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 50 to 100 of 2806 << Previous Next >>

Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
Arch Neurol 54:539-544, Basun,H.,et al, 1997

Clin Features of Early-Onset Alzheimer Disease in Large Kindred with an E280A Presenilin-1 Mutation
JAMA 277:793-799, Lopera,F.,et al, 1997

Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
Ann Neurol 41:150-159, Heutnik,P.,et al, 1997

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Whipple Disease Confined to the Central Nervous System in Childhood
AJNR 17:1589-1591, Duprez,T.P.J.,et al, 1996

BSE Linked to New Variant of CJD in Humans
BMJ 312:795, 791, 843, 85496., , 1996

A New Variant of Creutzfeldt-Jakob Disease in the UK
Lancet 347:921-925, 915, 916, 91796., Will,R.G.,et al, 1996

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

Creutzfeldt-Jakob Disease from Contaminated Growth Hormone Extracts in France
Neurol 47:690-695, Billette de Villemeur,T.,et al, 1996

Reversible Dementia and Chorea in a Young Woman with the Lupus Anticoagulant
Neurol 46:1599-1603, Van Horn,G.,et al, 1996

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
Ann Neurol 38:817-824, Hutchinson,M.,et al, 1995

Clinical Spectrum of CADASIL:A Study of 7 Families
Lancet 346:934-939, Chabriat,H.,et al, 1995

Creutzfeldt-Jakob Disease and Bovine Spongiform Encephalopathy:Any Connection?
BMJ 311:1415-1421, Almond,J.W., 1995

Sneddon's Syndrome is a Thrombotic Vasculopathy:Neuropathologic and Neuroradiologic Evidence
Neurol 45:557-560, Geschwind,D.H.,et al, 1995

Familial Alzheimer's Disease
Ann Neurol 36:335-336, Bird,T.D., 1994

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Chromosome 14-Encoded Alzheimer's Disease:Genetic and Clinicopathological Description
Ann Neurol 36:362-367, Haltia,M.,et al, 1994

Familial Progressive Subcortical Gliosis
Neurol 44:1633-1643, Lanska,D.J.,et al, 1994

Electroencephalography as an Aid in the Exclusion of Alzheimer's Disease
Arch Neurol 51:280-284, Robinson,D.J.,et al, 1994

Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
J Pediatr 123:242-247, Kelly,D.A.,et al, 1993

Clinicopath Conf
Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) , with Amyloid (KURU) Plaques, Case 17-1993, N, JM 328:66,1993., 1993

Pick's Disease Versus Alzheimer's Disease:A Comparison of Clinical Characteristics
Neurol 43:289-292, Mendez,M.F.,et al, 1993

Inherited Prion Disease (PrP lysine 200) in Britain:Two Case Reports
BMJ 306:301-302, 2881993., Collinge,J.,et al, 1993

Presenile-Onset Cerebral Adrenoleukodystrophy Presenting as Balint's Syndrome and Dementia
Neurol 43:1249-1251, Uyama,E.,et al, 1993

Small Infarctions of Cochlear, Retinal, and Encephalic Tissue in Young Women
Stroke 23:903-907, Schwitter,J.,et al, 1992

Epidemiology of Human Immunodeficincy Virus Encephalopathy in the United States
Neurol 42:1472-1476, Janssen,R.S.,et al, 1992

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Celiac Disease, Brain Atrophy, and Dementia
Neurol 41:372-375, Collin,P.,et al, 1991

Membranous Lipodystrophy:MR Imaging Appearance of the Brain
Radiology 180:793-797, Araki,T.,et al, 1991

Early-Onset Dementia & Extrapyramidal Disease:Clinicopath Variant of Gerstmann-Straussler-Scheinker or Alzheimer's Disease?
JNNP 53:932-934, Hart,J.Jr.&Gordon,B., 1990

Prion Dementia Without Characteristic Pathology
Lancet 336:7-9, 21-221990., Collinge,J.,et al, 1990

Transmission and Age-At-Onset Patterns in Familial Alzheimer's Disease:Evidence for Heterogeneity
Neurol 40:395-403, Farrer,L.A.,et al, 1990

Elevated Serum Levels of Tumor Necrosis Factor are Associated with Prog Encephalopathy in Children with AIDS
Am J Dis Child 143:771-774, Mintz,M.,et al, 1989

Magnetic Resonance Imaging in Pathologically Proven Hallervorden-Spatz Disease
Neurol 39:440-442, Schaffert,D.A.,et al, 1989

Cerebrovascular Disease & Antiphospholipis Antibodies in SLE, Lupus-Like Dis, & Primary Antiphospholipid Synd
Am J Med 86:391-399, Asherson,R.A.,et al, 1989

Predisposing Locus for Alzheimer's Disease on Chromosome 21
Lancet 1:352-355, Goate,A.M.,et al, 1989

Diagnostic Criteria for Rett Syndrome
The Rett Syndrome Diagnostic Criteria Work Group, Ann Neurol 23:425-4281988., , 1988

Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
Neurol 38:154-155, Tennison,M.B.,et al, 1988

Neurological Manifestations in Three German Children with AIDS
Neuropediatrics 18:99-106, Biggemann,B.,et al, 1987

Rett's Syndrome, Correlation of Electroencephalogram Characteristics with Clinical Staging
Arch Neurol 44:1053-1056, Glaze,D.G.,et al, 1987

Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome
Ann Neurol 18:560-566, Belman,A.L.,et al, 1985

Atypical Alzheimer's Disease with Spastic Paresis & Ataxia
Ann Neurol 17:297-300, Aikawa,H.,et al, 1985

Progressive Dementia, Visual Deficits, Amyotrophy, & Microinfarcts
Neurol 35:789-796, Kaplan,J.G.,et al, 1985

Creutzfeldt-Jakob Disease in a Young Adult with Idiopathic Hypopituitarism, Relation to Growth Hormone
NEJM 313:731-733, Koch,T.K.,et al, 1985

Creutzfeldt-Jakob Disease after Administration of Human Growth Hormone
Lancet 2:244-246, Powell-Jackson,J.,et al, 1985

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984

Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
Case 7-1984, NEJM 310:445-4551984., , 1984

Left-handedness in Early & Late Onset Dementia
Neurol 34:367-369, Seltzer,B.,et al, 1984

Lipomembranous Polycystic Osteodysplasia (Brain, Bone, & Fat Disease)
Neurol 33:81-86, Bird,T.D.,et al, 1983

Showing articles 50 to 100 of 2806 << Previous Next >>