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Differential
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abdominal reflex, absent

abducens nerve paralysis

abulia

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome myelopathy

acquired immunodeficiency syndrome, infants and children

acromicria

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

Africa

alcohol injection

alcohol intolerance

alcohol, neurologic complications with

alcoholism

Alexanders disease

Alexanders disease, adult onset

algorithm

alopecia

alternating rapid movement

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anemia

angiography, spinal

ankle reflex, absent

anterior horn cell disease

antioxidant

aphasia

aqueduct of Sylvius, stenosis

aqueductal stenosis

areflexia

arm weakness

Arnold Chiari malformation

atherosclerosis, generalized

atypical

auditory evoked brainstem potentials

autism

autoantibodies

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar impression

behavioral disorder

Behcet's syndrome

benign essential tremor

biotin

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

bladder dysfunction

blindness

brachial plexus neuropathy

brain atrophy

brain biopsy

brain biopsy, negative

brain biopsy, stereotaxic

brainstem

brainstem, atrophy

brainstem, dysfunction

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, ischemia

brainstem, lesion of

brainstem, neoplasms of

calcification, intracranial

carcinoma of pancreas

carotid angiogram

CAT scan

CAT scan, abnormal

CAT scan, emission, abnormal

CAT scan, spine

cataracts

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellar plaques, amyloid

cerebellar vermis

cerebral cortex

cerebral folate deficiency syndrome

cerebral palsy

cerebral palsy, associated problems with

cerebral venous thrombosis

cerebroretinal microangiopathy with calcifications and cysts

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, recurrent

cerebrovascular disease

cervical myelopathy

cervical spondylosis

chenodeoxycholic acid

chromosomal abnormality

chromosome 2

chromosome 6

chronic progressive external ophthalmoplegia

cirrhosis

Clinical Pathologic Conference(C.P.C.)

clonus

clubfoot as related to neurologic disease

cobalamin C deficiency

cognition

cold hands sign

color vision, impaired

coma

complications

concentration, impaired

confusion

congenital infection, CNS

consanguinity

constipation

controversies in neurology

conversion reaction

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cough

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

crossed adductor reflex

crying, pathologic

deafmute

deafness

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

deep gray nuclei

degenerative cervical myelopathy

degenerative diseases of CNS

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, treatment of

demyelinating disease

dentate nuclei, lesion of

depression

dermatitis

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

diplegia, spastic cerebral

diplopia

disability, neurological

disorientation

distal muscle atrophy

distal muscle weakness

Dravet syndrome

drug abuse, inhalation

dysarthria

dysarthria-clumsy hand syndrome

dystonia musculorum deformens

dystrophic calcification

ears of the Lynx MR sign

eczema

efficacy

electrical sensation

electroencephalogram, abnormalities of

encephalitis lethargica

enzyme, muscle disease

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

equinovarus

evoked potentials

executive dysfunction

exome sequencing

eye movement, disorders of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

fatal familial insomnia

fatigue

fatty acid, elevated plasma content

fever

fine motor function, impaired

finger nose finger test

finger tapping

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

fluctuate

fluorescent treponema antibody absorption(FTA-ABS)

folic acid

folic acid deficiency

Friedreich's ataxia, late onset

frontal lobe, pathologic signs of

fundus, abnormality of

gammaglobulin therapy, intravenous

genetic neurologic disorders

Gerstmann-Straussler-Scheinker disease

GFAP gene

girdle sensation

glioblastoma multiforme(astrocytoma Gr.III)

glioma

glioma, low-grade

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucagonoma

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

glycogen storage disease

granulomatosis with polyangiitis

granulomatous disease

grasp reflex

growth retardation

Guillain Barre syndrome

Hallervorden Spatz disease

headache, intermittent

health insurance

hearing loss

hearing problems in children

heel-knee-shin test

hemangioma

hemangioma, vertebral

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

hepatosplenomegaly

herniated disc

herniated disc, cervical

high arched feet

Hispanics

hoarseness

human immunodeficiency virus type 1

human T-lymphotropic virus type I(HTLV-I)

human T-lymphotropic virus type II(HTLV-II)

