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abscess, intracerebral

abscess, intracranial

abscess, retropharyngeal

abscess, sphenoid sinus

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome-related complex

addiction, heroin

adolescent medicine

advances in neurology

adverse drug reaction

Aicardi-Goutieres syndrome

airway obstruction

akinesia of eyelid function

alcohol, neurologic complications with

alcoholic withdrawal states, DT's, convulsions, etc.

alexia without agraphia

alien hand syndrome

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

alveolar hypoventilation

Alzheimer's disease

aminoacidopathies

AMPA receptor antibodies

amphetamines, dyskinesia associated with

amphiphysin antibodies

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

anemia, hemolytic

aneurysm, intracranial

anti basal ganglia antibodies

anti GQ1b IgG antibody

anticholinergic drugs

anticholinesterase

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, untoward effects of

anti-dopamine 2 receptor antibody

antistreptolysin titer

anxiolytic agents

aortic valve, lesion of

aphasia, progressive, primary

apraxia of eye movements

apraxia of eyelid opening

apraxia, constructional

arm swing, reduced

arrhythmia, cardiac

arteriovenous malformation

arteriovenous malformation, cerebral

arthrogryposis multiplex

arylsulfatase A

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, truncal

ataxic-dystonia syndromes

athetosis, causes of

atlanto-axial subluxation

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autoimmune basal ganglia encephalitis

autoimmune disease

automobile accidents

autonomic dysfunction

autonomic neuropathy

B 12 deficiency

bacterial infection

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery migraine

behavioral disorder

benign essential tremor

bent spine syndrome

beta adrenergic blocker

bilirubin encephalopathy

biopterin deficiency

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

bladder dysfunction

blinking, reduced

bone marrow biopsy

botulinum toxin

botulinum toxin, complications of

brainstem, atrophy

brainstem, dysfunction

brainstem, lesion of

Brueghel's syndrome

bulbar dysfunction

calcification, intracranial

calcium antagonist

calcium antagonist, side effects of

carbamazepine, toxicity

carbon monoxide poisoning

carcinoembryonic antigen

cardiac arrest and resuscitation

cardiopulmonary bypass

carotid artery occlusion, neck

carpal tunnel syndrome

CAT scan, abnormal

CAT scan, chest

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, isodense lesion with acute hemorrhage

CAT scan, muscle

caudate nucleus, atrophy

caudate nucleus, lesion of

cavernous hemangioma

cavernous sinus

cavernous sinus, metastasis to

cavernous sinus, syndrome

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar edema

cerebellar lesion

cerebellar pontine angle

cerebellar pontine angle tumor

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral ischemia

cerebral palsy, adults

cerebral palsy, associated problems with

cerebral peduncle

cerebral vasculature, calcification

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, biochemical markers of CNS tumors

cerebrospinal fluid, cell count, normal

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, complications with

cerebrovascular accident, infancy and childhood

cerebrovascular accident, young adult

ceruloplasmin, serum

cervical spine injury

cervical spondylosis

Charcot-Marie-Tooth

chelation therapy

chilbran skin lesions

chiropractic manipulation

chiropractic manipulation, neurologic complications with

chorea, causes of

chorea, familial

chorea, Sydenham's

chorea, treatment of

choreoathetosis

choreoathetosis, paroxysmal

chromosomal abnormality

chronic progressive external ophthalmoplegia

cirrhosis, causes of childhood

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

cold intolerance

collapsin response mediator protein 5 IgG

colloid cyst of third ventricle

coma, causes of

coma, unknown etiology

compression fracture

compression neuropathy

computers, neurologic diagnosis and

conjugate gaze, forced

contractures, joint

conversion reaction

copper metabolism, abnormal

cornea, opacity of

Cornelia de Lange syndrome

cortical blindness

cortical-basal ganglionic degeneration

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

crying, pathologic

cultured skin fibroblasts

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, childhood

dementia, presenile

dementia, treatment of

dental procedure, neurologic complications with

dentate nuclei, lesion of

dermatomyositis

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diagnostic criteria

differential diagnosis

dilantin, toxicity

diphenhydramine

disability, neurological

discectomy, cervical

distal muscle atrophy

diurnal variation

dopa responsive dystonia

dopamine agonist

dopamine antagonist

dopamine depleting agents

dopamine receptor, D2

dorsal column stimulator

down-beat nystagmus

DPPX, antibodies

DPPX, antibodies, encephalitis

drug abuse, neurologic complications of

drug induced neurologic disorders

drug overdose, accidental

drug withdrawal

dural sinus thrombosis

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dyskinesia, buccal lingual facial

