Neudle.com: dementia diagnostic classification

Differential
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abdominal distention

abdominal protrusion

abscess, intracerebral

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, older adults

acromicria

activities of daily living

addiction, heroin

Addison's disease

adolescent medicine

adrenal crisis, acute

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult-onset leukodystrophy, with neuroaxonal spheroids

advance directives

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement, impaired

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, driving with

Alzheimer's disease, early onset

Alzheimer's disease, early symptoms

Alzheimer's disease, familial

Alzheimer's disease, incidence

Alzheimer's disease, misdiagnosis

Alzheimer's disease, pathogenesis

Alzheimer's disease, preclinical

Alzheimer's disease, prognosis of

Alzheimer's disease, rapidly progressive

Alzheimer's disease, rate of clinical decline

Alzheimer's disease, risk factors in

Alzheimer's disease, staging

Alzheimer's disease, treating associated medical problems in

Alzheimer's disease, treatment of

Alzheimer's disease, vaccine

Alzheimer's disease, visual variant

aminoacidopathies

ammonia

AMPA receptor antibodies

amphiphysin antibodies

amygdala

amyloid

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

amyloid angiopathy, cerebral, inflammatory type

amyloid angiopathy, cerebral, tumefactive

amyloid angiopathy, hereditary cystatin C

amyloid beta protein

amyloid beta-related angiitis

amyloid imaging

amyloid plaques

amyloid-related imaging abnormalities

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, treatment of

anemia, megaloblastic

anesthesia, general

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiitis, isolated of CNS, tumefactive

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, false negative

angiography, cerebral, negative

antibodies to measles

anticholinergic drugs

anticholinesterase

anticoagulant, complications of

anticoagulant, contraindications

anticoagulant, discontinuation

anticoagulant, treatment

anticoagulant, treatment in CVD

anticonvulsants

anticonvulsants, untoward effects of

antidotes

antiphospholipid antibodies

antithyroid antibodies

anxiety

aphasia

aphasia, progressive

aphasia, progressive, non-fluent

aphasia, progressive, primary

apnea

apolipoprotein E

apolipoprotein E, false positive

apoliprotein E, plasma level

applause sign

apraxia

apraxia, constructional

aqueduct of Sylvius, obstruction

artificial intelligence

autoimmune basal ganglia encephalitis

autoimmune disease

autoimmune encephalopathy

autoimmune meningitis

automobile accidents

autonomic dysfunction

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavior

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

benign essential tremor

blood pressure, control

blood transfusion

bone biopsy

bone marrow biopsy

bone marrow transplantation

bovine spongiform encephalopathy

brain biopsy, complications of

brain biopsy, false negative

brain biopsy, indication

brain biopsy, negative

calcification, intracranial

carbamazepine, toxicity

carbon monoxide poisoning

cardiac surgery, neurologic complications with

cardiopulmonary bypass

caregiver

carotid artery disease

carotid artery stenosis

CAT scan

CAT scan, abnormal

CAT scan, angiography

CAT scan, angiography, false negative

CAT scan, chest

CAT scan, contrast enhanced

CAT scan, contrast enhanced, delayed

CAT scan, contrast enhanced, double dose

CAT scan, dementia

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, indications for

CAT scan, mass effect on

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

cavum septi pellucidi

CD4 counts

celiac disease, childhood

central hypoventilation

central nervous system, infection of

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellar tonsils

cerebral arteries

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral death

cerebral edema

cerebral edema, vasogenic

cerebral infarction

cerebral infarction, hemorrhagic

cerebral infarction, subcortical

cerebral ischemia

cerebral palsy

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebroretinal microangiopathy with calcifications and cysts

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, beta-D-glucan

cerebrospinal fluid, biochemical markers of CNS disease

cerebrospinal fluid, culture negative

cerebrospinal fluid, drainage of

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, leak

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, misdiagnosis

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, nonvascular territory

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, three territory involvement

cerebrovascular accident, topographic pattern

cerebrovascular accident, women

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, risk factors in

chemotherapy, CNS treatment and complications with

chromosomal abnormality

chromosome 17

chromosome 19

chromosome 20

chronic progressive external ophthalmoplegia

chronic traumatic encephalopathy

cingulate gyrus

cisterna magna

claustrophobia

Clinical Pathologic Conference(C.P.C.)

