Neudle.com: dementia young

Differential
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acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

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, preclinical

Alzheimer's disease, treatment of

amaurosis fugax

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

amyloid angiopathy, hereditary cystatin C

amyloid beta protein

amyloid plaques

amyloid-related imaging abnormalities

amyotrophic lateral sclerosis

ANA-negative systemic lupus erythematosus

anemia

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiitis, isolated of CNS, tumefactive

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, false negative

anomic aphasia

antibodies to measles

anticardiolipin antibodies

anticoagulant, treatment

antiphospholipid antibodies

antiphospholipid antibody syndrome

anxiety

aphasia

aphasia, logopenic, progressive

aphasia, progressive

aphasia, progressive, non-fluent

aphasia, progressive, primary

auditory evoked brainstem potentials

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

bone marrow transplantation

bone survey

bovine spongiform encephalopathy

bradykinesia

brain atrophy

brain biopsy

brain biopsy, negative

calcification, intracranial

cardiomyopathy

carotid artery occlusion, neck

carotid artery stenosis

case studies

CAT scan

CAT scan, abnormal

CAT scan, emission, abnormal

CAT scan, false negative

cataracts

caudate nucleus, lesion of, bilateral

celiac disease, adult

central nervous system, infection of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar infarction

cerebellar plaques, amyloid

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, hemorrhagic

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral ischemia

cerebroretinal microangiopathy with calcifications and cysts

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, atrial myxoma

cerebrovascular accident, bilateral

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, recurrent

cerebrovascular accident, three territory involvement

cerebrovascular accident, topographic pattern

cerebrovascular accident, women

cerebrovascular accident, work up for

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

children

chorea

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

clindamycin

Clinical Pathologic Conference(C.P.C.)

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical blindness, transient

cortical infarction

cortical infarction, small

coumarin

COVID-19

cranial nerve palsies

C-reactive protein, elevated

crying, pathologic

cultured skin fibroblasts

cyst, bone

deafness

degenerative diseases of CNS

delirium

delusion

dementia

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, childhood

dementia, clinical diagnosis

dementia, diagnostic evaluation of

dementia, differential diagnosis of

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, transmissible

dementia, treatment of

demyelinating disease

depression

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diet

differential diagnosis

diplopia

disability rating scale, neurological

disorientation

dizziness

dural graft, cadaveric

electroencephalogram, abnormalities of

electroencephalogram, focal delta activity

electroencephalogram, pediatric patients

electroencephalogram, periodic complexes

encephalopathy, metabolic

encephalopathy, progressive

enzyme, defect

epidemic

epidemiology of neurology

evoked potentials

executive dysfunction

familial hemiplegic migraine

farmer

fasciculation

fatty acid, elevated plasma content

frontal lobe, anatomy and physiology

frontal lobe, atrophy

frontal lobe, lesion of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

Gerstmann-Straussler-Scheinker disease

gliadin antibodies

gliosis

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

granular atrophy, cerebral cortex

Hallervorden Spatz disease

hallucination

hallucination, visual

hearing loss, bilateral

hearing problems in children

heart block

hemiparesis

hemiplegia

hemosiderosis of CNS, superficial

hepatitis

hepatosplenomegaly

heralding manifestation

Hodgkin's disease

human immunodeficiency virus type 1

Huntington's chorea

Huntington's disease, children

hydrocephalus

hydrocephalus, exvacuo

hydrocephalus, normal pressure

hypotension, systemic

hypotonia

iatrogenic neurologic disorders

imbalance

immunosuppressive agents

impaired vigilance

impulsivity

inappropriate behavior

inattention

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incoordination

infection

inflexibility, mental

intellectual deficit

intellectual deterioration

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, lobar

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

iron, brain

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, medical precaution with

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

Kearns-Sayre syndrome

language disorder in adults

language disorders in children

laughing, pathologic

Leber's hereditary optic neuropathy

lecanemab

leg weakness, bilateral

leukoencephalopathy, adult onset, sporadic

level of consciousness, decreased

Lewy body

life expectancy

lipid storage disorder of CNS

lipomembranous polycystic osteodysplasia

lymphoma involving CNS

manganese intoxication

mania

manic-depressive

MELAS syndrome

memory, defect of recent

memory, impairment of

memory, impairment of, subjective

meningeal biopsy

meningeal enhancement

meningovascular syphilis

mental retardation

mental status, abnormal

MERRF syndrome

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

microangiopathy, brain

microangiopathy, retina

microcephaly

microhemorrhage, intracerebral

microinfarcts

middle cerebral artery, occlusion of

middle cerebral artery, stenosis of

migraine

migraine, hemiplegic

mild cognitive impairment

mimics

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve lesion

molecular genetics

monoclonal antibodies

movement disorder, extrapyramidal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, functional

