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Found 22 publications

Disconnected Motor Intention and Spatial Attention in a Case of Probable Marchiafava-Bignami Disease.

Efficacy of virtual reality therapy in ideomotor apraxia rehabilitation: A case report.

A Homozygous Synonymous Variant Likely Cause of Severe Ciliopathy Phenotype.

Splinter haemorrhages and brain infarcts as an unusual presentation of sarcoidosis.

Heterozygous deletion in exon 6 of STEX gene causing ataxia with oculomotor apraxia type 2 (AOA-2) with ovarian failure.

Fatal insomnia: the elusive prion disease.

A molecular pathology, neurobiology, biochemical, genetic and neuroimaging study of progressive apraxia of speech.

An autopsy-proven case of Corticobasal degeneration heralded by Pontine infarction.

Posterior Cortical Atrophy phenotype in a GBA N370S mutation carrier: a case report.

New measures of agency from an adaptive sensorimotor task.

Creutzfeldt-Jakob Disease with a Five-Year Clinical Course, Multicentric Cerebellar Prion Plaques and Prior History of Biopsy-Proven Primary Angiitis of the Central Nervous System: A Case for Iatrogenic Exposure?

Complete monoplegia due to limb-kinetic apraxia in a patient with traumatic brain injury: A case report.

Showing 1-12 of 22