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Differential
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abscess, intracerebral

acquired immunodeficiency syndrome

addiction, heroin

addiction, heroin-neurologic complications with

adenine arabinoside

adrenoleukodystrophy

advances in neurology

adverse drug reaction

agnosia, visual

albumin transfusion

Alexanders disease

Alice in Wonderland syndrome

alien hand syndrome

alternating rapid movement, impaired

Alzheimer's disease

Alzheimer's disease, familial

Alzheimer's disease, rapidly progressive

Alzheimer's disease, rate of clinical decline

Alzheimer's disease, visual variant

AMPA receptor antibodies

amyloid angiopathy, cerebral

amyloid plaques

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, childhood

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, post-encephalitic

angiitis, isolated of CNS

animal exposure

anticonvulsants

anticonvulsants, untoward effects of

antithyroid antibodies

antiviral agents

aphasia, progressive

aphasia, progressive, primary

aphasia, transcortical

aphasia, transcortical-sensory

apolipoprotein E

apraxia, dressing

Arnold Chiari malformation

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

autoimmune disease

autonomic dysfunction

axonal degeneration

bacterial infection

Balint's syndrome

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

behavioral disorder

Behcet's syndrome

beriberi, infantile

biologic markers

blood dyscrasias, neurologic findings with

blood transfusion

bovine spongiform encephalopathy

brain biopsy, complications of

brain biopsy, false negative

brain biopsy, indication

brain biopsy, negative

brainstem, lesion of

burning paresthesia

calcification, intracranial

Canavan's disease

carbamazepine, toxicity

carbon monoxide poisoning

carcinoma of breast

cardiac transplantation

CAT scan, abnormal

CAT scan, contrast enhanced

CAT scan, demyelinating disease

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

caudate nucleus

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 atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar plaques, amyloid

cerebellum, disease of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral glucose metabolism

cerebral infarction

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, misdiagnosis

cerebrovascular accident, nonvascular territory

cerebrovascular accident, young adult

Charles Bonnet's syndrome

chemotherapy, CNS treatment and complications with

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cingulate gyrus

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

cognition, slowed

cogwheel rigidty

color vision, impaired

concentration, impaired

contactin associated protein like 2 antibodies

controversies in neurology

corneal transplant

cortical blindness

cortical infarction

cortical-basal ganglionic degeneration

Creutzfeldt-Jakob disease, genetic

cultured skin fibroblasts

cytochrome c oxidase

cytochrome c oxidase, deficiency

deafness, congenital

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, childhood

dementia, diagnostic evaluation of

dementia, differential diagnosis of

dementia, familial

dementia, frontotemporal

dementia, presenile

dementia, prevention of

dementia, rapidly progressive

dementia, reversible

dementia, screening for

dementia, transmissible

dementia, treatment of

demyelinating disease

denial of blindness(Antons syndrome)

dentate nuclei, lesion of

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

differential diagnosis

difficulty climbing stairs

dissociated sensory loss

drug abuse, neurologic complications of

drug induced neurologic disorders

drug withdrawal

dural graft, cadaveric

dyschromatopsia

dysdiadochokinesia

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, complications with

electroencephalogram, depth electrode

electroencephalogram, focal delta activity

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

electron microscopy

electrophoretic pattern, CSF

electrophoretic pattern, serum

emotional lability

encephalitis, autoimmune

encephalitis, bornavirus

encephalitis, Japanese

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis, postinfectious

encephalopathy, carcinomatous

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, neonatal

epidemiology of neurology

epilepsia partialis continua

episodic disorders

evoked potentials

executive dysfunction

experimental allergic encephalitis

eye movement, disorders of

Fabry's disease

faciobrachial dystonic seizure

failure to thrive

fatal familial insomnia

feeding disorder

finger nose finger test

flu-like illness

follicle stimulating hormone

fontanel, bulging

Friedreich's ataxia

frontal lobe, anatomy and physiology

frontal lobe, pathologic signs of

gamma amino butyric acid receptor antibody

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

Gerstmann syndrome

Gerstmann-Straussler-Scheinker disease

glutaric acidemia

glycine receptor antibodies

gyrus, abnormal

Hallervorden Spatz disease

hallucination, visual

hallucination, visual, benign

head circumference

headache, episodic

heel-knee-shin test

hemianopia, homonymous

hepatolenticular degeneration(Wilson's disease)

