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Journal of Medical Genetics|June 14, 2012
Intragenic CAMTA1 rearrangements cause non-progressive congenital ataxia with or without intellectual disabilityJulien Thevenon, Estelle Lopez, Boris Keren, et al.Journal of Alzheimer'S Disease : JAD|August 6, 2019
Causative Mutations and Genetic Risk Factors in Sporadic Early Onset Alzheimer's Disease Before 51 YearsMorgane Lacour, Olivier Quenez, Anne Rovelet-Lecrux, et al.Alzheimer'S Research & Therapy|May 11, 2023
Phenotype and imaging features associated with APP duplicationsLou Grangeon, Camille Charbonnier, Aline Zarea, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 6, 2017
Consensus classification of posterior cortical atrophySebastian J Crutch, Jonathan M Schott, Gil D Rabinovici, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 20, 2016
Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's diseaseJonathan M Schott, Sebastian J Crutch, Minerva M Carrasquillo, et al.Nature Communications|October 31, 2019
Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3Rahel T Florian, Florian Kraft, Elsa Leitão, et al.Brain : a Journal of Neurology|December 21, 2014
Adult-onset genetic leukoencephalopathies: a MRI pattern-based approach in a comprehensive study of 154 patientsXavier Ayrignac, Clarisse Carra-Dalliere, Nicolas Menjot de Champfleur, et al.Neurology|June 20, 2024
Cerebral Amyloid Angiopathy-Related Inflammation and Biopsy-Positive Primary Angiitis of the CNS: A Comparative StudyLou Grangeon, Grégoire Boulouis, Jean Capron, et al.Annals of Neurology|September 27, 2018
Prevalence of amyloid-β pathology in distinct variants of primary progressive aphasiaDavid Bergeron, Maria L Gorno-Tempini, Gil D Rabinovici, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 28, 2024
Assessment of Mendelian and risk-factor genes in Alzheimer disease: A prospective nationwide clinical utility study and recommendations for genetic screeningGaël Nicolas, Aline Zaréa, Morgane Lacour, et al.Pageof 8