cluster, geographic

coenzyme Q10 deficiency

collapsin response mediator protein 5 IgG

concentration, impaired

concussion

confusion

confusional state, acute

congenital infection, CNS

congenital malformation

congenital malformation, non CNS

contactin associated protein like 2 antibodies

controversies in neurology

coronary artery bypass

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical blindness, transient

cortical infarction

cortical infarction, small

cortical-basal ganglionic degeneration

cranial nerve palsies

cranial neuropathy

C-reactive protein

C-reactive protein, elevated

Creutzfeldt-Jakob disease, genetic

cryptococcal meningitis

cultured skin fibroblasts

cyanide poison

cyclophosphamide

cyst, cortical parenchyma

cyst, ventricular

cysticercosis

cysticercosis, cerebral

cysticercosis, intraventricular

cysticercosis, subarachnoid

degenerative diseases of CNS

delay in diagnosis

delirium

delirium, work up for

delusion

dementia

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, childhood

dementia, clinical diagnosis

dementia, diagnostic classification

dementia, diagnostic evaluation of

dementia, differential diagnosis of

dementia, early detection

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, mixed

dementia, presenile

dementia, prevalence of

dementia, rapidly progressive

dementia, reversible

dementia, screening for

dementia, subcortical

dementia, thalamic

dementia, transmissible

dementia, treatment of

dementia, unknown etiology

demyelinating disease

denervation of muscle

denervation potentials

dentate nuclei

dentate nuclei, lesion of

denture cream

depression

depth perception, impaired

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty climbing stairs

diplopia

disability rating scale, neurological

disability, neurological

disinhibition-dementia-parkinsonism-amyotrophic complex

DPPX, antibodies, encephalitis

drug induced neurologic disorders

dural arteriovenous malformation

dural graft, cadaveric

dural tear

dysarthria

dysdiadochokinesia

dysexecutive syndrome

dyskinesia

dyskinesia, buccal lingual facial

dystonia, drug induced

dystonia, focal

dystonia, truncal

dystonic reaction, acute

ears of the Lynx MR sign

electroencephalogram, abnormalities of

electroencephalogram, complications with

electroencephalogram, depth electrode

electroencephalogram, focal delta activity

electroencephalogram, periodic complexes

electroencephalogram, spike activity

electromyogram

electron microscopy

electrophoretic pattern, CSF

electrophoretic pattern, serum

encephalitis, autoimmune

encephalitis, bornavirus

encephalitis, clinical picture and treatment of

encephalitis, etiology

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, Japanese

encephalitis, paraneoplastic

encephalitis, viral

encephalopathy

encephalopathy, carcinomatous

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, post traumatic

encephalopathy, progressive

endemic area

endocarditis

endocarditis, infectious

endocarditis, subacute bacterial

enolase

enzyme, defect

eosinophilia

epidemiology of neurology

epidural blood patch

epilepsia partialis continua

episodic disorders

episodic neurologic deficits

esophageal varices

ethics in neurology

evidence-based research

executive dysfunction

exercise

exercise intolerance

exome sequencing

extralimbic encephalitis

eye movement, disorders of

eye, pain in

facial expression abnormality

facial movement disorder

facial weakness, bilateral

faciobrachial dystonic seizure

fatal familial insomnia

fatigue

fatty acid, elevated plasma content

fever

fibrillations

fine motor function, impaired

finger nose finger test

finger tapping

fistula, arterio-venous, dural

fluorescein angiography

fluorescent treponema antibody absorption(FTA-ABS)