dyskinesia, causes of

dyskinesia, drug induced

dyskinesia, facial

dystonia musculorum deformens

dystonia musculorum deformens, carrier

dystonia, axial

dystonia, cervical

dystonia, children

dystonia, classification

dystonia, delayed onset

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, focal

dystonia, focal lesion causing

dystonia, focal task specific

dystonia, infancy

dystonia, laryngeal

dystonia, painful

dystonia, paroxysmal

dystonia, post traumatic

dystonia, prevalence of

dystonia, psychogenic

dystonia, segmental

dystonia, symptomatic

dystonia, tongue

dystonia, treatment of

dystonia, truncal

dystonic lipidosis

dystonic reaction, acute

dystonic tremor

ectopic pinealoma

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

emergencies, neurologic

emotional lability

empyema, epidural

empyema, epidural-spinal

empyema, subdural

encephalitis lethargica

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, clinical picture and treatment of

encephalitis, etiology

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis, postinfectious

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, post anoxic

encephalopathy, progressive

entrapment neuropathy

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

epsilon sarcoglycan gene

esophageal varices

ethics in neurology

evoked potentials

exercise intolerance

exercise-induced neurologic dysfunction

exome sequencing

extralimbic encephalitis

extrapyramidal movement disorder, progressive

eye movement, disorders of

face, contractions

facial expression abnormality

facial nerve palsy

faciobrachial dystonic seizure

failure to thrive

feeding disorder

fine motor function, impaired

forceps delivery

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

frontal behavioral spatial syndrome

frontal lobe, pathologic signs of

fungal infection, CNS

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gamma hydroxybutyric acid

gammaglobulin therapy, intravenous

gangliosidosis GM1

gangliosidosis, generalized

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

gests antagoniste

Gilles de la Tourette syndrome

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

globus pallidus, stimulation

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

glutaric acidemia

glutaric aciduria

glycine receptor antibodies

growth retardation

Guillain Barre syndrome

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

head injury, pediatric

health insurance

hemianopia, homonymous

hemifacial spasm

hemiparesis, transient

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatosplenomegaly

heralding manifestation

herniated disc, cervical

Hodgkin's disease

homovanillic acid

human immunodeficiency virus type 1

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's disease, children

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperpyrexia, CNS disorder causing

