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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 22, 2016
The Contribution of the Corpus Callosum to Language LateralizationLeighton B N Hinkley, Elysa J Marco, Ethan G Brown, et al.
Radiology|October 21, 2014
Standardized MR terminology and reporting of implants and devices as recommended by the American College of Radiology Subcommittee on MR SafetyEmanuel Kanal, Jerry Froelich, A James Barkovich, et al.
Annals of Neurology|February 26, 2005
Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander diseaseRong Li, Anne B Johnson, Gajja Salomons, et al.
Plos One|August 8, 2012
The role of corpus callosum development in functional connectivity and cognitive processingLeighton B N Hinkley, Elysa J Marco, Anne M Findlay, et al.
Stroke|November 13, 2014
Arteriopathy diagnosis in childhood arterial ischemic stroke: results of the vascular effects of infection in pediatric stroke studyMax Wintermark, Nancy K Hills, Gabrielle A deVeber, et al.
Neurology|August 24, 2012
Peritrigonal and temporo-occipital heterotopia with corpus callosum and cerebellar dysgenesisTiziana Pisano, A James Barkovich, Richard J Leventer, et al.
Molecular Genetics and Metabolism|February 17, 2015
Disease specific therapies in leukodystrophies and leukoencephalopathiesGuy Helman, Keith Van Haren, Joshua L Bonkowsky, et al.
American Journal of Human Genetics|November 27, 2010
A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataractsGaneshwaran H Mochida, Vijay S Ganesh, Jillian M Felie, et al.
Neurology|October 1, 2013
Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humansL Benjamin Hills, Amira Masri, Kotaro Konno, et al.
Annals of Neurology|January 21, 2015
Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasiaAlissa M D'Gama, Ying Geng, Javier A Couto, et al.
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