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Annals of Neurology|February 1, 2011
Gait alterations in healthy carriers of the LRRK2 G2019S mutationAnat Mirelman, Tanya Gurevich, Nir Giladi, et al.Annals of Neurology|February 1, 2011
Ictal very low frequency oscillation in human epilepsy patientsLiankun Ren, Kiyohito Terada, Koichi Baba, et al.Annals of Neurology|February 1, 2011
Large genomic deletions: a novel cause of Ullrich congenital muscular dystrophyA Reghan Foley, Ying Hu, Yaqun Zou, et al.Annals of Neurology|September 21, 2010
Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA)Michael C Kruer, Coro Paisán-Ruiz, Nathalie Boddaert, et al.Annals of Neurology|September 25, 2010
Direct interaction between causative genes of DYT1 and DYT6 primary dystoniaSophie Gavarini, Corinne Cayrol, Tania Fuchs, et al.Annals of Neurology|September 7, 2010
Role of interleukin-1beta in postoperative cognitive dysfunctionMario Cibelli, Antonio Rei Fidalgo, Niccolò Terrando, et al.Annals of Neurology|December 15, 2010
Amantadine use associated with impulse control disorders in Parkinson disease in cross-sectional studyDaniel Weintraub, Mandy Sohr, Marc N Potenza, et al.Annals of Neurology|February 1, 1990
Age-related changes in the human nigrostriatal dopaminergic systemJ De Keyser, G Ebinger, G VauquelinAnnals of Neurology|July 1, 1978
Increased sodium plus potassium adenosine triphosphatase activity in erythrocyte membranes in Huntington's diseaseD A Butterfield, J Q Oeswein, M E Prunty, et al.Annals of Neurology|July 1, 1978
Angiotensin converting enzyme in kainic acid--injected striataE A Singh, E G McGeerPageof 982