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Differential
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acetazolamide

acetylcholine receptor antibody

Addison's disease

adrenergic blocker

advances in neurology

adverse drug reaction

agoraphobia

airway obstruction

alcohol

alcohol, neurologic complications with

alcoholism

Alexanders disease

Alexanders disease, adult onset

algorithm

alpha adrenergic blocker

alprazolam

alternating rapid movement

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, misdiagnosis

anatomy of

anemia

anemia, hemolytic

aneurysm, intracranial

anticholinergic drugs

anticonvulsants

anticonvulsants, untoward effects of

anxiety

aorta, atherosclerosis

aphonia

apraxia

areflexia

Arnold Chiari malformation

aspartate aminotransferase

ataxia telangiectasia

ataxic-dystonia syndromes

athetosis

athetosis, causes of

attention deficit disorder with hyperactivity

atypical

auditory evoked brainstem potentials

auditory evoked potentials

autism

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal spheroid

Babinski sign

basal ganglia

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

behavioral disorder

Behcet's syndrome

benign essential tremor

benign essential tremor, refractory

beta adrenergic blocker

biologic markers

blepharospasm

blinking, reduced

blood dyscrasias, neurologic findings with

bone marrow suppression

botulinum toxin

botulinum toxin, complications of

bradykinesia

brain atrophy

brain transplantation

calcification, intracranial

calcium antagonist

camptocormia

carbon monoxide poisoning

carbonic anhydrase inhibitor

carcinoma

carcinoma of pancreas

CAT scan, emission, abnormal

cataracts

catatonia

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellum, disease of

cerebral blood flow

cerebral cortex

cerebral cortical atrophy

cerebral infarction

cerebral infarction, hemorrhagic

cerebral palsy

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cherry red spot-myoclonus syndrome

chromosomal abnormality

chromosome 14

chromosome 3

chromosome 6

cingulate island sign

cirrhosis

cirrhosis, causes of childhood

claustrum

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

copper metabolism, abnormal

cornea, abnormal

coronary artery bypass

corpus callosum, lesion of

corpus callosum, thinning

degenerative diseases of CNS

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetic coma, diagnosis and treatment

diarrhea

diet

differential diagnosis

dilantin

disability, neurological

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dopamine agonist

dopamine receptor, D2

drooling

drug induced neurologic disorders

dysarthria

dysdiadochokinesia

dyskinesia

dyskinesia, buccal lingual facial

dyskinesia, causes of

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, cervical

dystonia, classification

dystonia, etiology of

dystonia, evaluation of

dystonia, face

dystonia, focal

dystonia, laryngeal

dystonia, post traumatic

dystonia, prevalence of

dystonia, symptomatic

dystonia, treatment of

DYT1 mutation

edema, pedal

efficacy

electroencephalogram, abnormalities of

electrolyte imbalance

electromyogram

electron microscopy

electronystagmography

emotional lability

encephalitis

encephalitis, Japanese

encephalitis, viral

encephalopathy

epidemiology of neurology

eye movement, disorders of

Fabry's disease

facial appearance, abnormal

facial expression abnormality

Fahr disease

failed medical management

failure to thrive

falling

familial

familial hemiplegic migraine

fasciculation

fatal familial insomnia

fatigue

fine motor function, impaired

finger nose finger test

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal lobe, lesion of

frontal lobe, pathologic signs of

gaze fixation, distractable

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

Gilles de la Tourette syndrome

glabellar sign

glioma

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucose tolerance test, abnormal

