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abducens nerve paralysis, bilateral

acute ataxia of childhood

acute cerebellar ataxia

acute disseminated encephalomyelitis

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

alcohol intolerance

alkalosis, respiratory

alpha-fetoprotein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

Alzheimer's disease

AMPA receptor antibodies

amyotrophic lateral sclerosis

aneurysm, children

aneurysm, fusiform

aneurysm, vertebral basilar system

Angelman syndrome

angiitis, granulomatous of CNS

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, negative

angiography, posterior fossa

angiotensin-converting enzyme

animal exposure

ankle reflex, absent

anti GQ1b IgG antibody

antibodies to measles

anticonvulsants

anticonvulsants, effectiveness

antithyroid antibodies

apraxia of eye movements

Arnold Chiari malformation

arterial dissection

arterial dissection, intracranial

arterial dissection, ruptured

arterial dissection, vertebral

arylsulfatase A

ascending paralysis

ataxia telangiectasia

ataxia, acute onset

ataxia, cerebellar

ataxia, congenital

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, truncal

autoimmune basal ganglia encephalitis

autoimmune disease

automobile accidents

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

bacterial infection

bacterial infection, CNS

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery migraine

basilar artery occlusion

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

behavioral disorder, acute

biotin deficiency

biotinidase deficiency

blindness, monocular

blindness, transient

blood dyscrasias, neurologic findings with

bone marrow biopsy

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, dysfunction

brainstem, glioma in children

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

calcification, intracranial

calcium antagonist

carcinoembryonic antigen

carcinoma of pancreas

carpo-pedal spasm

CAT scan, abnormal

CAT scan, angiography

CAT scan, dense artery sign

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, pelvis

cataracts, congenital

cat-scratch disease

cauda equina, enhancement

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar pontine angle

cerebellar pontine angle tumor

cerebellar vermis

cerebellitis, autoimmune

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, mechanical extraction

cerebral folate deficiency syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, bilateral

cerebrovascular accident, prognosis in

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

cerebrovascular disease, surgical treatment of

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

choreoathetosis

chorioretinitis

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

cognitive delay

conjunctival biopsy

corpus callosum, thinning

cortical ribbon sign

counterimmunoelectrophoresis

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cyst, parenchymal

cyst, subcortical

decerebrate posture

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delayed dentition

dementia, childhood

dementia, presenile

dementia, reversible

dementia, treatment of

demyelinating disease

dense basilar artery sign

dense middle cerebral artery sign

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatitis herpetiformis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diagnostic criteria

differential diagnosis

digital subtraction angiography

disability, neurological

disease modifying agents

diurnal variation

doll's head maneuver

down-beat nystagmus

Dravet syndrome

drug induced neurologic disorders

drug induced neurologic disorders in children

dysdiadochokinesia

dyskinesia, buccal lingual facial

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electron microscopy

embolism, paradoxical

embolism, vertebral-basilar artery

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, etiology

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, postinfectious

encephalomyopathy

encephalopathy, acute

encephalopathy, Hashimoto's

endovascular therapy

enterovirus infection of CNS

epicanthal folds

epidemiology of neurology

episodic disorders

episodic neurologic deficits

Epstein-Barr virus

evoked potentials

exercise intolerance

exome sequencing

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

feeding disorder

finger nose finger test

fingerprint bodies

Fisher's syndrome

flaccid paralysis

fluorescene in situ hybridization

folic acid deficiency

fornix, lesion of

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

fragile-X syndrome

Friedreich's ataxia

fundus, abnormality of

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic linkage

genetic neurologic disorders

genetic testing

Gillespie syndrome

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

gluten sensitivity

gluten-free diet

gram negative rod

granulomatous disease

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, variant forms of

hallucination, visual

hand-foot-mouth disease

Hartnup's disease

headache, bifrontal

headache, occipital

headache, recurrent

headache, severe

headache, sudden onset of

hearing problems in children

heavy metal intoxication

heel-knee-shin test

hemosiderosis of CNS, superficial

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

herniated disc, thoracic

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

Huntington's chorea

hydroxyglutaric aciduria

hyperintense vessel sign

hyperosmolality

hypertension, cerebrovascular disease with

hyperventilation

hypocalcemia, causes of

hypomyelination

hypoparathyroidism

hypopigmentation of skin

hypothalamus, disturbance of

hypotonia, infants

iatrogenic neurologic disorders

immunization, neurologic complications with

immunodeficiency

immunosuppression

inappropriate antidiuretic(A.D.H.)hormone

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic intranuclear

industrial neurologic disorders

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

internal capsule

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intracranial hypertension, benign

