Differential (Click to cross reference) acquired immunodeficiency syndrome acute ataxia of childhood acute cerebellar ataxia adverse drug reaction alcohol, neurologic complications with alcoholism alien hand syndrome alopecia alternating rapid movement ankle reflex, absent anterior horn cell disease anterior tibial muscle weakness anti Yo antibody antiviral agents aphasia apraxia areflexia arthralgia arthropathy asterixis ataxia ataxia telangiectasia ataxia, acute onset ataxia, cerebellar ataxia, hereditary ataxia, progressive ataxia, truncal ataxic gait attention deficit disorder with hyperactivity autoantibodies autonomic dysfunction autosomal rcessive spastic ataxia of Charlevoix-Saguenay axonal spheroid Babinski sign basal ganglia, calcification of basal ganglia, lesion of behavioral disorder benign essential tremor benign essential tremor, refractory beta adrenergic blocker biologic markers blindness bradykinesia brain atrophy brain biopsy CAG repeats calcification, intracranial carbamazepine carcinoma carcinoma of lung CAT scan CAT scan, abnormal central nervous system, infection of cerebellar ataxia, autosomal recessive cerebellar ataxia, hereditary cerebellar atrophy, primary cerebellar degeneration cerebellar disease, eye movement disorder in cerebellar hemorrhage cerebellar hypoplasia cerebellar lesion cerebellum, disease of cerebral cortical atrophy cerebrospinal fluid cerebrospinal fluid, abnormal cerebrospinal fluid, cytology cerebrospinal fluid, enzymes in cerebrospinal fluid, gammaglobulin of cerebrospinal fluid, gold sol.curve of cerebrospinal fluid, lactic acid concentration cerebrospinal fluid, oligoclonal IgG in cerebrospinal fluid, red cells in cerebrovascular accident chest x-ray, abnormal children chills chylomicron retention disease cirrhosis Clinical Pathologic Conference(C.P.C.) coagulopathy cogwheel rigidty Collier's sign confusion consanguinity corpus callosum, lesion of corpus callosum, thinning cortical-basal ganglionic degeneration cranial neuropathy, multiple creatine phosphokinase(CPK)elevated deafness decerebrate posture degenerative diseases of CNS dementia dentate nuclei developmental disability developmental milestones developmental milestones, loss of developmental retardation diabetes mellitus differential diagnosis difficulty going down stairs dilantin distal muscle weakness doriden drug induced neurologic disorders dysarthria dysdiadochokinesia dysmetria dysphagia dystonia, focal electroencephalogram, abnormalities of electroencephalogram, focal delta activity electromyogram encephalitis erythema nodosum exome sequencing eye movement, disorders of facial weakness facial weakness, bilateral failed medical management falling false positive VDRL familial fasciculation fever fine motor function, impaired finger nose finger test fingerprint bodies foot deformity Fragile-X associated tremor/ataxia-syndrome fragile-X syndrome fragile-X syndrome, carrier Friedreich's ataxia gait disorder gastrointestinal perforation gaze palsy gender gene gene mutation genetic neurologic disorders genetic screening genetic testing glucose tolerance test, abnormal granular osmiphilic material hallucination hammertoes handwriting head injury head injury, delayed deterioration following head nodding headache heavy metal intoxication hemiplegia hemochromatosis hemochromatosis, primary hepatic encephalopathy hepatitis hepatolenticular degeneration(Wilson's disease) hepatomegaly hepatosplenomegaly high arched feet hyperosmolality hyperreflexia hyperthyroidism hypocalcemia hypoparathyroidism hypotonia hypotonia, infants imbalance inborn errors of metabolism inclusion bodies inclusion bodies, eosinophilic cytoplasmic inclusion bodies, eosinophilic intranuclear inclusion bodies, intranuclear incoordination intellectual deficit intellectual deterioration Jakob-Creutzfeldt disease Jakob-Creutzfeldt disease, cerebellar variant Kernig's sign Krabbe's disease kuru plaques lactic acidemia lactic dehydrogenase(LDH) laughing, pathologic leg weakness, bilateral Leigh's disease leukodystrophy leukoencephalopathy leukoencephalopathy, hereditary diffuse leukopenia liver function enzymes low back pain lysosomal storage disease