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abiotrophy

abortion, spontaneous

acanthocytosis

acetaminophen

acetylcholine

acquired immunodeficiency syndrome

acrochordon

acromegaly

activities of daily living

acute disseminated encephalomyelitis

Addison's disease

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

alpha methyldopa hydrazine

alpha methyltyrosine

alpha-fetoprotein

alpha-synuclein

altered states of consciousness, driving with

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

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

analgesic

anasarca

anatomy of

anemia, iron deficiency

angiitis, isolated of CNS

angiofibroma, facial

angiography, cerebral

ankle edema

anomic aphasia

anosmia

anti basal ganglia antibodies

antibiotics

anticholinergic drugs

anticholinergic drugs, side effects of

anticonvulsants

anticonvulsants, untoward effects of

antidepressant

anti-dopamine 2 receptor antibody

aortic valve, lesion of

aphasia

aphasia, progressive

aphasia, progressive, primary

aphasia, rehabilitation

apnea

apnea, primary central

apraxia of eye movements

areflexia

arm swing, reduced

arrhythmia, cardiac

arterial dissection, aorta, cerebral symptoms with

arteriopathy

arthrogryposis multiplex

ataxia telangiectasia

attention deficit disorder with hyperactivity

attention span

atypical

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

automatic behavior

automobile accidents

autonomic dysfunction

autonomic nervous system

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

beta adrenergic blocker

biologic markers

bitemporal visual field defect

blood dyscrasias, neurologic findings with

bone marrow biopsy

botulinum toxin

bovine spongiform encephalopathy

brain implant, polymeric

brain transplantation

brainstem, atrophy

brainstem, neoplasms of

bromocriptine

bromocriptine, slow release

Brueghel's syndrome

bruxism

bulbar palsy

bulbar palsy, childhood

bulbar palsy, progressive

calcification, intracranial

carbon monoxide poisoning

carcinoma

carcinoma of breast

cardiomyopathy

carpal tunnel syndrome

CAT scan, emission, abnormal

catalepsy

cataplexy

cataracts

cataracts, congenital

catatonia

catecholamine

catechol-o-methyltransferase inhibitor

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 pontine angle

cerebellar pontine angle tumor

cerebellar vermis

cerebral cortex

cerebral cortical atrophy

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, leak

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, women

Charcot-Marie-Tooth

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

Chiari Frommel syndrome

chiasmal syndromes

children

chlorpromazine

choline acetyltransferase

chromophobe adenoma, treatment of

chromosomal abnormality

chromosome 14

chromosome 20

chromosome 5

chronic traumatic encephalopathy

cirrhosis

cisternogram, radionuclide

claustrophobia

Clinical Pathologic Conference(C.P.C.)

color vision, impaired

congenital birth defects

congenital malformation

congenital malformation, non CNS

congestive heart failure

conjunctival injection

consanguinity

constipation

contactin associated protein like 2 antibodies

controversies in neurology

conversion reaction

coprolalia

coronary artery disease

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cranial nerve palsies

crying, pathologic

cryosurgery

cryotherapy

cultured skin fibroblasts

degenerative diseases of CNS

delay in diagnosis

delusion

dementia

dementia, diagnostic evaluation of

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, screening for

dementia, thalamic

dementia, transmissible

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

deprenyl

depression

developmental milestones

developmental milestones, loss of

developmental retardation

dexamethasone suppression test

DHE

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

dialysis

diet

differential diagnosis

disability rating scale, neurological

disability, neurological

diurnal variation

domperidone

dopa responsive dystonia

dopamine

dopamine agonist

dopamine agonist withdrawal syndrome

dopamine antagonist

dopamine antagonist, peripheral

dopamine beta hydroxylase

dopamine depleting agents

dopamine receptor

dopamine receptor, D2

dopaminergic desensitization

dopaminergic dysfunction

dopaminergic neurons

doppler, transcranial

downward gaze

downward gaze, paralysis of

driving

drooling

droperidol

drug induced neurologic disorders

dyskinesia, buccal lingual facial

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, drug induced

dystonia, face

dystonia, focal

dystonia, treatment of

dystonic reaction, acute

echocardiogram

echocardiogram, transthoracic

edema, pedal

efficacy

electroconvulsive therapy

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electrophoretic pattern, CSF

