Differential (Click to cross reference) acquired immunodeficiency syndrome acquired immunodeficiency syndrome-related complex acrocyanosis Aicardi-Goutieres syndrome akathisia alcohol alcohol, neurologic complications with alien hand syndrome altered states of consciousness anemia anorexia anti basal ganglia antibodies anti IgLON5 anticholinergic drugs anxiety apraxia apraxia of eye movements apraxia, constructional astrocytoma asymptomatic ataxia athetosis atypical autoantibodies B 12 deficiency ballismus, bilateral basal ganglia basal ganglia, calcification of basal ganglia, infarction basal ganglia, lesion of basal ganglia, lesion, bilateral benign essential tremor beta adrenergic blocker blepharospasm blinking, reduced bradykinesia brain atrophy brain biopsy bruxism calcification, intracranial carbon monoxide poisoning cardiomyopathy CAT scan CAT scan, abnormal CAT scan, chest CAT scan, emission, abnormal cataracts central nervous system, infection of cerebral cortical atrophy 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dysphagia dyspraxia dystonia dystonia, children dystonia, delayed onset dystonia, face dystonia, focal dystonia, psychogenic dystonia, treatment of dystonic reaction, acute electroencephalogram electromyogram emergencies, neurologic encephalitis encephalitis lethargica encephalitis, paraneoplastic encephalitis, viral encephalopathy encephalopathy, post anoxic epileptic encephalopathy epsilon sarcoglycan gene extralimbic encephalitis face, contractions faciobrachial dystonic seizure familial feeding disorder fever frontal lobe, pathologic signs of gait disorder gamma amino butyric acid receptor antibody gaze palsy gaze palsy, supranuclear gene gene mutation genetic diagnosis, prenatal genetic neurologic disorders granuloma, pulmonary grasp reflex handedness head injury head lag head nodding headache hearing loss heart block hemiballismus hemichorea hemiparesis hepatic failure hepatolenticular degeneration(Wilson's disease) heralding manifestation human immunodeficiency virus type 1 hydrocephalus hydrocephalus, normal pressure hyperekplexia hyperpyrexia, CNS disorder causing hyperreflexia hypoglycorrhachia hypotonia hypotonia, infants hypoxia, newborn hypoxic encephalopathy imbalance immunotherapy intellectual deficit interferon alpha intestinal pseudoobstruction intracerebral hemorrhage intrauterine irritability Kayser-Fleischer ring Kearns-Sayre syndrome L-dopa Leber's hereditary optic neuropathy left handedness Leigh's disease leucine rich glioma inactivated 1 antibodies leukodystrophy leukoencephalopathy levitation Lewy body disease, diffuse liver disease lobar atrophy masked facies mediastinum, mass of medical-legal aspects of neurology MELAS syndrome memory, defect of recent memory, impairment of meningismus meningitis meningitis, fungal meningitis, syphilitic meningitis, TB MERRF syndrome microcephaly misdiagnosis mitochondrial disease mitochondrial encephalomyopathy molecular genetics mortality movement disorder movement disorder, delayed onset movement 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Showing articles 850 to 863 of 863 << Previous Startle Disease or Hyperkplexia Pathological Surprise Reaction J Neurol Sci 5:523, Villeneuve,A.,et al, 1967 Diseases of Muscles-Clinical Manifestations & Differential Diagnosis The New Physic 263, 1967, Oct., Boshes,L., 1967 Facial Myokymia JNNP 29:35, Mathews,W.B., 1966 Orthopaedic Aspects of Intraspinal Tumors in Infants & Children J Bone & Joint Surg 47A:223965., Tachdjian,M.&Matson,D., 1965 Hyperkplexia"Jumping Frenchman of Maine" Arch Neurol 12:311, Stevens,H., 1965 The Neurological Sequelae of Electrical Injury Can Med Assn J 91:195, Silversides,J., 1964 Syndrome of Intention of Action Myoclonus as a Sequel to Hypoxic Encephalopathy Brain 86:111, Lance,J.,et al, 1963 Neuro CPC of MGH Metachromatic Leukodystrophy, NEJM 267:1198-12041962., , 1962 Neuro CPC of MGH Jacob-Creutzfeldt Disease, NEJM 264:1359-13641961., , 1961 Diseases of the Basal Ganglia-Their Relation to Disorders of Movement Lancet 1099, 1960, Nov., Denny-Brown,D., 1960 Clinical Picture in Creutzfeldt-Jakob Disease Trans of Amer Neuro Assn 5:l47, Fisher,C.M., 1960 Neuro CPC of MGH Cerebral Infarcts Due to Paradoxical Emboli, NEJM 258:338-3451958., , 1958 Neuro CPC of MGH Meningeal Gliomatosis, NEJM 259:688-6931958., , 1958 Neurologic Manifestations of Chronic Pulmonary Insufficiency NEJM 257:579-590, Austen,F.K.,et al, 1957 Showing articles 850 to 863 of 863 << Previous