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abiotrophy

abortion, spontaneous

acanthocytosis

acute disseminated encephalomyelitis

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alternating rapid movement

Alzheimer's disease

Alzheimer's disease, familial

Alzheimer's disease, incidence

Alzheimer's disease, prognosis of

Alzheimer's disease, risk factors in

Alzheimer's disease, treatment of

Alzheimer's disease, visual variant

ammonia

amyloid plaques

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anatomy of

angiitis, isolated of CNS

aphasia, progressive, primary

apnea

apnea, primary central

apraxia of eye movements

areflexia

arm swing, reduced

arthrogryposis multiplex

aspartocyclase

aspiration

ataxia

ataxia telangiectasia

autonomic dysfunction

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

blood dyscrasias, neurologic findings with

bone marrow biopsy

bovine spongiform encephalopathy

brain transplantation

brainstem, atrophy

brainstem, neoplasms of

bruxism

bulbar palsy

bulbar palsy, childhood

bulbar palsy, progressive

cafe au lait spots

CAG repeats

calcification, intracranial

Canavan's disease

cane

carbon monoxide poisoning

CAT scan, emission, abnormal

catalepsy

cataplexy

cataracts

cataracts, congenital

caudate nucleus, atrophy

celiac disease, adult

central core disease

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebral cortex

cerebral cortical atrophy

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, bilateral

Charcot-Marie-Tooth

cherry red spot

cherry red spot-myoclonus syndrome

children

choline acetyltransferase

chorea

chorea, familial

choreoathetosis

chromosomal abnormality

chromosome 14

chromosome 20

chromosome 5

chronic traumatic encephalopathy

claustrophobia

Clinical Pathologic Conference(C.P.C.)

cognition

cogwheel rigidty

Collier's sign

color vision, impaired

compulsivity

confusion

congenital birth defects

congenital malformation

congenital malformation, non CNS

consanguinity

contactin associated protein like 2 antibodies

controversies in neurology

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cost

CPAP

crying, pathologic

cultured skin fibroblasts

deafness

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, cerebrovascular disease causing

dementia, diagnostic evaluation of

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, prevention of

dementia, rapidly progressive

dementia, screening for

dementia, thalamic

dementia, transmissible

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diet

differential diagnosis

diplopia

dopamine

dopamine agonist

dopaminergic dysfunction

electroencephalogram, abnormalities of

electromyogram

electrophoretic pattern, CSF

emotional lability

employment

encephalitis

encephalitis, Japanese

encephalitis, viral

encephalopathy

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, post traumatic

enkephalins

enzyme activity

enzyme, defect

epidemiology of neurology

executive dysfunction

exercise intolerance

eye movement, disorders of

familial periodic ataxia

fasciculation

Fazio-Londe's disease

feeding disorder

fetal tissue

fibrillations

fine motor function, impaired

football neurologic injuries

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

free radical

Friedreich's ataxia

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontotemporal dementia, behavioral variant

gamma amino butyric acid

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann syndrome

Gerstmann-Straussler-Scheinker disease

glabellar sign

gliadin antibodies

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid

glutamic acid decarboxylase

glutaric acidemia

gluten sensitivity

gluten-free diet

glycogen storage disease

granular osmiphilic material

grasp reflex

growth hormone

growth retardation

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

head injury, repetitive

heavy metal intoxication

hepatic encephalopathy

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

highly active antiretroviral therapy

human immunodeficiency virus type 1

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

huntingtin

Huntington's chorea

Huntington's chorea, genetic counselling

hypotension, systemic

hypothalamus

hypothermia

hypotonia

hypoxic encephalopathy

iatrogenic neurologic disorders

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

insular cortex, lesion

intellectual deficit

intellectual deterioration

internet

intrathecal medication

intrinsic hand muscles, wasting of

inverse association

iron, brain

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

Kugelberg-Welander syndrome

kuru

lactic acidemia

language disorder in adults

laughing

laughing, pathologic

L-dopa

L-dopa, drug interactions with and side effects of

learning disability, in children

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

Lesch-Nyhan syndrome

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

Lewy body disease, diffuse

life expectancy

life support, withdrawal of

limbic system

limbic-predominant age-related TDP-43 encephalopathy

liver disease

lobar atrophy

locus ceruleus, lesion of

logopenia

loss of sympathy

lysosomal storage disease

lysosomes, abnoral

macrocephaly

macular degeneration

magnetic susceptibility

maple syrup urine disease

Marinesco-Sjogren syndrome

masked facies

memory, defect of recent

memory, impairment of

meningitis

mental retardation

mental status, abnormal

metronidazole

Mexican

microhemorrhage, intracerebral

midbrain

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mimics

minocycline

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

modafinil

molecular genetics

Montreal cognitive assessment

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, complications with

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion weighted

MRI, eye of tiger sign

MRI, field strength

MRI, field strength, high

MRI, FLAIR

MRI, gradient-echo

MRI, hypointense signal foci on

MRI, paramagnetic effect

MRI, serial

MRI, spinal cord

MRI, spine

MRI, T1 weighted high signal foci

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, treatment of

multiple sleep latency test

multiple system atrophy

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle wasting, diffuse

muscular dystrophy

mutism

myasthenia gravis

myelination of nervous system

myoclonus, orthostatic

myopathy

myopathy, mitochondrial

myotonia dystrophica

N-acetyl-L-aspartic acid

narcolepsy

Native Americans

negative

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neuroaxonal dystrophy, infantile

