Differential (Click to cross reference) abdominal distention acral sensory symptoms adrenoleukodystrophy airway obstruction alopecia alternating rapid movement Alzheimer's disease Alzheimer's disease, familial amenorrhea anemia ankle reflex, absent anomic aphasia anorexia anosmia anterior tibial muscle weakness antibiotics antiviral agents aphasia apraxia areflexia arrhythmia, cardiac arteriopathy arthralgia arthritis arthrogryposis multiplex asthma asthma, poliomyelitis-like syndrome with asymptomatic ataxia ataxia, cerebellar ataxia, hereditary ataxia, truncal ataxic gait attention deficit disorder with hyperactivity autonomic dysfunction autonomic neuropathy autonomic neuropathy, idiopathic Babinski sign bacterial infection bacterial infection, CNS basal ganglia, infarction behavioral disorder benign essential tremor Bing-Neel syndrome blindness bradyphrenia brain biopsy bulbar palsy calf hypertrophy carcinoma carcinoma of thyroid cardiomyopathy CAT scan CAT scan, abnormal CAT scan, contrast enhanced CAT scan, demyelinating disease cataracts cataracts, congenital central core disease central nervous system, infection of cephalosporins cerebellar atrophy, primary cerebellar atrophy, secondary cerebellar lesion cerebellar plaques, amyloid cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy cerebral cortical atrophy cerebral embolism cerebral infarction cerebral infarction, small, deep cerebral infarction, subcortical cerebrospinal fluid cerebrospinal fluid, abnormal cerebrospinal fluid, cytology cerebrospinal fluid, elevated protein of cerebrospinal fluid, proteincytologic dissociation cerebrovascular accident cerebrovascular accident, familial occurrence cerebrovascular accident, multiple cerebrovascular accident, recurrent Charcot-Marie-Tooth children chorioretinitis chromosomal abnormality chromosome 17 chromosome 9 Clinical Pathologic Conference(C.P.C.) clubfoot as related to neurologic disease cognition cogwheel rigidty coma confusion congenital bilateral perisylvian syndrome congenital malformation congenital myasthenic syndromes congestive heart failure consanguinity constipation contractures, joint corpus callosum corpus callosum, atrophy of corpus callosum, lesion of corpus callosum, thinning creatine phosphokinase(CPK)elevated cry, abnormal deafness deep gray nuclei deep tendon reflexes degenerative diseases of CNS delay in diagnosis dementia dementia, cerebrovascular disease causing dementia, presenile dementia, rapidly progressive dementia, transmissible demyelinating disease dentate nuclei dentate nuclei, lesion of developmental abnormality of brain developmental disability developmental milestones, loss of developmental retardation dexterity, impaired diabetes insipidus diabetes mellitus diabetes mellitus, ocular complications in diabetic cranialneuropathies diarrhea differential diagnosis difficulty going down stairs diplopia dislocated hip, congenital disorientation distal muscle atrophy distal muscle weakness dizziness downward gaze, paralysis of drooling dysarthria dyskinesia, buccal lingual facial dysmorphic dysphagia electrocardiogram, abnormal electroencephalogram, abnormalities of electroencephalogram, triphasic delta waves electromyogram electron microscopy electrophoretic pattern, serum electroretinograph encephalopathy encephalopathy, progressive endocarditis, marantic enzyme, defect episodic neurologic deficits epistaxis evoked potentials exercise exercise intolerance exome sequencing eye movement, disorders of facial movement disorder facial weakness facial weakness, bilateral falling false negative familial fatigue feeding disorder fever fine motor function, impaired fingerprint bodies foot deformity foot drop frataxin Friedreich's ataxia frontal lobe, pathologic signs of fundus, abnormality of gag reflex, depressed gait disorder gait, spastic gait, waddling gangliosidosis GM2 gangliosidosis GM2-AB variant gaze palsy gaze palsy, supranuclear gaze palsy, vertical gene gene mutation genetic counselling genetic linkage genetic neurologic disorders genetic testing globoid cells glossitis glucose tolerance test, abnormal glycogen