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Differential
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adenylate kinase 5 autoantibodies

advances in neurology

agitation

agnosia, visual

akinetic mute

Alice in Wonderland syndrome

alien hand syndrome

alternating rapid movement

aluminum

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, familial

Alzheimer's disease, heterogeneity of

Alzheimer's disease, incidence

Alzheimer's disease, pathogenesis

Alzheimer's disease, preclinical

Alzheimer's disease, risk factors in

Alzheimer's disease, staging

Alzheimer's disease, treatment of

amnesia

AMPA receptor antibodies

amyloid

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, iatrogenic

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

aphasia, progressive, primary

apraxia of eyelid opening

apraxia, constructional

areflexia

arm swing, reduced

arthrogryposis multiplex

basal ganglia, lesion, bilateral

bovine spongiform encephalopathy

brain transplantation

CAT scan, emission, abnormal

cataplexy

cavum septi pellucidi

central core disease

central hypoventilation

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, secondary

cerebellar plaques, amyloid

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral edema, vasogenic

cerebral glucose metabolism

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, biochemical markers of CNS disease

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

Charcot-Marie-Tooth

choline acetyltransferase

chorea

choreoathetosis

chorioretinitis

chronic traumatic encephalopathy

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

cognition

color vision, impaired

complications

compulsivity

concussion

concussion, recurrent

confusion

controversies in neurology

cortical blindness

cortical ribbon sign

cortical-basal ganglionic degeneration

cough

cultured skin fibroblasts

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, diagnostic evaluation of

dementia, differential diagnosis of

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, screening for

dementia, subcortical

dementia, transmissible

depression

developmental milestones, loss of

differential diagnosis

electroencephalogram, abnormalities of

encephalitis

encephalitis, autoimmune

encephalitis, viral

encephalopathy

encephalopathy, post traumatic

epidemiology of neurology

executive dysfunction

eye movement, disorders of

falling

familial

Fazio-Londe's disease

fine motor function, impaired

finger nose finger test

flortaucipir

foam cells

football neurologic injuries

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

gait disorder

gait, apraxic

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

Gerstmann-Straussler-Scheinker disease

granulovacuolar degeneration

grasp reflex

Hallervorden Spatz disease

handwriting

head injury

head injury, mild

head injury, repetitive

head injury, return to play following

headache

headache, frontal

heavy metal intoxication

heel-knee-shin test

hemianopia, homonymous

hemifacial spasm

hepatic failure

hepatosplenomegaly

heralding manifestation

herpes virus infection

hippocampal atrophy

hippocampus

hippocampus, hyperintense

hydrocephalus, normal pressure

hypophonia

iatrogenic neurologic disorders

immunoperoxidase staining

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

intellectual deterioration

interferon

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

jaundice

Kluver-Bucy syndrome

Kugelberg-Welander syndrome

language disorder in adults

L-dopa

lead poisoning

Lewy body

Lewy body disease, diffuse

limbic encephalitis

lipid storage disorder of CNS

manganese intoxication

masked facies

memory, defect of recent

memory, impairment of

meningitis

mental status, abnormal

mild cognitive impairment

mild cognitive impairment converting to Alzheimer's disease

mimics

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

molecular genetics

mongolism

Montreal cognitive assessment

movement disorder, extrapyramidal

MRI

MRI pattern

MRI, abnormal

MRI, diffusion weighted

MRI, diffusion weighted, pattern

MRI, voxel-based morphometry

multiple system atrophy

nerve conduction studies

neurofibrillary degeneration

neurofibrillary degeneration, causes of

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic signs

neurologic symptoms

neurologic testing

neuron specific enolase

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

nucleus basalis of Meynert

obsessive-compulsive disorder

old age, neurology of

olfactory bulb

ophthalmoplegia

ophthalmoplegia, total

