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Aicardi-Goutieres syndrome

altered states of consciousness

alternating hemiplegia

amobarbitol interview

AMPA receptor antibodies

amphiphysin antibodies

amyloid angiopathy, cerebral

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, Parkinson-dementia-complex

anesthesia, spinal

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral, beaded vessels

angiography, cerebral

animal exposure

anti basal ganglia antibodies

antibiotics, neurologic complications with

antibodies to measles

antiphospholipid antibodies

antithyroid antibodies

arrhythmia, cardiac

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

autonomic nervous system

autonomic neuropathy

B 12 deficiency

bacterial infection

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

blood brain barrier

Borrelia miyamotoi infection

bovine spongiform encephalopathy

brain biopsy, false negative

brainstem, infarction of

brainstem, lesion of

Brueghel's syndrome

burning feet, differential diagnosis of

calcification, intracranial

carbon monoxide poisoning

carcinoma of lung

carotid angiogram

carpo-pedal spasm

CAT scan, abnormal

CAT scan, chest

CAT scan, complication with

CAT scan, contrast enhanced

CAT scan, emission, abnormal

CAT scan, pelvis

celiac disease, adult

central nervous system, infection of

central pontine myelinolysis

cerebellar degeneration

cerebellar lesion

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral infarction

cerebral ischemia

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gamma amino butyric acid

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, intraventricular

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, young adult

cervical spondylosis

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chilbran skin lesions

choreoathetosis

chronic progressive external ophthalmoplegia

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

coccidioidomycosis

cogwheel rigidty

collapsin response mediator protein 5 IgG

congenital infection, CNS

congenital paresis

contactin associated protein like 2 antibodies

conversion reaction

cortical blindness

cortical ribbon sign

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

cytomegalic inclusion disease

cytomegalovirus infection

deep gray nuclei

delay in diagnosis

dementia, childhood

dementia, differential diagnosis of

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, transmissible

dementia, treatment of

demyelinating disease

dentate nuclei, lesion of

dermatomyositis

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

differential diagnosis

disability, neurological

distal muscle atrophy

distal muscle weakness

doll's head maneuver

downward gaze, paralysis of

DPPX, antibodies, encephalitis

dysequilibrium syndrome

dyskinesia, facial

dystonia, children

electrical injury of nervous system

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

encephalitis lethargica

encephalitis, autoimmune

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encephalitis, diagnosis of

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encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalitis, Powassan

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encephalomyelitis

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encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, parainfectious

encephalopathy, progressive

enterovirus infection of CNS

epidemiology of neurology

epilepsia partialis continua

episodic disorders

episodic neurologic deficits

episodic unconsciousness

extralimbic encephalitis

eye movement, disorders of

eye movement, painful

facial movement disorder

facial nerve palsy

faciobrachial dystonic seizure

feeding disorder

fine motor function, impaired

flaccid paralysis

frontal lobe, pathologic signs of

fungal infection, CNS

F-wave response

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

geographic location

gliadin antibodies

gliomatosis cerebri

glutamic acid decarboxylase, antibody

gram positive rod

granuloma, pulmonary

hallucination, olfactory

hallucination, visual

hand-foot-mouth disease

headache, severe

headache, sudden onset of

headache, throbbing

headache, vascular

hemimyoclonic jerks

hemiparesis, transient

hepatosplenomegaly

heralding manifestation

herpes simplex encephalitis

herpes simplex virus

human immunodeficiency virus type 1

hydrocephalus, normal pressure

hydroxyindole acetic acid 5(5HIAA)

hydroxytryptophan L-5(L-5 HTP)

