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Publications by SHINO SHIMADA
PRRT2 Mutation in a Sporadic Case of Paroxysmal Kinesigenic Dyskinesia
Juntendo Medical Journal
Related publications
A Common PRRT2 Mutation in Familial Paroxysmal Kinesigenic Dyskinesia in Hong Kong: A Case Series of 16 Patients
Hong Kong Medical Journal
Medicine
Paroxysmal Kinesigenic Dyskinesia
Intronic PRRT2 Mutation Generates Novel Splice Acceptor Site and Causes Paroxysmal Kinesigenic Dyskinesia With Infantile Convulsions (PKD/IC) in a Three Generation Family
BMC Medical Genetics
Genetics
Novel Locus for Paroxysmal Kinesigenic Dyskinesia Mapped to Chromosome 3q28-29
Scientific Reports
Multidisciplinary
Paroxysmal Kinesigenic Choreoathetosis.
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Aberrant Sensory Gating of the Primary Somatosensory Cortex Contributes to the Motor Circuit Dysfunction in Paroxysmal Kinesigenic Dyskinesia
Frontiers in Neurology
Neurology
Generalized Epilepsy-Paroxysmal Dyskinesia Syndrome
Somatic SMARCB1 Mutation in Sporadic Multiple Meningiomas: Case Report
Frontiers in Neurology
Neurology
A Novel CACNA1A Nonsense Variant in a Patient Presenting With Paroxysmal Exertion-Induced Dyskinesia
Journal of the Neurological Sciences
Neurology
