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Neurology|November 1, 2013
Can the DSM-5 framework enhance the diagnosis of MCI?Mary Ganguli
Neurology|November 1, 2013
De novo INF2 mutations expand the genetic spectrum of hereditary neuropathy with glomerulopathyInès Mademan, Tine Deconinck, Argirios Dinopoulos, et al.
Neurology|November 13, 2013
Unilateral leukonychia and hair depigmentation in multifocal motor neuropathyMartin R Turner
Neurology|November 8, 2013
Practice variability in brain death determination: a call to actionClaire N Shappell, Jeffrey I Frank, Khalil Husari, et al.
Neurology|November 8, 2013
Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutationsGerald Pfeffer, Ailbhe Burke, Patrick Yu-Wai-Man, et al.
Neurology|November 12, 2013
Nonamnestic mild cognitive impairment progresses to dementia with Lewy bodiesTanis J Ferman, Glenn E Smith, Kejal Kantarci, et al.
Neurology|November 12, 2013
Prognosis of juvenile myoclonic epilepsy 45 years after onset: seizure outcome and predictorsPhiline Senf, Bettina Schmitz, Martin Holtkamp, et al.
Neurology|October 25, 2013
Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutationsKarine Auré, Odile Dubourg, Claude Jardel, et al.
Neurology|August 6, 2013
Dose dependence of fetal malformations associated with valproateFrank J Vajda, Terence J O'Brien, Janet E Graham, et al.
Neurology|September 27, 2013
Unrecognized vitamin D3 deficiency is common in Parkinson disease: Harvard Biomarker StudyHongliu Ding, Kaltra Dhima, Kaitlin C Lockhart, et al.
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