Differential (Click to cross reference) adverse drug reaction amyotrophic lateral sclerosis amyotrophic lateral sclerosis, bulbar amyotrophic lateral sclerosis, atypical amyotrophic lateral sclerosis, diagnosis of amyotrophic lateral sclerosis, etiology of amyotrophic lateral sclerosis, prognosis amyotrophic lateral sclerosis, treatment of ANA antibodies to voltage-gated calcium channels antispasticity drugs areflexia autonomic dysfunction Babinski sign baclofen basal ganglia, lesion of basal ganglia, lesion, bilateral blepharospasm botulinum toxin botulinum toxin, complications of Brueghel's syndrome bulbar palsy CAG repeats camptocormia carcinoma carcinoma of lung carnitine deficiency myopathy carpal tunnel syndrome CAT scan, chest chewing, impaired children Clinical Pathologic Conference(C.P.C.) clonus complications creatine phosphokinase(CPK)elevated developmental milestones, loss of developmental retardation diabetes mellitus differential diagnosis distal muscle weakness drooling dropped head syndrome drug induced neurologic disorders dysarthria dysphagia dystonia dystonia, cervical dystonia, drug induced dystonia, face dystonia, focal dystonia, treatment of electromyogram electromyogram, decremental response electromyogram, incremental response entrapment neuropathy enzyme, defect enzyme, muscle disease enzyme, serum exercise exercise intolerance exercise-related muscle strength increase familial fasciculation fatigable chewing fatigue flexor spasm foot drop gait disorder gamma amino butyric acid-mimetic drug gangliosidosis GM2 gemfibrozil gene mutation genetic neurologic disorders genetic testing gynecomastia hand pain hand weakness hemifacial spasm hemiparesis hexosaminidase-A hip flexor weakness histochemistry of muscle HMGcoA reductase inhibitors H-reflex testing hyperparathyroidism hyperreflexia hypomyelination hypoparathyroidism hyporeflexia intrathecal antispasticity drugs intrinsic hand muscles, wasting of ischemic exercise test jaw jerk, abnormal Jewish lactic acidemia lactic dehydrogenase(LDH) leg weakness, bilateral lipid lowering agent lipid storage disorder of CNS lovastatin lysosomal storage disease McArdle's disease McArdle's disease, adult onset Mills syndrome misdiagnosis mitochondrial disease molecular genetics motor neuron disease MRI, abnormal MRI, hypointense signal foci on multiple sclerosis multiple sclerosis, treatment of muscle atrophy, progressive muscle biopsy muscle cramp muscle pain muscle phosphorylase deficiency muscle spasm muscle stiffness muscle strength, testing muscle tenderness muscle weakness muscle weakness, proximal muscle weakness, sudden onset of myasthenic syndrome myoglobinuria myopathy myopathy, hypocalcemic myopathy, metabolic myopathy, mitochondrial myopathy, proximal myositis neck weakness neoplasm, primary of CNS-intraventricular nerve conduction studies neurologic complications of, surgery neurologic disease, diagnoses of neuromuscular disease, electrodiagnosis of neuromuscular junction, abnormality of neuropathology neuropathy overlap syndrome pain pain, leg paraparesis, spastic paresthesias paresthesias, feet paresthesias, hands pediatric neurology prognosis progressive neurologic disorder proteinuria proximal muscle atrophy pyramidal tract dysfunction recurrent repetitive nerve stimulation review article rhabdomyolysis rigidity sedimentation rate, elevated seizure spastic dysphonia spasticity spasticity, treatment of spinal cord, injury of spinal cord, injury, management of standing difficulty startle reaction statin therapy stiff joints Tay-Sachs disease temporalis muscle wasting thalamus, lesion of thalamus, lesion of-bilateral tone, muscle, increased tongue, fasciculations of tongue, weakness treatment of neurologic disorder trinucleotide repeats undiagnosed urine, dark weakness weakness, fatiguable weakness, generalized weakness, progressive weakness, proximal white matter disease xerostomia X-linked bulbospinal neuronopathy

Showing articles 700 to 705 of 705 << Previous Epilepsy in Children Current Therapy, 1966, p. 574., Scholl,M.L., 1966 Facial Myokymia JNNP 29:35, Mathews,W.B., 1966 Recognition, Prognosis, & Treatment of the Guillain-Barre Syndrome (Acute Idiopathic Polyneuritis) Med Clin North Am 47:1371, Eiben,R.,et al, 1963 The Natural Hx of Infantile Spasms Arch Dis Child 36:17, Jeavons,P.M.,et al, 1961 Occlusive Cerebrovascular Disease Am J Med 30:577, Meyer,J.S., 1961 Five Types of Dystrophy Together with Other Conditions Producing Insidious Muscle Weakness-Table 1-Hospital Med p. 60., , 1850 Showing articles 700 to 705 of 705 << Previous