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypertensive encephalopathy

hyperthyroidism

hypoglycorrhachia

hypothalamus, disturbance of

iatrogenic neurologic disorders

immunohistochemistry

immunologic disease

immunology and the nervous system

immunosuppression

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

interferon alpha

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

juvenile distal and segmental muscular atrophy

juvenile paresis

Kearns-Sayre syndrome

Krabbe's disease

lactic dehydrogenase(LDH)

laminectomy, cervical

Leber's hereditary optic neuropathy

Leigh's disease

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

limbic encephalitis

liver function enzymes

lymphadenopathy

lymphoma involving CNS

lymphoma, primary of CNS

malignancy screen

malignancy, occult

meconium staining

mediastinum, mass of

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, fungal

meningitis, neutrophilic

meningitis, syphilitic

meningitis, treatment of

meningoencephalitis

meningoencephalomyelitis

mental status, abnormal

mesial temporal lobe

midbrain, infarction of

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoclonal antibodies

motor neuron disease

motor neuron disease, misdiagnosis

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, hypointense signal foci on

MRI, spinal cord

MRI, sulcal hyperintensity

multiple sclerosis

muscle tenderness

myasthenia gravis, paraneoplastic

myasthenic syndrome

mycoplasma pneumoniae

myelitis, longitudinal

myelitis, transverse

myelitis, transverse, recurrent

myoclonic ataxia

myoclonic jerks

myoclonus, abdominal

myoclonus, cortical

myoclonus, epilepsy

myoclonus, segmental

myoclonus, treatment of

myopathy, mitochondrial

nausea and vomiting

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve conduction studies

neurexin-3 alpha antibodies

neurologic complications of, burns

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular junction

neuronal cell surface antigen

neuronopathy, sensory

neuropathology, brain

neuropathy, paraneoplastic

NMDA antagonists

nystagmus, vertical

occupational neurologic disorders

ocular motility, disorders of

oculogyric crisis

oculomasticatory myorhythmia

old age, neurology of

olivary degeneration, hypertrophic

onconeural antibodies

ophthalmoplegia

opportunistic infection

opsoclonus-myoclonus syndrome

optic chiasm, enlarged

optic nerve, enlarged

optic neuropathy

oral ulcerations

ovary, enlarged

pain, abdominal

palatal myoclonus

paralysis, acute

paralysis, acute areflexic

paraneoplastic cerebellar degeneration

Parkinson disease, postencephalitic

Parkinsonism syndrome

PAS positive material in the brain

patient information and support

periarteritis nodosa

peripheral nerve, lesion of

personality change

phenylketonuria

pigmentary retinopathy

pituitary, hormones of

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pneumoencephalogram(PEG)

poliomyelitis-like illness

polymerase chain reaction

polyneuropathy, uremic

pons, lesion of

posterior inferior cerebellar artery syndrome

posterior leukoencephalopathy syndrome

precipitating factors

prevention of neurologic disorders

progressive multifocal leucoencephalopathy

progressive neurologic disorder

protein 14-3-3, cerebrospinal fluid

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary embolism

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pyramidal tract

pyramidal tract dysfunction

rabies, nervous system involvement with

radiation therapy, CNS treatment and complications with

ragged-red fibers

Ramsay Hunt syndrome

rapidly progressing neurologic illness

real-time quaking-induced conversion

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal transplantation

respiratory failure

restless leg syndrome

reticulum cell sarcoma

retro-orbital pain

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

sarcoidosis, CNS

Schilder's disease

sedimentation rate, elevated

seizure, drug resistance

seizure, precipitating factors

seizure, spinal

seizure, stimulus sensitive

seizure, treatment of

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

skin, lesions in neurologic disorders

sleep pathology and physiology

slow virus infection of CNS

sodium valproate

speech disorder, childhood

spinal cord, injury of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal cord, vascular malformation of

