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abscess, intracranial

achilles tendon, enlarged

acute disseminated encephalomyelitis

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

adverse drug reaction

alternating hemiplegia

alternating hemiplegia of childhood

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

anterior tibial muscle weakness

antiviral agents

arthrogryposis multiplex

ataxia, cerebellar

ataxia, progressive

ataxic-dystonia syndromes

attention deficit disorder with hyperactivity

autoimmune basal ganglia encephalitis

autoimmune disease

autoimmune meningitis

autonomic dysfunction

axonal degeneration

axonal spheroid

basal ganglia, lesion, bilateral

bladder dysfunction

brain biopsy, false negative

brain biopsy, indication

brainstem, atrophy

brainstem, lesion of

calcification, gyral

calcification, intracranial

candida albicans

CAT scan, abnormal

CAT scan, disappearing lesion on

CAT scan, emission, abnormal

central nervous system, infection of

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral infarction, subcortical

cerebral palsy, etiology

cerebral palsy, work up

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, beta-D-glucan

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, cryptogenic

cerebrovascular accident, mimics

cerebrovascular accident, nonvascular territory

cerebrovascular accident, young adult

chemical meningitis

chest x-ray, abnormal

chewing movements

choreoathetosis

chromosomal abnormality

cingulate gyrus

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

cold intolerance

collagen vascular disease

coma, sudden onset

congenital myasthenic syndromes

corpus callosum

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cranial nerve enhancement

cranial neuropathy

creatine phosphokinase(CPK)elevated

crying, pathologic

cryptococcal meningitis

cyst, benign intracranial

cyst, cortical parenchyma

cyst, parenchymal

cystatin C mutation

degenerative diseases of CNS

delay in diagnosis

delayed muscle relaxation

dementia, presenile

dementia, rapidly progressive

dental infection

developmental disability

developmental retardation

diabetes mellitus

diagnostic criteria

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

double-cortex syndrome

drug induced neurologic disorders

dysdiadochokinesia

dysferlinopathy

dystonia, children

Ehlers-Danlos syndrome

Ehlers-Danlos syndrome, classification

empyema, subdural

encephalitis, acute

encephalitis, autoimmune

encephalitis, diagnosis of

encephalitis, etiology

encephalitis, Japanese

encephalitis, viral-causes of

encephalopathy, acute

Erdheim-Chester disease

exome sequencing

Fabry's disease

facial appearance, abnormal

facial weakness

fatal familial insomnia

feeding disorder

fine motor function, impaired

fourth ventricle, compression

fungal infection

fungal infection, CNS

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

geographic location

globus pallidus, lesion of, bilateral

GLUT1 deficiency syndrome

glycogen storage disease

gram positive cocci

headache, awakening with

headache, positional

headache, progressive

helminthic infection of CNS

hemianopia, homonymous

hemiparesis, transient

hemophagocytic lymphohistiocytosis

heralding manifestation

herpes simplex encephalitis

high arched feet

high arched palate

hydrocephalus, non-communicating(obstructive)

hyperammonemic encephalopathy

hyperhomocysteinemia

hypoglycorrhachia

hypogonadism, hypogonadotropic

hypotonia, causes of

hypotonia, infants

immunocompetent

immunomodulation

immunosuppression

immunosuppressive agents

inborn errors of metabolism

inclusion bodies, intranuclear

insular cortex, lesion

intellectual deficit

interstitial pulmonary fibrosis

intracerebral hemorrhage

intravenous drug abuse

intrinsic hand muscles, wasting of

joint hypermobility

Krabbe's disease

lactic acidemia

lacunar infarction

laughing, pathologic

Leber's hereditary optic neuropathy

leg weakness, bilateral

leukoencephalopathy

leukoencephalopathy with calcification and cysts

level of consciousness, decreased

lid abnormalities

limb-girdle weakness

lung-brain syndromes

lysosomal storage disease

malformation, CNS, congenital

malignancy screen

McLeod syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningeal sarcomatosis

meningitis, aseptic

meningitis, bacterial

meningitis, basilar

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, diagnosis

meningitis, fungal

meningitis, helminthic

meningitis, neutrophilic

meningitis, noninfectious

meningitis, parameningeal

meningitis, parasitic

meningitis, treatment of

meningitis, treatment of, empirical

meningitis, viral

meningitis, viral etiology in

meningitis-encephalitis PCR panel

mental retardation

mental status, abnormal

metabolic acidosis

methylmalonic acidemia

microhemorrhage, intracerebral

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

motor neuron disease

movement disorder

moyamoya, adult

MRI, blooming effect

MRI, contrast enhanced

MRI, diffusion weighted

MRI, mass effect on

MRI, nodular enhancement

MRI, spinal cord

muscle atrophy, progressive

muscle stiffness

muscle twitching

muscle wasting, diffuse

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, misdiagnosis of

myasthenia gravis, seronegative

myasthenia gravis, treatment of

myeloneuropathy

myoclonic jerks

myopathy, vacuolar

nausea and vomiting

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neuromyotonia and axonal neuropathy