fluorescent treponema antibody absorption/false positive

folic acid

folic acid deficiency

follicle stimulating hormone

fourth ventricle, cyst

fracture, long bone

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

frontal behavioral spatial syndrome

frontal lobe, anatomy and physiology

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal brain sagging syndrome

frontotemporal dementia, behavioral variant

frozen section

fundus, abnormality of

funduscopic exam

fungal infection

fungal infection, CNS

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, supranuclear

general paresis of the insane

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

Gerstmann syndrome

Gerstmann-Straussler-Scheinker disease

glutamic acid decarboxylase, antibody

glutaric acidemia

glycine receptor antibodies

GM antigen test

GM1 ganglioside antibodies

Google

gram positive rod

grandiosity

granular osmiphilic material

granulomatous disease

hallucination, visual

head injury, repetitive

hearing loss, bilateral

hearing loss, sudden, bilateral

heel-knee-shin test

helminthic infection of CNS

hematuria, microscopic

hemianopia

hemianopia, homonymous

hemifacial spasm

hemiparesis

hemiparesis, recurrent

hemiplegia

hemorrhage, thalamic

hemosiderosis of CNS, superficial

hemosiderosis, subarachnoid

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniation syndromes, intracranial

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

herpes simplex encephalitis, differential diagnosis of

highly active antiretroviral therapy

hippocampal atrophy

hippocampus

hippocampus, hyperintense

Hispanics

histamine-2 receptor blockers

histopathology

HIV CSF viral escape syndrome

Hodgkin's disease, neurologic involvement with

homograft

homosexual

human immunodeficiency virus type 1

human immunodeficiency virus type 1, testing

Huntington's chorea

Huntington's disease, children

hydrocephalus

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydrocephalus, normal pressure, etiology