neuroaxonal leukodystrophy

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurogenic bladder

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

neurologic signs

neurologic symptoms

neuronal cell death

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal loss

neuronal migration disorder

neurons

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuroprotective agents

neurotoxic

neurotoxin

neurotransmitter

next-generation sequencing

Niemann-Pick disease

nigrostriatal pathway

NMDA antagonists

NMDA receptors

nucleus basalis of Meynert

nystagmus

nystagmus, rotary

nystagmus, vertical

obsessive-compulsive disorder

ocular motility, disorders of

old age, neurology of

ophthalmoplegia

ophthalmoplegia, total

optic atrophy

optic atrophy, hereditary

orthostatic hypotension

osmotic demyelination syndrome

oxidative phosphorylation

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

Parkinson disease

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, familial

Parkinson disease, L-dopa nonresponsive

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism-dementia complex

PAS positive

PAS positive material in the brain

pathologic reflex

patient information and support

penguin silhouette sign

peptides, brain

perseveration

persistent vegetative state

persistent vegetative state, children

persistent vegetative state, etiology of

personality change

phakomatoses

phobias

physician assisted suicide

Pick bodies

Pick's disease

pigmentary retinopathy

pneumonia

poison, mercury

poison, neurologic problems with

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polysomnogram

pontocerebellar atrophy

posterior column disease

posterior cortical atrophy

prevention of neurologic disorders

primary lateral sclerosis

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

protein 14-3-3, cerebrospinal fluid

protein 14-3-3, cerebrospinal fluid, false positive

pruritus

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

rapidly progressing neurologic illness

release phenomena

REM sleep

remote effect of cancer on the nervous system

saccadic eye movements, abnormal

seizure, drug resistance

seizure, laughing as manifestation

semantic dementia

senile plaques

sensorineural hearing loss

sequencing difficulty

short stature

sinemet

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

sleep

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

SMN1 gene

soccer

sodium-glucoe cotransporter-2 inhibitors

speech disorder, childhood

speech, loss of

spinal cord

spinal cord degeneration

spinal cord, infarction of

spinal cord, injury of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, intramedullary

spinal cord, vascular disorders Affecting

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 12

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

splenomegaly

spongy degeneration of brain

sports medicine, neurology of

standing difficulty

startle myoclonus

status epilepticus

stem cell transplantation

stillbirth

stimulant drugs

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

stridor

stuttering

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

survival motor neuron gene

symmetric brain lesions

temporal lobe, atrophy

tetracycline

thalamus, lesion of

thalamus, lesion of-bilateral

treatment of neurologic disorder

trinucleotide repeats

ventricular enlargement

vestibular function, tests of

visual acuity, decreased

visual evoked response

visual fields, constricted

visual impairment

visual loss

visual symptoms

visuospatial disturbance

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

web sites

weight gain

weight loss

Werdnig-Hoffman disease

West disease

West Nile fever

Western immunoblot test

word-finding difficulty

workup

writing

X-linked bulbospinal neuronopathy

Showing articles 200 to 250 of 873 << Previous Next >>

Degenerative Diseases of the Nervous System, Werdnig-Hoffman Disease, Spinal Muscular Atrophy
Adams & Victors Principles of Neurology, Chp 39, pg 1116, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Kugelberg-Welander Syndrome SMAIII
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Neuropsychiatric Changes Precede Classic Motor Symptoms in ALS and Do Not Affect Survival
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Comparison of Pregabalin with Pramipexole for Restless Legs Syndrome
NEJM 370:621-631,667, Allen, R.P.,et al, 2014

ICU-Acquired Weakness and Recovery from Critical Illness
NEJM 370:1626-1635, Kress, J.P. & Hall, J.B., 2014

Venous Thromboembolism in Amyotrophic Lateral Sclerosis
Neurol 82:1674-1677, Gladman, M.,et al, 2014

Brugada Syndrome in Spinal and Bulbar Muscular Atrophy
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Blood Biomarkers for Brain Injury in Concussed Professional Ice Hockey Players
JAMA Neurol 71:684-692,677, Shahim, P.,et al, 2014

Long-Term Effectivenss of Dopamine Agonists and Monoamine Oxidase B Inhibitors Compared with Levodopa as Initial Treatment for Parkinsons Disease (PD MED): A Large, Open-Label, Pragmatic Randomised Trial
Lancet 383: Doi: 10.1016/S0140-6736, PD MED Collaborative Group, 2014

Palliative Care and Neurology
Neurol 83:561-567, Boersma, I.,et al, 2014

Motor Neurone Disease
BMJ 349:g4052, Nageshwaran, S.,et al, 2014

Restless Genital Syndrome in Parkinson Disease
JAMA Neurol 71:1559-1561, Aquino, C.C.,et al, 2014