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuroophthalmology

neuropathy, demyelinating

newborn, evaluation of

next-generation sequencing

night blindness

nystagmus, gaze-evoked

ocular motility, disorders of

ophthalmoplegia

opportunistic infection

opportunistic infection, CNS

ornithine transcarbamylase deficiency

ovarian dysgenesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

parasitic infection, CNS

Parkinsonism syndrome

paroxysmal neurologic deficits

pathologic reflex

peripheral blood smear

Perrault syndrome

philtrum, tented

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

polyglucosan body disease

polymerase chain reaction

Pompe's disease of glycogen storage

pons, lesion of

precipitating factors

progressive neurologic disorder

proximal muscle atrophy

pseudobulbar palsy

pseudoxanthoma elasticum

psychiatric problems in neurologic disorders

ptosis, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

ragged-red fibers

release phenomena

respiratory tract infection

salivation, excessive

sarcoidosis, CNS

sedimentation rate, elevated

sensorineural hearing loss

shunt procedure, ventricular

shunt procedure, ventricular-complications of

skin, hyperextensible

skin, lesions in neurologic disorders

skin, translucent

sleep pathology and physiology

small vessel disease

small vessel disease, cerebral

spastic paraplegia, type 7

speech disorder

speech, absence of

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 28

spinocerebellar degeneration

standing difficulty

status epilepticus

striatal encephalitis

strokelike episodes

subarachnoid hemorrhage

symmetric brain lesions

systemic illness

tandem gait, ataxic

telangiectases, retinal

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

tone, muscle, increased

tongue, enlarged

treatment of neurologic disorder

treatment, empirical

tremor, intention

trinucleotide repeats

tumefactive lesion

urea-cycle enzymopathies

urinary incontinence

urinary urgency

vestibular migraine

viral infection

viral infection, CNS

vision loss, sequential

vision, blurred

visual field defect

visual loss, progressive

visual loss, transient

visual obscurations, transient

walking, delayed

walking, difficulty with

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

white matter disease

white matter disease, subcortical

white matter disease, unilateral

whole genome sequencing

wide based gait

winging of scapula

wound healing, poor

x-linked intellectual deficit

x-linked mental retardation

Showing articles 200 to 250 of 290 << Previous Next >>

Survival of Implanted Fetal Dopamine Cells & Neuro Improvement 12 to 46 Months after Transpl for Parkinson's
NEJM 327:1549-1555, 15891992., Freed,C.R.,et al, 1992

Bilateral Fetal Mesencephalic Grafting in Two Patients with Parkinsonism Induced by MPTP
NEJM 327:1556-1563, 15891992., Widner,H.,et al, 1992

Cerebral Glucose Metabolism in Parkinson's Disease with and without Dementia
Arch Neurol 49:1262-1268, Peppard,R.F.,et al, 1992

HIV Encephalopathy and Dementia
Psychiatr Clin North Am 15:455-466, Pajeau,A.K.&Roman,G.C., 1992

Striatal D2 Receptor Status in Patients with Parkinson's Disease, Striatonigral Degeneration, and PSP, (PET)
Ann Neurol 31:184-192, Brooks,D.J.,et al, 1992

Transplantation of Fetal Dopamine Neurons in Parkinson's Disease:PET Studies in 2 Pts with Putaminal Implants
Ann Neurol 31:166-173, Sawle,G.V.,et al, 1992

FDG-PET in Pediatric Posterior Fossa Brain Tumors
J Comput Assist Tomogr 16:62-68, Hoffman,J.M.,et al, 1992

Infantile Spasms:II. Lenticular Nuclei and Brain Stem Activation on Positron Emission Tomography
Ann NEurol 31:212-219, Chugani,H.T.,et al, 1992

Crossed Cerebellar Diaschisis and Crossed Cerebellar Atrophy:MR Findings & Clin Symptoms in 26 Pts
AJR 158:1155-1159, Tien,R.D.&Ashdown,B.C., 1992

Hypertensive Encephalopathy:Findings on CT, MR Imaging, and SPECT Imaging in 14 Cases
AJR 159:379-383, Schwartz,R.B.,et al, 1992

New Anatomical and Functional Imaging Methods
Ann Neurol 32:395-400, Prichard,J.W.&Brass,L.M., 1992

Advances in Neurology
NEJM 326:1608-1616, 1671-16761992., Gilman,S., 1992

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

Cerebral Brain Metabolism in Adult Dyslexic Subj Assessed with PET Scan During Auditory Task
ARch Neurol 49:734-739, Hagman,J.O.,et al, 1992

The Biology of Developmental Dyslexia
JAMA 268:912-915, Rumsey,J.M., 1992

Blinded Clinical Evaluation of Positron Emission Tomography for Diagnosis of Probable Alzheimer's Disease
Neurol 42:765-770, Powers,W.J.,et al, 1992