storage disease gram positive rod granular osmiphilic material granulomatous disease growth retardation Guillain Barre syndrome hallucination hallucination, visual hammertoes hand deformity hand weakness hands, fisted head lag hearing loss hemiparesis hemiplegia hemorrhagic diathesis hepatomegaly hepatosplenomegaly high arched feet high arched palate hippocampus hippocampus, hyperintense hydrocephalus hydrocephalus, normal pressure hyperphagia hyperpigmentation of skin hyperreflexia hypertonia hyperviscosity hypoalbuminemia hypodontia hypogonadism hypogonadism, hypogonadotropic hypomyelination hyporeflexia hyposmia hypothalamus, damage to hypothalamus, disturbance of hypotonia hypotonia, infants immunofluorescence immunosuppressive agents impotence impulsivity inclusion bodies inclusion bodies, eosinophilic cytoplasmic inclusion bodies, intracytopasmic incoordination infection insomnia intellectual deficit intellectual deterioration intestinal biopsy intracerebral hemorrhage intrinsic hand muscles, wasting of iritis irritability ischemic exercise test Jakob-Creutzfeldt disease Krabbe's disease kuru kuru plaques kyphoscoliosis, neurologic causes of kyphosis Lafora body Lafora's disease leg numbness leg weakness, bilateral leg weakness, unilateral Leigh's disease lethargy leukocyte enzyme abnormality leukocytosis leukodystrophy leukoencephalopathy level of consciousness, decreased light-near dissociation, causes of limbic encephalitis lordosis lumbosacral plexopathy lymph node biopsy lymphadenopathy lysosomal storage disease macroglobulinemia malabsorption malabsorption syndrome malaise malformation, CNS, congenital malignant hyperpyrexia McArdle's disease meconium staining memory, defect of recent memory, impairment of meningitis meningitis, aseptic mental retardation mental status, abnormal mestinon micrognathia migraine misdiagnosis mitochondrial disease mitochondrial encephalomyopathy mitochondrial recessive ataxic syndrome mitral valve prolapse mitral valve vegetation molecular genetics monomelic amyotrophy mononeuritis multiplex mononeuropathy mortality motor neuron disease movement disorder movement disorder, extrapyramidal MRI MRI, abnormal MRI, diffusion weighted MRI, disappearing lesion on MRI, hypointense signal foci on MRI, peripheral nerve MRI, spinal cord MRS multiple endocrine neoplasia multiple sclerosis multiple sclerosis, differential diagnosis of multiple sclerosis, familial multiple sclerosis, misdiagnosis muscle atrophy, progressive muscle atrophy, static muscle biopsy muscle cramp muscle pain muscle phosphorylase deficiency muscle spasm muscle stiffness muscle weakness muscle weakness, proximal muscular dystrophy muscular dystrophy, Becker mycobacterium avium-intracellulare myelomalacia myelopathy myoclonus myoclonus, epilepsy myoglobinuria myopathy myotonia congenita myotonia dystrophica narcolepsy nasal speech negative nerve biopsy nerve conduction studies nerve hypertrophy nerve root hypertrophy neuroendocrinology neurologic complications of, systemic disease neurologic disease, diagnoses of neurologic examination neurologic signs neuroma neuronal ceroid-lipofuscinosis neuropathology neuropathy neuropathy, amyloid neuropathy, ataxic neuropathy, demyelinating neuropathy, hereditary peripheral neuropathy, hypertrophic neuropathy, onion bulb neuropathy, peripheral neuropathy, sensory neuropathy, sensory, hereditary night blindness night sweats nonverbal Notch3 gene nystagmus nystagmus, rotary nystagmus, upbeating-in primary position of gaze nystagmus, vertical ocular motility, disorders of oculomasticatory myorhythmia opened mouth operculum syndrome, bilateral ophthalmoplegia ophthalmoplegia, total opisthotonus optic ataxia optic atrophy optic chiasm, enlarged optic disc cup optic nerve, enlarged pain pain, abdominal pain, foot papilledema paralysis paraparesis paraparesis, familial spastic paraparesis, spastic paresthesias paresthesias, feet paresthesias, lower extremity Parkinson disease PAS positive PAS positive material in the brain Pelizaeus Merzbacher pericarditis peroneal muscle atrophy, causes of peroxisomal disease personality change pes