granular osmiphilic material

grimacing

gynecomastia

Hallervorden Spatz disease

heavy metal intoxication

heel-knee-shin test

hemochromatosis

hemochromatosis, primary

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), late onset

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

hepatosplenomegaly

heralding manifestation

hypotension, neurologic causes of

hypotension, systemic

hypothyroidism

hypotonia

hypoxic encephalopathy

iatrogenic neurologic disorders

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

intellectual deterioration

intelligence quotient

intracerebral hemorrhage

intrinsic hand muscles, wasting of

iron, brain

Jakob-Creutzfeldt disease

jaundice

jaw contractures

joint hypermobility

Kayser-Fleischer ring

kinesia paradoxica

kyphoscoliosis, neurologic causes of

L-dopa, drug interactions with and side effects of

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

lethargy

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

leukopenia

level of consciousness, decreased

Lewy body

Lewy body disease, diffuse

lightheaded

lipid storage disorder of CNS

liver biopsy

liver disease

liver function enzymes

liver transplantation

locus ceruleus, lesion of

lymphoma involving CNS

lysosomal storage disease

macrocephaly

marche a petits pas

Marinesco-Sjogren syndrome

masked facies

memory, impairment of

mental retardation

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, treatment of

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, face of giant panda sign on

MRI, false negative

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, negative

MRI, paramagnetic effect

MRI, T1 weighted high signal foci

MRS

multiple sclerosis

multiple sclerosis, cognitive presenttion

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

neoplasm, intracranial

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

neuroaxonal leukodystrophy

neuroendocrinology

neurofibromatosis 1

neurologic complications of, burns

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuronopathy

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral

neuropathy, sensory

neuropsychiatry

neurotoxin

nigrostriatal pathway

nimodipine

nutritional deficiency

nystagmus

nystagmus, pendular

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

obsessive-compulsive disorder

ocular motility, disorders of

oculogyric crisis

old age, neurology of

opened mouth

optic atrophy

organ transplantation

orthostatic hypotension

osmotic demyelination syndrome

ovarian insufficiency

parenteral alimentation

paresthesias

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, atypical

Parkinson disease, benign tremulous

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, familial

Parkinson disease, fluctuations in

Parkinson disease, freezing phenomena in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

past pointing

patient information and support

phenylketonuria, adult onset

pheochromocytoma

phlebotomy

poison, neurologic problems with

positional head-hanging test

postoperative neurologic complications

postural abnormality

practice guidelines

pregnancy, neurologic complications in

prion disease

PRKN gene

prognosis

progressive neurologic disorder

progressive supranuclear palsy

propranolol

prothrombin time, prolonged

pruritus

pseudobulbar palsy

psychiatric disorder

psychiatric manifestations of brain tumors

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

psychosis, cause of

psychosocial aspects

pulmonary function tests

Purkinje cell

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

quality of life

radiation therapy, stereotactic

radiculopathy

raphe nuclei

reading disorder, acquired

reflex sympathetic dystrophy

rehabilitation for neurologic disorders

remote effect of cancer on the nervous system

renal failure

renal stones

respirations in CNS disease

reversible neurologic disorder

saccadic eye movements, abnormal

safety

salivation, excessive

seizure, differential diagnosis of

seizure, psychomotor-temporal lobe

sensory tricks

serum alanine aminotransferase

single photon emission computed tomography

skin, biopsy

skin, darkening of

sleep pathology and physiology

slit lamp examination

smell

Smell Identification Test

SNCA duplication

somatosensory evoked potentials

spastic dysphonia

spasticity

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

speech, slowed

speech, soft

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 12

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spinopontine atrophy, dominant

