Latest Articles
- ArticleAxon reflex–mediated vasodilation is reduced in proportion to disease severity in TTR-FAPIrène Calero-Romero, Marc R. Suter, Bernard Waeber, et al.August 03, 2018
- Clinical/Scientific NotesDe novo DNM1L mutation associated with mitochondrial epilepsy syndrome with fever sensitivityEmma Ladds, Andrea Whitney, Eszter Dombi, et al.August 03, 2018
- ArticleAssociation study between multiple system atrophy and TREM2 p.R47HKotaro Ogaki, Michael G. Heckman, Shunsuke Koga, et al.August 01, 2018
- ArticleConfirming TDP2 mutation in spinocerebellar ataxia autosomal recessive 23 (SCAR23)Guido Zagnoli-Vieira, Francesco Bruni, Kyle Thompson, et al.August 01, 2018
- EditorialThese violent repeats have violent extendsJulien Couthouis, Aaron D. GitlerAugust 01, 2018
- ArticlePopulation genealogy resource shows evidence of familial clustering for Alzheimer diseaseLisa Anne Cannon-Albright, Sue Dintelman, Tim Maness, et al.August 01, 2018
- ArticleNoncoding repeat expansions for ALS in Japan are associated with the ATXN8OS geneMakito Hirano, Makoto Samukawa, Chiharu Isono, et al.August 01, 2018
- Clinical/Scientific NotesCase of late-onset Sandhoff disease due to a novel mutation in the HEXB geneAngela R. Sung, Paolo Moretti, Aziz ShaibaniJuly 30, 2018
- ArticleASFMR1 splice variantA predictor of fragile X-associated tremor/ataxia syndromePadmaja Vittal, Shrikant Pandya, Kevin Sharp, et al.July 30, 2018
- Clinical/Scientific NotesNovel ELOVL4 mutation associated with erythrokeratodermia and spinocerebellar ataxia (SCA 34)Pierre R. Bourque, Jodi Warman-Chardon, Daniel A. Lelli, et al.July 26, 2018
Pages
Advertisement