emergencies, neurologic

encephalitis, autoimmune

encephalitis, Japanese

encephalitis, viral

encephalopathy

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, post traumatic

encephalopathy, progressive

epidemiology of neurology

executive dysfunction

exercise intolerance

extrapyramidal

eye movement, disorders of

familial periodic ataxia

fasciculation

fatigue

Fazio-Londe's disease

fine motor function, impaired

follicle stimulating hormone

foot deformity

foot drop

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 bleeding

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann syndrome

Gerstmann-Straussler-Scheinker disease

Gilles de la Tourette syndrome

glabellar sign

gliadin antibodies

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glomus jugulare tumor

glutamic acid

glutamic acid decarboxylase

granular osmiphilic material

grasp reflex

growth hormone

growth hormone deficiency

growth retardation

guanfacine

hair, loss

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination

hallucination, auditory

head injury, repetitive

head nodding

headache

headache, drug induced

headache, emergency

headache, episodic

headache, evaluation of

headache, prophylaxis

headache, treatment of

health insurance

hearing loss

heavy metal intoxication

hemiballismus

hemidystonia

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

hiccoughs

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

hypothalamus, damage to

hypothermia

hypothyroidism

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

intellectual deterioration

internet

internuclear ophthalmoplegia

intracerebral hemorrhage

intrathecal medication

inverse association

iron, brain

iron, serum

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

Kugelberg-Welander syndrome

kuru

lactic acidemia

language disorder in adults

lanreotide

laughing, pathologic

L-dopa

L-dopa, controlled release

L-dopa, drug interactions with and side effects of

L-dopa, potentiators of

learning disability, in children

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

Lewy body

Lewy body disease, diffuse

life support, withdrawal of

limbic system

limbic-predominant age-related TDP-43 encephalopathy

locus ceruleus, lesion of

logopenia

loss of sympathy

lumbar puncture, indications for

luteinizing hormone

lysosomal storage disease

lysosomes, abnoral

macrocephaly

macular degeneration

magnetic susceptibility

manic-depressive

maple syrup urine disease

marche a petits pas

Marinesco-Sjogren syndrome

masked facies

medication withdrawal

mellaril

memory, defect of recent

memory, impairment of

meningitis

menses

mental retardation

mental status, abnormal

microhemorrhage, intracerebral

microsurgery

microsurgery, transsphenoidal

midbrain

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

migraine, biochemical abnormalities with

migraine, menses

migraine, pregnancy

migraine, prophylaxis

migraine, treatment of

mimics

minocycline

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve lesion

mitral valve regurgitation

modafinil

molecular genetics

monoamine oxidase inhibitors

monoamines

monoamines, brain

Montreal cognitive assessment

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, post hemiplegic

movement disorder, treatment of

MPTP

MRI

MRI, abnormal

MRI, complications with

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, field strength

MRI, field strength, high

MRI, FLAIR

MRI, gradient-echo

MRI, hypointense signal foci on

MRI, indications for

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

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS-treatment of

neoplasm, pituitary

neoplasm, pituitary, incidental

neoplasm, pituitary, treatment of

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-treatment of

neuroaxonal dystrophy, infantile

neuroaxonal leukodystrophy

neurochemistry

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neuroleptic

neuroleptic malignant syndrome

neuroleptic, atypical

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

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

nonsteroidal anti-inflammatory drug

norepinephrine

nucleus basalis of Meynert

nystagmus

nystagmus, rotary

nystagmus, vertical

obsessive-compulsive disorder

octreotide

ocular motility, disorders of

oculogyric crisis

olanzapine

old age, neurology of

oligospermia

ophthalmoplegia

ophthalmoplegia, total

opiate

opisthotonus

optic atrophy

optic atrophy, hereditary

optic chiasm

optic chiasm, herniation

oral contraceptives

oral contraceptives, neurologic complications with

orthostatic hypotension

osmotic demyelination syndrome

Othello syndrome

oxidative phosphorylation

paraparesis, familial spastic

paraparesis, familial spastic, classification

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, driving with

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, early symptoms

Parkinson disease, etiology of

Parkinson disease, exacerbation

Parkinson disease, familial

Parkinson disease, fluctuations in

Parkinson disease, freezing phenomena in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, nonmotor problems of

Parkinson disease, on-off phenomena in

Parkinson disease, pathogenesis of

Parkinson disease, presymptomatic detection

Parkinson disease, prognosis of

Parkinson disease, progression

Parkinson disease, sensory symptoms in

Parkinson disease, surgical treatment of

Parkinson disease, transient

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism-dementia complex

parsidol

PAS positive

PAS positive material in the brain

pathologic gambling

pathologic reflex

pathology

patient information and support

penguin silhouette sign

persistent vegetative state

persistent vegetative state, children

persistent vegetative state, etiology of

PHNO, enteral infusion, continuous

PHNO, intravenous

phobias

physician assisted suicide

physostigmine

Pick bodies

Pick's disease

pigmentary retinopathy

pimozide

pituitary

pituitary, adenoma

pituitary, adenoma, giant

pituitary, enlargement

pituitary, hormones of

pituitary, lesion of

pituitary, microadenoma

placebo effect

pleocytosis of cerebrospinal fluid

poison, neurologic problems with

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polyps, gastrointestinal tract