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, dementia with

Parkinson disease, L-dopa nonresponsive

Parkinson disease, postencephalitic

Parkinson disease, tremor, absence of

Parkinsonism syndrome

PAS positive material in the brain

pathologic reflex

pathology

penguin silhouette sign

Pittsburgh Compound B

PLEDs

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

positional head-hanging test

preclinical

pregnancy, neurologic complications in

prion disease

prognosis

progressive neurologic disorder

progressive supranuclear palsy

prosopagnosia

protein 14-3-3, cerebrospinal fluid

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

proteinopathy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis

pugilistic parkinsonism

punch-drunk syndrome

pursuit eye movements, abnormal

rapidly progressing neurologic illness

reading disorder, acquired

reading problem, causes of

real-time quaking-induced conversion

release phenomena

respirations in CNS disease

retrocollis

review article

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

saccadic eye movements

saccadic eye movements, abnormal

salivation, excessive

screening

semantic dementia

senile plaques

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

sinemet

single photon emission computed tomography

sleep apnea, obstructive

sleep pathology and physiology

smell

Smell Identification Test

soccer

speech disorder

speech disorder, non aphasic

splenomegaly

spongy degeneration of brain

sports medicine, neurology of

square wave jerks

staining reactions in neuropathology

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

subacute sclerosing panencephalitis, adult onset

substantia nigra

symmetric brain lesions

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of-bilateral

toxoplasmosis, CNS

trauma

treatment of neurologic disorder

vibratory sensation, abnormal

visuospatial disturbance

vocal cord paralysis

voice, abnormality of

walking frame

walking, difficulty with

war

weight loss

Werdnig-Hoffman disease

word-finding difficulty

Showing articles 50 to 100 of 1020 << Previous Next >>

Clinicopath Conf:Multisystem Neurodegenerative Disease with Dementia Pugilistica
NEJM 340:1269-1277, Case 12-1999, 1999

Longitudinal Study of CSF Levels of Tau, A beta 1-40, and A beta 1-42 (43) in Alzheimer's Disease
Ann Neurol 44:17-26, 61998., Kanai,M.,et al, 1998

Clinicopath Conf
Subacute Sclerosing Panencephalitis, Case 15-1998, NEJM 338:1448-1456998., , 1998

New Neuropathological Criteria for Alzheimer Disease
Arch Neurol 55:1174-1176, Hyman,B.T., 1998

Assessment of CSF Levels of Tau Protein in Mildly Demented Patients with Alzheimer's Disese
Neurol 48:632-635, Galasko,D.,et al, 1997

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

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Apolipoprotein E, Dementia, and Cortical Deposition of B-Amyloid Protein
NEJM 333:1242-1247, 12831995., Polvikoski,T.,et al, 1995

Regional Distrib of Neurofibrillary Tangles & Senile Plaques in Cerebral Cortex of Very Old Pts
Arch Neurol 52:1150-1159, Gioannakopoulos,P.,et al, 1995

The Neuropathology of Williams Syndrome
Arch Neurol 52:209-212, Golden,J.A.,et al, 1995

Is Alzheimer's Disease an Apolipoprotein E Amyloidosis?
Lancet 345:956-958, Wisniewski,T.,et al, 1995

Alzheimer's-Disease-Like Changes in Tau Protein Processing:Assoc with Aluminium Accum in Brains of Dialysis Pts
Lancet 343:993-997, 9891994., Harrington,C.R.,et al, 1994

Gerstmann-Straussler-Scheinker Disease, II, Neurofibrillary Tangles & Plaques with PrP-amyloid in an Affected Family
Neurol 39:1453-1461, Ghetti,B.,et al, 1989

Dementia in Down's Syndrome:Cerebral Glucose Utilization, Neuropsychological Assessment, and Neuropathology
Neurol 38:938-942, Schapiro,M.B.,et al, 1988

Aluminium, Chemical Physiology and Alzheimer's Disease
Lancet 2:1008-1010, Birchall,J.D.&Chappell,J.S., 1988

Immunocytochemistry of Neurofibrillary Tangles in Dementia Pugilistica and Alzheimer's Disease:Evidence for Common Genesis
Lancet 2:1456-1458, Roberts,G.W., 1988

Clinico-Pathologic Studies in Dementia:Nondemented Subjects with Pathologically Confirmed Alzheimer's Disease
Neurol 38:1682-1687, Crystal,H.,et al, 1988

Brain Amyloid and Alzheimer Disease
Ann Int Med 109:41-54, Vinters,H.V.,et al, 1988

Clinical, Path, & Neurochem Changes in Dementia:Subgroup with Preserved Mental Status & Neocortical Plaques
Ann Neurol 23:138-144, Katzman,R.,et al, 1988

Alzheimer's Disease
NEJM 314:964-973, Katzman,R., 1986

Clinicopath. Conference
Subacute Sclerosing Panencephalitis, Due to Measles Virus, Case 25-1986, NEJM 314:1689-170086., , 1986