MRI, gradient-echo

MRI, high signal foci on

MRI, linear enhancement

MRI, punctate pattern

MRI, ring sign, open

MRI, serial

MRI, spinal cord

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle atrophy, progressive

muscle biopsy

muscle weakness

muscle weakness, proximal

mutism

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelomalacia

myelopathy

myocardial infarction

myoclonic jerks

myoclonus

myopathy

myopathy, mitochondrial

nausea and vomiting

negative

neologism

neoplasm, intracranial, differential diagnosis of

neoplastic angioendotheliosis

nerve biopsy

nerve conduction studies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal leukodystrophy

neurocutaneous disease

neurocutaneous melanosis

neuroendocrinology

neurofibrillary degeneration

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral

nutritional deficiency

nystagmus

obsessive-compulsive disorder

occipital lobe, lesion of

occupational neurologic disorders

ophthalmoplegia

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic neuritis

optic neuritis, bilateral

optic neuropathy

pain

pain, increased response

pancytopenia

papilledema

paranoia

paraparesis, familial spastic

Parkinson disease, dementia with

Parkinson disease, familial

Parkinson disease, rapid progression

Parkinson disease, young onset

Parkinsonism syndrome

Parkinsonism-dementia complex

PAS positive

PAS positive material in the brain

pathologic reflex

peripheral vascular disease

pigmentary retinopathy

Pittsburgh Compound B

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

polycystic lipomembranous osteodysplasia

polymerase chain reaction

posterior cortical atrophy

practice guidelines

preclinical

prenatal diagnosis by amniocentesis

presenilin-1 gene

presenilin-2 gene

prevention of neurologic disorders

prion disease

prognosis

progressive myoclonic epilepsy

progressive neurologic disorder

progressive subcortical gliosis

protein 14-3-3, cerebrospinal fluid

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

ptosis

pulmonary infiltrates

pyramidal tract dysfunction

quadriparesis

quadriplegia

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapidly progressing neurologic illness

real-time quaking-induced conversion

respirations in CNS disease

reticulum antibodies

retinal branch artery occlusion

sedimentation rate, elevated

seizure

seizure, children

seizure, diagnosis of

sensorineural hearing loss

sensory symptoms

serologic testing

short stature

single photon emission computed tomography

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

small vessel disease

Sneddon's syndrome

somatosensory evoked potentials

spasticity

speech disorder

spinal cord, embolism of

spinal cord, infarction of

spinal cord, lesion of

spinal cord, pathologic exam of

splenomegaly

spongy degeneration of brain

startle myoclonus

status epilepticus

status epilepticus, intractable

stereotyped behavior

steroid therapy, CNS treatment and complications with

strokelike episodes

stuttering

stuttering following CVA

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

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

substantia nigra

sural nerve

Susac's syndrome

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

tau protein

tauopathy

temporal lobe, atrophy

testicular atrophy

thalamus, lesion of

thalamus, lesion of-bilateral

Three territory sign

thromboangiitis obliterans cerebri

thrombophlebitis

tinnitus

tissue plasminogen activator, intravenous

titubation

tongue, fasciculations of

toxoplasmosis, CNS

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

treatment of neurologic disorder

tumor necrosis factor

vanishing white matter

vision, failure of in childhood

visual acuity, decreased

visual evoked response

word-finding difficulty

workup

Showing articles 1800 to 1850 of 2806 << Previous Next >>

Blinded Clinical Evaluation of Positron Emission Tomography for Diagnosis of Probable Alzheimer's Disease
Neurol 42:765-770, Powers,W.J.,et al, 1992

Comparative Analysis of Computed Tomographic and Magnetic Resonance Imaging Scans in Alzheimer Patients and Controls
Arch Neurol 49:381-384, Sandor,T.,et al, 1992

Stroke in a Cohort of Patients with Homozygous Sickle Cell Disease
J Pediatr 120:360-366, Balkaran,B.,et al, 1992

Lupus Anticoagulant and Anticardiolipin Antibodies in Young Adults with Cerebral Ischemia
Stroke 23:189-193, Nencini,P.,et al, 1992

Cerebral Infarction Associated with Protein C Deficiency
Stroke 23:108-111, Matsushita,K.,et al, 1992

Progressive Language Disorder Due to Lobar Atrophy
Ann Neurol 31:174-183, Snowden,J.S.,et al, 1992

Clinicopath Conf
Pick's Diseae, Case 6-1992, NEJM 326:397-405992., , 1992

Bilateral Middle Cerebral Artyery Occlusions in Neurocysticercosis
Stroke 23:280-283, terPenning,B.,et al, 1992

Cerebral Cysticercosis and Stroke. Alarcon
F. , et al, Stroke 23:224-22892., , 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

Cerebral Infarction in Young Men with Nephrotic Syndrome
Stroke 23:295-297, Fuh,J.L.,et al, 1992

Clinicopath Conf
Huntington's Diseae, Case2-1992, NEJM 326:117-125992., , 1992

Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
NEJM 326:444-449, Medori,R.,et al, 1992

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992

Fatal Familial Insomnia:A Second Kindred with Mutation of Prion Protein Gene at Codon 178
Neurol 42:669-670, 1992, Medori,R.,et al, 1992