heralding manifestation

herpes simplex encephalitis

herpes simplex virus

herpes virus infection

histochemistry of muscle

hockey stick sign

hot cross bun sign

human immunodeficiency virus type 1

Huntington's chorea

hydrocephalus, normal pressure

hyperthyroidism

hypoparathyroidism

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

immunocompetent

immunodeficiency

immunohistochemistry

immunologic disease

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

incubation period

infant and newborn with distress, neurologic prognosis in

infant, evaluation of

intellectual deterioration

internuclear ophthalmoplegia

internuclear ophthalmoplegia, unilateral

interobserver agreement

intestinal pseudoobstruction

intracerebral hemorrhage

intrathecal chemotherapy

intraventricular hemorrhage

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, conjugal

Jakob-Creutzfeldt disease, Heidenhain variant

Jakob-Creutzfeldt disease, medical precaution with

Jakob-Creutzfeldt disease, unilateral

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

Kearns-Sayre syndrome

Krabbe's disease

lactic acidemia

laminar necrosis, cortical

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

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalitis, acute necrotizing hemorrhagic

leukoencephalopathy

leukoencephalopathy, differential diagnosis

Lewy body disease, diffuse

life expectancy

limbic encephalitis

lipid storage disorder of CNS

liver transplantation

lymphoma involving CNS

lymphoma, primary of CNS

lysosomes, abnoral

magnetic susceptibility

malignancy screen

maple syrup urine disease

Marinesco-Sjogren syndrome

memory, defect of recent

memory, impairment of

meningoencephalitis

mental retardation

mental status, abnormal

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

microhemorrhage, intracerebral

midbrain, lesion of

Mini Mental Status Examination

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molecular genetics

Morvan's fibrillary chorea

motor neuron disease

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

MRI, abnormal, seizure causing

MRI, CAT scan compared to

MRI, cerebrovascular disease

MRI, complications with

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion tensor

MRI, diffusion weighted

MRI, diffusion weighted, pattern

MRI, early changes in CVA

MRI, false negative

MRI, false positive

MRI, functional

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, indications for

MRI, lesion burden

MRI, paramagnetic effect

MRI, proton density

MRI, punctate pattern

MRI, spinal cord

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRI, target sign

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple system atrophy

muscle twitching

myelitis, longitudinal

myelitis, transverse

myoclonic jerks

myoclonus, action

myoclonus, cortical

myoclonus, differential diagnosis of

myoclonus, epilepsy

myoclonus, stimulus sensitive

myopathy, mitochondrial

nasal brushings

neoplasm, intracranial

neoplasm, metastatic to CNS

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary of CNS

nerve conduction studies

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic testing

neuron specific enolase

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuropathology, brain

neuropathy, ataxia, retinitis pigmentosa

neuropathy, peripheral

Niemann-Pick disease

NMDA antagonists

nucleus basalis of Meynert

nutritional deficiency

nystagmus, periodic alternating

nystagmus, rotary

occipital cortex

occipital lobe, lesion of

occupational neurologic disorders

ocular motility, disorders of

old age, neurology of

olfactory biopsy

olfactory cortex

olfactory mucosa

olfactory pathway

olfactory tract

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

optic atrophy, hereditary

optic neuropathy

organ transplantation

orthostatic hypotension

osmotic demyelination syndrome

overlap syndrome

owl's eye sign of spinal cord

palmomental response

paraparesis, spastic

parietal lobe, lesion of

parietal lobe, syndromes of

Parkinson disease

Parkinson disease, misdiagnosis

Parkinson disease, motor neuron disease with

Parkinson disease, postencephalitic

Parkinsonism plus syndrome

Parkinsonism syndrome

PAS positive material in the brain

pathologic reflex

peduncular hallucinosis

Pelizaeus Merzbacher

personality change

pigmentary retinopathy

pituitary, hormones of

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

pons, lesion of

posterior cortical atrophy

posterior leukoencephalopathy syndrome

postictal encephalopathy

potassium channel antibodies

practice guidelines

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

prion protein gene

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

protein 14-3-3, cerebrospinal fluid

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

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

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychotic behavior

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapidly fatal neurologic illness