hyperthyroidism

hypoalbuminemia

hypoglycorrhachia

hypometric saccades

hypoparathyroidism

hypopituitarism

hypotension, systemic

hypotonia, infants

hypoxia, newborn

hypoxic encephalopathy

iatrogenic neurologic disorders

ideomotor apraxia

imbalance, postural

immunodeficiency

immunologic disease

immunosuppression

immunosuppressive agents

inappropriate antidiuretic(A.D.H.)hormone

inborn errors of metabolism

inclusion bodies, intranuclear

incontinence, fecal

infantile bilateral striatal necrosis

infantile hemiplegia

infantile spasm

intellectual deficit

intellectual deterioration

interferon alpha

internal capsule

internal cerebral vein

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial pressure, increased

intrathecal antispasticity drugs

islet cell tumor

Jakob-Creutzfeldt disease

jaw jerk, abnormal

jugular foramen syndrome

Kayser-Fleischer ring

Kearns-Sayre syndrome

Klinefelter's syndrome

klippel feil syndrome

lactic acidemia

lacunar infarction

laminectomy, lumbar

laryngismus stridulus

laughing, pathologic

L-dopa, drug interactions with and side effects of

L-dopa, enteral infusion, continuous

Leber's hereditary optic neuropathy

left handedness

leg spasms, painful

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukoencephalopathy

level of consciousness, decreased

Lewy body disease, diffuse

lid abnormalities

life expectancy

limb immobilization

limbic encephalitis

lipid storage disorder of CNS

liver function enzymes

liver transplantation

lumbar puncture

lysosomal storage disease

malformation, vascular

malformation, vascular, cerebral

manganese intoxication

mediastinum, mass of

medical-legal aspects of neurology

memory, defect of recent

memory, impairment of

meningitis, carcinomatous

mental retardation

mental retardation, etiology of

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methylmalonic acidemia

midbrain, atrophy

midbrain, infarction of

migraine, children

migraine, chronic

migraine, hemiplegic

migraine, treatment of

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoclonal antibodies

motor dysfunction

motor neuron disease

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, hyperkinetic

movement disorder, paroxysmal

movement disorder, psychogenic

movement disorder, treatment of

MRI, blooming effect

MRI, CAT scan compared to

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, gradient-echo

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, mouse ears

MRI, paramagnetic effect

MRI, spinal cord

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, paroxysmal symptoms in

multiple system atrophy

Munchausen syndrome

muscle diseases, characteristics of

muscle hypertrophy

muscle stiffness

muscle weakness

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

musician's dystonia

myasthenia gravis

myasthenia gravis, drug induced

myasthenia gravis, unmasked

myasthenic crisis

mycoplasma pneumoniae

myelopathy, chronic progressive

myeloradiculopathy

myoclonic dystonia

myoclonic jerks

myoclonus, action

myoclonus, cortical

myoclonus, segmental

myopathy, carcinomatous

myopathy, metabolic

myopathy, mitochondrial

myopathy, thyroid disease causing

myotonia dystrophica

nasal stuffiness

neoplasm, intracranial

neoplasm, intracranial with metastasis extracranially

neoplasm, metastatic to CNS

neoplasm, peripheral nerve

neoplasm, posterior fossa

neoplasm, primary intracerebral

neoplasm, primary intracranial-treatment of

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-infants

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

nerve conduction studies

neuritis, causes of

neurocutaneous disease

neurodegeneration with brain iron accumulation

neuroendocrinology

neurofibrillary degeneration

neuroleptic malignant syndrome

neuroleptic, atypical

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, multifocal

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

neurologic symptoms, unexplained

neurologic testing

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology, brain

neuropathy, diabetic

neuropathy, peripheral

neurotransmitter

next-generation sequencing

Niemann-Pick disease

nitroproprionic acid

NMDA antagonists

nonsteroidal anti-inflammatory drug

numb clumsy hands syndrome

nystagmus, congenital

nystagmus, infancy

nystagmus, monocular

nystagmus, periodic

nystagmus, vertical

obsessive-compulsive disorder

occipital lobe, lesion of

occupational neurologic disorders

occupational neuropathies

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculogyric crisis

old age, neurology of

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, progressive external

optic neuropathy

optokinetic nystagmus, abnormal

oral contraceptives

oral contraceptives, choreiform movements with

orthostatic hypotension

osteomyelitis, skull

osteomyelitis, spinal

otitis, neurologic complications with

overuse syndrome

paraspinal muscle

paraspinal muscle weakness

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, familial

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, postencephalitic

Parkinson disease, prognosis of

Parkinson disease, progression

Parkinson disease, psychogenic

Parkinson disease, rapid onset

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal exertion-induced dyskinesia

paroxysmal hemiplegia

paroxysmal hypnogenic dyskinesia

paroxysmal kinesigenic dyskinesia

paroxysmal neurologic deficits

paroxysmal neurologic disorder

paroxysmal nonkinesigenic dyskinesia

patient information and support

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

pediatric opioid use associated neurotoxicity

penguin silhouette sign

perineural invasion

peripheral nerve, lesion of

peroxisomal disease

personality change

personality disorder

phencyclidine poisoning

phenothiazine, dyskinesia associated with

phenylketonuria

pigmentary retinopathy

pituitary, adenoma

pituitary, microadenoma

pleocytosis of cerebrospinal fluid

pleural effusion

poison, neurologic problems with

polycythemia, primary

polycythemia, secondary

pons, lesion of

position sensation

posterior cerebral artery

posterior cerebral artery embolism

posterior cerebral artery territory infarction

postoperative neurologic complications

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

premature infant

pretectal syndrome

prevention of neurologic disorders

primary episodic ataxia

primary familial brain calcification

progressive neurologic disorder

progressive supranuclear palsy

prolactin, elevated

proprioception, abnormal

pseudoathetosis

pseudobulbar palsy

pseudohypoparathyroidism

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis, acute

psychosomatic disease

psychotic behavior

ptosis, bilateral

pulmonary edema

pupil, abnormality in neurologic disorders

pure sensory stroke

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quality of life

radial nerve, palsy of

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reflex sympathetic dystrophy

release phenomena

remote effect of cancer on the nervous system

repetition strain injury

repetitive nerve stimulation

reserpine treatment in movement disorder

respiratory failure

respiratory tract infection

restless leg syndrome

retinal degeneration

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

rigidity, axial

Riley-Day syndrome

saccadic eye movements, abnormal

salivation, excessive

Schilder's disease

sea-blue histiocytes

sedimentation rate, elevated

seizure, adult onset

seizure, children

seizure, differential diagnosis of

seizure, dystonic

seizure, neonatal

seizure, psychomotor-temporal lobe

seizure, stimulus sensitive

seizure, unknown origin

selective serotonin reuptake inhibitors

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory loss, cortical

sequencing difficulty

serologic testing

serologic testing, false negative

sexual behavior, disorder of

shoulder, elevation

single photon emission computed tomography

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

sleep apnea, obstructive

sleep pathology and physiology

slit lamp examination

spastic dysphonia

spasticity, treatment of

speech disorder

speech disorder, childhood

speech disorder, non aphasic

spinal cord, compression of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, infants and children

