Browsing eNauka

Browsing by Project NINDS

Showing results 1 to 8 of 8
Issue DateTitleAuthor(s)TypeМp-cat.
2012A Fluorescent, Genetically-Encoded Voltage Probe Capable of Resolving Action PotentialsBarnett, Lauren; Platisa, Jelena; Popovic, Marko; Pieribone, Vincent A; Hughes, ThomasArticle
21aM21a
2024An update on multiple system atrophyStankovic, Iva D; Kuijpers, Mechteld; Kaufmann, HoracioArticle
21aM21a
2024Developmental delay can precede neurologic regression in early onset metachromatic leukodystrophyAdang, Laura Ann; ...; Potic, Ana D; ...; (broj, koautora 48)Article
21M21
2013Genetically Targeted Optical Electrophysiology in Intact Neural CircuitsCao, G; Platisa, Jelena; Pieribone, Vincent A; Raccuglia, Davide; Kunst, Michael; Nitabach, Michael NArticle
21a+M21a+
2024Genotype-phenotype correlation in PRKN-associated Parkinson's diseaseMenon, Poornima Jayadev; ...; Jovanović, Čarna; Svetel, Marina V.  ; ...; (broj koautora 53)Article
21aM21a
2025High-density multielectrode arrays bring cellular resolution to neuronal activity and network analyses of corticospinal motor neuronsQuintanilla, Christopher A; Fitzgerald, Zachary; Kashow, Omar; Radojicic, Mihailo S; Ulupinar, Emel; Bitlis, Dila; Genc, Baris; Andjus, Pavle  ; Van, Drongelen Wim; Ozdinler, Hande PArticle
21M21
2013Intracranial vessel localization with power motion Doppler (PMD-TCD) compared with CT angiography in patients with acute ischaemic strokeBarlinn, Kristian B; Zivanovic, Zeljko D; Zhao, Limin; Kesani, Maruthi; Balucani, Clotilde; Tsivgoulis, Georgios; Alexandrov, Andrei VArticle
21M21
2012Novel PRRT2 mutation in an African-American family with paroxysmal kinesigenic dyskinesiaHedera, Peter; Xiao, Jianfeng; Puschmann, Andreas; Momcilovic, Dragana R; Wu, Steve W; LeDoux, Mark SArticle
21M21