Multiple Sclerosis Dementia
Neurol 42:696, Mendez,M.D.&Frey,W.F., 1992

Criteria for the Diagnosis of Ischemic Vascular Dementia Proposed by St of CA Alzheimer's Disease Diag Treat Ctrs
Neurol 42:473-480, Chui,H.C.,et al, 1992

Evaluation of Cerebral Biopsies for the Diagnosis of Dementia
Arch Neurol 49:28-31, Hulette,C.M.,et al, 1992

Physicians, Elderly Drivers, and Dementia
Lancet 339:41-43, O'Neill,D., 1992

Prion Disease
NEJM 326:486-487, Johnson,R.T., 1992

Creutzfeldt-Jakob Disease in a Pathologist
Neurol 42:463, Gorman,D.G.,et al, 1992

Spinal Cord Syphilis Associated with Human Immunodeficiency Virus Infection:A Treatable Myelopathy
Am J Med 91:101-103, Berger,J.R., 1992

Clinical Features of Vascular Thrombosis Following Varicella
Am J Dis Child 146:100-102, Bodensteiner,J.B.,et al, 1992

Encephalitis in Cat Scratch Disease with Persistent Dementia
JNNP 55:133-135, Revol,A.,et al, 1992

The Neuropsychological Features of Mitochondrial Myopathies and Encephalomyopathies
Arch Neurol 49:158-160, Kartsounis,L.D.,et al, 1992

Shunting Normal-Pressure Hydrocephalus:Do the Benefits Outweigh the Risks? A Multicenter Study and Literatire Review
Neurol 42:54-59, Vanneste,J.,et al, 1992

Idiopathic Hemiparetic Parkinsonism, A Syndrome Distinct from Idiopathic Parkinsonism
Lancet 339:149-150, DeKeyser,J.,et al, 1992

A Quantitative MRI Study of Vascular Dementia
Neurol 42:138-142, Liu,C.K.,et al, 1992

Is Aluminium a Dementing Ion?
Editorial, Lancet 339:713-7141992., , 1992

Should Patients with Alzheimer's Disease be Told Their Diagnosis
NEJM 326:947-951, Drickamer,M.A.&Lachs,M.S., 1992

A Familial Disorder with Subcortical Ischemic Strokes, Dementia, and Leukoencephalopathy
Neurol 42:1015-1019, Mas,J.L.,et al, 1992

Idiopathic Childhoos Stroke is Associated with Human Leukocyte Antigen (HLA) -B51
Ann Neurol 31:675-677, Mintz,M.,et al, 1992

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

The Agraphia of Alzheimer's Disease
Neurol 42:776-784, Henderson,V.W.,et al, 1992

Sleep in Alzheimer's Disease and the Sundown Syndrome
Neurol 42:83-94, Vitiello,M.V.,et al, 1992

Does Computed Tomographic Brain Imaging Have a Place in the Diagnosis of Dementia
Arch Int Med 152:1437-1440, Engel,P.A.&Gelber,J., 1992

Cranial Computed Tomographic Ovservations in Multi-Infarct Dementia
Stroke 23:804-811, Gorelick,P.B.,et al, 1992

Preventable Senility:A Call for Action Against the Vascular Dementias
Lancet 340:645-648, Hachinski,V., 1992

Dementia After Stroke:Baseline Frequency, Risks, and Clinical Features in a Hospitalized Cohort
Neurol 42:1185-1193, 1992. a, Tatemichi,T.K.,et al, 1992

Cysticercosis and Cerebrovascular Disease:A Review
JNNP 55:252-254, DelBrutto,O.H., 1992

Cerebellar Infarction in the Young
Stroke 23:763-766, Rosman,N.P.,et al, 1992

Dementia Associated with lacunar Infarction
Stroke 23:1225-1229, Loeb,C.,et al, 1992

Hypertension and the Brain
Arch Int Med 152:938-945, Phillips,S.J.,et al, 1992

The Older Driver, Clinical Assessment and Injury Prevention
Arch Int Med 152:735-740, Underwood,M., 1992

Personality Changes in Alzheimer's Disease
Arch Neurol 49:486-491, Chatterjee,A.,et al, 1992

Stroke in an Early Adolescent with Systemic Lupus Erythematosus and Coexistent Antiphospholipid Antibodies
Pediatrics 90:96-99, Dungan,D.D., 1992

Brain Imaging in Human Immunodeficiency Virus Infection
Semin Neurol 12:57-69, Ketonen,L.&Tuite,M.J., 1992

The Diagnostic Utility of Elevation in Cerebrospinal Fluid B2-Microglobulin in HIV-1 Dementia
Neurol 42:1707-1712, McArthur,J.C.,et al, 1992

HIV Encephalopathy and Dementia
Psychiatr Clin North Am 15:455-466, Pajeau,A.K.&Roman,G.C., 1992

Showing articles 1800 to 1850 of 2806 << Previous Next >>