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abortion, spontaneous

acute disseminated encephalomyelitis

adult polyglucosan body disease

advances in neurology

adverse drug reaction

agnosia, visual

Alexanders disease

alien hand syndrome

alpha-fetoprotein

alpha-synuclein

alternating rapid movement

Alzheimer's disease

Alzheimer's disease, familial

Alzheimer's disease, incidence

Alzheimer's disease, prognosis of

Alzheimer's disease, risk factors in

Alzheimer's disease, treatment of

Alzheimer's disease, visual variant

amyloid plaques

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

angiitis, isolated of CNS

angiofibroma, facial

aphasia, progressive

aphasia, progressive, primary

apnea, primary central

apolipoprotein E

apraxia of eye movements

arm swing, reduced

arthrogryposis multiplex

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

autoimmune disease

automatic behavior

automobile accidents

autonomic dysfunction

axonal degeneration

axonal spheroid

Balint's syndrome

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

Behcet's syndrome

biologic markers

bladder dysfunction

blood dyscrasias, neurologic findings with

bone marrow biopsy

bovine spongiform encephalopathy

brain transplantation

brainstem, atrophy

brainstem, neoplasms of

bulbar palsy, childhood

bulbar palsy, progressive

cafe au lait spots

calcification, intracranial

Canavan's disease

carbon monoxide poisoning

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

cataracts, congenital

caudate nucleus, atrophy

celiac disease, adult

central core disease

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebral cortex

cerebral cortical atrophy

cerebral dominance

cerebral infarction

cerebral vasculature

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, bilateral

Charcot-Marie-Tooth

cherry red spot

cherry red spot-myoclonus syndrome

choline acetyltransferase

chorea, familial

choreoathetosis

chromosomal abnormality

chronic traumatic encephalopathy

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

color vision, impaired

congenital birth defects

congenital malformation

congenital malformation, non CNS

contactin associated protein like 2 antibodies

controversies in neurology

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

crying, pathologic

cultured skin fibroblasts

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, cerebrovascular disease causing

dementia, diagnostic evaluation of

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, prevention of

dementia, rapidly progressive

dementia, screening for

dementia, thalamic

dementia, transmissible

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

differential diagnosis

dopamine agonist

dopaminergic dysfunction

dopaminergic neurons

dystonia, focal

electroencephalogram

electroencephalogram, abnormalities of

electrophoretic pattern, CSF

emotional lability

encephalitis, Japanese

encephalitis, viral

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, post traumatic

enzyme activity

epidemiology of neurology

erectile dysfunction

ethics in neurology

evoked potentials

executive dysfunction

exercise intolerance

eye movement, disorders of

failure to thrive

familial periodic ataxia

Fazio-Londe's disease

feeding disorder

fine motor function, impaired

fingerprint bodies

flail arm syndrome

football neurologic injuries

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

Friedreich's ataxia

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontotemporal dementia, behavioral variant

gamma amino butyric acid

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann syndrome

Gerstmann-Straussler-Scheinker disease

gliadin antibodies

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase

glutaric acidemia

gluten sensitivity

gluten-free diet

glycogen storage disease

granular osmiphilic material

growth retardation

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

head circumference

head injury, mild

head injury, repetitive

headache, episodic

health insurance

heavy metal intoxication

hepatic encephalopathy

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

highly active antiretroviral therapy

hippocampal atrophy

hockey stick sign

human immunodeficiency virus type 1

human T-lymphotropic virus type II(HTLV-II)