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 16

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spongy degeneration of brain

sports medicine, neurology of

sprain, cervical

startle reaction

status dystonicus

status epilepticus

status epilepticus, intractable

stem cell transplantation

stereotaxic surgery

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulation, deep brain

stimulation, deep brain, bilateral

stimulation, thalamic

stooped posture

streptococcal infection

streptococcus pyogens

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

subarachnoid hemorrhage

subdural hematoma

substantia nigra

subthalamic nucleus

sugarcane, mildewed

suprasellar lesion

swallow evaluation

symmetric brain lesions

systemic illness

tardive akathisia

tardive dyskinesia

tardive dyskinesia, treatment of

tardive dystonia

teratoma, ovarian

tetrahydrobiopterin

thalamic dystonia

thalamic tumors

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

thoracic outlet syndromes

thrombocytopenia

tongue, protrusion of

tonic foot response

torticollis, acute infectious

torticollis, benign paroxysmal

torticollis, familial

torticollis, infants and children

torticollis, natural history

torticollis, ocular

torticollis, post traumatic

toxic encephalopathy

toxins, nervous system

toxoplasmosis, CNS

transcutaneous electrical nerve stimulation

transient neurologic deficit

transient paroxysmal dystonia in infancy

treatment failure

treatment of neurologic disorder

treatment, empirical

tremor, post traumatic

tremor, postural

tremor, psychogenic

tremor, resting

tremor, thalamic

tremor, treatment of

tricyclic antidepressant

trientine dihydrochloride

trigeminal neuralgia

trinucleotide repeats

tyrosine hydroxylase deficiency

ulnar neuropathy

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urinary sulfatidase excretion

urine test for metabolic disorders

urine test in toxic screen

vasospasm, cerebral

viral infection

viral infection, CNS

vision, blurred

visual evoked response

visual field defect

visual impairment

visual symptoms

visuospatial disturbance

vitamin E deficiency

walking, difficulty with

weakness, generalized

weakness, progressive

Werdnig-Hoffman disease

Whipple's disease

white matter disease

wide based gait

Wolfram syndrome

writhing movements

X-linked dystonia-parkinsonism syndrome

x-linked mental retardation

Showing articles 600 to 650 of 797 << Previous Next >>

Pernicious Anemia with Neuropsychiatric Dysfunction in a Patient with Sickle Cell Anemia Treated with Folate Supplementation
NEJM 348:2204-2207, Dhar,M.,et al, 2003

A Longitudinal Study of Gait and Balance Dysfunction in Normal Older People
Arch Neurol 60:835-839, Baloh,R.W.,et al, 2003

Autoantibodies to Glutamic Acid Decarboxylase in Downbeat Nystagmus
JNNP 74:998-999, Antonini,G.,et al, 2003

Abnormality of Gait as a Predictor of Non-Alzheimer's Dementia
NEJM 347:1761-1768, Verghese,J.,et al, 2002

Clinicopath Conf., Acute Disseminated Encephalomyelitis
NEJM 347:1433-1440, Case 34-2002, 2002

Clinicopath Conf, Primary Lymphoma of CNS
NEJM 346:1009-1015, Case 10-2002, 2002

Clinicopath Conf., Cerebral Venous Thrombosis, Resulting in Hemorrhagic Infarction of the Posterior Left Temporal Lobe
NEJM 346:1651-1658, Case 16-2002, 2002

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Clinicopath Conf, Traumatic Perilymphatic Fistula, Bacterial Labyrinthitis, Meningitis Due to Streptococcus Pneumoiae
NEJM 345:1901-1907, Case 40-2001, 2001

Headache and CNS White Matter Abnormalities Associated with Gluten Sensitivity
Neurol 56:385-388, Hadjivassiliou,M.,et al, 2001

Mild Guillain-Barre Syndrome
Arch Neurol 58:1098-1101, Green,D.M. &Ropper,A.H., 2001

Computerized Posturography Analysis of Progressive Suprnuclear Palsy
Arch Neurol 57:1464-1469, Ondo,W.,et al, 2000

