Publications by authors named "Gulzar Karim"

Objective: To retrospectively report prVEPs in SPG11 ARHSP-TCC.

Background: ARHSPTCC is characterized by a thin corpus callosum, progressive spastic paraparesis, cognitive decline,and axonal neuropathy by SPG11 mutations. Additionally, seizures, cerebellar ataxia, speech and swallowing problems, extrapyramidal signs, and skeletal deformities may occur.

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