Huntington's chorea

Huntington's chorea, genetic counselling

hypotension, systemic

hypoxic encephalopathy

iatrogenic neurologic disorders

ideomotor apraxia

imbalance, postural

immunodeficiency

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

initiative, lack of

insular cortex, lesion

intellectual deficit

intellectual deterioration

intrathecal medication

intrinsic hand muscles, wasting of

inverse association

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

Krabbe's disease

Kugelberg-Welander syndrome

lactic acidemia

language disorder in adults

laughing, pathologic

L-dopa, drug interactions with and side effects of

learning disability, in children

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

Lesch-Nyhan syndrome

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

Lewy body disease, diffuse

life expectancy

life support, withdrawal of

limbic-predominant age-related TDP-43 encephalopathy

locus ceruleus, lesion of

loss of sympathy

lysosomal storage disease

lysosomes, abnoral

macular degeneration

magnetic susceptibility

maple syrup urine disease

Marinesco-Sjogren syndrome

memory, defect of recent

memory, impairment of

mental retardation

mental status, abnormal

microhemorrhage, intracerebral

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

Montreal cognitive assessment

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, complications with

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion weighted

MRI, eye of tiger sign

MRI, field strength

MRI, field strength, high

MRI, gradient-echo

MRI, hypointense signal foci on

MRI, paramagnetic effect

MRI, spinal cord

MRI, T1 weighted high signal foci

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, treatment of

multiple sleep latency test

multiple system atrophy

muscle atrophy, progressive

muscle wasting, diffuse

muscular dystrophy

myasthenia gravis

myelination of nervous system

myeloneuropathy

myoclonic jerks

myoclonus, epilepsy

myoclonus, orthostatic

myopathy, mitochondrial

myotonia dystrophica

N-acetyl-L-aspartic acid

Native Americans

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neuroaxonal dystrophy, infantile

neuroaxonal leukodystrophy

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurogenic bladder

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

neurologic signs

neurologic symptoms

neuronal cell death

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal migration disorder

neuroophthalmology

neuropathology, brain

neuroprotective agents

neurotransmitter

next-generation sequencing

Niemann-Pick disease

nigrostriatal pathway

NMDA antagonists

nucleus basalis of Meynert

nystagmus, rotary

nystagmus, vertical

obsessive-compulsive disorder

ocular motility, disorders of

old age, neurology of

ophthalmoplegia

ophthalmoplegia, total

optic atrophy, hereditary

orthostatic hypotension

osmotic demyelination syndrome

oxidative phosphorylation

pain, sensation

palatal myoclonus

palliative care

palmomental response

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

Parkinson disease

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, familial

Parkinson disease, L-dopa nonresponsive

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism-dementia complex

PAS positive material in the brain

pathologic reflex

patient information and support

penguin silhouette sign

peptides, brain

persistent vegetative state

persistent vegetative state, children

persistent vegetative state, etiology of

personality change

physician assisted suicide

pigmentary retinopathy

poison, mercury

poison, neurologic problems with

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

pontocerebellar atrophy

posterior column disease

posterior cortical atrophy

postural abnormality

practice guidelines

pretectal syndrome

prevention of neurologic disorders

primary lateral sclerosis

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

protein 14-3-3, cerebrospinal fluid

protein 14-3-3, cerebrospinal fluid, false positive

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pulmonary infection

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

ragged-red fibers

rapidly progressing neurologic illness

release phenomena

remote effect of cancer on the nervous system

respiratory failure

retinal degeneration

retinitis pigmentosa

rigidity, axial

saccadic eye movements, abnormal

sarcoidosis, CNS

sea-blue histiocytes

seizure, children

seizure, drug resistance

seizure, laughing as manifestation

semantic dementia

sensorineural hearing loss

sequencing difficulty

single photon emission computed tomography

skin, lesions in neurologic disorders

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

sodium-glucoe cotransporter-2 inhibitors

spastic diplegia

speech disorder

speech disorder, childhood

speech, loss of

spinal cord degeneration

spinal cord, infarction of

spinal cord, injury of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, intramedullary

spinal cord, vascular disorders Affecting

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 12

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spongy degeneration of brain

