Differential (Click to cross reference) abducens nerve paralysis acoustic nerve acral sensory symptoms Adies pupil advances in neurology alcohol intolerance alkylating agents altered states of consciousness amyloidosis amyotrophic lateral sclerosis amyotrophic lateral sclerosis, epidemiology of amyotrophic lateral sclerosis, familial amyotrophic lateral sclerosis, guamian type of ankle reflex, absent anterior tibial muscle weakness antimetabolite areflexia arthrogryposis multiplex asparginase ataxia ataxia, cerebellar atonic bladder autonomic dysfunction Babinski sign benign essential tremor blood dyscrasias, neurologic findings with burning paresthesia caloric testing CAT scan, abnormal CAT scan, metrizamide CAT scan, myelogram with cauda equina cauda equina, enhancement cauda equina, lesion of cavernous sinus cavernous sinus, lesion of central core disease cerebrospinal fluid, pressure low Charcot-Marie-Tooth chemotherapy, CNS treatment and complications with children chromosomal abnormality chromosome 17 claudication, intermittent of cauda equina Clinical Pathologic Conference(C.P.C.) clubfoot as related to neurologic disease corpus callosum, lesion of cranial nerve enlargement cranial nerves cranial neuropathy cranial neuropathy, multiple deafness degenerative diseases of CNS Dejerine-Sottas syndrome dementia dermatomyositis differential diagnosis diplopia diplopia, transient disability, neurological distal muscle atrophy distal muscle weakness DNA probes dysarthria dysphagia electroencephalogram, inflammatory disease electromyogram encephalopathy epidemiology of neurology episodic neurologic deficits evoked potentials facial nerve palsy, bilateral facial pain falling familial fasciculation Fazio-Londe's disease fever fine motor function, impaired fluorouracil flush syndrome foot deformity foot drop gadolinium gait disorder gene gene mutation genetic counselling genetic diagnosis genetic diagnosis, prenatal genetic linkage genetic neurologic disorders genetic testing genu of corpus callosum Guillain Barre syndrome hallucination hammertoes hand deformity hand weakness headache hearing loss heavy metal intoxication hemiparesis hemiparesis, transient high arched feet human genome hyperreflexia hyponatremia hyporeflexia imbalance impotence inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with inclusion bodies inclusion bodies, eosinophilic cytoplasmic incoordination intrinsic hand muscles, wasting of isoniazid jaw pain klippel feil syndrome Korsakoff's psychosis Kugelberg-Welander syndrome kyphoscoliosis, neurologic causes of laminectomy, cervical laminectomy, lumbar leg weakness, bilateral leukemia, neurologic findings assoc.with leukoencephalopathy lumbosacral plexopathy meningismus meningoencephalopathy methotrexate methylhydrazine derivatives misdiagnosis molecular genetics monoamine oxidase inhibitors mononeuropathy monoparesis motor neuron disease MRI MRI, abnormal MRI, contrast enhanced MRI, cranial nerves MRI, diffusion tensor MRI, diffusion weighted MRI, disappearing lesion on MRI, peripheral nerve MRI, spinal cord MRI, spine muscle cramp muscle diseases, characteristics of muscle pain muscle weakness muscle weakness, proximal muscle, metabolic disorders of muscular dystrophy muscular dystrophy, Duchenne muscular dystrophy, facioscapulohumeral muscular dystrophy, limb-girdle myasthenia gravis myasthenic crisis myelin protein zero gene myelogram myelopathy myeloradiculopathy myopathy myopathy, carcinomatous myopathy, thyroid disease causing myositis myotonia dystrophica nausea and vomiting nerve biopsy nerve conduction studies nerve growth factor nerve hypertrophy nerve root enhancement nerve root hypertrophy neuritis, causes of neurofibrillary degeneration neurologic complications