Differential (Click to cross reference) acanthocytosis acetylcholine acoustic neurinoma, bilateral adrenoleukodystrophy advances in neurology adverse drug reaction albinism alcohol intolerance alcohol, neurologic complications with algorithm alpha-fetoprotein alternating rapid movement Alzheimer's disease amantadine aminoacidopathies amyotrophic lateral sclerosis anemia antibodies to voltage-gated calcium channels anticholinesterase anticonvulsants anticonvulsants, selection of antioxidant apraxia of eye movements areflexia Arnold Chiari malformation arrhythmia, cardiac asymptomatic ataxia ataxia telangiectasia ataxia, cerebellar ataxia, hereditary ataxia, paroxysmal ataxia, progressive ataxia, sensory ataxia, truncal ataxic gait ataxic-dystonia syndromes ataxin ataxin-2 atypical auditory evoked brainstem potentials autonomic dysfunction Babinski sign baclofen bacterial infection basal ganglia, degeneration Bassen-Kornzweig syndrome benign essential tremor biologic markers blindness blood dyscrasias, neurologic findings with bradykinesia brain atrophy brainstem, atrophy brainstem, lesion of CAG repeats calcium channel dysfunction carcinoembryonic antigen carcinoma carcinoma of lung cardiomyopathy CAT scan CAT scan, abnormal CAT scan, emission CAT scan, emission, abnormal cataracts celiac disease, adult central core disease cerebellar ataxia, autosomal recessive cerebellar ataxia, children cerebellar ataxia, children, differential diagnosis of cerebellar ataxia, hereditary cerebellar ataxia, primary cerebellar atrophy, primary cerebellar atrophy, secondary cerebellar degeneration cerebellar vermis cerebral cortical atrophy cerebral glucose metabolism cerebro hepato renal syndrome cerebrovascular accident Chediak-Higashi syndrome cherry red spot-myoclonus syndrome children chloride channel dysfunction choking chorea choreoathetosis chromosomal abnormality chromosome 11 chromosome 12 chromosome 14 chromosome 6 chromosome 9 cigarette smoking cirrhosis Clinical Pathologic Conference(C.P.C.) clonus clubfoot as related to neurologic disease Cockayne's syndrome cognition Collier's sign cone-rod dystrophy congestive heart failure consanguinity controversies in neurology conversion reaction copper deficiency cornea, abnormal cranio-cervical junction creatine phosphokinase(CPK)elevated Cuba cystic fibrosis, neurologic complications with deafmute deafness deep tendon reflexes degenerative diseases of CNS delay in diagnosis dementia dentate nuclei, lesion of dentatorubral-pallidoluysian atrophy depression dexterity, impaired diabetes mellitus diabetes mellitus, chemical dilantin diplopia disability, neurological distal muscle atrophy DNA probes down-beat nystagmus down-beat nystagmus, primary position of gaze drooling drug induced neurologic disorders dwarfism dysarthria dysdiadochokinesia dysmetria dysmorphic dysphagia dyspraxia dystonia echocardiogram echocardiogram, LVH electrocardiogram, abnormal electrocardiogram, LVH electroencephalogram, abnormalities of electromyogram electronystagmography electronystagmography, abnormal electroretinograph endocardial fibrosis enzyme, defect epidemiology of neurology episodic neurologic deficits ethics in neurology evoked potentials excitotoxin exome sequencing eye movement, disorders of falling familial familial hemiplegic migraine family planning fasciculation fatigue fever finger nose finger test foot numbness Fragile-X associated tremor/ataxia-syndrome fragile-X syndrome fragile-X syndrome, carrier frataxin Friedreich's ataxia Friedreich's ataxia, late onset fundus, abnormality of gait disorder gangliosidosis GM2 gargoylism gastrectomy, neurologic complications following gaze palsy gaze palsy, supranuclear gene gene mutation genetic