cavus phosphorylase b kinase deficiency phytanic acid pleocytosis of cerebrospinal fluid pleural effusion pleurisy pneumonia POLR3B polydipsia polymerase chain reaction polymicrogyria polyneuropathy polyneuropathy, familial polyps, gastrointestinal tract prognosis progressive myoclonic epilepsy progressive neurologic disorder pseudobulbar palsy pseudohypertrophy psychiatric disorder psychiatric problems in neurologic disorders psychological testing, neurologic problems ptosis ptosis, bilateral pupil, abnormality in neurologic disorders pupil, light reflex, abnormal pyramidal tract pyramidal tract dysfunction recurrent Red flags Refsum's disease release phenomena renal failure respiratory failure retinal hemorrhages retinitis pigmentosa retinopathy reversible neurologic disorder review article Romberg's sign scoliosis scoliosis, neurologic association with sea-blue histiocytes second wind phenomena sedimentation rate, elevated seizure seizure, children seizure, intractable seizure, teenager senile plaques sensorineural hearing loss sensory loss skin, biopsy skin, darkening of skin, lesions in neurologic disorders sleep pathology and physiology slow virus infection of CNS small vessel disease smell somnolence spastic ataxia spasticity sphingolipodoses spinal cord, lesion of spinocerebellar ataxia splenomegaly spongy degeneration of brain spontaneous remission startle myoclonus startle reaction steatorrhea steppage gait storage disease of CNS stuttering subarachnoid hemorrhage subcortical U fibers sudden death superior cerebellar peduncle symmetric brain lesions synkinesis systemic illness tandem gait, ataxic tapetoretinal degeneration teeth, abnormal teeth, number of in infants temporal lobe, lesion temporal lobe, lesion, bilateral temporalis muscle wasting term infant testicular biopsy thalamus, lesion of-bilateral tinnitus toe walking transient neurologic deficit treatment of neurologic disorder tremor tremor, intention trimethoprim-sulfamethoxazole trinucleotide repeats tripping ultrasonography, nerve upgaze upgaze, paralysis of urinary 17 hydroxycorticosteroids urinary 17 ketosteroids urinary incontinence urine, dark uveitis vasculopathy vertical gaze vibratory sensation, abnormal viral infection, CNS vision, blurred visual acuity, decreased visual evoked response visual fields, constricted visual loss visual loss, slow vitamin deficiency vitamin E vitamin E deficiency vitreous opacities vitritis Waldenstrom's macroglobulinemia walking, delayed walking, difficulty with weakness weakness, fatiguable weakness, generalized weakness, progressive weakness, proximal weight loss wheelchair Whipple's disease white matter disease wide based gait Wolfram syndrome

Showing articles 50 to 63 of 63 << Previous A Syndrome of Progressive Muscle Spasm, Alopecia, & Diarrhea Neurol 28:458, Satoyoshi,E., 1978 Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978 Ocular Involvement in Whipple's Disease Arch Ophthalmol 96:1431-1436, Font,R.L.,et al, 1978 Adult-onset GM2 Gangliosidosis Neurol 28:1117-1123, O'Neill,B.,et al, 1978 The Spectrum of Mild X-Linked Recessive Muscular Dystrophy Arch Neurol 34:408, Ringer,S.P.,et al, 1977 Clinical Pathologic Conference, Creutzfeldt-Jakob Disease, (Case record 43-1977) NEJM 297:930, Scully,R.E.,et al, 1977 Juvenile Diabetes Mellitus & Optic Atrophy Arch Neurol 34:759, Lessell,S.,et al, 1977 CT Scanning & Diagnosis of Adrenoleukodystrophy Neurol 27:884, Greenberg,H.S.,et al, 1977 Whipple's Disease of the Central Nervous System Acta Neuropath 36:31, Silbert,S.W.,et al, 1976 Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients Medicine 55:467, Knox,D.L.,et al, 1976 Charcot-Marie-Tooth Disease Associated With"Essential Tremor" Neurol Sciences 28:17-40, Salisachs,P.J., 1976 Isolation & Characterization of an Aetiological Agent in Whipple's Disease BMJ 3:568, Clancy,R.L.,et al, 1975 Whipple's Disease:A Review of 19 Pnts from one Hospital & a Review of the Literature since 1950 Medicine 49:175, Maizel,H.,et al, 1970 Cerebral Complications of Whipple's Disease Brain 88:137, Smith,W.T.,et al, 1965 Showing articles 50 to 63 of 63 << Previous