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abducens nerve paralysis

aceruloplasminemia

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome myelopathy

activities of daily living

activities of daily living scale

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

affect, inappropriate

alcohol intolerance

alcohol intoxication

alcohol, blood level of

alcohol, neurologic complications with

alcoholic blackout

alcoholic dementia

alcoholic polyneuropathy

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

Alexanders disease

alkylating agents

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

Alzheimer's disease

Alzheimer's disease, age of onset

Alzheimer's disease, conjugal

Alzheimer's disease, diagnosis of

Alzheimer's disease, early onset

Alzheimer's disease, familial

Alzheimer's disease, familial, late onset

Alzheimer's disease, heterogeneity of

Alzheimer's disease, incidence

Alzheimer's disease, misdiagnosis

Alzheimer's disease, pathogenesis

Alzheimer's disease, preclinical

Alzheimer's disease, risk factors in

Alzheimer's disease, treatment of

aminoacidopathies

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

amyloid angiopathy, hereditary cystatin C

amyloid beta protein

amyloid imaging

amyloid plaques

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

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

anemia, megaloblastic

anesthesia, general

aneurysm, intracranial

angiography, cerebral

angioid streaks

animal exposure

ankle, swelling of

anticholinergic drugs

anticholinesterase

anticonvulsants, selection of

aphasia, progressive

aphasia, progressive, primary

apolipoprotein E

apraxia, constructional

Arnold Chiari malformation

arylsulfatase A

asterixis, causes of

asterixis, unilateral

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atherosclerosis, premature

auditory evoked brainstem potentials

autonomic dysfunction

axonal degeneration

axonal spheroid

B 12 deficiency

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

behavior, combative

behavioral disorder

Behcet's syndrome

benign essential tremor

biologic markers

bladder dysfunction

blinking, reduced

blood dyscrasias, neurologic findings with

blood transfusion

bone marrow transplantation

botulinum toxin

bovine spongiform encephalopathy

brain transplantation

brainstem, atrophy

brainstem, lesion of

calcification, intracranial

Canavan's disease

carbon monoxide poisoning

carcinoma of pancreas

carotid artery disease

carotid artery occlusion, bilateral

CAT scan, abnormal

CAT scan, contrast enhanced

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

cell fusion test

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellar plaques, amyloid

cerebellum, disease of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema, vasogenic

cerebral glucose metabolism

cerebral infarction

cerebral infarction, subcortical

cerebral vasculature, calcification

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, amonia

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, glutamine

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

ceruloplasmin, serum

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chewing movements

choline acetyltransferase

chorea, causes of

chorea, familial

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cigarette smoking

cingulate gyrus

cingulate island sign

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

coat-hanger pain

cobalamin C deficiency

coenzyme Q10 deficiency

cognition, slowed

cogwheel rigidty

cold hands sign

color vision, impaired

compression neuropathy

conjunctival biopsy

copper deficiency

copper metabolism, abnormal

corneal dystrophy

corneal transplant

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical blindness, transient

cranial neuropathy, multiple

Creutzfeldt-Jakob disease, genetic

crying, pathologic

cultured skin fibroblasts

Cushing's syndrome

decerebrate posture

deep gray nuclei

degenerative diseases of CNS

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, childhood

dementia, diagnostic evaluation of

dementia, differential diagnosis of

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, screening for

dementia, subcortical

dementia, thalamic

dementia, transmissible

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

differential diagnosis

difficulty climbing stairs

disability rating scale, neurological

disinhibition-dementia-parkinsonism-amyotrophic complex

dopamine agonist

down-beat nystagmus

dysdiadochokinesia

dyskinesia, drug induced

dyssynergia cerebellaris myoclonica

dystonia, cervical

dystonia, focal

dystonia, post traumatic

dystonia, treatment of

ears of the Lynx MR sign

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, pediatric patients

electroencephalogram, periodic complexes

electroencephalogram, video monitoring with

electron microscopy

electroretinograph

emotional lability

encephalitis, Japanese

encephalitis, viral

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

epidemiology of neurology

episodic neurologic deficits

erectile dysfunction

esophageal varices

ethics in neurology

evoked potentials

executive dysfunction

exercise intolerance

exome sequencing

eye movement, disorders of

Fabry's disease

facial expression abnormality

facial nerve palsy, bilateral

familial hemiplegic migraine

fatal familial insomnia

fatty acid, elevated plasma content

feeding disorder

ferritin, elevated

fetal alcohol syndrome

finger nose finger test

fingerprint bodies

flail arm syndrome

fracture, long bone

fracture, pathologic

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal lobe, anatomy and physiology

