Latest Articles

Subject

Article
Clinical and imaging findings in Parkinson disease associated with the A53E SNCA mutation
Mika H. Martikainen, Markku Päivärinta, Marja Hietala, et al.

October 15, 2015
Article
Alzheimer risk genes modulate the relationship between plasma apoE and cortical PiB binding
Andreas Lazaris, Kristy S. Hwang, Naira Goukasian, et al.

October 15, 2015
Article
Dyslexia susceptibility genes influence brain atrophy in frontotemporal dementia
Donata Paternicó, Enrico Premi, Antonella Alberici, et al.

October 08, 2015
Clinical/Scientific Notes
Spinocerebellar ataxia type 10 in Chinese Han
Kang Wang, Karen N. McFarland, Jilin Liu, et al.

October 08, 2015
Article
Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum of SPG11
Ceren Iskender, Ece Kartal, Fulya Akcimen, et al.

October 08, 2015
Clinical/Scientific Notes
GYG1 gene mutations in a family with polyglucosan body myopathy
Marina Fanin, Annalaura Torella, Marco Savarese, et al.

September 24, 2015
Article
Isolated inclusion body myopathy caused by a multisystem proteinopathy–linked hnRNPA1 mutation
Rumiko Izumi, Hitoshi Warita, Tetsuya Niihori, et al.

September 24, 2015
The Helix
A lot of nextsNext-generation sequencing, databases, and neurologists
Stefan M. Pulst

August 20, 2015
Editorial
Next-generation sequencing still needs our generation's clinicians
A. Reghan Foley, Sandra Donkervoort, Carsten G. Bönnemann

August 13, 2015
Article
Expanding genotype/phenotype of neuromuscular diseases by comprehensive target capture/NGS
Xia Tian, Wen-Chen Liang, Yanming Feng, et al.

August 13, 2015

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