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advances in neurology

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alternating hemiplegia

alternating hemiplegia of childhood

AMPA receptor antibodies

amphiphysin antibodies

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anti IgLON5

anticholinergic drugs

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

basal ganglia

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

carbon monoxide poisoning

cardiac arrest

cardiac arrest and resuscitation

CAT scan

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CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, muscle

catalepsy

cataplexy

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cerebellar degeneration

cerebral cortical atrophy

cerebral palsy

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrovascular accident

cerebrovascular accident, infancy and childhood

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clonazepam

clozapine

cognition

collapsin response mediator protein 5 IgG

coma

complications

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creatine phosphokinase(CPK)elevated

cyanide poison

degenerative diseases of CNS

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developmental retardation

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dopa responsive dystonia

dopamine agonist

dopamine depleting agents

DPPX

DPPX, antibodies

DPPX, antibodies, encephalitis

drug induced neurologic disorders

dysarthria

dyskinesia

dyskinesia, buccal lingual facial

dyskinesia, drug induced

dysphagia

dystonia

dystonia musculorum deformens

dystonia, classification

dystonia, delayed onset

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, face

dystonia, focal

dystonia, treatment of

dystonia, truncal

dystonic reaction, acute

DYT1 mutation

efficacy

electroencephalogram, abnormalities of

electromyogram

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalopathy

encephalopathy, neonatal

encephalopathy, post anoxic

enzyme, defect

executive dysfunction

exome sequencing

eye movement, disorders of

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

gests antagoniste

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

glycine receptor antibodies

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hepatolenticular degeneration(Wilson's disease)

Huntington's disease, children

hypoxic encephalopathy

iatrogenic neurologic disorders

inborn errors of metabolism

inclusion bodies, intranuclear

intellectual deterioration

internal cerebral vein

L-dopa, delayed treatment in Parkinsonism

L-dopa, drug interactions with and side effects of

left handedness

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukodystrophy

life expectancy

limbic encephalitis

lipid storage disorder of CNS

low back pain

lumbar puncture

lysosomal storage disease

masked facies

mellaril

memory

memory, impairment of

meningitis, carcinomatous

mental retardation

mental status, abnormal

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

mitochondrial disease

monoclonal antibodies

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, hyperkinetic

movement disorder, treatment of

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, eye of tiger sign

MRI, negative

MRI, paramagnetic effect

neuroleptic, atypical

neurologic disease, diagnoses of

neurologic signs

neuronal intranuclear inclusion disease

obsessive-compulsive disorder

oculogyric crisis

old age, neurology of

paraspinal muscle weakness

Parkinson disease

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, fluctuations in

Parkinson disease, freezing phenomena in

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, mode of onset

Parkinson disease, on-off phenomena in

Parkinson disease, prognosis of

Parkinson disease, rapid onset

Parkinson disease, treatment of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

phenothiazine

phenothiazine, dyskinesia associated with

pigmentary retinopathy

Pisa syndrome

pleocytosis of cerebrospinal fluid

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

prevention of neurologic disorders

PRKN gene

prognosis

progressive neurologic disorder

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

putamen, lesion of, bilateral

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quality of life

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

recurrent

remote effect of cancer on the nervous system

reserpine treatment in movement disorder

salivation, excessive

seizure, laughing as manifestation

seizure, neonatal

seizure, unknown origin

sensorineural hearing loss

sensory tricks

serologic testing

serologic testing, false negative

seronegative

sinemet

sleep pathology and physiology

stem cell transplantation

steroid

steroid therapy, CNS treatment and complications with

stimulation, deep brain

stooped posture

streptococcal infection

streptococcus pyogens

striatal encephalitis

tardive dyskinesia, treatment of

tardive dystonia

tardive pain syndrome

tetrabenazine

tetrahydrobiopterin

thalamus, infarction of

thalamus, lesion of-bilateral

tonic foot response

torticollis

torticollis, benign paroxysmal

torticollis, familial

torticollis, infants and children

toxic encephalopathy

toxins, nervous system

treatment of neurologic disorder

tricyclic antidepressant

trinucleotide repeats

urinary sulfatidase excretion

walking, difficulty with

weakness, progressive

white matter disease

whole genome sequencing

wide based gait

workup

writers cramp

Showing articles 1250 to 1300 of 1853 << Previous Next >>

Cerebrovascular Complications of Primary Herpes Varicella-Zoster Infection
Editorial, Lancet 339:1449-14501992., , 1992

Rasmussen's Encephgalitis:Neuroimaging Findings in Four Patints
AJR 158:1329-1332, Tien,R.D.,et al, 1992

Clinicopath Conf
Cat-Scratch Disease, with Encephalopathy, Case 22-1992, NEJM 326:1480-148992., , 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

Coeliac Disease, Epilepsy, and Cerebral Calcifications
Lancet 340:439-443, Gobbi,G.,et al, 1992

Epidemiology of Human Immunodeficincy Virus Encephalopathy in the United States
Neurol 42:1472-1476, Janssen,R.S.,et al, 1992

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992

Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings
Ann Neurol 31:64-68, Perlman,J.M.&Argyle,C., 1992

