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	1.	Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in France. [electronic resource] by Lattante, Serena Le Ber, Isabelle Camuzat, Agnès Brice, Alexis Kabashi, Edor Producer: 20131211 In: Neurobiology of aging vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Screening UBQLN-2 in French frontotemporal lobar degeneration and frontotemporal lobar degeneration-amyotrophic lateral sclerosis patients. [electronic resource] by Lattante, Serena Le Ber, Isabelle Camuzat, Agnès Pariente, Jérémie Brice, Alexis Kabashi, Edor Producer: 20131104 In: Neurobiology of aging vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	The PSP-associated MAPT H1 subhaplotype in Guadeloupean atypical parkinsonism. [electronic resource] by Camuzat, Agnès Romana, Marc Dürr, Alexandra Feingold, Josué Brice, Alexis Ruberg, Merle Lannuzel, Annie 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)
	4.	G303V tau mutation presenting with progressive supranuclear palsy-like features. [electronic resource] by Choumert, Ariane Poisson, Alice Honnorat, Jérôme Le Ber, Isabelle Camuzat, Agnes Broussolle, Emmanuel Thobois, Stéphane Producer: 20120808 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)
	5.	Spinocerebellar ataxia type 10 in the French population. [electronic resource] by Fujigasaki, Hiroto Tardieu, Sandrine Camuzat, Agnès Stevanin, Giovanni LeGuern, Eric Matsuura, Tohru Ashizawa, Tetsuo Dürr, Alexandra Brice, Alexis Producer: 20020328 In: Annals of neurology vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy-like tauopathy. [electronic resource] by Caparros-Lefebvre, Dominique Sergeant, Nicolas Lees, Andrew Camuzat, Agnes Daniel, Susan Lannuzel, Annie Brice, Alexis Tolosa, Eduardo Delacourte, Andre Duyckaerts, Charles Producer: 20020510 In: Brain : a journal of neurology vol. 125 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	New Antibody-Free Mass Spectrometry-Based Quantification Reveals That C9ORF72 Long Protein Isoform Is Reduced in the Frontal Cortex of Hexanucleotide-Repeat Expansion Carriers. [electronic resource] by Viodé, Arthur Fournier, Clémence Camuzat, Agnès Fenaille, François Latouche, Morwena Elahi, Fanny Le Ber, Isabelle Junot, Christophe Lamari, Foudil Anquetil, Vincent Becher, François Publication details: Frontiers in neuroscience 2018 In: Frontiers in neuroscience vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes. [electronic resource] by Stevanin, Giovanni Fujigasaki, Hiroto Lebre, Anne-Sophie Camuzat, Agnes Jeannequin, Cecile Dode, Catherine Takahashi, Junko San, Chankranira Bellance, Robert Brice, Alexis Durr, Alexandra Producer: 20030916 In: Brain : a journal of neurology vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Prevalence of dentatorubral-pallidoluysian atrophy in a large series of white patients with cerebellar ataxia. [electronic resource] by Le Ber, Isabelle Camuzat, Agnès Castelnovo, Giovanni Azulay, Jean-Philippe Genton, Pierre Gastaut, Jean-Louis Broglin, Dominique Labauge, Pierre Brice, Alexis Durr, Alexandra Producer: 20030916 In: Archives of neurology vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	TREM2 mutations are rare in a French cohort of patients with frontotemporal dementia. [electronic resource] by Lattante, Serena Le Ber, Isabelle Camuzat, Agnès Dayan, Sarah Godard, Chloé Van Bortel, Inge De Septenville, Anne Ciura, Sorana Brice, Alexis Kabashi, Edor Producer: 20140325 In: Neurobiology of aging vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Genetic analysis of matrin 3 gene in French amyotrophic lateral sclerosis patients and frontotemporal lobar