rapidly progressing neurologic illness

real-time quaking-induced conversion

release phenomena

remote effect of cancer on the nervous system

respiratory failure

restless leg syndrome

retinal degeneration

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

risk-benefit assessment

roving eye movements

saccadic eye movements, abnormal

sarcoidosis, CNS

seizure, children

seizure, nonconvulsive

sensorineural hearing loss

sensory symptoms

serum S100 protein

simultanagnosia

single photon emission computed tomography

sleep pathology and physiology

slow virus infection of CNS

spastic diplegia

speech, loss of

speech, pressured

spinal cord, lesion of

spinocerebellar degeneration

spongy degeneration of brain

spongy degeneration of brain, differential diagnosis of

square wave jerks

startle myoclonus

startle reaction

status epilepticus

status epilepticus, nonconvulsive

steroid therapy, CNS treatment and complications with

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

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

substantia nigra

symmetric brain lesions

tandem gait, ataxic

temporal lobe, status

thalamic tumors

thalamic tumors, bilateral

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine deficiency

toxic encephalopathy

treatment of neurologic disorder

tremor, intention

tuberous sclerosis

twitching, face

upgaze, paralysis of

urinary incontinence

urine test for metabolic disorders

vertigo, episodic

vibratory sensation

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

visual distortions

visual evoked response

visual field defect

visual impairment

visual loss, progressive

vitamin deficiency

Von Hippel Lindau

walking, difficulty with

Wallerian degeneration

weakness, acute

weakness, focal

weakness, progressive

Wernicke's aphasia

Wernicke's encephalopathy

West Nile fever

Western immunoblot test

white matter disease

white matter disease, periventricular

wide based gait

Showing articles 550 to 600 of 3442 << Previous Next >>

Neuropathy, Encephalopathy, Status Epilepticus, and Acute Intermittent Porphyria
Lancet 395:e101, Ahmed, M.A.,et al, 2020

CASPR2 Autoimmunity in Children Expanding to Mild Encephalopathy with Hypertension
Neurol 94:e2290-e2301,953, Syrbe, S.,et al, 2020

Contrast-Induced Encephalopathy Following Coronary Angiography
Neurol 94:e2491-e2494, Harada, Y.,et al, 2020

Vitamin B6 Deficiency Presenting with New-Onset Epilepsy and Status Epilepticus in a Patient with Parkinson Disease
Neurol 94:e2605-e2607, Modica, J.S.,et al, 2020

Choosing Anticonvulsant Medications to Manage Status Epilepticus
NEJM 382:2569-2572, Wu, K., 2020

COVID-19: A Global Threat to the Nervous System
Ann Neurol 88:1-11, Koralnik, I.J. & Tyler, K.L., 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Pathophysiology and Management of Hyperammonemia in Organ Transplant Patients
Am J Kidney Dis PMID:31040091, Seethapathy, H. & Fenves, A.Z., 2019

An Intracerebral Hemorrhage Care Bundle is Associated with Lower Case Fatality
Ann Neurol 86:495-493, Parry-Jones, A.R.,et el, 2019

A Case of Acute Encephalopathy and Rigidity in a 30-Year-Old Man
Neurol 93:759-763, Hurtubise, B. & MacLellan, A., 2019

Prolonged Microgravity Affects Human Brain Structure and Function
AJNR 40:1878-1885, Roberts,D.R.,et al, 2019

Randomized Trial of Three Anticonvulsant Medications for Status Epilepticus
NEJM 381:2103-2113,2171, Kapur, J.,et al, 2019

Lyme Disease: What the Neuroradiologist Needs to Know
AJNR 40:1998-2000, Valand, H.A.,et al, 2019

A 23-Year-Old Man with Headaches, Confusion, and Lower Extremity Weakness
Neurol 92:863-867, Patel, N.M.,et al, 2019

Treatment of Patients with Psychogenic Nonepileptic Attacks
JAMA 321:1967-1968, Tolchin, B.,et al, 2019

A 68-year-old Man with Rapid Cognitive Decline
Neurol 93:315-318, Berth, S.H.,et al, 2019