Huntington's chorea

Huntington's disease, children

hydrocephalus

hydrocephalus, non-communicating(obstructive)

hyperammonemic encephalopathy

hyperhidrosis

hyperhomocysteinemia

hyperpigmentation of skin

hypotension, systemic

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic intranuclear

intellectual deterioration

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jamaica ginger paralysis

laminectomy, cervical

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leuko-araiosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukopenia

level of consciousness, decreased

lymphoma involving CNS

lymphomatoid granulomatosis

macrocephaly

Madonna facies

Maghreb

malformation, vascular

mania

marche a petits pas

marihuana

medulla oblongata, lesion of

megalencephaly

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal gliomatosis

meningitis, CSF cell count-normal

meningomyelitis

mental retardation

mental status, abnormal

metabolic disorder, primary

methylglutaconic aciduria

methylmalonic acidemia

microangiopathy, brain

microcephaly

microdontia

middle cerebellar peduncle

middle cerebellar peduncle, lesion, bilateral

Mills syndrome

mimics

misdiagnosis

mitochondrial disease

mobility

mobility aids

molecular genetics

mononeuritis multiplex

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, emergent

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, negative

MRI, paramagnetic effect

MRI, spinal cord

MRI, spine

MRI, T1 weighted high signal foci

MRS

multinucleated giant cell

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle weakness, proximal

mutism

myasthenia gravis

myelitis, longitudinal

myelomalacia

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myelopathy, hepatic

myelopathy, tract-specific

myxedema, neurologic manifestations of

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-treatment of

nerve biopsy

nerve conduction studies

neurocutaneous disease

neuroendocrinology

neurogenic bladder

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuronal intranuclear inclusion disease

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, peripheral

neuropathy, sensory

neurosyphilis

neurotoxin

next-generation sequencing

night blindness

nitrous oxide

numb clumsy hands syndrome

numbness, extremity

nystagmus

nystagmus, dissociated

ocular motility, disorders of

oculodentodigital dysplasia

oculogyric crisis

ophthalmoplegia

ophthalmoplegia, progressive external

optic ataxia

optic atrophy

optic atrophy, hereditary

optic neuritis

optic neuropathy

optical coherence tomography

oral ulcerations

orthostatic hypotension

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, spastic

paraparesis, spastic, tropical

Parkinson disease, arteriosclerotic

Parkinson disease, asymmetric onset

Parkinson disease, L-dopa nonresponsive

Parkinson disease, postencephalitic

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

photosensitivity, skin

physical therapy

pleocytosis of cerebrospinal fluid

poison, organophosphate

POLR3B

polyglucosan body

polyglucosan body disease

polymerase chain reaction

posterior column disease

postural abnormality

practice guidelines

precipitating factors

primary lateral sclerosis

prion disease

prisoners of war, neurologic complications in

prognosis

progressive neurologic disorder

proprioception, abnormal

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis

ptosis

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pursuit eye movements, abnormal

pyramidal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, progressive

quadriplegia

radiation therapy, CNS treatment and complications with

radiculopathy

Rankin score

rapidly progressing neurologic illness

remote effect of cancer on the nervous system

renal stones

respiratory dyskinesias

reticulum cell sarcoma

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

review article

rigidity

risk factors

risk-benefit assessment

Romberg's sign

Rosenthal fibers

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

rubella virus

saccadic eye movements, abnormal

safety

Saudi Arabia

scissors gait

sclerae, hyperpigmented

scleritis

scleroderma

scleroderma, neurologic involvement with

SCN1A gene

scoliosis

scoliosis, neurologic association with

sedimentation rate, elevated

seizure, tonic-clonic

sensorineural hearing loss

sensory level

sensory loss

sensory loss, cutaneous

serologic testing

serologic testing of cerebrospinal fluid

short stature

shunt procedure, ventricular

sinusitis

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep apnea

sleep pathology and physiology

slow virus infection of CNS

snout reflex

sodium channel dysfunction

solitary scerlosis

somatosensory evoked potentials

spastic paraplegia, type 11

spastic paraplegia, type 7

spasticity

spasticity, treatment of

spastin

speech disorder

speech disorder, childhood

speech, loss of

spinal cord

spinal cord, cervical

spinal cord, compression of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal cord, vascular disorders Affecting

spinal cord, vascular malformation of

spinal xanthomatosis

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spinocerebellar degeneration