polysomnogram

pontocerebellar atrophy

posterior column disease

posterior cortical atrophy

postpartum

postpartum cerebral angiopathy

postural abnormality

practice guidelines

pramipexole

pramipexole, extended release

pregabalin

pregnancy, neurologic complications in

pretectal syndrome

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

proton beam therapy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

pyruvate-kinase deficiency anemia

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

rapidly progressing neurologic illness

release phenomena

REM sleep

remote effect of cancer on the nervous system

renal failure

reserpine and reserpine like drugs

reserpine treatment in movement disorder

respirator

respiratory failure

restless arms syndrome

restless genital syndrome

restless leg syndrome

retroperitoneal fibrosis

risk-benefit assessment

ritalin

ropinirole

ropinirole, prolonged release

rotigotine

saccadic eye movements, abnormal

seizure, drug resistance

seizure, laughing as manifestation

sella turcica, enlargement of

semantic dementia

senile plaques

sensorineural hearing loss

sequencing difficulty

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

skull x-ray

skull x-ray, abnormal

sleep

sleep apnea

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

smell

Smell Identification Test

SMN1 gene

soccer

somatostatin analogue

speech disorder, childhood

speech, loss of

speech, soft

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

stem cell transplantation

stereotyped behavior

stereotyped behavior, drug induced

stereotypy

steroid

steroid therapy, CNS treatment and complications with

stillbirth

stimulant drugs

stimulation, deep brain

storage disease of CNS

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

stridor

stuttering

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

subclavian steal syndrome, causes of

substantia nigra

subthalamic nucleus

subthalamic nucleus deep brain stimulation

survival motor neuron gene

symmetric brain lesions

tardive dyskinesia, treatment of

tardive dystonia

tardive pain syndrome

temporal lobe, atrophy

testosterone, serum, low

thalamus, lesion of-bilateral

thiothixene

thyroiditis

tic

tic, chronic multiple

tic, classification of

transdermal medication

trauma

treatment of neurologic disorder

tremor, thalamic stimulation for suppression of

trichopoliodystrophy

tricresylphosphate

tricuspid valve, lesion of

tricyclic antidepressant

trifluoperazine

trinucleotide repeats

Unified Parkinson Rating Scale

ventricular enlargement

vestibular function, tests of

visual acuity, decreased

visual evoked response

visual field defect

visual fields

visual fields, constricted

visual impairment

visual loss

visual symptoms

visuospatial disturbance

walking, difficulty with

weakness

weakness, generalized

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 0 to 50 of 434 Next >>

Cognitive and Clinical Characteristics of Patients with Limbic-Predominant Age-Related TDP-43 Encephalopathy
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Risk of First Ischaemic Stroke and Use of Antidopaminergic Antiemetics: Nationwide Case-Time-Control Study
BMJ 376:e061921, Benard-Laribiere, A.,et al, 2022

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

Sport Associated Dementia
BMJ 372:N168, Stewart, W., 2021

Single Photon Emission Computed Tomography/Positron Emission Tomography Molecular Imaging for Parkinsonism: A Fast-Developing Field
Ann Neurol 90:711-719, Verger, A.,et al, 2021

Changing Gears - DBS for Dopaminergic Desensitization in Parkinsons Disease?
Ann Neurol 90:699-710, Weiss, D.,et al, 2021

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Stridor in Multiple System Atrophy
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Neurodegenerative Disease Mortality Among Former Professional Soccer Players
