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Brain : a Journal of Neurology
|
March 5, 2020
Recommendations to distinguish behavioural variant frontotemporal dementia from psychiatric disorders
Simon Ducharme, Annemiek Dols, Robert Laforce, et al.
Neurology
|
July 5, 2022
Differences in Motor Features of <i>C9orf72</i>, <i>MAPT</i>, or <i>GRN</i> Variant Carriers With Familial Frontotemporal Lobar Degeneration
Philip Wade Tipton, Angela B Deutschlaender, Rodolfo Savica, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 1, 2020
Comprehensive Analysis of Familial Parkinsonism Genes in Rapid-Eye-Movement Sleep Behavior Disorder
Kheireddin Mufti, Uladzislau Rudakou, Eric Yu, et al.
Neurology
|
December 24, 2010
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers
N Finch, M M Carrasquillo, M Baker, et al.
Neurobiology of Aging
|
May 16, 2020
SMPD1 variants do not have a major role in rapid eye movement sleep behavior disorder
Uladzislau Rudakou, Naomi C Futhey, Lynne Krohn, et al.
Journal of Alzheimer'S Disease : JAD
|
November 19, 2025
Neurodevelopmental effects of genetic frontotemporal dementia mutations revealed by total intracranial volume differences
Isis So, Arabella Bouzigues, Lucy L Russell, et al.
Annals of Neurology
|
March 11, 2024
Presynaptic Dopaminergic Imaging Characterizes Patients with REM Sleep Behavior Disorder Due to Synucleinopathy
Dario Arnaldi, Pietro Mattioli, Stefano Raffa, et al.
Annals of Neurology
|
November 7, 2025
Association between Human Leukocyte Antigen Alleles and Neuropathological Outcomes in Lewy Body Disease
Marios Gavrielatos, Michael G Heckman, Alexandra I Soto-Beasley, et al.
Alzheimer'S Research & Therapy
|
March 15, 2019
Lewy Body Dementia Association's Research Centers of Excellence Program: Inaugural Meeting Proceedings
Bethany Peterson, Melissa Armstrong, Douglas Galasko, et al.
Neurobiology of Aging
|
May 29, 2014
Ataxin-2 as potential disease modifier in C9ORF72 expansion carriers
Marka van Blitterswijk, Bianca Mullen, Michael G Heckman, et al.
Page
of 96
Search research articles
Search
Showing results (841-850 of 957) with videos related to
Sort By:
Page
of 96
Brain : a Journal of Neurology
|
March 5, 2020
Recommendations to distinguish behavioural variant frontotemporal dementia from psychiatric disorders
Simon Ducharme, Annemiek Dols, Robert Laforce, et al.
Neurology
|
July 5, 2022
Differences in Motor Features of <i>C9orf72</i>, <i>MAPT</i>, or <i>GRN</i> Variant Carriers With Familial Frontotemporal Lobar Degeneration
Philip Wade Tipton, Angela B Deutschlaender, Rodolfo Savica, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 1, 2020
Comprehensive Analysis of Familial Parkinsonism Genes in Rapid-Eye-Movement Sleep Behavior Disorder
Kheireddin Mufti, Uladzislau Rudakou, Eric Yu, et al.
Neurology
|
December 24, 2010
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers
N Finch, M M Carrasquillo, M Baker, et al.
Neurobiology of Aging
|
May 16, 2020
SMPD1 variants do not have a major role in rapid eye movement sleep behavior disorder
Uladzislau Rudakou, Naomi C Futhey, Lynne Krohn, et al.
Journal of Alzheimer'S Disease : JAD
|
November 19, 2025
Neurodevelopmental effects of genetic frontotemporal dementia mutations revealed by total intracranial volume differences
Isis So, Arabella Bouzigues, Lucy L Russell, et al.
Annals of Neurology
|
March 11, 2024
Presynaptic Dopaminergic Imaging Characterizes Patients with REM Sleep Behavior Disorder Due to Synucleinopathy
Dario Arnaldi, Pietro Mattioli, Stefano Raffa, et al.
Annals of Neurology
|
November 7, 2025
Association between Human Leukocyte Antigen Alleles and Neuropathological Outcomes in Lewy Body Disease
Marios Gavrielatos, Michael G Heckman, Alexandra I Soto-Beasley, et al.
Alzheimer'S Research & Therapy
|
March 15, 2019
Lewy Body Dementia Association's Research Centers of Excellence Program: Inaugural Meeting Proceedings
Bethany Peterson, Melissa Armstrong, Douglas Galasko, et al.
Neurobiology of Aging
|
May 29, 2014
Ataxin-2 as potential disease modifier in C9ORF72 expansion carriers
Marka van Blitterswijk, Bianca Mullen, Michael G Heckman, et al.
Page
of 96