Macroglossia in Amyotrophic Lateral Sclerosis
JAMA Neurol 70:1432-1435, McKee, H.R.,et al, 2013

Clinical Features of Dopamine Agonist Withdrawal Syndrome in a Movement Disorders Clinic
JNNP 84:130-135, Pondal, M.,et al, 2013

Owls Eye in Spinal Magnetic Resonance Imaging
Arch Neurol 69:407-408, Ghosh,P.S. and Mitra,S., 2012

Imaging Findings in Tick-Borne Encephalitis with Differential Diagnostic Considerations
AJR 199:420-427, Horger, M.,et al, 2012

Bright Tongue Sign in ALS
Neurol 79:1520, Fox, M.D. & Cohen, A.B., 2012

Extended-Release Pramipexole in Advanced Parkinson Disease
Neurol 77:767-774, Schapira, A.H.V.,et al, 2011

Spinal Muscular Atrophy A Timely Review
Arch Neurol 68:979-984, Kolb, S.J.,et al, 2011

Spectrum of Paraneoplastic Disease Associated With Lymphoma
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Tourettes Syndrome
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Predictors of Neurologic Outcome in Hypothermia After Cardiac Arrest
Ann Neurol 68:907-914, Fugate,J.E.,et al, 2010

Prolactinomas
NEJM 362:1219-1226, Klibanski,A., 2010

Dopamine Agonist Withdrawal Syndrome in Parkinson Disease
Arch Neurol 67:58-63, Rabinak,C. &Nirenberg,M., 2010

Othello Syndrome in Parkinson Disease Patients Without Dementia
The Neurologist 15:34-36, Cannas,A.,et al, 2009

Long-Term Effect of Initiating Pramipexole vs Levodopa in Early Parkinson Disease
Arch Neurol 66:563-570, Parkinson Sutdy Group CALM Cohort Investigators, 2009

Neurologic Prognosis After Cardiac Arrest
NEJM 361:605-611, Young,G.B., 2009

Practice Parameter Update: The Care of the Patient with Amyotrophic Lateral Sclerosis: Drug, Nutritional, and Respiratory Therapies (An Evidence-Based Review)
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A Large-Scale International Meta-Analysis of Paraoxonase Gene Polymorphisms in Sporadic ALS
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Parkinsons Disease
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The Floppy Infant: Evaluation of Hypotonia
Pediatrics in Review 30:e66-e76, Peredo, D. & Hannibal M., 2009

Functional Abnormalities Underlying Pathological Gambling in Parkinson Disease
Arch Neurol 65:1604-1611, Cilia,R.,et al, 2008

Levodopa for the Treatment of Parkinsons Disease
NEJM 359:2468-2476, LeWitt,P.A., 2008

Fourteen-Year Final Report of the Randomized PDRG-UK Trial Comparing Three Treatments in PD
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Invited Article: Changing Concepts in Parkinson Disease: Moving Beyond the Decade of the Brain
Neurol 70:1996-2003, Marras,C. &Lang,A., 2008

Restless Arms
Lancet 371:530, Horvath,J.,et al, 2008

Primary Lateral Sclerosis With HIV-1 Infection
Neurol 70:575-577, Verma,A. &Berger,J.R., 2008

Diagnosis and Management of Motor Neurone Disease
BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 2008

Headache and Pregnancy
The Neurologist 14:108-119, Menon,R. &Bushnell,C.D., 2008

Genetics of Familial Amyotrophic Lateral Sclerosis
Neurol 70:144-152, Valdmanis,P.N. &Rouleau,G.A., 2008

Neonatal Diagnosis and Treatment of Menkes Disease
NEJM 358:605-614, Kaler, S.G.,et al, 2008

Compulsive Singing: Another Aspect of Punding in Parkinsons Disease
Ann Neurol 62:525-528, Bonvin,C.,et al, 2007

Clinicopath Conf., Multifocal Motor Neuropathy With Conduction Block
NEJM 357: 2707-2715, Case 40-2007, 2007

Clinicopath conf., Human Prion Disease, Sporadic CJD
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Treatment Options in the Modern Management of Parkinson Disease
Arch Neurol 64:1083-1088, Schapira,A.H.V., 2007

Cerebral Cortical and White Matter Lesions in Amyotrophic Lateral Sclerosis With Dementia; Correlation With MR and Pathologic Examinations
AJNR 28:1505-1510, Matsusue,E.,et al, 2007

Lead Poisoning From the Beauty Case: Neurologic Manifestations in an Elderly Woman
Neurol 69:929-930, Fluri,F.,et al, 2007

Risk Factors for the Development of Pedal Edema in Patients Using Pramipexole
Arch Neurol 64:820-824, Kleiner-Fisman,G. &Fisman,D.N., 2007

Transdermal Rotigotine: Double-Blind, Placebo-Controlled Trial in Parkinson Disease
Arch Neurol 64:676-682, Jankovic,J.,et al, 2007

Advanced Parkinson Disease Treated with Rotigotine Transdermal System PREFER Study
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Showing articles 200 to 250 of 873 << Previous Next >>