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Treatable Bilateral Striatal Lesions Related to Anti-Dopamine 2 Receptor
Neurol 91:98-101, Marques-Matos, C.,et al, 2018

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
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Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
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Amyotrophic Lateral Sclerosis
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Conversion to Parkinson Disease in the PARS Hyposmic and Dopamine Transporter-Deficit Prodromal Court
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Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
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Neuroimaging Changes in Menkes Disease, Part 1
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Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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Leukodystrophy and Progressive Myoclonic Epilepsy Disclosing DRPLA
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Orthostatic Myoclonus Associated with CASPR2 Antibodies
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A Young Man with Progressive Language Difficulty and Early-Onset Dementia
JAMA Neurol 73:595-599, Botha, H.,et al, 2016

Practice Guideline Summary: Treatment of Restless Leg Syndrome in Adults
Neurol 87:2585-2593, Winkelman, J.W.,et al, 2016

Multiple-System Atrophy
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Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
NEJM 372:1151-1162, Miller, B.L.,et al, 2015

Degenerative Diseases of the Nervous System, Parkinson Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1082, Ropper, A.H.,et al, 2014

Comparison of Pregabalin with Pramipexole for Restless Legs Syndrome
NEJM 370:621-631,667, Allen, R.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

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

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

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

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
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Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
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Inverse Association between Cancer and Alzheimers Disease: Results from the Framingham Heart Study
BMJ 344:e1442, Driver,J.A.,et al, 2012

Neurodegenerative causes of death among retired National Football League Players
Neurol 79:1970-1974, Lehman, E.,et al, 2012

Treatment of Multiple System Atrophy Using Intravenous Immunoglobulin
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Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
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Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus
RadioGraphics 31:5-30, Hegde,A.N.,et al, 2011

Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease
Neurol 76:1372-1376, Sone, J.,et al, 2011

Extended-Release Pramipexole in Advanced Parkinson Disease
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Dopamine Agonist Withdrawal Syndrome in Parkinson Disease
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The Spectrum of Mutations in Progranulin: A Collaborative Study Screening 545 Cases of Neurodegeneration
Arch Neurol 67:161-170,145, Yu,C.-E.,et al, 2010

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

Huntingtons Disease
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010

Tourettes Syndrome
NEJM 363:2332-2338, Kurlan,R., 2010

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

Rapidly Progressive Neurodegenerative Dementias
Arch Neurol 66:201-207, Josephs,K.A.,et al, 2009

Long-Term Effect of Initiating Pramipexole vs Levodopa in Early Parkinson Disease
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Showing articles 0 to 50 of 434 Next >>