hydrocephalus, transient

hyperpigmentation of skin

hypotension, systemic

hypothalamus, disturbance of

hypothalamus, lesion of

hypothyroidism

hypotonia

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

ideomotor apraxia

imbalance

imbalance, postural

immune reconstitution inflammatory syndrome

immunization, neurologic complications with

immunosuppressive agents

immunotherapy

impaired vigilance

impulsivity

inappropriate antidiuretic(A.D.H.)hormone

inappropriate behavior

inattention

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion bodies, location of

incontinence, fecal

incoordination

infection

inflexibility, mental

initiative, lack of

insomnia

insular cortex

insular cortex, lesion

insular cortex, lesion, bilateral

intellectual deficit

intellectual deterioration

interferon

interferon alpha

intermittent positive pressure breathing

internal carotid artery

internet

interobserver agreement

interpeduncular cistern, compressed

intestinal biopsy

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, lobar

intracerebral hemorrhage, multiple

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, small

intracerebral hemorrhage, young adult

intracranial hypertension, benign

intracranial pressure, increased

intravenous drug abuse

iron, brain

irritability

ischemic score

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, Heidenhain variant

Jakob-Creutzfeldt disease, medical precaution with

Jakob-Creutzfeldt disease, unilateral

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

jaundice

Kayser-Fleischer ring

Kearns-Sayre syndrome

kinesia paradoxica

Kleine-Levin syndrome

Kluver-Bucy syndrome

kuru

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction

laminar necrosis, cortical

L-dopa

Leber's hereditary optic neuropathy

lecanemab

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

lethargy

leucine rich glioma inactivated 1 antibodies

leuko-araiosis

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, hereditary diffuse

leukoencephalopathy, toxic

leukopenia

level of consciousness, decreased

Lewy body

Lewy body disease, diffuse

Lhermitte's sign

life expectancy

life support, withdrawal of

limbic encephalitis

limbic system

limbic-predominant age-related TDP-43 encephalopathy

lipid lowering agent

lipid storage disorder of CNS

listeria monocytogenes

listeriosis, CNS

lithium

liver disease

liver function enzymes

lumbar puncture, complications of

lymphadenopathy

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

macrocephaly

maculopathy

magnetic susceptibility

maple syrup urine disease

marche a petits pas

masked facies

masseter muscle wasting

mediastinum, mass of

medical-legal aspects of neurology

memory, defect of recent

memory, impairment of

memory, impairment of, subjective

memory, recent

meningeal biopsy

meningeal enhancement

meningitis

meningitis, aseptic

meningitis, aspergillus

meningitis, bacterial

meningitis, basilar

meningitis, carcinomatous

meningitis, chronic

meningitis, cysticercosis

meningitis, eosinophilic

meningitis, fungal

meningitis, fungal-negative CSF culture

meningitis, granulomatous

meningitis, helminthic

meningitis, neurologic aspects and complications of

meningitis, neutrophilic

meningitis, neutrophilic, persistent

meningitis, noninfectious

meningitis, parameningeal

meningitis, parasitic

meningitis, spinal fluid smear and culture-negative

meningitis, syphilitic

meningitis, TB

meningitis, treatment of

meningitis, treatment of, empirical

meningitis, viral etiology in

meningitis-encephalitis PCR panel

meningoencephalitis

meningovascular syphilis

mental retardation

mental status, abnormal

MERRF syndrome

mesial temporal lobe

mesial temporal sclerosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metformin

methotrexate

methylmalonic acid, serum

metronidazole

Mexican

Mexico

microabscesses, cerebral

microangiopathy, brain

microangiopathy, retina

microcephaly

micrographia

microhemorrhage, intracerebral

midbrain

midbrain, atrophy

midbrain, swollen

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

migraine with aura

mild cognitive impairment

mild cognitive impairment converting to Alzheimer's disease

mimics

Mini Mental Status Examination

miosis

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monoparesis

Montreal cognitive assessment

mood change

mortality

Morvan's fibrillary chorea

mosquito

motor neuron disease

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, hyperkinetic

movement disorder, treatment of

MRI, angiography, false negative

MRI, cerebrovascular disease

MRI, complications with

MRI, contrast enhanced

MRI, diffusion weighted

MRI, diffusion weighted, pattern

MRI, disappearing lesion on

MRI, early changes in CVA

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, indications for

MRI, lesion burden

MRI, magnetization transfer sequence

MRI, mass effect on

MRI, negative

MRI, paramagnetic effect

MRI, proton density

MRI, punctate pattern

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, sulcal hyperintensity

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRI, venography

MRI, vessel wall enhancement

MRI, volumetry

MRI, voxel-based morphometry

MRS

multinucleated giant cell

multiple sclerosis

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

mutism

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

mycophenolate

myelitis, longitudinal

myelitis, transverse, recurrent

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, mitochondrial

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS-treatment of

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-treatment of

neoplastic angioendotheliosis

nerve agents

nerve biopsy

nerve conduction studies

neurexin-3 alpha antibodies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal leukodystrophy

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neuroleptic

neuroleptic sensitivity

neuroleptic, atypical

neurologic complications

neurologic complications of, chronic pulmonary disease

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, multifocal

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic examination, focal

neurological intensive care

neurologist

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuron specific enolase

neuronal cell surface antigen

neuronal intranuclear inclusion disease

neuronopathy

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, ataxia, retinitis pigmentosa