splenium of corpus callosum

splenomegaly

spongy degeneration of brain

stimulation, deep brain

stimulation, thalamic

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

stridor

striopallidodentate calcifications, familial idiopathic

stuttering

substantia nigra

subthalamic nucleus

subthalamic nucleus deep brain stimulation

suicide

sural nerve

symmetric brain lesions

syncope

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

teeth, number of in infants

testicular enlargement

tetrabenazine

tetrathiomolybdate

thalamic tumors

thalamic tumors, bilateral

thalamotomy

thalamotuberal artery

thalamus

thalamus, focused ultrasound ablation

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thiazide diuretic

thrombocytopenia

thrombus, mural

thymus and neuromuscular function

tongue, fasciculations of

tongue, protrusion of

tonic foot response

topiramate

torticollis

torticollis, post traumatic

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, classification

tremor, differential diagnosis of

tremor, post traumatic

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

trientine dihydrochloride

trinucleotide repeats

twins

ultrasonography

ultrasonography, head

ultrasonography, high-intensity focused

uric acid, low

urine test for metabolic disorders

urine, dark

ventricular enlargement

vertigo

vertigo, migraine causing

vestibulopathy

vibratory sensation, abnormal

viral infection

visual acuity, decreased

visual evoked response

visual fields, constricted

voice, abnormality of

Von Hippel Lindau

walking frame

walking, difficulty with

weakness

weight loss

Wernicke's encephalopathy

X-linked bulbospinal neuronopathy

x-linked intellectual deficit

x-linked mental retardation

zinc

Showing articles 1500 to 1550 of 2512 << Previous Next >>

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Lancet 340:987-991, Tienari,P.J.,et al, 1992

Tardive Dyskinesia Presenting as Severe Dysphagia
JNNP 55:1203-1204, Gregory,R.P.,et al, 1992

Tardive Dyskinesia Associated with Use of Metoclopramide in a Child
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Multiple Sclerosis in 54 Twinships:Concordance Rate is Independent of Zygosity
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Botulinum Toxin, Useful in Adult Onset Focal Dystonias
BMJ 305:1169-1170, Lees,A.J., 1992

Analysis of the Prion Protein Gene in Thalamic Dementia
Neurol 42:1859-1863, Petersen,R.B.,et al, 1992

Familial Alzheimer's Disease:Second Gene Locus Located, Markers for Familial Disease May be Available
BMJ 305:1108-1109, Mullan,M., 1992

Leksell's Posteroventral Pallidotomy in the Treatment of Parkinson's Disease
J Neurosurg 76:53-61, Laitinen,L.V.,et al, 1992

Recovery From Experimental Parkinsonism in Primates with GM1 Ganglioside Treatment
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The Biology of Developmental Dyslexia
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Causal Heterogeneity in Isolated Lissencephaly
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Population Screening for Fragile X
Lancet 339:1210-1213, Turner,G.,et al, 1992

Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992

Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
Neurol 42:897-902, Nevile,H.E.,et al, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
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Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992

De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
Lancet 339:1081-1082, Hoogendijk,J.E.,et al, 1992

Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
Ann Neurol 32:404-407, Boylan,K.B.&Cornblath,D.R., 1992

Genetic Diagnosis of Gaucher's Disease
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Parkinson's Disease in Twins
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Detection of Full Fragile X Mutation
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Cerebromeningeal Haemophagocytic Lymphohistiocytosis
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Comparison of Magnetic Resonance Angiography, Conventional Angiography, and Duplex Scanning
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Psychiatric Disturbances in Metachromatic Leukodystrophy
Arch Neurol 49:401-406, Hyde,T.M.,et al, 1992

Recent Progress Toward Understanding the Molecular Biology of Von Recklinghausen Neurofibromatosis
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Paramedian Thalamopeduncular Infarction:Clinical Syndromes and Magnetic REsonance Imaging
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Midbrain Syndromes of Benedikt, Claude, and Nothnagel:Setting the Record Straight
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Familial Intracranial Aneurysms, A Review
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Protein S Deficiency in Middle-Aged Women with Stroke
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Familial Intracranial Haemorrhage Due to Factor V Deficiency
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A Familial Disorder with Subcortical Ischemic Strokes, Dementia, and Leukoencephalopathy
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New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
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The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
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Myelopathy Associated with Human T Cell Lymphotropic Virus Type 1 in a White European Native to England
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Unstable DNA Sequence in Myotonic Dystrophy
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Progressive Language Disorder Due to Lobar Atrophy
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Showing articles 1500 to 1550 of 2512 << Previous Next >>