Assessment:Positron Emission Tomography
Report of Therapeutics & Technology Assessment Subcommittee of the AAN, Neurol 41:163-16791., , 1991

PET:Its Clinical Role in Neurology
JNNP 54:1-5, Brooks,D.J., 1991

Widespread Functional Effects of Discrete Thalamic Infarction
Arch Neurol 48:178-182, Szelies,B.,et al, 1991

Identification of Early Recurrence of Primary Central Nervous System Tumors by (18F) Fluorodeoxyglucose PET
Ann Neurol 29:347-355, 3451991., Glantz,M.J.,et al, 1991

Posterior Cortical Dementia with Alexia:Neurobehavioural, MRI, and PET Findings
JNNP 54:443-448, Freedman,L.,et al, 1991

Positron Emission Tomography in Progressive Supranuclear Palsy
Arch Neurol 48:389-391, Bhatt,M.H.,et al, 1991

Dopa-responsive Dystonia:[18F]Dopa Positron Emission Tomography
Ann Neurol 30:24-30, Sawle,G.V.,et al, 1991

Preclinical Detection of Parkinson's Disease
Neurology Suppl 2, 41:5-921991., Koller,W.C.&Langston,J.W., 1991

Technology Assessment Revisited:Does Positron Emission Tomography Have Proven Clinical Efficacy?
Neurol 41:1339-1340, Powers,W.J.,et al, 1991

Visual Loss in Tuberous Sclerosis
Neurol 41:1915-1917, Dotan,S.A.,et al, 1991

Positron Emission Tomography in Neuropsychiatric Lupus Erythematosus
Neurol 40:304-308, Stoppe,G.,et al, 1990

Preliminary Report:Activation of the Cerebellum in Essential Tremor
Lancet 336:1028-1030, Colebatch,J.G.,et al, 1990

Cerebral Glucose Hypermetabolism in Friedreich's Ataxia Detected with Positron Emission Tomography
Ann Neurol 28:750-757, Gilman,S.,et al, 1990

Clinical & PET Studies in the'Extrapyramidal Syndrome'of Dementia of the Alzheimer Type
Arch Neurol 47:1318-1323, Tyrrell,P.J.,et al, 1990

Plasticity in the Aging Brain
Arch Neurol 47:1336-1341, Kaye,J.A.,et al, 1990

The Nigrostriatal Dopaminergic System Assessed in Vivo by PET Volunteers & Pts with Parkinson's Disease
Arch Neurol 47:1290-1298, Leenders,K.L.,et al, 1990

Cerebral Glucose Metabolism in Adults with Hyperactivity of Childhood Onset
NEJM 323:1361-1366, 1413-14151990., Zametkin,A.J.,et al, 1990

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

A Brain Transplant that Works
Lancet 335:445-446, , 1990

Positron Emission Tomography in Shy-Drager Syndrome
Ann Neurol 28:101-103, Bhatt,M.H.,et al, 1990

PET Study in Progressive Supranuclear Palsy, Hypometabolic Pattern
Arch Neurol 47:747-752, Blin,J.,et al, 1990

Positron Emission Tomography in Creutzfeldt-Jakob Disease
Arch Neurol 47:1035-1038, Holthodd,V.A.,et al, 1990

Transplantation of Human Fetal Dopamine Cells for Parkinson's Disease
Arch Neurol 47:505-512, Freed,C.R.,et al, 1990

National Cancer Institute Workshop Statement
Advances in Clinical Imaging Using Positron Emission Tomography, Arch Int Med 150:735-739, 729990., , 1990

Cerebral Metabolic Asymmetries & Assoc Neuro-psych Patterns in Early Dementia of the Alzheimer Type
Arch Neurol 47:753-760, Haxby,J.V., 1990

Infantile Spasms:I. PET Identified Focal Cortical Dysgenesis in Cryptogenic Cases for Surgical Treatment
Ann Neurol 27:406-413, Shields,W.D.,et al, 1990

Slowly Progressive Aphasia:Three Cases with Language, Memory, CT and PET Data
JNNP 53:987-993, Kempler,D.,et al, 1990

Pituitary Microadenomas:A PET Study
Radiology 177:39-44, DeSouza,B.,et al, 1990

The Brain in Schizophrenia
JNNP 53:725-726, Ron,M.A.&Harvey,I., 1990

The Evaluation and Treatment of Seizures
NEJM 323:1468-1474, Scheuer,M.L.&Pedley,T.A., 1990

PET Scanning, Provides Information on Function
BMJ 298:692-694, Frackowiak,R.S.J.&Jones,T., 1989

SPECT and PET in Epilepsy
Editorial, Lancet 1:135-1371989., , 1989

A Referendum on Clinical Trial Research in Multiple Sclerosis:Opinion of Jekyll Island Workshop
Neurol 39:977-981, Noseworthy,J.H.,et al, 1989

Immunological Treatment for Multiple Sclerosis
Editorial, Lancet 1:699-7011989., , 1989

Showing articles 200 to 250 of 290 << Previous Next >>