neuropathy, motor, multifocal

neurosyphilis

neurotoxic

neurotoxin

new onset refractory status epilepticus

newborn, evaluation of

next-generation sequencing

nonvasculitic autoimmune inflammatory meningoencephalitis

nutritional deficiency

nystagmus

nystagmus, monocular

obsessive-compulsive disorder

occipital lobe, lesion of

occupational neurologic disorders

ocular motility, disorders of

oculomasticatory myorhythmia

olanzapine

old age, neurology of

ophthalmoplegia, progressive external

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic chiasm

optic chiasm, lesion of

optic neuritis

optic neuritis, bilateral

optic neuropathy

optokinetic nystagmus, abnormal

organ transplantation

orthostatic hypotension

osmotic demyelination syndrome

pain, increased response

pain, leg

pallido-ponto-nigral degeneration

paralysis, acute areflexic

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, spastic

paraphasias

parasitic infection, CNS

parasomnia

paresthesias

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, asymmetric onset

Parkinson disease, axial symptoms

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, freezing phenomena in

Parkinson disease, heterogeneity of

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinson disease, unilateral

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

pathognomonic

pathologic reflex

pathology

patient information and support

penguin silhouette sign

penicillamine

periaqueductal lesion

perihippocampal fissure

pernicious anemia

peroxisomal disease

perseveration

persistent vegetative state

persistent vegetative state, children

persistent vegetative state, etiology of

personality change

phenylketonuria

phenylketonuria, adult onset

Pittsburgh Compound B

pituitary, hormones of

platelet inhibiting drugs

platelet inhibiting drugs, contraindications

pleocytosis of cerebrospinal fluid

pleural effusion

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polyneuropathy

pons, flattened

positive sharp waves

posterior column disease

posterior cortical atrophy

posterior leukoencephalopathy syndrome

postoperative neurologic complications

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

preclinical

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prepontine cistern, effaced

presenilin-2 gene

prevention of neurologic disorders

primary intracranial hypotension

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive subcortical gliosis

progressive supranuclear palsy

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

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

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

proteinopathy

proteinuria

proton pump inhibitors

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, dilated, bilateral

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

radiation encephalopathy, delayed

radiation necrosis

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly fatal neurologic illness

rapidly progressing neurologic illness

reading

reading disorder, acquired

reading problem, causes of

real-time quaking-induced conversion

remote effect of cancer on the nervous system

respirations in CNS disease

respiratory arrest

respiratory failure

respiratory tract infection

retinal artery occlusion

retinal branch artery occlusion

reversible neurologic disorder

risk factors, modification

risk-benefit assessment

rubella encephalitis, progressive

rubella syndrome

rubella virus

rubeola virus

saccadic eye movements, abnormal

safety

sagging of the brain

salivation, excessive

scoliosis, neurologic association with

scotomata, scintillating

scrapie

screening

sedation

sedimentation rate, elevated

seizure, nonconvulsive

seizure, psychomotor-temporal lobe

seizure, surgical treatment of

seizure, treatment of

seizure, treatment of, first

seizure, unknown origin

semantic dementia

senile plaques

sensorineural hearing loss

sensory loss

sensory loss, cutaneous

sensory symptoms

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum S100 protein

sexual behavior, disorder of

sexual dysfunction in neurologic disease

short stature

short steps

shunt procedure, lumboperitoneal

shunt procedure, ventricular

shunt procedure, ventricular-complications of

simultanagnosia

sinemet

single photon emission computed tomography

single photon emission computed tomography, false negative

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

sleep apnea

sleep apnea, obstructive

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

small vessel disease

small vessel vasculitis

smell

Smell Identification Test

snoring

somnolence

spastic paraplegia, type 11

spasticity

speech disorder

speech, soft

spinal cord, lesion of

spirochete infection

splenium of corpus callosum

splenium of corpus callosum, displaced

splenomegaly

spongy degeneration of brain

sports medicine, neurology of

statin therapy, discontinuation

status epilepticus

status epilepticus, intractable

status epilepticus, nonconvulsive

steatorrhea

stem cell transplantation

stereotyped behavior

steroid

steroid dementia

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

stridor

stroke center

strokelike episodes

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

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subcortical hemorrhage

subinsular cortex

substantia nigra

Susac's syndrome

symmetric brain lesions

syncope

syphilis, asymptomatic

syphilis, congenital

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

temporal artery, biopsy

temporal lobe

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thyroid function tests

thyroid peroxidase antibodies

tongue, fasciculations of

tonic spasms

tonsil biopsy

tonsillar herniation of cerebellum

toxic encephalopathy

toxins, nervous system

toxoplasmosis, CNS

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

trauma

treatment of neurologic disorder

tricyclic antidepressant

trientine dihydrochloride

trifluoperazine

trinucleotide repeats

urea-cycle enzymopathies

urinary incontinence

urinary sulfatidase excretion

urine test for metabolic disorders

uveitis

vaccination, neurologic complications with

Venereal Disease Research Laboratory test

venous hypertension

venous ischemia

ventricular enlargement

vibratory sensation, abnormal

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visuospatial disturbance

vitamin deficiency

vocal cord paralysis

voriconazole

Waldenstrom's macroglobulinemia

walking frame

walking, difficulty with

war

water channel antibodies

weakness

weakness, generalized

weakness, progressive

weight loss

West Nile fever

Western immunoblot test

wheelchair

Whipple's disease

white matter disease

white matter disease, subcortical

white matter, dirty-appearing

wide based gait

Wingspan study

word-finding difficulty

workup

writing

X-linked bulbospinal neuronopathy

zinc

Showing articles 200 to 250 of 5115 << Previous Next >>

Treatment-Induced Leukoencephalopathy in Primary CNS Lymphoma,A Clinical and Autopsy Study
Neurol 62:451-456, Lai,R.,et al, 2004