counselling genetic linkage genetic neurologic disorders genetic screening genetic testing glaucoma globus pallidus, lesion of glutamate dehydrogenase deficiency glutamic acid glycogen storage disease growth retardation Guillain Barre syndrome Hallervorden Spatz disease Hallgren's syndrome hammertoes handwriting head injury head nodding hearing loss heart block heel-knee-shin test hepatolenticular degeneration(Wilson's disease) hexosaminidase-A and B HLA hot cross bun sign huntingtin Huntington's chorea Hurler's syndrome hydroxytryptophan L-5(L-5 HTP) hyperreflexia hypertonia hypokalemic periodic paralysis hyposmia hypotonia hypoxia imbalance imbalance, postural immunodeficiency immunosuppression inclusion bodies inclusion bodies, intracytopasmic inclusion bodies, ubiquitin incoordination intellectual deficit internuclear ophthalmoplegia internuclear ophthalmoplegia, bilateral intestinal lymphangiectasia jaw jerk, abnormal Kearns-Sayre syndrome keratoconus kyphoscoliosis, neurologic causes of kyphosis Lafora's disease Laurence-Moon-Bardet-Biedl syndrome L-dopa lecithin leg weakness, bilateral Leigh's disease leukemia leukocyte peroxidase leukodystrophy leukoencephalopathy life expectancy lipid storage disorder of CNS lipid storage myopathy liver disease low back pain lymphoma macular degeneration malabsorption malabsorption syndrome malformation, CNS, congenital malignant hyperpyrexia malondialdehyde Marinesco-Sjogren syndrome memory, impairment of mental retardation MERRF syndrome metabolic disorder, primary Mexican middle cerebellar peduncle middle cerebellar peduncle, lesion migraine migraine, hemiplegic mimics mirror writing misdiagnosis mitochondrial disease molecular genetics mortality motor neuron disease movement disorder movement disorder, extrapyramidal MRI MRI, abnormal MRI, FLAIR MRI, negative MRI, spinal cord mucopolysaccharidoses multiple sclerosis multiple sclerosis, differential diagnosis of multiple sclerosis, misdiagnosis multiple system atrophy muscle biopsy muscle cramp muscle weakness muscle weakness, proximal muscular dystrophy muscular dystrophy, Becker muscular dystrophy, cardiovascular changes with muscular dystrophy, Duchenne myasthenic syndrome myelogram myelomalacia myeloneuropathy myelopathy myoclonic jerks myoclonus myoclonus, epilepsy myopathy myopathy, mitochondrial myopia myotonia congenita myotonia dystrophica neoplasm, primary intracranial neoplasm, primary of CNS nerve conduction studies neuritis neurocutaneous disease neuroendocrinology neurologic disease neurologic disease, diagnoses of neurologic signs neuronal ceroid-lipofuscinosis neuronal migration disorder neuronopathy neuroophthalmology neuropathology neuropathy neuropathy, amyloid neuropathy, hereditary peripheral neuropathy, peripheral neurotoxin neurotransmitter neutropenia nicotine night blindness numbness, extremity nystagmus nystagmus, primary position of gaze nystagmus, upbeating-in primary position of gaze nystagmus, vertical obesity ocular motility, disorders of ocular myopathy old age, neurology of ophthalmoplegia ophthalmoplegia, progressive external optic atrophy optic nerve optic neuropathy optical coherence tomography orbit, tomograms of orthostatic hypotension pain pain, management of chronic palatal myoclonus pancytopenia paramyotonia congenita paraparesis, familial spastic Parkinson disease Parkinson disease, familial Parkinsonism multiple-system atrophy Parkinsonism syndrome paroxysmal neurologic deficits pathologic reflex pathology periodic paralysis peroxisomal disease pes cavus photophobia physostigmine pigmentary retinopathy polydactyly polymerase chain reaction polymyositis polyneuropathy pons, atrophy pontocerebellar atrophy posterior column disease