Results 281 to 285 of about 600,045 (285)

Large-scale mitochondrial DNA deletion underlying familial multiple system atrophy of the cerebellar subtype

Clinical Case Reports (discontinued), 2016
Abdulaziz Alsemari
exaly  

Morphological changes of cerebellar substructures in temporal lobe epilepsy: A complex phenomenon, not mere atrophy.

Seizure, 2018
V. Marcián, R. Mareček, E. Koriťáková, M. Pail, M. Bareš, M. Brázdil   +5 more
semanticscholar   +1 more source

Subacute cerebellar ataxia and atrophy developed in a young woman with systemic lupus erythematosus whose cerebrospinal fluid was positive for antineuronal cell antibody

Lupus, 2012
Keishi Fujio, Yukiko Iwasaki, Hirofumi Shoda   +2 more
exaly  

De novo KIF1A mutations cause intellectual deficit, cerebellar atrophy, lower limb spasticity and visual disturbance

Journal of Human Genetics, 2015
Chihiro Ohba, K. Haginoya, H. Osaka, K. Kubota, A. Ishiyama, Takuya Hiraide, H. Komaki, M. Sasaki, S. Miyatake, M. Nakashima, Y. Tsurusaki, N. Miyake, F. Tanaka, H. Saitsu, N. Matsumoto   +14 more
semanticscholar   +1 more source

The role of CYP2C9 polymorphisms in phenytoin-related cerebellar atrophy

Seizure: the Journal of the British Epilepsy Association, 2013
Luciano de Paola, Rosana Herminia Scola, Carlos Silvado   +2 more
exaly