degeneration with amyotrophic lateral sclerosis patients. [electronic resource] by Millecamps, Stéphanie De Septenville, Anne Teyssou, Elisa Daniau, Mailys Camuzat, Agnès Albert, Mélanie LeGuern, Eric Galimberti, Daniela Brice, Alexis Marie, Yannick Le Ber, Isabelle Producer: 20151109 In: Neurobiology of aging vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions. [electronic resource] by Lattante, Serena Le Ber, Isabelle Galimberti, Daniela Serpente, Maria Rivaud-Péchoux, Sophie Camuzat, Agnès Clot, Fabienne Fenoglio, Chiara Scarpini, Elio Brice, Alexis Kabashi, Edor Producer: 20151019 In: Neurobiology of aging vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia. [electronic resource] by Dürr, Alexandra Camuzat, Agnès Colin, Emilie Tallaksen, Chantal Hannequin, Didier Coutinho, Paula Fontaine, Bertrand Rossi, Annick Gil, Roger Rousselle, Christophe Ruberg, Merle Stevanin, Giovanni Brice, Alexis Producer: 20050111 In: Archives of neurology vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulin. [electronic resource] by Caroppo, Paola Le Ber, Isabelle Camuzat, Agnès Clot, Fabienne Naccache, Lionel Lamari, Foudil De Septenville, Anne Bertrand, Anne Belliard, Serge Hannequin, Didier Colliot, Olivier Brice, Alexis Producer: 20150306 In: JAMA neurology vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Posterior cortical atrophy as an extreme phenotype of GRN mutations. [electronic resource] by Caroppo, Paola Belin, Catherine Grabli, David Maillet, Didier De Septenville, Anne Migliaccio, Raffaella Clot, Fabienne Lamari, Foudil Camuzat, Agnès Brice, Alexis Dubois, Bruno Le Ber, Isabelle Producer: 20150415 In: JAMA neurology vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Is the saitohin gene involved in neurodegenerative diseases? [electronic resource] by Verpillat, Patrice Ricard, Sylvain Hannequin, Didier Dubois, Bruno Bou, Jacqueline Camuzat, Agnès Pradier, Laurent Frebourg, Thierry Brice, Alexis Clerget-Darpoux, Françoise Deleuze, Jean-François Campion, Dominique Producer: 20021230 In: Annals of neurology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Age at onset variance analysis in spinocerebellar ataxias: a study in a Dutch-French cohort. [electronic resource] by van de Warrenburg, Bart P C Hendriks, Harrie Dürr, Alexandra van Zuijlen, Martin C A Stevanin, Giovanni Camuzat, Agnès Sinke, Richard J Brice, Alexis Kremer, Berry P H Producer: 20050520 In: Annals of neurology vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Homozygous TREM2 mutation in a family with atypical frontotemporal dementia. [electronic resource] by Le Ber, Isabelle De Septenville, Anne Guerreiro, Rita Bras, José Camuzat, Agnès Caroppo, Paola Lattante, Serena Couarch, Philippe Kabashi, Edor Bouya-Ahmed, Kawtar Dubois, Bruno Brice, Alexis Producer: 20150209 In: Neurobiology of aging vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis. [electronic resource] by Verpillat, Patrice Camuzat, Agnès Hannequin, Didier Thomas-Anterion, Catherine Puel, Michèle Belliard, Serge Dubois, Bruno Didic, Mira Lacomblez, Lucette Moreaud, Olivier Golfier, Véronique Campion, Dominique Brice, Alexis Clerget-Darpoux, Françoise Producer: 20030519 In: European journal of human genetics : EJHG vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients. [electronic resource] by Chaussenot, Annabelle Le Ber, Isabelle Ait-El-Mkadem, Samira Camuzat, Agnès de Septenville, Anne Bannwarth, Sylvie Genin, Emmanuelle C Serre, Valérie Augé, Gaëlle Brice, Alexis Pouget, Jean Paquis-Flucklinger, Véronique Producer: 20151109 In: Neurobiology of aging vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 57 results.