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Fabienne Clot

Showing results (1-10 of 40) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|January 2, 2009
Myoclonus-dystonia: an updateKiyoka Kinugawa, Marie Vidailhet, Fabienne Clot, et al.
Journal of Neurology|January 17, 2025
Respiratory failure as main presentation sign of MAPT-related disorderMaud Favier, Maité Formaglio, Anne Cosson, et al.
Journal of Alzheimer'S Disease : JAD|July 2, 2023
Atypical White Matter Hyperintensities Markedly Impact Plasma Neurofilament Light Chain Variability in GRN PatientsJoana Vítor, Dario Saracino, Sebastian Ströer, et al.
Journal of the Neurological Sciences|August 5, 2008
[123I]-FP-CIT and [99mTc]-HMPAO single photon emission computed tomography in a new sporadic case of rapid-onset dystonia-parkinsonismPaolo Zanotti-Fregonara, Marie Vidailhet, Aurélie Kas, et al.
Sleep|March 27, 2010
Sleep and rhythm consequences of a genetically induced loss of serotoninSmaranda Leu-Semenescu, Isabelle Arnulf, Caroline Decaix, et al.
Human Immunology|March 26, 2003
HLA types in celiac disease patients not carrying the DQA1*05-DQB1*02 (DQ2) heterodimer: results from the European Genetics Cluster on Celiac DiseaseKati Karell, Andrew S Louka, Simon J Moodie, et al.
Neurology. Genetics|December 30, 2020
Who and Why? Requests for Presymptomatic Genetic Testing for Amyotrophic Lateral Sclerosis/Frontotemporal Dementia vs Huntington DiseaseMaria Del Mar Amador, Marcela Gargiulo, Christilla Boucher, et al.
Neurobiology of Aging|August 3, 2014
Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansionsSerena Lattante, Isabelle Le Ber, Daniela Galimberti, et al.
JAMA Neurology|December 30, 2014
Posterior cortical atrophy as an extreme phenotype of GRN mutationsPaola Caroppo, Catherine Belin, David Grabli, et al.
JAMA Neurology|October 16, 2014
Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulinPaola Caroppo, Isabelle Le Ber, Agnès Camuzat, et al.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
Movement Disorders : Official Journal of the Movement Disorder Society|January 2, 2009
Myoclonus-dystonia: an updateKiyoka Kinugawa, Marie Vidailhet, Fabienne Clot, et al.
Journal of Neurology|January 17, 2025
Respiratory failure as main presentation sign of MAPT-related disorderMaud Favier, Maité Formaglio, Anne Cosson, et al.
Journal of Alzheimer'S Disease : JAD|July 2, 2023
Atypical White Matter Hyperintensities Markedly Impact Plasma Neurofilament Light Chain Variability in GRN PatientsJoana Vítor, Dario Saracino, Sebastian Ströer, et al.
Journal of the Neurological Sciences|August 5, 2008
[123I]-FP-CIT and [99mTc]-HMPAO single photon emission computed tomography in a new sporadic case of rapid-onset dystonia-parkinsonismPaolo Zanotti-Fregonara, Marie Vidailhet, Aurélie Kas, et al.
Sleep|March 27, 2010
Sleep and rhythm consequences of a genetically induced loss of serotoninSmaranda Leu-Semenescu, Isabelle Arnulf, Caroline Decaix, et al.
Human Immunology|March 26, 2003
HLA types in celiac disease patients not carrying the DQA1*05-DQB1*02 (DQ2) heterodimer: results from the European Genetics Cluster on Celiac DiseaseKati Karell, Andrew S Louka, Simon J Moodie, et al.
Neurology. Genetics|December 30, 2020
Who and Why? Requests for Presymptomatic Genetic Testing for Amyotrophic Lateral Sclerosis/Frontotemporal Dementia vs Huntington DiseaseMaria Del Mar Amador, Marcela Gargiulo, Christilla Boucher, et al.
Neurobiology of Aging|August 3, 2014
Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansionsSerena Lattante, Isabelle Le Ber, Daniela Galimberti, et al.
JAMA Neurology|December 30, 2014
Posterior cortical atrophy as an extreme phenotype of GRN mutationsPaola Caroppo, Catherine Belin, David Grabli, et al.
JAMA Neurology|October 16, 2014
Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulinPaola Caroppo, Isabelle Le Ber, Agnès Camuzat, et al.
Pageof 4