splenomegaly

spondylolysis

spongy degeneration of brain

startle reaction

status epilepticus

stereotyped behavior

steroid therapy, CNS treatment and complications with

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

subcortical U fibers

substantia nigra

superior cerebellar peduncle

symmetric brain lesions

syndactyly

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

teeth, number of in infants

tone, muscle, increased

tongue, enlarged

tongue, impaired movements of

tongue, ulcer

tonic foot response

tonsillar herniation of cerebellum

toxins, nervous system

transient ischemic attack

treatment of neurologic disorder

trinucleotide repeats

urea-cycle enzymopathies

vibratory sensation, abnormal

visual acuity, decreased

visual evoked response

walking, difficulty with

war

weakness

weakness, progressive

weakness, proximal

weight loss

Western immunoblot test

wheelchair

white matter disease

wide based gait

word-finding difficulty

Showing articles 900 to 950 of 2715 << Previous Next >>

Stalevo for Parkinson's Disease
The Medical Letter 46:39, , 2004

Acute Cerebellar Ataxia Due to Sjogren Syndrome
Neurol 62:2332-2333, Wong,S.,et al, 2004

Hereditary Spastic Paraplegia
Arch Neurol 61:849-855,830, Orlacchio,A.,et al, 2004

Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
Arch Neurol 61:875-880, Smith,C.O.,et al, 2004

Acute Bilateral Inferior Cerebellar Infarction in a Patient With Neurosyphillis
Arch Neurol 61:953-956, Umashankar,G.,et al, 2004

Idiopathic Hyposmia As a Preclinical Sign of Parkinson's Disease
Ann Neurol 56:173-181,169, Ponsen,M.M.,et al, 2004

The Neurological Complications of Bariatric Surgery
Arch Neurol 61:1185-1189, Berger,J.R., 2004

Surgical and Hardware Complications of Subthalamic Stimulation
Neurol 63:612-616, Lyons,K.E.,et al, 2004

Five New Cases of a Recently Described Leukoencephalopathy with High Brain Lactate
Neurol 63:688-692, Linnankivi,T.,et al, 2004

Pathogenetic Mechanisms of Parkin in Parkinson's Disease
Lancet 364:722-724, Hattori,N. &Mizuno,Y., 2004

Clinicopath Conf, Multiple-System Atrophy
NEJM 351:912-921, Case 27-2004, 2004

Monoamine Oxide Type B Inhibitors in Early Parkinson's Disease:Meta-Analysis of 17 Randomised Trials Involving 3525 Patients
BMJ 329:593-596, Ives,N.J.,et al, 2004

Clinicopath Conf, Pernicious Anema with Autoimmune Gastritis and B12 Deficiency
NEJM 351:1333-1341, Case 30-2004, 2004

Oral Antispastic Drugs in Nonprogressive Neurologic Diseases
Neurol 63:1357-1363, Montane,E.,et al, 2004

Frequency of Orthostatic Hypotension in a Community Based Cohort of Patients with Parkinson's Disease
JNNP 75:1470-1471, Allcock,L.M.,et al, 2004

Autonomic Failure as the Initial Presentation of Parkinson Disease and Dementia with Lewy Bodies
Neurol 63:1093-1095, Kaufmann,H.,et al, 2004

Glabellar and Palmomental Reflexes in Parkinsonian Disorders
Neurol 63:1096-1098, Brodsky,H.,et al, 2004

Post-Stroke Movement Disorders; Report of 56 Patients
JNNP 75:1568-1574, Alarcon,F.,et al, 2004

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
Pract Neurology 4:50-55, Razvi,S.S.M. &Muir,K.W., 2004

Reversible Corpus Callosum Lesion in Legionnaires Disease
JNNP 75:651-654, Morgan, J.C.,et al, 2004

Morning Glory Sign: A Particular MR Finding in Progressive Supranuclear Palsy
Magn Reson Med Sci 3:125-132, Adachi, M., et al, 2004

Heterozygous Niemann-Pick Disease Type C Presenting with Tremor
Neurol 63:2189-2190, Josephs,K.A.,et al, 2004

Silent Infarcts Demonstrated by Diffusion-Weighted MRI in CADASIL
Eur Neurol 49: 178-180, Moon,S.Y.,et al, 2003