Clinical Features of Vascular Thrombosis Following Varicella
Am J Dis Child 146:100-102, Bodensteiner,J.B.,et al, 1992

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation
Neurol 42:545-550, Goto,Y.,et al, 1992

GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
Ann Neurol 31:328-332, Yoshida,K.,et al, 1992

Idiopathic Hemiparetic Parkinsonism, A Syndrome Distinct from Idiopathic Parkinsonism
Lancet 339:149-150, DeKeyser,J.,et al, 1992

Headaches in Children Younger than 7 Years of Age
Arch Neurol 49:79-82, Chu,M.L.&Chinnar,S., 1992

Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992

Pharmacologic Treatment of Childhood Migraine
J Pediatr 120:653-657, Ingarashi,M.,et al, 1992

Mumps-Associated Acute Cerebellar Ataxia
Am J Dis Child 146:930-931, Cohen,H.A.,et al, 1992

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

Acute Cerebellar Ataxia in a Child with Transient Pontine Lesions Demonstrated by MRI
Neuropediatrics 22:225-227, Groen,R.J.M.,et al, 1991

Central Nervous System Complications of Infective Endocarditis
Stroke 22:1461-1463, Salgado,A.V., 1991

Essential Tremor:Clinical Correlates in 350 Patients
Neurol 41:234-238, Lou,J.&Jankovic,J., 1991

MRI in the Diagnosis of Heterotopic Gray Matter, Report of Three Cases First Discovered in Adulthood
Neuroradiology 33:527-528, Zisch,R.&Artmann,W., 1991

Does Ageing Aggravate Parkinsonisn Disability?
JNNP 54:780-782, Blin,J.,et al, 1991

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Clinicopath Conf
Case 40-1991, Inclusion-Body Myositis, NEJM 325:1026-1035991., , 1991

Clinical Correlates of Response to Botulinum Toxin Injections
Arch Neurol 48:1253-1256, Jankovic,J.&Schwartz,K.S., 1991

Vertebrobasilar Ischemia after Neck Motion
Stroke 22:1452-1460, Frisoni,G.B.&Anzola,G.P., 1991

Late-Life Migraine
Arch Neurol 48:1174-1177, Aring,C.D., 1991

Clinical Use of Botulinum Toxin
National Institutes of Health Consensus Develop Conf Stmt, Nov 12-14, 1990, Arch Neurol 48:1294-1298, 199, 1991

The Bioloigcal Basis for the Treatment of Acute Stroke
Neurol 41:1867-1873, Scheinberg,P., 1991

Cocaine as a Risk Factor for Acute Dystonic Reactions
Neurol 41:1670-1672, Hegarty,A.M.,et al, 1991

Thalamic Ischemia in Transient Global Amnesia:A SPECT Study
Neurol 41:1748-1752, Goldenberg,G.,et al, 1991

A Genetic Study of Idiopathic Focal Dystonias
Ann Neurol 29:320-324, Waddy,H.M.,et al, 1991

Posttraumatic Torticollis
Arch Neurol 48:221-223, Truong,D.D.,et al, 1991

Cat Scratch Disease, Acute Encephalopathy & Other Neurologic Manifestations
Am J Dis Child 145:98-101, Carithers,H.A.&Margileth,A.M., 1991

Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
Neurol 41:174-181, Nygaard,T.G.,et al, 1991

Cortical Resection for Children with Epilepsy
Am J Dis Child 145:314-320, Wyllie,E., 1991

Medical Assessment and Treatment of Chronic Epilepsy
BMJ 302:363-366, Shorvon,S.D., 1991

Celiac Disease, Brain Atrophy, and Dementia
Neurol 41:372-375, Collin,P.,et al, 1991

Idiopathic First Seizure in Adult Life:Who Should be Treated?
BMJ 302:620-623, vanDonselaar,C.A.,et al, 1991

Clinicopath Conf
Renal Cholesterol Embolism (after CABG) , Case 2-1991, NEJM 324:113-1201., , 1991

Transient Global Amnesia, Recurrences are Rare and Patients May Drive
BMJ 302:62-63, Cartlidge,N.E.F., 1991

Diagnostic Tests for Choreoacanthocytosis
Neurol 41:1000-1006, Feinberg,T.E.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Internal Capsule Plaque and Tonic Spasms in Multiple Sclerosis
Arch Neurol 48:427-429, Maimone,D.,et al, 1991

The Coexistence of Tics and Dystonia
Arch Neurol 48:862-865, Stone,L.A.&Jankovic,J., 1991

Therapeutic Uses Of Botulinum Toxin
NEJM 324:1186-1194, Jankovic,J.&Brin,M.F., 1991

Usefulness of a Writing Device in Writer's Cramp
Neurol 41:1136-1138, Ranawaya,R.&Lang,A., 1991

Hemidystonia Due to a Contralateral Parietooccipital Metastasis:Disappearance after Removal of the Mass Lesion
Neurol 41:1519-1520, Krauss,J.K.,et al, 1991

The Relationship Between Trauma and Idiopathic Torsion Dystonia
JNNP 54:713-717, Fletcher,N.A.,et al, 1991

Showing articles 1250 to 1300 of 1853 << Previous Next >>