sports medicine, neurology of

standing difficulty

startle myoclonus

status epilepticus

stem cell transplantation

stimulant drugs

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

substantia nigra

subthalamic nucleus

survival motor neuron gene

symmetric brain lesions

synucleinopathy

systemic illness

tandem gait, ataxic

TDP-43 proteinopathy

temporal lobe, atrophy

thalamus, lesion of

thalamus, lesion of-bilateral

tongue, atrophy

toxic encephalopathy

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trichopoliodystrophy

tricresylphosphate

trinucleotide repeats

tuberous sclerosis

upgaze, paralysis of

urinary incontinence

ventricular enlargement

vestibular function, tests of

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

visual evoked response

visual fields, constricted

visual impairment

visual symptoms

visuospatial disturbance

walking, difficulty with

weakness, generalized

weakness, progressive

Werdnig-Hoffman disease

West Nile fever

Western immunoblot test

white matter disease

wide based gait

Wolfram syndrome

word-finding difficulty

X-linked bulbospinal neuronopathy

Showing articles 450 to 500 of 873 << Previous Next >>

Dopamine, Dystonia, and the Deficient Co-Factor
Lancet 345:1130, Williams,A.C., 1995

Multifocal Motor Neuropathy with Conduction Block:A Study of 24 Patients
JNNP 59:38-44, Bouche,P.,et al, 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Increased Incidence of Levodopa Therapy Following Metoclopramide Use
JAMA 274:1780-1782, Avorn,J.,et al, 1995

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Oral and Genital Tardive Pain Syndromes
Neurol 44:2115-2119, Ford,B.,et al, 1994

Reverse Shapiro's Syndrome:Hirayama
K. , et al, Arch Neurol 51:494-49694., , 1994

Bilateral Distal Upper Limb Amyotrophy and Watershed Infarcts from Vertebral Dissection
Stroke 25:1870-1872, Pullicino,P., 1994

Treatment with D-penicillamine Improves Dopamine D2-Receptor Binding and T2-Signal Intensity in de novo Wilson's Disease
Neurol 44:1079-1082, Schwarz,J.,et al, 1994

Detection of Cortical Neuron Loss in Motor Neuron Disease by Proton Magnetic Resonance Spectroscopic Imaging in Vivo
Neurol 44:1933-1938, Pioro,E.P.,et al, 1994

Superoxide Dismutase and ALS
Lancet 344:1651-1652, Orrell,R.W.&deBelleroche,J.S., 1994

Intestinal Pseudo-Obstruction in Adult Spinal Muscular Atrophy
Muscle & Nerve 17:946-948994., Ionasescu,V.,et al, 1994

Location of the Corticospinal Tract in the Internal Capsule at MR Imaging
Radiology 191:455-460, Yagishita,A.,et al, 1994

Motor Neuron Disease
JNNP 57:886-896, Leigh,P.N.&Ray-Chaudhuri,K., 1994

Recent Developments in the Drug Treatment of Motor Neurone Disease
BMJ 309:140-141, , 1994

Sequences Specific for Enterovirus Detected in Spinal Cord from Patients with Motor Neurone Disease
BMJ 308:1541-1543, Woodall,C.J.,et al, 1994

Diagnosis and Management of Pituitary Tumours
BMJ 308:1087-1091, Levy,A.&Lightman,S.L., 1994

Dopa-Responsive Dystonia:Pathological and Biochemical Observations in a Case
Ann Neurol 35:396-402, 3811994., Rajput,A.H.,et al, 1994

A Multicenter Double-Blind Placebo-Controlled Trial of Pergolide as an Adjunct to Sinemet in Parkinson's Disease
Movement Disorders, 9:40-471994., Olanow,C.W.,et al, 1994

Parkinson's Disease
JNNP 57:672-681, Marsden,C.D., 1994

The Clinical Correlates of High-Titer IgG Anti-GM1 Antibodies
Ann Neurol 35:234-237, Kornberg,A.J.,et al, 1994

Intravenous Immunoglobulin Trtm in Pts with Motor Neuron Syndromes Assoc with Anti-GM Antibodies:A Contrld Study
Neurol 44:429-432, Azulay,J-P.,et al, 1994

Neuron-Specific Enolase & Myelin Basic Protein:Relation of CSF Concentr to Neuro Cond of Asphyx Full-Term Infants
Pediatrics 93:234-240, Garcia-Alix,A.,et al, 1994

Amyotrophic Lateral Sclerosis Patient Antibodies Label CA2+Channel a1 Subunit
Ann Neurol 35:164-171, 1311994., Fumiharu,K.,et al, 1994

