoise Bourbonneux, Valery Cartier, Régine Morin, Christine Szymanowicz, Anton Vuillaume, Isabelle Producer: 20160926 In: Annales de biologie clinique vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Gentle blood aspiration and tube cushioning reduce pneumatic tube system interference in lactate dehydrogenase assays. [electronic resource] by Strubi-Vuillaume, Isabelle Carlier, Valentine Obeuf, Catherine Vasseur, Francis Maury, J-Claude Maboudou, Patrice Mangalaboyi, Jacques Durocher, Alain Launay, David Noel, Christian Brousseau, Thierry Producer: 20161028 In: Annals of clinical biochemistry vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe. [electronic resource] by Klebe, Stephan Lacour, Arnaud Durr, Alexandra Stojkovic, Tanya Depienne, Christel Forlani, Sylvie Poea-Guyon, Sandrine Vuillaume, Isabelle Sablonniere, Bernard Vermersch, Patrick Brice, Alexis Stevanin, Giovanni Producer: 20080123 In: Neurogenetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1. [electronic resource] by Vuillaume, Isabelle Devos, David Schraen-Maschke, Susanna Dina, Christian Lemainque, Arnaud Vasseur, Francis Bocquillon, Guy Devos, Patrick Kocinski, Carole Marzys, Christiane Destée, Alain Sablonnière, Bernard Producer: 20021203 In: Annals of neurology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Expanding the phenotype of SCA19/22: Parkinsonism, cognitive impairment and epilepsy. [electronic resource] by Huin, Vincent Strubi-Vuillaume, Isabelle Dujardin, Kathy Brion, Marine Delliaux, Marie Dellacherie, Delphine Cuvellier, Jean-Christophe Cuisset, Jean-Marie Riquet, Audrey Moreau, Caroline Defebvre, Luc Sablonnière, Bernard Devos, David Producer: 20180806 In: Parkinsonism & related disorders vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	New syndromic form of benign hereditary chorea is associated with a deletion of TITF-1 and PAX-9 contiguous genes. [electronic resource] by Devos, David Vuillaume, Isabelle de Becdelievre, Alix de Martinville, Berengère Dhaenens, Claire-Marie Cuvellier, Jean-Christophe Cuisset, Jean-Marie Vallée, Louis Lemaitre, Marie-Pierre Bourteel, Hélène Hachulla, Eric Wallaert, Benoit Destée, Alain Defebvre, Luc Sablonnière, Bernard Producer: 20070220 In: Movement disorders : official journal of the Movement Disorder Society vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment. [electronic resource] by Delplanque, Jérôme Devos, David Huin, Vincent Genet, Alexandre Sand, Olivier Moreau, Caroline Goizet, Cyril Charles, Perrine Anheim, Mathieu Monin, Marie Lorraine Buée, Luc Destée, Alain Grolez, Guillaume Delmaire, Christine Dujardin, Kathy Dellacherie, Delphine Brice, Alexis Stevanin, Giovanni Strubi-Vuillaume, Isabelle Dürr, Alexandra Sablonnière, Bernard Producer: 20141104 In: Brain : a journal of neurology vol. 137 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	A genetic variation in the ADORA2A gene modifies age at onset in Huntington's disease. [electronic resource] by Dhaenens, Claire-Marie Burnouf, Sylvie Simonin, Clémence Van Brussel, Edwige Duhamel, Alain Defebvre, Luc Duru, Cécile Vuillaume, Isabelle Cazeneuve, Cécile Charles, Perrine Maison, Patrick Debruxelles, Sabrina Verny, Christophe Gervais, Hélène Azulay, Jean-Philippe Tranchant, Christine Bachoud-Levi, Anne-Catherine Dürr, Alexandra Buée, Luc Krystkowiak, Pierre Sablonnière, Bernard Blum, David Producer: 20091203 In: Neurobiology of disease vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene. [electronic resource] by Gras, Domitille Jonard, Laurence Roze, Emmanuel Chantot-Bastaraud, Sandra Koht, Jeanette Motte, Jacques Rodriguez, Diana Louha, Malek Caubel, Isabelle Kemlin, Isabelle Lion-François, Laurence Goizet, Cyril Guillot, Loic Moutard, Marie-Laure Epaud, Ralph Héron, Bénédicte Charles, Perrine Tallot, Marilyn Camuzat, Agnès Durr, Alexandra Polak, Michel Devos, David Sanlaville, Damien Vuillaume, Isabelle Billette de Villemeur, Thierry Vidailhet, Marie Doummar, Diane Producer: 20121127 In: Journal of neurology, neurosurgery, and psychiatry vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Targeting chelatable iron as a therapeutic modality in Parkinson's disease. [electronic resource] by Devos, David Moreau, Caroline Devedjian, Jean Christophe Kluza, Jérome Petrault, Maud Laloux, Charlotte Jonneaux, Aurélie Ryckewaert, Gilles Garçon, Guillaume Rouaix, Nathalie Duhamel, Alain Jissendi, Patrice Dujardin, Kathy Auger, Florent Ravasi, Laura Hopes, Lucie Grolez, Guillaume Firdaus, Wance Sablonnière, Bernard Strubi-Vuillaume, Isabelle Zahr, Noel Destée, Alain Corvol, Jean-Christophe Pöltl, Dominik Leist, Marcel Rose, Christian Defebvre, Luc Marchetti, Philippe Cabantchik, Z Ioav Bordet, Régis Producer: 20150330 In: Antioxidants & redox signaling vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Singular DYT6 phenotypes in association with new THAP1 frameshift mutations. [electronic resource] by Blanchard, Arnaud Roubertie, Agathe Simonetta-Moreau, Marion Ea, Vuthy Coquart, Coline Frederic, Melissa Y Gallouedec, Gael Adenis, Jean-Paul Benatru, Isabelle Borg, Michel Burbaud, Pierre Calvas, Patrick Cif, Laura Damier, Philippe Destee, Alain Faivre, Laurence Guyant-Marechal, Lucie Janik, Piotr Janoura, Samer Kreisler, Alexandre Lusakowska, Anna Odent, Sylvie Potulska-Chromik, Anna Rudzińska, Monika Thobois, Stephane Vuillaume, Isabelle Tranchant, Christine Tuffery-Giraud, Sylvie Coubes, Philippe Sablonnière, Bernard Claustres, Mireille Collod-Béroud, Gwenaelle Producer: 20111208 In: Movement disorders : official journal of the Movement Disorder Society vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Methylphenidate for gait hypokinesia and freezing in patients with Parkinson's disease undergoing subthalamic stimulation: a multicentre, parallel, randomised, placebo-controlled trial. [electronic resource] by Moreau, Caroline Delval, Arnaud Defebvre, Luc Dujardin, Kathy Duhamel, Alain Petyt, Gregory Vuillaume, Isabelle Corvol, Jean-Christophe Brefel-Courbon, Christine Ory-Magne, Fabienne Guehl, Dominique Eusebio, Alexandre Fraix, Valérie Saulnier, Pierre-Jean Lagha-Boukbiza, Ouhaid Durif, Frank Faighel, Mirela Giordana, Caroline Drapier, Sophie Maltête, David Tranchant, Christine Houeto, Jean-Luc Debû, Bettina Sablonniere, Bernard Azulay, Jean-Philippe Tison, François Rascol, Olivier Vidailhet, Marie Destée, Alain Bloem, Bastiaan R Bordet, Régis Devos, David Producer: 20120920 In: The Lancet. Neurology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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