Differential (Click to cross reference) abducens nerve paralysis, bilateral acanthocytosis adrenoleukodystrophy adverse drug reaction agammaglobulinemia aminoacidopathies ANA arrhythmia, cardiac ataxia ataxia, cerebellar atrial fibrillation basal ganglia, calcification of basal ganglia, lesion, bilateral Bassen-Kornzweig syndrome blindness botulism brainstem, lesion of brainstem, tuberculoma of calcification, intracranial cardiomegaly cardiomyopathy CAT scan CAT scan, abnormal CAT scan, dense artery sign cataracts cerebral cortical atrophy cerebral embolism cerebral embolism, cardiac origin cerebral infarction cerebro hepato renal syndrome cerebrospinal fluid, elevated protein of cerebrovascular accident cerebrovascular accident, young adult children chronic progressive external ophthalmoplegia Chvostek sign Clinical Pathologic Conference(C.P.C.) Cockayne's syndrome coenzyme Q10 deficiency collagen vascular disease congestive heart failure conjunctival biopsy consanguinity cornea, abnormal corpus callosum, lesion of creatine phosphokinase(CPK)elevated cyst, parenchymal deafmute deafness deep gray nuclei dementia diabetes mellitus diplopia DNA probes drug induced neurologic disorders dwarfism dysphagia dystonia electrocardiogram, abnormal electroencephalogram, abnormalities of electron microscopy electronystagmography electroretinograph encephalopathy extraocular muscle atrophy extraocular muscle lesion eye closure eye movement, disorders of face, numbness of facial nerve palsy facial nerve palsy, bilateral facial nerve, lesion of facial weakness familial fatigue Friedreich's ataxia fundus, abnormality of gangliosidosis GM1 gangliosidosis, generalized gargoylism gaze palsy, horizontal gene mutation gene therapy genetic counselling genetic linkage genetic neurologic disorders glaucoma Hallervorden Spatz disease Hallgren's syndrome headache hearing loss heart block heart murmur histochemistry of muscle Hurler's syndrome hypocalcemia hypoglycorrhachia hypomagnesemia hypoparathyroidism hypoparathyroidism, idiopathic hypothyroidism hypotonia intestinal pseudoobstruction Kearns-Sayre syndrome keratoconus Laurence-Moon-Bardet-Biedl syndrome Leber's hereditary optic neuropathy Leigh's disease leukocyte enzyme abnormality leukodystrophy lid closure, weakness of macular degeneration malformation, CNS, congenital medulla oblongata, lesion of MELAS syndrome Melkersson's syndrome meningitis mental retardation MERRF syndrome metabolic acidosis metachromatic leukodystrophy middle cerebellar peduncle, lesion middle cerebellar peduncle, lesion, bilateral misdiagnosis mitochondrial disease mitochondrial encephalomyopathy mitral valve lesion mitral valve prolapse MNGIE syndrome molecular genetics MRI MRI pattern MRI, abnormal MRI, contrast enhanced MRI, diffusion weighted mucopolysaccharidoses muscle biopsy muscle biopsy, extraocular muscle cramp muscle weakness, proximal muscular dystrophy muscular dystrophy, congenital myasthenia gravis myasthenia gravis, differential diagnosis myasthenia gravis, misdiagnosis of myasthenia gravis, ocular myasthenia gravis, seronegative myasthenic syndrome myelopathy myoclonus myoclonus, epilepsy myopathy myopathy, mitochondrial myopia myotonia myotonia dystrophica neck weakness neuritis neuroaxonal dystrophy neuroendocrinology neurologic complications of, systemic cancer neurologic disease, diagnoses of neurologic symptoms neuromuscular blockade neuromuscular disease, electrodiagnosis of neuromuscular junction, abnormality of neuronal ceroid-lipofuscinosis neuroophthalmology neuropathy neuropathy, ataxia, retinitis pigmentosa neuropathy, hereditary peripheral Niemann-Pick disease night blindness obesity ocular myopathy oculopharyngeal muscular dystrophy ophthalmoplegia ophthalmoplegia, plus syndrome ophthalmoplegia, progressive external optic atrophy optic nerve optic neuropathy orbicularis oculi muscle pancytopenia peroxisomal disease pigmentary retinopathy pleocytosis of cerebrospinal fluid polydactyly pons, lesion of prognosis prostigmine pseudomyasthenia pseudoretinitis pigmentosa psychiatric disorder psychiatric problems in neurologic disorders ptosis ptosis, bilateral pulmonary infiltrates pyruvate metabolism, abnormality of radiculopathy ragged-red fibers Raynaud's phenomenon refractive errors Refsum's disease renal tubular acidosis retinal degeneration retinal lesion retinitis pigmentosa retinopathy review article schizophrenia scleroderma scleroderma, neurologic involvement with sedimentation rate seizure sensorineural hearing loss seronegative short stature skin, biopsy skin, tight Southern immunoblot test Spielmeyer Vogt syndrome spinocerebellar degeneration spongy degeneration of brain Stephens syndrome succinate dehydrogenase deficiency sudden death symmetric brain lesions tapetoretinal degeneration tetany thalamus, lesion of-bilateral tongue, fasciculations of treatment of neurologic disorder tuberculoma of CNS tuberculosis tuberculosis, miliary Usher's syndrome visual field defect visual fields, constricted visual loss weakness weakness, fatiguable weakness, generalized weight loss white matter disease white matter disease, pattern

Showing articles 750 to 757 of 757 << Previous Abducens Nerve Palsy in Dilantin Intoxication J Pediatr 55:73-77, Manlapaz,J.S., 1959 Zoster Sine Herpete BMJ 418, 1958 Aug., Lewis,G.W., 1958 An Unusual Variant of Acute Idiopathic Polyneuritis (Syndrome of Ophthalmoplegia, Ataxia, & Areflexia) NEJM 255:57, Fisher,C.M., 1956 Neoplasms within the Midbrain Arch Neurol & Psych 68:116952., Netsky,M.G.,et al, 1952 Ocular Palsy in Temporal Arteritis Minn Med 42:1258, 1430, 1617952., Fisher,C.M., 1952 Ocular Motor Manifestations of Brainstem & Cerebellar Dysfunction Chap 9, p 104 Neuro-Ophthalmol ed J. L. Smith., Daroff,R.B., 1850 An 81-Year-Old Man with Imbalance and Memory Impairment , Golbe,L.I.,et al, Ophthalmoplegia with Isolated Extraocular Muscle Hypertropny JAMA Neurol 81:190-191, Li,C.M.F., et al, Showing articles 750 to 757 of 757 << Previous