A Controlled Trial of Riluzole in Amyotrophic Lateral Sclerosis
NEJM 330:585-591, Bensimon,G.,et al, 1994

Conjugal Amyotrophic Lateral Sclerosis:A Report on Two Couples from Southern France
Neurol 44:547-548, Camu,W.,et al, 1994

Fluctuating Parkinson's Disease:Treatment with the Long-Acting Dopamine Agonist Cabergoline
Arch Neurol 51:1236-1241, Ahlskog,J.E.,et al, 1994

Growth Factors:Potential Therapeutic Applications in Neurology
JNNP 54:1445-1450, Drago,J.,et al, 1994

Monomelic Amyotrophy
Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994

Clinical Significance of Hypointensity in the Motor Cortex on T2-Weighted Images
Neurol 44:1181, Iwasaki,Y.,et al, 1994

Conjugal Amyotrophic Lateral Sclerosis:Report of a Young Married Couple
Neurol 43:2378-2380, Cornblath,D.R.,et al, 1993

Drug Therapy of Migraine
NEJM 329:1476-1483, Welch,K.M.A., 1993

Differential Diagnosis of Guillain-Barre Synd, In Guillain-Barre Synd
Thieme Med Publ, Ch 3, p 42993., Parry,G.J., 1993

Amyotrophic Lateral Sclerosis:T2 Shortening in Motor Cortex at MR Imaging
Radiology 189:843-846, Oba,H.,et al, 1993

Lymphocytic Infiltrates in the Spinal Cord in Amyotrophic Lateral Sclerosis
Arch Neurol 50:30-36, Engelhardt,J.I.,et al, 1993

Motor Neuron Diseases and Amyotrophic Lateral Sclerosis:GM1 Antibodies and Paraproteinemia
Neurol 43:418-420, Sanders,K.A.,et al, 1993

Poliomyelitis:Hyperintensity of the Anterior Horn Cells on MRI Images of the Spinal Cord
AJR 161:863-865, Malzberg,M.S.,et al, 1993

Comparisons of Therapeutic Effects of Levodopa
Levodopa & Selegiline, & Bromocriptine in Pts with Early, Mild Parkinson's, Parkinson's Res Grp in U, , BMJ 372,1993., 1993

Defecatory Function in Parkinson's Disease:Response to Apomorphine
Ann Neurol 33:490-493, Edwards,L.L.,et al, 1993

Multiple System Atrophy & Prog Supranuc Palsy, Dimin Striatal D2 Dopamine Receptor Act by SPECT
Arch Neurol 50:513-516, vanRoyen,E.,et al, 1993

Treatment of Parkinson's Disease
NEJM 329:1021-1027, Calne,D.B., 1993

Do Alcoholics Drink Their Neurons Away?
Lancet 342:1201-1204, Jensen,G.B.&Pakkenberg,B., 1993

The Prevalence of Metoclopramide-Induced Tardive Dyskinesia and Acute Extrapyramidal Movement Disorders
Arch Int Med 153:1469-1475, Ganzini,L.,et al, 1993

Acute Paralytic Syndrome in Three American Men:Comparison with Chinese Cases
Arch Neurol 50:732-735, Jackson,C.E.,et al, 1993

Polyglucosan Body Disease Simulating Amyotrophic Lateral Sclerosis
Neurol 43:785-790, McDonald,T.D.,et al, 1993

Single-Photon Emission Computed Tomographic Investigation of Patients with Motor Neuron Disease
Neurol 43:1569-1573, Abe,K.,et al, 1993

Spinal Fluid Cells and Protein in Amyotrophic Lateral Sclerosis
Arch Neurol 50:489-491, Norris,F.H.,et al, 1993

The Natural History of Amyotrophic Lateral Sclerosis
Neurol 43:1316-1322, Ringel,S.P.,et al, 1993

Vaccine-Associated Paralytic Poliomyelitis
NEJM 329:810-811, Mermel,L.,et al, 1993

Rapidly Progressive Aphasic Dementia and Motor Neuron Disease
Ann Neurol 33:200-207, Caselli,R.J.,et al, 1993

Showing articles 450 to 500 of 873 << Previous Next >>