Cerebellum

Latest Articles

Article
Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48)
David Genis, Sara Ortega-Cubero, Hector San Nicolás, et al.

Neurology October 31, 2018
Resident & Fellow Section
Clinical Reasoning: Transient speech deficits in a patient with history of medulloblastoma
Jessica D. Schulte, Gunnar Hargus, Peter Canoll, et al.

Neurology September 17, 2018
Clinical/Scientific Notes
The cerebellar histiocytosisProgressive ataxia is not always a genetic disease
Igor de Assis Franco, Marcelo de Melo Aragão, Pedro Braga-Neto, et al.

Neurology July 18, 2018
Article
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration
Valentina Muto, Elisabetta Flex, Zachary Kupchinsky, et al.

Neurology June 29, 2018