Prion Deposition in Olfactory Biopsy of Sporadic Creutzfeldt-Jakob Disease
Ann Neurol 55:294-296, Tabaton,M.,et al, 2004

Extraneural Pathologic Prion Protein in Sporadic Creutzfeldt-Jakob Disease
NEJM 349:1812-1820, Glatzel,M.,et al, 2003

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

Challenging the Clinical Utility of the 14-3-3 Protein for the Diagnosis of Sporadic Creutzfeldt-Jakob Disease
Arch Neurol 60:813-816,803, Geschwind,M.D.,et al, 2003

Early Alzheimer's Disease
NEJM 349:1056-1063, Kawas,C.H., 2003

Primary Progressive Aphasia--A Language-Based Dementia
NEJM 349:1535-1542, Mesulam,M.-M., 2003

Operational Definitions for the NINDS-AIREN Criteria for Vascular Dementia
Stroke 34:1907-1912, van Straaten,E.C.W.,et al, 2003

Identification of New Presenilin Gene Mutations in Early-Onset Familial Alzheimer Disease
Arch Neurol 60:1541-1544,1521, Tedde,A.,et al, 2003

Diffusion-Weighted Imaging Discriminates Progressive Supranuclear Palsy from PD, But Not From the Parkinson Variant of Multiple System Atrophy
Neurol 60:922-927, Seppi,K.,et al, 2003

Antivonvulsants for Creutzfeldt-Jakob Disease?
Lancet 361:224, Fioel,A.,et al, 2003

Detection of Pathologic Prion Protein in the Olfactory Epithelium in Sporadic Creutzfeldt-Jakob Disease
NEJM 348:711-719,681, Zanusso,G.,et al, 2003

Neuroimaging and Early Diagnosis of Alzheimer Disease: A Look to the Future
Radiology 226:315-336, Petrella,J.R.,et al, 2003

Subacute Meningoencephalitis in a Subset of Patients with AD After AB42 Immunization
Neurol 61:46-54,7, Orgogozo,J.M.,et al, 2003

Tau Protein and 14-3-3 Protein in the Differential Diagnosis of Creutzfeldt-Jakob Disease
Neurol 58:192-197, Otto,M.,et al, 2002

Recombinant Interferon-a-induced Chorea and Frontal Subcortical Dementia
Neurol 58:328-330, Moulignier,A.,et al, 2002

Research Evaluation and Prospective Diagnosis of Dementia With Lewy Bodies
Arch Neurol 59:43-46,29, Lopez,O.L,et al, 2002

The Neurological Masquerade of Intravascular Lymphomatosis
Arch Neurol 59:439-443, Beristain,X.&Azzarelli,B., 2002

Epilepsy Presenting as AD: Neuroimaging, Electroclinical Features, and Response to Treatment
Neurol 58:298-301, Hogh,P.,et al, 2002

Alzheimer Disease
JAMA 287:2335-2338, Cummings,J.L. &Cole,G., 2002

Abnormal Diffusion-Weighted Magnetic Resonance Imaging in Creutzfeldt-Jakob Disease Following Corneal Transplantations
Arch Neurol 59:637-639, Rabinstein,A.A.,et al, 2002

Conspicuity and Evolution of Lesions in Creutzfeldt-Jakob Disease at Diffusion-Weighted Imaging
AJNR 23:1164-1172,1070, Murata,T.,et al, 2002

Sporadic Creutzfeldt-Jakob Disease and Surgery
Neurol 59:543-548, Ward,H.J.T.,et al, 2002

Effect of Radiotherapy and Other Treatment-Related Factors on Mid-Term to Long-Term Cognitive Sequelae in Low-Grade Gliomas: A Comparative Study
Lancet 360:1361-1368, Klein,M.,et al, 2002