memory, impairment of meningeal enhancement meningismus meningitis, carcinomatous meningoencephalitis middle cerebellar peduncle middle cerebellar peduncle, lesion middle cerebellar peduncle, lesion, bilateral misdiagnosis molecular genetics mosquito movement disorder movement disorder, delayed onset movement disorder, drug induced movement disorder, extrapyramidal MRI MRI, abnormal MRI, diffusion weighted MRI, negative multiple sclerosis multiple sclerosis, treatment of multiple system atrophy muscle biopsy muscle cramp muscle stiffness muscle weakness, proximal myelinolysis, extrapontine myelomalacia myelopathy myoclonic jerks myoclonus myoclonus, epilepsy mysoline negative nerve conduction studies neuroaxonal leukodystrophy neuronal ceroid-lipofuscinosis neuronal intranuclear inclusion disease neuropathology neuropathy neuropathy, demyelinating neuropathy, peripheral nursing home nutritional deficiency nystagmus nystagmus, rotary nystagmus, vertical oculogyric crisis ophthalmoplegia optic atrophy optic neuropathy optic neuropathy, bilateral osmotic demyelination syndrome pain, back paraplegia paresthesias Parkinson disease Parkinson disease, benign tremulous Parkinson disease, L-dopa nonresponsive Parkinsonism multiple-system atrophy Parkinsonism syndrome PAS positive PAS positive material in the brain past pointing pericarditis pes cavus phlebotomy pleocytosis of cerebrospinal fluid pneumoencephalogram(PEG) poison, neurologic problems with polymerase chain reaction, false negative polymyositis pons, lesion of prevention of neurologic disorders prognosis progressive neurologic disorder propranolol prothrombin time, prolonged psychosis purpura pyramidal tract dysfunction pyruvate metabolism, abnormality of quadriparesis quadriplegia rash Raynaud's phenomenon rectal biopsy remote effect of cancer on the nervous system review article rigidity Sabin-Feldman dye test saccadic eye movements, abnormal sciatica sedimentation rate, elevated seizure seizure, children serum glutamic oxaloacetic transaminase skin, biopsy skin, darkening of spasticity speech disorder, childhood speech, delayed development of speech, loss of spinocerebellar ataxia spinocerebellar ataxia type 12 spinocerebellar ataxia type 3/Machado Joseph disease splenomegaly stage-fright staggering startle myoclonus startle reaction status epilepticus stimulation, deep brain storage disease of CNS striatonigral degeneration striatonigral degeneration, infantile stuttering systemic lupus erythematosus systemic lupus erythematosus, neurologic complications with systemic lupus erythematosus, skin changes in tandem gait, ataxic tauopathy terfenadine tetany thalamotomy thalamus, focused ultrasound ablation thrombocytopenia thrombotic thrombocytopenia purpura thyrotoxicosis titubation toe walking toxoplasma complement fixation test toxoplasmosis, acquired toxoplasmosis, CNS treatment of neurologic disorder tremor tremor, cerebellar tremor, classification tremor, differential diagnosis of tremor, intention tremor, orthostatic tremor, physiologic tremor, post traumatic tremor, postural tremor, psychogenic tremor, resting tremor, rubral tremor, surgical treatment of tremor, thalamic stimulation for suppression of tremor, treatment of tremor, voice tremor, writing trimethoprim-sulfamethoxazole trinucleotide repeats tripping urticaria uveitis vagus nerve stimulation Venereal Disease Research Laboratory test vertigo viral infection viral infection, CNS visual loss vitamin E deficiency walking, delayed walking, difficulty with weight loss West Nile fever wheelchair white matter disease wide based gait workup writing

Showing articles 900 to 904 of 904 << Previous Metabolic Defects Associated with Mental Retardation Am J Dis Child 104:401, Garell,D., 1962 Diseases of the Basal Ganglia-Their Relation to Disorders of Movement Lancet 1099, 1960, Nov., Denny-Brown,D., 1960 Neurologic Manifestations of Chronic Carbon Monoxide Poisoning NEJM 261:1217-1220, Gilbert,G.J.,et al, 1959 Neurologic Manifestations of Chronic Pulmonary Insufficiency NEJM 257:579-590, Austen,F.K.,et al, 1957 Cerebellar Ataxia in Children Handout & References., Gilbert,J.J., 1850 Showing articles 900 to 904 of 904 << Previous