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Neurology|December 24, 2013
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopiesDavina J Hensman Moss, Mark Poulter, Jon Beck, et al.
Neurology|July 9, 2014
Structural and functional brain connectivity in presymptomatic familial frontotemporal dementiaElise G P Dopper, Serge A R B Rombouts, Lize C Jiskoot, et al.
Neurology|December 20, 2013
Higher risk of progression to dementia in mild cognitive impairment cases who revert to normalRosebud O Roberts, David S Knopman, Michelle M Mielke, et al.
Neurology|August 16, 2015
The unruptured intracranial aneurysm treatment score: a multidisciplinary consensusNima Etminan, Robert D Brown, Kerim Beseoglu, et al.
Neurology|September 4, 2015
Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathiesCatherine Labbé, Kotaro Ogaki, Oswaldo Lorenzo-Betancor, et al.
Neurology|March 11, 2016
Sex differences in comorbidity at diagnosis of multiple sclerosis: A population-based studyRuth Ann Marrie, Scott B Patten, Helen Tremlett, et al.
Neurology|March 11, 2016
Health-related quality of life in multiple sclerosis: Direct and indirect effects of comorbidityLindsay I Berrigan, John D Fisk, Scott B Patten, et al.
Neurology|February 5, 2016
Cutaneous adverse events in multiple sclerosis patients treated with daclizumabIrene Cortese, Joan Ohayon, Kaylan Fenton, et al.
Neurology|February 7, 2016
Integrated systems of stroke care and reduction in 30-day mortality: A retrospective analysisAravind Ganesh, Patrice Lindsay, Jiming Fang, et al.
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