intracranial pressure, increased

intrathecal medication

Jakob-Creutzfeldt disease

Kearns-Sayre syndrome

lactic acidemia

language disorders in children

laryngismus stridulus

laughing, pathologic

lead and the nervous system

lead line, gingival

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukoencephalopathy

level of consciousness, decreased

limbic encephalitis

lipid storage disorder of CNS

liver function enzymes

locked-in syndrome

lymphadenopathy

lysosomal storage disease

macular degeneration

maple syrup urine disease

marche a petits pas

Marinesco-Sjogren syndrome

mediastinum, mass of

memory, impairment of

meningitis, aseptic

meningitis, carcinomatous

meningitis, recurrent

meningoencephalitis

meningoencephalitis, mumps

meningovascular syphilis

mental retardation

mental status, abnormal

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, children

migraine, visual symptoms in

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

molecular genetics

monoclonal antibodies

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, angiography

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR, hyperintense vessels

MRI, high signal foci on

MRI, spinal cord

multimodal neuroimaging

multiple sclerosis

multiple sclerosis, children

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, presenting manifestations

multiple sclerosis, prognosis

multiple system atrophy

muscle weakness

mycoplasma pneumoniae

myelinolysis, extrapontine

myoclonic jerks

myoclonus, epilepsy

myopathy, mitochondrial

myotonia dystrophica

nausea and vomiting

neonatal screening, genetic neurologic disorders

neoplasm, posterior fossa

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-treatment of

nephrotic syndrome

nerve conduction studies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neurocutaneous disease

neuroendocrinology

neurologic complications

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination, focal

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuropathology, brain

neuropathy, acute

neurotoxicity, acute

neurotransmitter

Niemann-Pick disease

NMDA antagonists

nystagmus, hereditary

nystagmus, monocular

nystagmus, periodic

nystagmus, rotary

nystagmus, vertical

ocular motility, disorders of

oculodentodigital dysplasia

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, progressive external

opsoclonus-myoclonus syndrome

optic disc edema

optic neuritis, children

optic neuropathy

optical coherence tomography

oral ulcerations

osmotic demyelination syndrome

ovary, enlarged

pain, abdominal

paralysis, acute

paralysis, acute areflexic

paraparesis, familial spastic

paraparesis, spastic

Parkinson disease

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

paroxysmal tonic upgaze

patent foramen ovale

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

Penumbra System

personality change

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

polymerase chain reaction

pons, infarction of

pons, lesion of

Poretti-Boltshauser syndrome

posterior leukoencephalopathy syndrome

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prevention of neurologic disorders

primary episodic ataxia

progressive multifocal leucoencephalopathy

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

ptosis, bilateral

puberty, delayed

pulmonary edema

pulmonary infection

pulmonary infiltrates

Purkinje cell surface antibody

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

Refsum's disease

remote effect of cancer on the nervous system

respirations in CNS disease

respiratory failure

respiratory tract infection

retina, abnormal

retinal degeneration

retinitis pigmentosa

Rett's syndrome

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

rubella encephalitis, progressive

salivation, excessive

sarcoidosis, CNS

seizure, children

seizure, differential diagnosis of

seizure, drug-induced

seizure, familial

seizure, febrile

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, tonic-clonic

seizure, treatment of

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

serologic testing

serologic testing, false negative

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

sodium channel dysfunction

speech disorder

speech disorder, childhood

speech, delayed development of

speech, loss of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinocerebellar degeneration

spongy degeneration of brain

startle myoclonus

status epilepticus

status tetanicus

steroid therapy, CNS treatment and complications with

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

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

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subarachnoid hemorrhage, recurrent