frontal lobe, atrophy

frontal lobe, lesion of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

fundus, abnormality of

gait, festinating

gangliosidosis GM2

Gaucher's disease

Gaucher's disease, adult onset

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

Gerstmann-Straussler-Scheinker disease

Gilles de la Tourette syndrome

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutaric acidemia

glycogen storage disease

granular osmiphilic material

growth retardation

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, visual

head circumference

health insurance

hearing loss, bilateral

hearing problems in children

heel-knee-shin test

hemochromatosis

hemochromatosis, primary

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

hexosaminidase-A

hockey stick sign

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's chorea, late onset

Huntington's chorea, misdiagnosis of

Huntington's disease, children

hydrocephalus, exvacuo

hyperadrenalism

hyperhomocysteinemia

hyperparathyroidism

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hyperthyroidism

hypoalbuminemia

hypometric saccades

hypoparathyroidism

hypotension, neurologic causes of

hypotension, systemic

hypothalamus, disturbance of

hypothermia, causes of

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

ileus, paralytic

imbalance, postural

immunofluorescence

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inappropriate behavior

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incontinence, fecal

infantile spasm

inflexibility, mental

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, lobar

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intrinsic hand muscles, wasting of

iron, serum, low

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, conjugal

Jakob-Creutzfeldt disease, medical precaution with

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

jaw contractures

Kayser-Fleischer ring

Kearns-Sayre syndrome

kinesia paradoxica

Kluver-Bucy syndrome

Korsakoff's psychosis

Krabbe's disease

lactic acidemia

lacunar infarction

Lafora's disease

laminectomy, lumbar

language disorder in adults

laughing, pathologic

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukodystrophy, pigmented orthochromatic

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

Lewy body disease, diffuse

libido, decreased

life expectancy

limbic-predominant age-related TDP-43 encephalopathy

lipid storage disorder of CNS

lipomembranous polycystic osteodysplasia

livedo reticularis

liver function enzymes

liver transplantation

lymphoma involving CNS

lysosomal storage disease

magnetic susceptibility

malformation, vascular

malformation, vascular, cerebral

manic-depressive

maple syrup urine disease

marche a petits pas

Marinesco-Sjogren syndrome

medical-legal aspects of neurology

memory, defect of recent

memory, impairment of

meningitis, carcinomatous

meningoencephalopathy

meningomyelitis

meningovascular syphilis

mental retardation

mental status, abnormal

mesial temporal lobe

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methylhydrazine derivatives

methylmalonic acidemia

microangiopathy, brain

microhemorrhage, intracerebral

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine with aura

migraine, hemiplegic

mild cognitive impairment

Minamata disease

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoamine oxidase inhibitors

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

moyamoya, adult

MRI, CAT scan compared to

MRI, complications with

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, functional

MRI, gradient-echo

MRI, indications for

MRI, paramagnetic effect

MRI, punctate pattern

MRI, spinal cord

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRI, target sign

multiple sclerosis

multiple sclerosis, cognitive presenttion

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Duchenne

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelitis, longitudinal

myeloneuropathy

myelopathy, vacuolar

myoclonic jerks

myoclonus, cortical

myoclonus, epilepsy

myoclonus, stimulus sensitive

myopathy, alcoholic

myopathy, mitochondrial

myotonia dystrophica

nausea and vomiting

neoplasm, intracranial

neoplasm, primary of CNS

nerve conduction studies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroaxonal leukodystrophy

