Latest Articles

Subject

Article
Tongue atrophy and fasciculations in transthyretin familial amyloid neuropathyAn ALS mimicker
Namita A. Goyal, Tahseen Mozaffar

July 30, 2015
Article
Late-onset Alzheimer disease risk variants mark brain regulatory loci
Mariet Allen, Michaela Kachadoorian, Minerva M. Carrasquillo, et al.

July 23, 2015
Article
Epileptic spasms are a feature of DEPDC5 mTORopathy
Gemma L. Carvill, Douglas E. Crompton, Brigid M. Regan, et al.

July 23, 2015
Clinical/Scientific Notes
Posterior reversible encephalopathy syndrome is not associated with mutations in aquaporin-4
Marcelo Matiello, Rajanandini Muralidharan, David Sun, et al.

July 16, 2015
Clinical/Scientific Notes
A novel DYNC1H1 mutation causing spinal muscular atrophy with lower extremity predominance
Qi Niu, Xingxia Wang, Mingchao Shi, et al.

July 16, 2015
Article
Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 loss
Ashley P.L. Marsh, Vesna Lukic, Kate Pope, et al.

July 16, 2015
Editorial
Are migraineurs naturally born “well-hearted”?
Anne Ducros

July 02, 2015
Editor's Note
Spotlight on the June 2015 issue
Stefan M. Pulst

July 02, 2015
Article
Genetic analysis for a shared biological basis between migraine and coronary artery disease
Bendik S. Winsvold, Christopher P. Nelson, Rainer Malik, et al.

July 02, 2015
Clinical/Scientific Notes
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease
Suzanne Lesage, Jose Bras, Florence Cormier-Dequaire, et al.

June 18, 2015

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