A M Halliday. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdolescentAdultAgedAthetosis/geneticsAtrophy/complicationsBrain Diseases/complicationsCerebellar Ataxia/complicationsCerebrovascular Disorders/complicationsChildElectroencephalographyElectromyographyEpilepsy/complicationsEpilepsy/diagnosisFemaleFriedreich Ataxia/complicationsHumansHuntington DiseaseHypoxia, Brain/complicationsInfantLipidoses/complicationsMaleMiddle AgedMucopolysaccharidoses/complicationsMyoclonus/complicationsMyoclonus/diagnosisMyoclonus/etiologyMyoclonus/geneticsOculomotor MusclesParkinson Disease/geneticsPrognosisRetinitis Pigmentosa/complicationsSubacute Sclerosing Panencephalitis/complicationsSyndrome
Year: 1967 PMID: 4277685
Source DB: PubMed Journal: Mod Trends Neurol ISSN: 0544-6872