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

teeth, wide-spaced

temporal lobe, lesion

teratoma, ovarian

tetany, normocalcemic

thalamus, lesion of

tongue, protrusion of

toxins, nervous system

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trinucleotide repeats

Trousseau's sign

upgaze, paralysis of

upgaze, sustained

urinary incontinence

urinary retention

urine test for metabolic disorders

urine test in toxic screen

vaccination, neurologic complications with

vasospasm, cerebral

vertebral-basilar insufficiency

vertigo, episodic

violent behavior

viral infection

viral infection, CNS

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual impairment

visual loss, progressive

visual loss, slow

visual loss, sudden-unilateral

visual loss, transient

visual obscurations, transient

visuospatial disturbance

von Bonsdorff's sign

Von Hippel Lindau

walking, difficulty with

weakness, generalized

white matter disease

wide based gait

Wolfram syndrome

X-linked bulbospinal neuronopathy

Showing articles 450 to 500 of 4289 << Previous Next >>

Clinical and MRI Findings in Spinocerebellar Ataxia Type 5
Neurol 53:1355-1357, Stevanin,G.,et al, 1999

Cerebellar Ataxia Associated with Subclinical Celiac Disease Responding to Gluten-Free Diet
Neurol 53:1606-1608, Pellecchia,M.T.,et al, 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

N-Acetylcysteine Therapy for Unverricht-Lundborg Disease
Neurol 52:426-427, Selwa,L.M., 1999

Leukoencephalopathy and Raised Brain Lactate from Heroin Vapor Inhalation ("Chasing the Dragon")
Neurol 53:589-1048, Kriegstein,A.R., et al, 1999

Opsoclonus as a Dominant Sign in Primary Sjogrens Syndrome
Neuro-Opthlhal 22:135-138, Lubec,D.,et al, 1999

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Susac Syndrome
Medicine 77:3-11, Papo,T.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

Chronic Progressive Leukoencephalopathy in Adult Celiac Disease
Neurol 50:820-822, Beyenburg,S.,et al, 1998

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998

Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
AJR 171:1131-1137, Antunez, E.,et al, 1998

Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
, Ghika,J. &Bogousslavsky, J., 1998

Adult Brainstem Gliomas
Neurol 51:1136-1139, Landolfi,J.C.,et al, 1998

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
Lancet 352:1582-1585, Hadjivassiliou,M.,et al, 1998

Ataxic Hemiparesis,Critical Appraisal of a Lacunar Syndrome
Stroke 29:2549-2555, Gorman,M. J.,et al, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
Neurol 51:882-884, Abe,Y.,et al, 1998

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Myelopathy Caused by Nitrous Oxide Toxicity
AJNR 19:894-896, 9941998., Pema,P.J.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998

Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998

Lateral Medullary Infarction
Stroke, Pathophysiology, Diagnosis and management, Churchhill Livingstone, NY 3rd Ed, Ch 22, p. 534, Amarenco,P.,et al, 1998

Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 1998

Hypophosphatemia-Induced Neuropathy: Clinical and Electrophysiologic Findings
Muscle Nerve 21:650-652, Siddiqui,M.F. &Bertorini,T.E., 1998

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Ocular Findings in Ramsay Hunt Syndrome
J Neuro-Ophthalmol 17:199-201, Mansour,A.M.&Bailey,B.J., 1997

Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

Causes and Mechanisms of Cerebellar Infarction in Young Patients
Stroke 28:2400-2404, Barinagarrementeria,F.,et al, 1997

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997

Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,et al, 1997

Is There a Gulf War Syndrome? Searching for Syndromes by Factor Analysis of Symptoms
JAMA 227:215-222, 2591997., Haley,R.W.,et al, 1997

Self-Reported Exposure to Neurotoxic Chemical Combinations in the Gulf War:A Cross-Sectional Epidemiologic Study
JAMA 227:231-237, 2591997., Haley,R.W.&Kurt,T.L., 1997

Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
Neurol 48:645-649, Kobari,M.,et al, 1997

MR of Childhood Metachromatic Leukodystrophy
AJNR 18:733-738, Kim,T.S.,et al, 1997

A 36-Year-Old Woman Recuperating From a Stroke
JAMA 277:1970-1976, Alexander,M., 1997

Pure or Predominant Sensory Stroke Due to Brain Stem Lesion
Stroke 28:1761-1764, Kim,J.S.&Bae,Y.H., 1997

Showing articles 450 to 500 of 4289 << Previous Next >>