Utility of Clinical Criteria in Differentiating Frontotemporal Lobar Degeneration (FTLD) From AD
Neurol 58:1608-1615, Rosen,H.J.,et al, 2002

Potentially Reversible Conditions in 1000 Consecutive Memory Clinic Patients
JNNP 73:390-394, Hejl,A.,et al, 2002

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Subacute Sclerosing Panencephalitis
Postgrad Med J 78:63-70, Garg, R.K.,et al, 2002

Drug-Induced Pisa Syndrome (Pleurothotomus)
CNS Drugs 10:166-174, Suzuki, T. & Matsuzaka, H., 2002

Quantitation of 14-3-3 and Neurol-Specific Enolase Proteins in CSF in Creutzfeldt-Jakob Disease
Neurol 57:728-730, Aksamit,A.L.,et al, 2001

Use of 14-3-3 and Other Brain-specific Proteins in CSF in the Diagnosis of Variant Creutzfeldt-Jakob Disease
JNNP 70:744-748, Green,A.J.E.,et al, 2001

Anosmia in Dementia is Associated with Lewy Bodies Rather Than Alzheimer's Pathology
JNNP 70:739-743,720, McShane,R.H.,et al, 2001

Positron Emission Tomography in Evaluation of Dementia
JAMA 286:2120-2127,2194, Silverman,D.H.S.,et al, 2001

Phenylketonuria Presenting in Adulthood as Progressive Spastic Paraparesis With Dementia
JNNP 71:795-797, Kasim,S.,et al, 2001

14-3-3 Protein Cerebrspinal Fluid Detection in Human Growth Hormone-Treated Creutzfeldt-Jakob Disease Patients
Ann Neurol 49:257-260, Brandel,J.,et al, 2001

Mesiotemporal T2-Weighted Hyperintensity: Neurosyphilis Mimicking Herpes Encephalitis
AJNR 22:314-316, Bash,S.,et al, 2001

Magnetic Resonance Spectroscopy in AD
Neurol 56:592-598, Valenzuela,M.J.,et al, 2001

Evaluation of CSf-tau and CSF-AB42 as Diagnostic Markers for Alzheimer Disease in Clinical Practice
Arch Neurol 58:373-379,349, Andreasen,N.,et al, 2001

Practice Parameter: Diagnosis of Dementia (an Evidence-Based Review)
Neurol 56:1143-1153, Knopman,D.S.,et al, 2001

CSF Detection of the 14-3-3 Protein in Unselected Patients with Dementia
Neurol 56:1528-1533, Burkhard,P.R.,et al, 2001

Diagnosis of New Variant Creutzfeldt-Jakob Disease
Ann Neurol 47:575-582, Will,R.G.,et al, 2000

Progressive Dementia and Gait Disorder in a 78 Year Old Woman
JNNP 68:526-531, Tagliati,M.,et al, 2000

Treating Nondementia Illnesses in Patients With Dementia
JAMA 283:3230-3235, Brauner,D.J. et al, 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Relation Between Cholinesterase Inhibitor and Pisa Syndrome
Lancet 355:2222, Kwak,Y.T. et al, 2000

Current Clinical Diagnosis in Creutzfeldt-Jakob Disease; Identification of Uncommon Variants
Ann Neurol 48:323-329, Zerr,I. et al, 2000

14-3-3 Testing in Diagnosing Creutzfeldt-Jakob Disease
Neurol 55:514-516, Lemstra,A.W. et al, 2000

Analysis of EEG and CSF 14-3-3 proteins as adis to the diagnosis of Creutzfeldt-Jakob Disease
Neurol 55:811-815, Zerr,I. et al, 2000

Misleading Results With the 14-3-3 Assay for the Diagnosis of Creutzfeldt-Jakob Disease
Neurol 55:1396-1397, Chapman,T.,et al, 2000

Dementia with Lewy Bodies in a Neuropathologic Series of Suspected Creutzfeldt-Jakob Disease
Neurol 55:1401-1404, Haik,S.,et al, 2000

Showing articles 200 to 250 of 5115 << Previous Next >>