spirochete infection

spongy degeneration of brain

startle myoclonus

startle reaction

status epilepticus, intractable

steroid therapy, CNS treatment and complications with

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

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

subacute sclerosing panencephalitis, adult onset

subdural hematoma

symmetric brain lesions

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

teratoma, ovarian

thalamus, lesion of-bilateral

thrombocytopenia

tonic cerebellar fits

toxoplasmosis, acquired

toxoplasmosis, CNS

transient neurologic deficit

transplacental virus infections

treatment of neurologic disorder

triangle of Guillain and Mollaret

Trousseau's sign

unconsciousness

unconsciousness, episodic

unconsciousness, transient

upgaze, paralysis of

uremic encephalopathy

uremic twitching

varicella zoster virus

viral infection

viral infection, CNS

viral isolation

vision, blurred, monocular

visuospatial disturbance

vitreous opacities

walking, difficulty with

weakness, generalized

Wernicke's encephalopathy

West Nile fever

Whipple's disease

white matter disease

white matter disease, subcortical

wide based gait

word-finding difficulty

zoster sine herpete

Showing articles 3550 to 3600 of 5034 << Previous Next >>

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Paraparesis During Myelography Associated with a Ruptured Thoracic Intervertebral Disc
Neurosurgery 24:912-914, Lehman,L.B., 1989

Internuclear Ophthalmoplegia in Tuberculous Meningitis
Tubercle 70:61-64, Teoh,R.,et al, 1989

Magnetic Resonance Imaging in Asymptomatic Disseminated Vasculomyelinopathy
J Neurol Sci 94:69-77, Poster, C.M., 1989

New-Onset Seizures Associated with Human Immunodeficiency Virus Infection: Causation and Clinical Features in 100 Cases
Am J Med 87:173-177, Holtzman, D.M.,et al, 1989

Cervical Myelopathy Secondary to Movement Disorders:Case Report
Neurosurgery 24:902-905, El-Mallakh,R.S.,et al, 1989

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

Headaches in Pregnancy
Semin Neurol 8:187-192, Reik,L., 1988

CT, MR, and Pathlogy in HIV Encephalitis and Meningitis
AJR 151:373-380, Post,M.J.D.,et al, 1988

Rapidly Progressive Dementia Caused by Spongiform Encephalopathy
West J Med 148:313-319, Enos,B.E.&Vinters,H.V., 1988

Postmarketing Surveillance for Neurologic Adverse Events after Hepatitis B Vaccination, Exp of the First 3 Yrs
Am J Epidemiol 127:337-352, Shaw,F.E.,et al, 1988

Paraplegia and Quadriplegia after Intrathecal Chemotherapy
Arch Phys Med Rehabil 69:1054-1056, Werner,R.A., 1988

Serum Antibodies to GM1 Ganglioside in Amytrophic Lateral Sclerosis
Neurol 38:1457-1461, Pestronk,A.,et al, 1988

Amyotrophic Lateral Sclerosis Presenting with Sleep Hypopnea Syndrome
Chest 93:1309-1312, Carre,P.C.,et al, 1988

Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988

A Creutzfeldt-Jakob Like Syndrome Due to Lithium Toxicity
JNNP 51:120-123, Smith,S.J.M.&Kocen,R.S., 1988

Myoclonus During Combined Tricyclic Antidepressant and Lithium Treatment
J Clin Psychopharmacol 8:446-447, Devanand,D.P.,et al, 1988

Creutzfeldt-Jakob Disease without Periodic Sharp Wave Complexes:A Clinical, EEG, and Path Study
Neurol 38:1056-1060, Zochodne,D.W.,et al, 1988

Neurologic Complications of Bone marrow Transplantation
In Neurol Complic of Transplants, Neurologic Clinics, 6:377-378988., Davis,D.G.&Patchell,R.A., 1988

MR Imaging of the Brain in Myelopathy Associated with Human T-Cell Lymphotropic Virus Type I
J Comput Assist Tomogr 12:750-754, Hara,Y.,et al, 1988

HTLV-I-Associated Myelopathy:Oligoclonal Immunoglobulin G Bands Contain Anti-HTLV-I-p24 Antibody
Ann Neurol 24:727-731, Grimaldi,L.M.E.,et al, 1988

Plasmapheresis in Treatment of Human T-Lymphotropic Virus Type-I Associated Myelopathy
Lancet 2:1109-1113, Matsuo,H.,et al, 1988

Human Immunodeficiency Virus in Vacuolar Myelopathy of the Acquired Immunodeficiency Syndrome
NEJM 319:1667-1668, Budka,H.,et al, 1988

Elevated Serum Antibody Titers to Epstein-Barr Virus in HTLV-I Associated Myelopathy (HAM)
Neurol 38:1650-1653, Itoyama,Y.,et al, 1988