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurogenic bladder

neurologic complications of, systemic cancer

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic testing

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology, brain

neuropathy, amyloid

neuropathy, ataxia, retinitis pigmentosa

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropsychiatry

neurotransmitter

next-generation sequencing

Niemann-Pick disease

nitrogen mustard

nystagmus, monocular

nystagmus, rotary

obsessive-compulsive disorder

occipital lobe, lesion of

occupational neurologic disorders

ocular motility, disorders of

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, hereditary

optic neuropathy

optokinetic nystagmus, abnormal

orthostatic hypotension

osmotic demyelination syndrome

overlap syndrome

owl's eye sign of spinal cord

pain, abdominal

pain, increased response

palatal myoclonus

pallido-ponto-nigral degeneration

palmoplantar keratoderma

paraparesis, familial spastic

paraparesis, spastic

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, atypical

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, familial

Parkinson disease, freezing phenomena in

Parkinson disease, misdiagnosis

Parkinson disease, pathogenesis of

Parkinson disease, rapid progression

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism-dementia complex

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive material in the brain

patient information and support

Pelizaeus Merzbacher

pernicious anemia

peroxisomal disease

personality change

phenylketonuria

phenylketonuria, adult onset

pheochromocytoma

photosensitivity, skin

pigmentary retinopathy

Pittsburgh Compound B

pituitary, hormones of

pleocytosis of cerebrospinal fluid

poison, mercury

poison, neurologic problems with

polycystic lipomembranous osteodysplasia

polyglucosan body

polyglucosan body disease

polymerase chain reaction

pons, lesion of

pontocerebellar atrophy

port wine nevus

postoperative neurologic complications

postural abnormality

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

presenilin-1 gene

presenilin-2 gene

prevention of neurologic disorders

primary lateral sclerosis

prion protein gene

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

progressive subcortical gliosis

progressive supranuclear palsy

protein 14-3-3, cerebrospinal fluid

pseudobulbar palsy

pseudoxanthoma elasticum

psychiatric disorder

psychiatric manifestations of brain tumors

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis, acute

psychosis, cause of

psychotic behavior

ptosis, bilateral

pulmonary embolism

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

radiation encephalopathy, delayed

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

real-time quaking-induced conversion

recombinant DNA

reflex sympathetic dystrophy

release phenomena

remote effect of cancer on the nervous system

respiratory depression

respiratory failure

retina, abnormal

retinal degeneration

retinal hemorrhages

retinitis pigmentosa

Rett's syndrome

roving eye movements

Schilder's disease

scoliosis, neurologic association with

sea-blue histiocytes

seizure, children

seizure, intractable

seizure, teenager

sensorineural hearing loss

shoulder, pain in

single photon emission computed tomography

skin, darkening of

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

small vessel disease

small vessel disease, cerebral

SNCA duplication

Sneddon's syndrome

somatosensory evoked potentials

spastic diplegia

spastic paraplegia, type 11

speech disorder

speech disorder, childhood

speech, loss of

sphingolipodoses

spinal cord, infarction of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 17

spinocerebellar ataxia type 7

spinocerebellar degeneration

spinopontine atrophy, dominant

spongy degeneration of brain

sports medicine, neurology of

startle myoclonus

startle reaction

status epilepticus

stereotyped behavior

steroid therapy, CNS treatment and complications with

stimulation, deep brain

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

strokelike episodes

Sturge-Weber syndrome

subarachnoid hemorrhage

subdural hematoma

substantia nigra

symmetric brain lesions

syphilis, meningomyelitis

syphilis, neurologic complications with

systemic lupus erythematosus

tandem gait, ataxic

tapetoretinal degeneration

Tay-Sachs disease

TDP-43 proteinopathy

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

testicular atrophy

thalamic tumors

thalamic tumors, bilateral

thalamus, atrophy of

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thromboangiitis obliterans cerebri

thrombocytopenia

thrombophlebitis

tongue, atrophy

tongue, fasciculations of

tonic foot response

torticollis, post traumatic

toxins, nervous system

transient ischemic attack

transient ischemic attack, recurrent

treatment of neurologic disorder

tremor, intention

tremor, post traumatic

tremor, resting

tremor, wing beating

trientine dihydrochloride

trinucleotide repeats

tuberous sclerosis

unconsciousness

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urine test for metabolic disorders

vanishing white matter

venous thrombosis, non-cerebral

ventricular enlargement

vertigo, episodic

very long chain fatty acids

vibratory sensation, abnormal

vincristine neurotoxicity

violent behavior

viral infection, CNS

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual fields, constricted

visual loss, progressive

visual loss, slow

visuospatial disturbance

vocal cord paralysis

Von Hippel Lindau

walking, difficulty with

weakness, acute

weakness, focal

weakness, progressive

Wernicke's aphasia

Wernicke's encephalopathy

white matter disease

white matter disease, subcortical

wide based gait

word-finding difficulty

xeroderma pigmentosa

Showing articles 1100 to 1150 of 3811 << Previous Next >>

Genetic Screening for a Single Common LRRK2 Mutation in Familial Parkinson's Disease
Lancet 365:410-412, Nichols, W.C., et al, 2005