A 44-Year-Old Woman with Difficulty Walking
JAMA 284:2632-2639, Iezzoni,L.I., 2000

What Contributes to Quality of Life in Patients with Parkinson's Disease?
JNNP 69:308-312,289, Schrag,A. et al, 2000

Rhombencephalitis Caused by West Nile Fever Virus
Neurol 55:153, Nichter,C.A. et al, 2000

Progressive Dementia and Gait Disorder in a 78 Year Old Woman
JNNP 68:526-531, Tagliati,M.,et al, 2000

Very Late-Onset Friedreich Ataxia Despite Large GAA Triplet Repeat Expansions
Arch Neurol 57:246-251, Bidichandani,S.I.,et al, 2000

Spontaneous and Reflex Movements in Brain Death
Neurol 54:221-223, Saposnik,G.,et al, 2000

A Six-Year-Old Girl with Tick paralysis
NEJM 342:90-94, Felz,M.W.,et al, 2000

Benign Acute Childhood Myositis, Laboratory and Clinical Features
Neurol 53:2127-2131, Mackay,M.T.,et al, 1999

Optimality Score for the Neurologic Examination of the Infant at 12 and 18 Months of Age
J Pediatr 135:153-161,140, Haataja,L.,et al, 1999

Clinical Correlates of Vascular Parkinsonism
Arch Neurol 56:98-102, Winikates,J.&Jancovic,J., 1999

Clumsiness, Confusion, Coma, and Valproate
Lancet 353:1408, Ellaway,C.J.,et al, 1999

Catalepsy After Stroke
Neurol 53:1132-1135, Saposnik,G.,et al, 1999

Paroxysmal Dyskinesias in Patients with HIV Infection
Neurol 52:109-114, Mirsattari,S.M.,et al, 1999

Diagnostic Criteria for Parkinson Disease
Arch Neurol 56:33-39, Gelb,D.J.,et al, 1999

Review of 23 Patients Affected by the Stiff Man Syndrome:Clinical Subdivision into Stiff Trunk (man) Syndrome,Stiff Limb Syndrome,and Progressive Encephalopmyelitis with Rigidity
JNNP 65:633-640, Barker,R.A.et al, 1998

Clinicopath Conf,Sarcoidosis,with Involvement of Spinal Cord,Brain,Mediastinal Lymph Nodes and ? Lung,Case 35-1998
NEJM 339:1534-1541, , 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Aggressive Approach in the Treatment of Acute Lead Encephalopathy with an Extraordinarily High Concentration of Lead
Arch Pediatr Adolesc Med 152:1100-1104, Gordon,R.A.,et al, 1998

Disequilibrium in Patients with Atherosclerosis; Relevance of Pontine Ischemic Rarefaction
Neurol 51:570-573, Kwa,V.I.H.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

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

Clinicopath Conf
Chronic Inflammatory Demyelinating Polyneuropathy, Case 13-1998, NEJM 338:1212-1219998., , 1998

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

Acute Vestibular Syndrome
NEJM 339:680-685, Hotson,J.R.&Baloh,R.W., 1998

Clinicopath Conf
Wegener's Granulomatosis Involving Sinuses, Skull, and Cranial Nerves, Case 28-1998, NEJM 339:755-76, , 199, 1998

Relationship Between Balance & Abnormalities in Cerebral MRI in Older Adults
Arch Neurol 55:73-79, Tell,G.S.,et al, 1998

Cerebral Oedema and Increased Intracranial Pressure in Chronic Liver Disease
Lancet 351:719-721, Donovan,J.P.,et al, 1998

Dropped Head Synd & Bent Spine Synd:Two Separate Clin Entities or Different Manifest of Axial Myopathy
JNNP 65:258-259, Oerlemans,W.G.H.&Visser,M., 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

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

Neurofibromatosis:An Unusual Cause of Cervical Myopathy
J Spine Cord Med 21:148-150, Barber,D.B.,et al, 1998

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

Balance in the Healthy Elderly
Arch Neurol 54:976-981, Camicioli,R.,et al, 1997

Clinicopath Conf
Hodgkin's Disease, Paraneoplastic Cerebellar Degeneration, Case 21-1997, NEJM 337:115-12297., , 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

Clinicopath Conf
Progressive Supranuclear Palsy, Case 26, 1997, NEJM 337:549-55697., , 1997

Epidemiology, Pathophysiology, & Management of Hyponatremic Encephalopathy
Am J Med 102:67-77, Fraser,C.L.,et al, 1997

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