Differential (Click to cross reference) acetazolamide acid maltase deficiency advances in neurology adverse drug reaction airway obstruction amyotrophic lateral sclerosis amyotrophic lateral sclerosis, epidemiology of amyotrophic lateral sclerosis, familial amyotrophic lateral sclerosis, guamian type of anesthesia, general antiarrhythmic drugs antibodies to voltage-gated calcium channels anticonvulsants antihistamines arrhythmia, cardiac arthrogryposis multiplex ataxia ataxia, paroxysmal autoimmune disease baldness botulism brainstem, lesion of calcium antagonist calcium channel dysfunction carbamazepine carcinoma cardiac surgery, neurologic complications with cardiac transplantation cardiomyopathy CAT scan CAT scan, muscle cataracts central core disease central nervous system, infection of Charcot-Marie-Tooth chewing, impaired children chloride channel dysfunction chronic progressive external ophthalmoplegia clubfoot as related to neurologic disease complications congenital birth defects congenital heart disease congenital myopathy controversies in neurology corpus callosum corpus callosum, thinning creatine phosphokinase(CPK)elevated degenerative diseases of CNS differential diagnosis dilantin dropped head syndrome drug induced neurologic disorders electrocardiogram, abnormal electromyogram electron microscopy encephalopathy encephalopathy, anoxic encephalopathy, neonatal epidemiology of neurology eye closure facial appearance, abnormal facial nerve palsy facial nerve palsy, bilateral facial nerve, lesion of facial weakness facial weakness, bilateral falling familial familial hemiplegic migraine Fazio-Londe's disease floppy infant frontal balding gene mutation genetic neurologic disorders genetic testing heavy metal intoxication high arched feet high arched palate Huntington's chorea hydrocephalus hyperkalemic periodic paralysis hypokalemia hypokalemic periodic paralysis hypotonia hypotonia, causes of hypotonia, infants hypoxic encephalopathy inclusion bodies inclusion bodies, eosinophilic cytoplasmic inclusion body myositis kaliuresis Kearns-Sayre syndrome Kugelberg-Welander syndrome lid closure, weakness of lordosis malignant hyperpyrexia Melkersson's syndrome metabolic acidosis mexiletine micrognathia migraine mitochondrial disease mitochondrial encephalomyopathy molecular genetics motor neuron disease MRI MRI, abnormal MRI, muscle muscle biopsy muscle cramp muscle hypertrophy muscle pain muscle stiffness muscular dystrophy muscular dystrophy, Becker muscular dystrophy, congenital muscular dystrophy, Duchenne myasthenia gravis myoglobinuria myopathy myopathy, drug-induced myopathy, mitochondrial myotonia myotonia congenita myotonia dystrophica myotonia dystrophica, classification myotonia, treatment of neck weakness neoplasm, metastatic to CNS neoplasm, primary of CNS neurofibrillary degeneration neurologic disease, diagnoses of neurologic evaluation newborn, evaluation of nifedipine ocular myopathy orbicularis oculi muscle paramyotonia congenita paresthesias paroxysmal neurologic deficits percussion induced muscle contraction periodic paralysis poison, mercury poison, neurologic problems with polymerase chain reaction polymerase chain reaction, false negative polymerase chain reaction, false positive polymyositis postoperative neurologic complications potassium channel antibodies potassium channel dysfunction procainamide prognosis respiratory failure review article rhabdomyolysis seizure sodium channel dysfunction spinal muscular atrophy spinocerebellar ataxia spinocerebellar ataxia type 6 temporalis muscle wasting term infant tocainide treatment of neurologic disorder tricresylphosphate trinucleotide repeats tubular aggregates, muscle viral infection, CNS weakness weaning from respirator, failure to Werdnig-Hoffman disease workup

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