Bone Mineral Density and the Risk of Alzheimer Disease
Arch Neurol 62:107-111, Tan,Z.S.,et al, 2005

A 32-Year Prospective Study of Change in Body Weight and Incident Dementia
Arch Neurol 62:55-60,20, Stewart,R.,et al, 2005

Meningovascular syphilis as a cause of basilar artery stenosis
Neurol 64:391-392, Flint, A.C., et al, 2005

A Variant in the HS1-BP3 Gene is Associated with Familial Essential Tremor
Neurol 64:417-421, Higgins, J.J., et al, 2005

Unawareness of Cognitive Deficit (Cognitive Anosognosia) in Probable AD and Control Subjects
Neurol 64:693-699, Barrett, A.M., et al, 2005

Steroid Dementia: an Overlooked Diagnosis?
Neurol 64:707-709, Sacks,O. & Shulman,M., 2005

Fatal Avian Influenza A (H5N1) in a Child Presenting with Diarrhea Followed by Coma
NEJM 352:686-691, de Jong,M.D., et al, 2005

Specialist Palliative Care in Dementia
BMJ 330:57-58, Chen,F. & Majeed,A., 2005

Unusual Variants of Alexander's Disease
Ann Neurol 57:327-338, van der Knaap,M.S., et al, 2005

Recent Developments in Pain in Dementia
BMJ 330:461-464, Scherder,E., et al, 2005

Sensorineural Hearing Loss in Children
Lancet 365:879-890, Smith, R.J.H.,et al, 2005

Atypical Antipsychotic Drugs and Risk of Ischaemic Stroke: Population Based Retrospective Cohort Study
BMJ 330:445-448, Gill,S.S., et al, 2005

Heritability of Carotid Artery Atherosclerotic Lesions
Stroke 36:5-8, Moskau,S.,et al, 2005

Metabolic Patterns Associated with the Clinical Response to Galantamine Therapy
Arch Neurol 62:721-728, Mega,M.S.,et al, 2005

Atorvastatin for the Treatment of Mild to Moderate Alzheimer Disease
Arch Neurol 62:753-757, Sparks,D.L.,et al, 2005

Proton MR Spectroscopy in Wilson Disease: Analysis of 36 Cases
AJNR 26:1066-1071, Lucato,L.T.,et al, 2005

Deaths with Antipsychotics in Elderly Patients with Behavioral Disturbances
Dept Health & Human Services (Apr), FDA Public Health Advisory, 2005

Donepezil for Dementia in Parkinsons Disease: A Randomised, Double Blind, Placebo Controlled, Crossover Study
JNNP 76:934-939,903, Ravina,B.,et al, 2005

The "Pulvinar Sign" in a Case of Paraneoplastic Limbic Encephalitis Associated with Non-Hodgkins Lymphoma
JNNP 76:882-884, Mihara,M.,et al, 2005

Vitamin E and Donepezil for the Treatment of Mild Cognitive Impairment
NEJM 352:2379-2388,2439, Petersen,R.C.,et al, 2005

Frontotemporal Lobar Degeneration
Arch Neurol 62:925-930, Johnson,J.K.,et al, 2005

Malignant Hyperthermia, Update on Susceptibility Testing
JAMA 293:2918-2924,2958, Litman,R.S.&Rosenberg,H., 2005

Diffusion-Weighted and Fluid-Attenuated Inversion Recovery Imaging in Creutzfeldt-Jakob Disease:High Sensitivity and Specificity for Diagnosis
AJNR 26:1551-1562, Young,G.S.,et al, 2005

Practice Parameter:Therapies for Essential Tremor
Neurol 64:2008-2020, Zesiewicz,T.A.,et al, 2005