Case 27-2019:A 16-Year-Old Girl with Head Trauma During a Sailboat Race
CPC,Concussion,Benign Paroxysmal Positional Vertigo, Case 27-2019, NEJM 381:863-871, Iaccarino,M.A.,et al, 2019

Childhood Primary Angiitis of the Central Nervous System
www.UptoDate.com, Dec, Twilt, M. & Benseler, S., 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

Acute Toxic Limbic Encephalopathy Following Glyphosate Intoxication
Neurol 92:534-536, Planche, V.,et al, 2019

Bismuth Neurotoxicity from Use of Topical Bismuth Dressing for Burns
Neurol 92:680-681, Saini, V.,et al, 2019

Cerebral Ischemia in Patients on Direct Oral Anticoagulants
Stroke 50:873-879, Macha, K.,et al, 2019

A 71-year-old Man Receiving Treatment for Cryptococcal Meningitis, Developing New-Onset Lethargy
Neurol 92:815-820, Peng, T.J.,et al, 2019

Long-Term Treatment Effect in Cerebrotendinous Xanthomatosis Depends on Age at Treatment Start
Neurol 92:e83-e95, Stelten, B.M.L.,et al, 2019

"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019

The Dangers of PRES
Neurol 92:e282-e285, Chaterine, C.,et al, 2019

A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
Neurol 92:e274-e281, Chen, Z. & Neo, S., 2019

Encephalopathy in a Large Cohort of British Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Patients
Stroke 50:283-290, Drazyk, A.M.,et al, 2019

Contemporary Reversal of Oral Anticoagulation in Intracerebral Hemorrhage
Stroke 50:529-536, Bower, M.M.,et al, 2019

Acute Encephalitis in Immunocompetent Adults
Lancet 393:702-716, Venkatesan, A.,et al, 2019

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Cerebellar Hippocampal and Basal Nuclei Transient Edema with Restricted Diffusion (CHANTER) Syndrome
Neurocrit Care 31:228-296, Jasne, A.S.,et al, 2019

Clinicopathologic Conference, Ingestion of Isopropyl Alcohol
NEJM 380:1657-1665, Case 13-2019, 2019

Clinicopathologic Conference, Adenovirus Meningoencephalitis
NEJM 381:1459-1470, Case 31-2019, 2019

Effects of Tranexamic Acid on Death, Disability, Vascular Occlusive Events and Other Morbidities in Patients with Acute Traumatic Brain Injury (CRASH-3): A Randomised, Placebo-Controlled Trial
Lancet 394:1713-1723,1687, The CRASH-3 trial collaborators, 2019

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Nivolumab-Induced Autoimmune Encephalitis in Two Patients with Lung Adenocarcinoma
Case Rep Neurol Med 2018;doi:10.1155/2018/2548528, Shah, S.,et al, 2018

Cerebral Fat Embolism Syndrome in Sickle Cell Disease Without Evidence of Shunt
eNeurologicSci 14:19-20, Nathan, C.L.,et al, 2018

Bilateral Basal Ganglia Necrosis Secondary to Methamphetamine
MDCP 5:55-556, Sanchez,A. et al, 2018

Intrasellar Herniation
Neurol 91:889-890, Pacheco, F.T.,et al, 2018

A 22-year-old Man Presenting with Headache and Right Leg Jerks
Neurol 91:891-895, Schupper, A.J.,et al, 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Surviving Cerebral Malaria
Neurol 91:978-979, Wijdicks, E.F.M. & Park, J.G., 2018

Japanese Encephalitis
Neurol 91:e2031-e2032, Zhang, B.,et al, 2018

Efficacy and Tolerability of Erenumab in Patients with Episodic Migraine in Whom Two-of-Four Previous Preventive Treatments were Unsuccessful: A Randomised, Double-Blind, Placebo-Controlled, Phase 3b Study
Lancet 392:2280-2287,2241, Reuter, U.,et al, 2018

Clinicopathologic Conference, Susacs Syndrome
NEJM 379:2152-2159, Case 37-2018, 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Tocilizumab Treatment for New Onset Refractory Status Epilepticus
Ann Neurol 84:940-945, Jun, J.,et al, 2018

Showing articles 550 to 600 of 3442 << Previous Next >>