potassium channel antibodies potassium channel dysfunction prevention of neurologic disorders progeria prognosis progressive myoclonic epilepsy progressive neurologic disorder proprioception, abnormal pseudobulbar palsy pseudoretinitis pigmentosa psychiatric disorder psychiatric problems in neurologic disorders psychological testing psychological testing, neurologic problems Purkinje cell putamen, lesion of putamen, lesion of, bilateral pyramidal tract pyramidal tract dysfunction radiation hypersensitivity Red flags refractive errors Refsum's disease remission remote effect of cancer on the nervous system retina, abnormal retinal degeneration retinal lesion retinitis pigmentosa retinopathy review article risk factors Romberg's sign saccadic eye movements, abnormal schizophrenia scoliosis seizure seizure, paradoxical seizure, treatment of sensorineural hearing loss sensory loss Shy-Drager syndrome sinemet skew deviation skew deviation, alternating skin, biopsy skin, lesions in neurologic disorders sleep apnea sleep pathology and physiology sodium channel dysfunction spastic ataxia spasticity sphingolipodoses Spielmeyer Vogt syndrome spinal cord, cervical spinal cord, lesion of spinal cord, neoplasm spinal cord, neoplasm, intramedullary spinal muscular atrophy spinocerebellar ataxia spinocerebellar ataxia type 1 spinocerebellar ataxia type 10 spinocerebellar ataxia type 12 spinocerebellar ataxia type 14 spinocerebellar ataxia type 16 spinocerebellar ataxia type 17 spinocerebellar ataxia type 2 spinocerebellar ataxia type 28 spinocerebellar ataxia type 3/Machado Joseph disease spinocerebellar ataxia type 5 spinocerebellar ataxia type 6 spinocerebellar ataxia type 7 spinocerebellar ataxia type 8 spinocerebellar degeneration spinopontine atrophy, dominant staggering steatorrhea striatonigral degeneration syphilis, neurologic complications with tandem gait, ataxic tapetoretinal degeneration telangiectases thalamus thyrotropin-releasing hormone tinnitus trazodone treatment of neurologic disorder tremor tremor, cerebellar tremor, intention trimethoprim-sulfamethoxazole trinucleotide repeats Unverricht-Lundborg disease upgaze, paralysis of Usher's syndrome vertigo vertigo, episodic vestibulopathy vibratory sensation vibratory sensation, abnormal visual acuity, decreased visual evoked response visual field defect visual fields, constricted visual loss visual loss, progressive visual loss, slow vitamin deficiency vitamin E vitamin E deficiency vitamin supplementation Von Hippel Lindau walking, difficulty with wheelchair white matter disease wide based gait workup X-linked bulbospinal neuronopathy

Showing articles 150 to 159 of 159 << Previous Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing NEJM 296:1138, Jackson,J.F.,et al, 1977 Azorean Disease of the Nervous System NEJM 296:1505, Romanul,F.C.A.,et al, 1977 Lower Motor Neuron Disease with Spinocerebellar Degeneration Ann Neurol 2:524, Page,R.W.,et al, 1977 Low Activities of the Pyruvate & Oxoglutarate Dehydrogenase Complexes in Five Patients with Friedreich's Ataxia NEJM 295:62, Blass,J.P.,et al, 1976 Machado Disease-a Hereditary Ataxia in Portuguese Emigrants to Mass Neurol 22:49, Nakano,K.K.,et al, 1972 Genetic Counseling in Retinitis Pigmentosa MCV Quart 8:283, Noah,V., 1972 Olivopontocerebellar Atrophies:A Review Medicine 49:227, Konigsmark,B., 1970 A Case of Cerebellar Ataxia, with a Discussion of Classification Arch Neurol 3:71, Locke,S.,et al, 1960 Cerebellar Ataxia in Children Handout & References., Gilbert,J.J., 1850 Hereditary Ataxias Genetics & the Inheritance of Integrated Neurol & Psych. Patterns-Vol 33, Proceed. Assoc. for Resear, h in NerSchut, J., 1850 Showing articles 150 to 159 of 159 << Previous