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

Intrathecal Baclofen Withdrawal Mimicking Sepsis
J Emerg Med 24:423-427, Kao,L.W.,e tal, 2003

Encephalitis lethargica syndrome:20 new cases and evidence of basal ganglia autoimmunity
Brain 127, 21-33, Dale, R.C., et al, 2003

Staging of Brain Pathology Related to Sporadic Parkinsons Disease
Neurobiol Aging 24:197-211, Braak,H.,et al, 2003

A Controlled Trial of Rotigotine Monotherapy in Early Parkinson's Disease
Arch Neurol 60:1721-1728, The Parkinson Study Group, 2003

Treatments of Parkinson Disease
Arch Neurol 60:1680-1684, Shults,C.W., 2003

Long-Term Follow-Up of Thalamic Deep Brain Stimulation for Essential and Parkinsonian Tremor
Neurol 61:1601-1604, Kumar,R.,et al, 2003

Prevalence and Clinical Features of HTLV Neurologic Disease in the HTLV Outcomes Study
Neurol 61:1588-1594, Orland,J.R.,et al, 2003

Vascular Parkinsonism in Moyamoya: Microvascular Biopsy and Imaging Corrleates
Ann Neurol 54:836-840, Tan,E.,et al, 2003

Dementia with Lewy Bodies
Lancet 362:1689-1690, Wilcock,G.K., 2003

Severe Worsening of Parkinsonism in Lewy Body Dementia Due to Donepezil
Neurol 61:1452, Onofri,M. & Thomas,A., 2003

Clinicopath Conf., Giant-Cell Arteritis
NEJM 349:170-180, Case 21-2003, 2003

Clinical Manifestations of Sarin Nerve Gas Exposure
JAMA 290:659-662, Lee,E.C., 2003

Post-transplantation HTLV-1 Myelopathy in Three Recipients From a Single Donor
JNNP 74:1080-1084, Zarranz Imirizaldu,J.J., et al, 2003

Neurologic Manifestations and Outcome of West Nile Virus Infection
JAMA 290:511-515,524,558, Sejvar,J.J.,et al, 2003

Biochemical And Clinical Aspects of Methotrexate Neurotoxicity
Chemotherapy 49:92-104, Vezmar,S.,et al, 2003

Pathological Gambling Associated with Dopamine Agonist Therapy in Parkinson's
Neurol 61:422-423, Driver-Dunckley,E.,et al, 2003

Orthostatic Hypotension in De Novo Parkinson Disease
Arch Neurol 60:1400-1404, Bonuccelli,U.,et al, 2003

Disappearance of Resting Tremor After "Stereotaxic" Thalamic Stroke
Neurol 61:1014-1015, Probst-Cousin,S.,et al, 2003

Spinal Dural Arteriovenous Fistulas: Clinical Features in 80 Patients
JNNP 74:1438-1440, Jellema,K.,et al, 2003

Symmetric Deep Cerebellar Lesions After Smoking Heroin
Arch Neurol 60:1605-1606, Ropper,A.H. &Blair,R., 2003

Bickerstaff's Brainstem Encephalitis: Clinical Features of 62 Cases and a Subgroup Associated with Guillain-Barre Syndrome
Brain 126:2279-2290, Odaka,M.,et al, 2003

Nonsteroidal Anti-Inflammatory Drugs and the Risk of Parkinson Disease
Arch Neurol 60:1059-1064,1043, Chen,H.,et al, 2003

Language Function and Dysfunction in Corticobasal Degeneration
Neurol 61:493-499, Graham,N.L.,et al, 2003

MR Imaging in the Differential Diagnosis of Neurogenic Foot Drop
AJNR 24:1283-1289,1273, Bendszus,M.,et al, 2003

Clinical Features and Neuropathology of Autosomal Dominant Spinocerebellar Ataxia (SCA17)
Ann Neurol 43:367-375, Rolfs,A.,et al, 2003

A Double-Blind Controlled Trial of Bilateral Fetal Nigral Transplantation in Parkinson's Disease
Ann Neurol 54:403-414, Olanow,C.W.,et al, 2003

Showing articles 900 to 950 of 2715 << Previous Next >>