Differential (Click to cross reference) acetazolamide amyotrophic lateral sclerosis amyotrophic lateral sclerosis, etiology of antibodies to voltage-gated calcium channels areflexia arrhythmia, cardiac ataxia ataxia, paroxysmal autoantibodies autoimmune disease autonomic dysfunction azathioprine calcium channel dysfunction carcinoma carcinoma of lung CAT scan, chest central core disease cerebellar degeneration cerebrospinal fluid, childhood children chloride channel dysfunction chromosomal abnormality ciguatera poisoning Clinical Pathologic Conference(C.P.C.) concentration, impaired confusion dementia dementia, autoimmune dementia, rapidly progressive dichlorphenamide difficulty climbing stairs diplopia electroencephalogram, abnormalities of electromyogram electromyogram, decremental response electromyogram, incremental response encephalitis, autoimmune encephalopathy epidemiology of neurology episodic neurologic deficits exercise-related muscle strength increase familial familial hemiplegic migraine fatigue gamma amino butyric acid receptor antibody gammaglobulin therapy, intravenous gene gene mutation genetic neurologic disorders hallucination headache hemiparesis hemiparesis, transient H-reflex testing hyperkalemic periodic paralysis hypokalemic periodic paralysis hyporeflexia immunologic disease immunology and the nervous system immunosuppressive agents insomnia intellectual deterioration limbic encephalitis lymphadenopathy, hilar malignancy, occult malignant hyperpyrexia memory, impairment of mexiletine migraine migraine, hemiplegic molecular genetics MRI, abnormal muscle cramp muscle diseases, characteristics of muscle strength, testing muscle weakness muscle weakness, proximal muscle weakness, sudden onset of myasthenic syndrome myasthenic syndrome, etiology myasthenic syndrome, seronegative myotonia myotonia congenita neck weakness nerve conduction studies neuroblastoma neurologic disease neurologic disease, diagnoses of neurologic signs neuromuscular disease, electrodiagnosis of neuromuscular junction, abnormality of paralysis paramyotonia congenita paraneoplastic cerebellar degeneration paroxysmal neurologic deficits periodic paralysis personality change plasmapheresis pleocytosis of cerebrospinal fluid potassium channel antibodies potassium channel dysfunction precipitating factors prognosis ptosis rapidly progressing neurologic illness remote effect of cancer on the nervous system repetitive nerve stimulation review article seizure serologic testing sodium channel dysfunction spinocerebellar ataxia spinocerebellar ataxia type 6 steroid steroid therapy, CNS treatment and complications with stop working thiazide diuretic transient neurologic deficit treatment of neurologic disorder weakness weakness, fatiguable weakness, generalized weakness, progressive weakness, proximal weight loss white matter disease xerostomia

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