Clinicopath Conf
Chronic Meningitis in a 68-Year Old Man, Granulomatous Angitis of the Central Nervous System, Am J M, d :407-413,1988., 1988

Familial Alzheimer's Disease with Myoclonus and'Spongy Change'
Arch Neurol 45:1097-1100, Duffy,P.,et al, 1988

Pain Syndromes in Multiple Sclerosis
Neurol 38:1830-1834, Moulin,D.E.,et al, 1988

Granulomatous Angiitis of the Central Nervous System:Protean Manifestations and Response to Treatment
JNNP 51:1126-1133, Koo,E.H.&Massey,E.W., 1988

Diagnostic Classification of Stroke, Especially Lacunes
Stroke 19:1071-1073, 1074-1083, 1988, Weisberg,L.A., 1988

The Clinical Spectrum of Alcoholic Pellagra Encephalopathy, A Retrospective Analysis of 22 Cases Studied Pathologically
Brain 111:829-842, Serdaru,M.,et al, 1988

Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
Arch Neurol 45:1118-1122, Uitti,R.J.,et al, 1988

Clinicopath Conf
Progressive Multifocal Leukoencephalopathy, Chronic Lymphocytic Leukemia, Case Record 45-1988, NEJM, 19:8-1280,1988., 1988

Tumors of the Brain and Nervous System After Radiotherapy in Childhood
NEJM 319:1033-1039, Ron,E.,et al, 1988

MR Imaging of Neurocysticercosis
J Comput Assist Tomogr 12:927-934, Zee,C.S.,et al, 1988

Leptomeningeal Dissemination of Low-Grade Gliomas in Childhood
Neurol 38:562-566, Civitello,L.A.,et al, 1988

Treatment Response in Malignant Optic Glioma of Adulthood
Neurol 38:1071-1074, Albers,G.W.,et al, 1988

Neck-Cracker Neuropathy
NEJM 318:1072, Nelson,K.R.&Tibbs,P., 1988

Magnetic Resonance Imaging in the Assessment of Medullary Compression in Achondroplasia
Am J Dis Child 142:989-992, Thomas,I.T.,et al, 1988

Undiagnosed Spinal Cord Injuries in Brain-Injured Children
Am J Dis Child 142:965-967, Sneed,R.C.&Stover,S.L., 1988

Microdiscectomy for Treating Lumbar Disc Protrusion, An Important Advance that Merits Wide Adoption
BMJ 297:5, Evans,G.&Jackson,R.K., 1988

Spinal Cord Infarction
Stroke 19:529-532, Satran,R., 1988

Steroid-Induced Spinal Epidural Lipomatosis:CT Survey
J Comput Assist Tomogr 12 501-503, Buthiau,D.,et al, 1988

Neurological Deterioration after Laminectomy for Spondylotic Cervical Myeloradiculopathy:Role of Sp Cord Ischaemia
JNNP 51:717-718, Cybulski,G.R.,et al, 1988

Odontoid Fracture in a Child Occupying a Child Restraint Seat
Pediatrics 82:117-118, Diekema,D.S.&Allen,D.B., 1988

Acute Paraplegia:A Presenting Manifestation of Aortic Dissection
Am J Med 84:765-770, Zull,D.N.&Cydulka,R., 1988

Long-Term Follow-Up of 71 Patients with Thunder-Clap Headache Mimicking Subarachnoid Haemorrhage
Lancet 2:68-70, Wijdicks,E.F.M.,et al, 1988

Outcome from Coma After Cardiopulmonary Resuscitation:Relation to Seizures & Myoclonus
Neurol 38:401-405, Krumholz,A.,et al, 1988

Clinicopath Conf
Wegner's Granulomatosis Involving Paranasal Sinuses & Leptomeninges, Case Record 12-1988, NEJM 318:7, 0-7688., 1988

Weakness of the Lower Extremity in Carotid Occlusive Disease
Arch Neurol 45:297-301, Yanagihara,T.,et al, 1988

Showing articles 3550 to 3600 of 5034 << Previous Next >>