Neuronal Pathology in the Nucleus Basalis & Associated Cell Groups in Senile Dementia of the Alzheimer's Type
Neurol 35:1089-1095, Saper,C.B.,et al, 1985

The Olfactory Bulbs in Alzheimer's Disease
JNNP 47:56-60, Esiri,M.M.&Wilcock,G.K., 1984

Presenile Alzheimer Disease:Amyloid Plaques in the Cerebellum
Neurol 30:820-825, Pro,J.D.,et al, 1980

Dementia From Aluminum Pots
NEJM 303:164, Levick,S.E., 1980

Relationship between plaques, tangles, & dementia in Down syndrome
Neurol 30:639-644, Ropper,A.H.,et al, 1980

Alzheimer Neurofibrillary Tangles in Diseases Other Than Senile & Presenile Dementia
Ann Neurol 5:288-294, Wisniewski,K.,et al, 1979

Cerebral Amyloid Angiopathy:Possible Relationship to Rheumatoid Vasculitis
Neurol 29:1336-1340, Mandybur,T.I., 1979

Dementia in Parkinson Disease:A Neuropathologic Study
Neurol 29:1209-1214, Hakim,A.M.,et al, 1979

Huntington Disease Associated with Alzheimer Disease
Ann Neurol 3:545, McIntosh,G.C.,et al, 1978

Presenile Dementia with Lewy Bodies & Neurofibrillary Tangles
Arch Neurol 35:818-822, Forno,L.S.,et al, 1978

Elevated Manganese Levels Associated with Dementia & Extrapyramidal Signs
Neurol 27:213, Banta,R.G.,et al, 1977

Alzheimer Neurofibrillary Change in Subacute Sclerosing Panencephalitis
Ann Neurol 1:103, Mandybur,T.I.,et al, 1977

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

Alzheimers Disease with Abnormal CSF Flow
Neurol 23:1058, Sohn,R.S.,et al, 1973

Peripheral Neuropathy, A Review
JAMA 335:255-266, Mauermann,M.L. & Staff,N.P., 2026

Clinical Insights Into CASPR1 and CASPR1/Contactin1 Com-lex Autoimmune Nodopathies
Neurol 106:e214403, Paramasivan,N.K.,et al, 2026

Polymyalgia Rheumatica
NEJM 394:1097-1109, Dejaco,C.,et al, 2026

Cerebral Amyloid Angiopathy
NEJM 394:1836-1845, Greenberg,S.M., 2026

A 32-Year-Old Woman with Progressive Vision Loss and Confusion
Neurol 106:e214988, Kumar,A.B.,et al, 2026

A 55-Year-Old Man with Rapidly Progressive Weakness and Numbness
Neurol 106:e218063, Li,X.,et al, 2026

Next-Day Serum Glial Fibrillary Acidic Protein Levels to Aid Diagnosis of Sport-Related Concussion
Neurol 104:e210308, OBrien,W.T.,et al, 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

A 69-Year-Old Woman with Ophthalmoplegia
Neurol 104:e213763, Yu, H & Frey, J, 2025

Rapid Diagnosis of Intracerebral Hemorrhage in Patients with Acute Stroke by Measuring Prehospital GFAP Levels on a Point-of-Care Device (DETECT)
Neurol 105: e213823, Kalra,L-P.,et al, 2025

Acute and Progressive Cognitive Decline in a 38-Year-Old Man
Neurol 105: e213871, Wu,L.,et al, 2025

Clinicopathologic Features, Pathogenesis, and Treatment of Monoclonal Gammopathy-Associated Myopathies
Neurol 105:213101, Soontrapa,P.,et al, 2025

Neuroimaging Findings in Children and Young Adults with Neurotoxicity after CAR T-Cell Therapy for B-Cell Malignancies
Neurol 105:e214086, McGuire,J.L.,et al, 2025

A 10-Year-Old Boy with Progressive Tremor, Insomnia and Autonomic Dysfunction
Neurol 105:e214297, Chen,Z., et al, 2025

Trident Sign in GFAP-Associated Meningoencephalomyelitis
Neurol 106:e214566, Mallett,N.S.,et al, 2025

Showing articles 50 to 100 of 1020 << Previous Next >>