A 10-Item Smell Identification Scale Related to Risk for Alzheimers Disease
Ann Neurol 58:155-160, Taberr,M.H.,et al, 2005

Statin Use and the Risk of Incident Dementia
Arch Neurol 62:1047-1051, Rea,T.D.,et al, 2005

Different Patterns of Magnetic Resonance Imaging Atrophy for Frontotemporal Lobar Degeneration Syndromes
Arch Neurol 62:1106-1110, Short,R.A.,et al, 2005

Delusions and Hallucinations in Dementia with Lewy Bodies: Worsening with Memantine
Neurol 65:481-482, Ridha,B.H.,et al, 2005

Creutzfeldt-Jakob Disease Mimicking Radiologic Posterior Reversible Leukoencephalopathy
Neurol 65:329, Sibon,I.,et al, 2005

Brain Magnetic Resonance Imaging in Patients with Cowden Syndrome
Medicine 84:129-136, Lok,C.,et al, 2005

Psychosocial Impact of Screening for Intracranial Aneurysms in Relatives with Familial Subarachnoid Hemorrhage
Stroke 36:836-840, Wermer,M.J.H.,et al, 2005

Pharmacological treatment of Neuropsychiatric Symptoms of Dementia
JAMA 293:596-608, Sink,K.M.,et al, 2005

The Clinical and Genetic Spectrum of Spinocerebellar Ataxia 14
Neurol 64:1258-1260, Chen,D-H.,et al, 2005

Autonomic Dysfunction in Machado-Joseph Disease
Arch Neurol 62:630-636, Yeh,T-H.,et al, 2005

Value of Gradient-Echo Magnetic REsonance Imaging in the Diagnosis of Familial Cerebral Cavernous Malformation
Arch Neurol 62:653-658, Lehnhardt,F-G.,et al, 2005

Autonomic Peripheral Neuropathy
Lancet 365:1259-1270, Freeman,R., 2005

The Role of Levodopa in the Management of Dementia With Lewy Bodies
JNNP 76:1200-1203, Moloy,S.,et al, 2005

Cholinesterase Inhibitors for Patients with Alzheimers Disease: Systematic Review of Randomised Clinical Trials
BMJ 331:321-323, Kaduszkiewicz,H.,et al, 2005

Carbamazepine Encephalopathy Masquerading as Creutzfeldt-Jakob Disease
Neurol 65:650-651, Horvath,J.,et al, 2005

Phaeochromocytoma
Lancet 366:665-675, Lenders,J.W.M.,et al, 2005

Clinicopath Conf, Prion Disease (Sporadic Creutzfeldt-Jakob Disease)
NEJM 353:1042-1050, Case 27-2005, 2005

NT-3 Promotes Nerve Regeneration and Sensory Improvement in CMT1A Mouse Models and in Patients
Neurol 65:681-689, 662, Sahenk,Z.,et al, 2005

Quality of Life in Patients with Charcot-Marie-Tooth Disease
Neurol 65:922-924, Vinci,P.,et al, 2005

Neuropathology of Dementia in Parkinsons Disease: A Prospective, Community-Based Study
Ann Neurol 58:773-776,663, Aarsland,D.,et al, 2005

Risk of Death With Atypical Antipsychotic Drug Treatment for Dementia, Meta-analysis of Randomized Placebo-Controlled Trials
JAMA 294:1934-1943,1963, Schneider,L.S.,et al, 2005

Delayed Neurotoxicity in Primary Central Nervous System Lymphoma
Arch Neurol 62:1595-1600, Omuro,A.M.P.,et al, 2005

Hereditary Motor and Sensory Neuropathies
Peripheral Neuropathy, Dyck,P.J. & Thomas,P.K. (Ed). Elsevier Publ, Vol 2, Ch 69: 1623-1635, Shy,M.E., et al, 2005

Lipid Lowering Agents Are Associated With a Slower Cognitive Decline in Alzheimers Disease
JNNP 76:1624-1629, Masse,I.,et al, 2005

Central Nervous System Involvement in Hereditary Neuropathy With Liability to Pressure Palsies
Arch Neurol 62:1911-1914, Sanahuja,J.,et al, 2005

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