of, systemic cancer neurologic disease neurologic disease, diagnoses of neuromuscular disease, electrodiagnosis of neuropathy neuropathy, classification of neuropathy, demyelinating neuropathy, diabetic neuropathy, hereditary peripheral neuropathy, hypertrophic neuropathy, onion bulb neuropathy, peripheral neuropathy, work up for neurotoxin neurotrophin-3 night blindness nitrogen mustard numbness, extremity optic atrophy optic atrophy, hereditary orthostatic hypotension pain pain, foot paralysis paralysis, recurrent paraparesis paresthesias paresthesias, feet paresthesias, lower extremity patient information and support peroneal muscle atrophy, causes of pes cavus pleocytosis of cerebrospinal fluid poison, mercury poison, neurologic problems with poliomyelitis polymerase chain reaction polymyositis polyneuropathy polyneuropathy, chronic inflammatory demyelinating polyneuropathy, familial porphyria pregnancy, neurologic complications in procarbazine prognosis progressive neurologic disorder proptosis ptosis ptosis, bilateral pulmonary function tests pupil pupil, dilated and fixed, bilateral pyramidal tract dysfunction quadriparesis quadriplegia, transient quality of life radiculopathy recombinant DNA recurrent Refsum's disease respiratory failure reversible neurologic disorder review article RFLPs Romberg's sign Roussy Levy syndrome sarcoidosis seizure sensorineural hearing loss sensory loss spinal cord, compression of spinal stenosis spinal stenosis, familial splenium of corpus callosum spontaneous remission steppage gait stiff man syndrome strokelike episodes subdural hematoma symmetric brain lesions syncope tinnitus toe walking tomaculous neuropathy torticollis transient neurologic deficit treatment of neurologic disorder tremor tricresylphosphate trigeminal nerve trigeminal nerve, hypertrophy trigeminal neuralgia trinucleotide repeats ultrasonography, nerve vestibular function, tests of vinblastine vincristine neurotoxicity visual evoked response visual impairment vocal cord paralysis weakness weakness, generalized weakness, progressive Werdnig-Hoffman disease white matter disease wrist drop X-linked neuropathy x-ray, spine

Showing articles 150 to 164 of 164 << Previous Clin. Path. Conference Olivopontocerebellar atrophy, sporadic form. Case Record 39-1980, NEJM 303:803-80980., , 1980 Masticatory Spasm in Facial Hemiatrophy Ann Neurol 7:585-587, Kaufman,M.D., 1980 Cranial Computerized Tomography & Marie's Ataxia Arch Neurol 35:55, Aita,J.F., 1978 Dominant Spinopontine Atrophy Arch Neurol 35:156, Pogacar,S.,et al, 1978 Computerized Tomography & Auditory-evoked Potentials:Use in the Diagnosis of Olivopontocerebellar Degeneration Arch Neurol 35:143, Gilroy,J.,et al, 1978 Physostigmine in Familial Ataxias Neurol 27:70, Kark,R.A.,et al, 1977 Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing NEJM 296:1138, Jackson,J.F.,et al, 1977 Lingual Exposure During Mandibular Third Molar Surgery Int J Oral Surg 6:334-339, Stacy,G.C., 1977 Shoulder Enlargement as the Presenting Sign in Syringomyelia JAMA 236:2878, Sackellares,J.C.,et al, 1976 Progressive Supranuclear Palsy-Case Study NEJM 293:346, Richardson,E.P., 1975 Trigeminal Neuralgia & Dental Malocclusions BMJ 4:38-40, Blair,G.A.S.,et al, 1973 Olivopontocerebellar Atrophies:A Review Medicine 49:227, Konigsmark,B., 1970 Progressive Facial Hemiatrophy (Parry-Romberg Syndrome) Am J Ophthalmol 67:561, Johnson,R.V.,et al, 1969 Ophthalmic Hazards of Neurodiagnostic Proc & Surgical Treatment, Clinical Neuroophthalmology The Williams & Wilkins Co, 1969, V-3:2501-2517., Walsh,F.B.&Hoyt,W.F., 1969 A Case of Cerebellar Ataxia, with a Discussion of Classification Arch Neurol 3:71, Locke,S.,et al, 1960 Showing articles 150 to 164 of 164 << Previous