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Differential
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abstract reasoning

acrocyanosis

activities of daily living scale

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

affect, flat

age associated memory impairment

Alzheimer's disease, age of onset

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, familial, late onset

Alzheimer's disease, heterogeneity of

Alzheimer's disease, noncognitive symptoms

Alzheimer's disease, pathogenesis

Alzheimer's disease, preclinical

Alzheimer's disease, risk factors in

Alzheimer's disease, staging

Alzheimer's disease, treatment of

amyloid

amyloid angiopathy, cerebral

amyloid-related imaging abnormalities

amyotrophic lateral sclerosis

aneurysm, intracranial, familial

angiitis, granulomatous of CNS

angiography, cerebral

anomic aphasia

anosmia

anticholinesterase

anticoagulant, treatment

antiphospholipid antibody syndrome

anxiety

aphasia

aphasia, logopenic, progressive

aphasia, progressive

aphasia, progressive, non-fluent

aphasia, progressive, primary

apolipoprotein E

apoliprotein E, plasma level

autonomic dysfunction

basal ganglia, calcification of

brain biopsy, negative

brain volume

C9orf72

calcification, intracranial

CAT scan, emission, abnormal

CAT scan, false negative

catalepsy

cataplexy

caudate nucleus, lesion of, bilateral

celiac disease, adult

central nervous system, infection of

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar plaques, amyloid

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebroretinal microangiopathy with calcifications and cysts

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, biochemical markers of CNS disease

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, young adult

children

chorea

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

controversies in neurology

corneal dystrophy

corpus callosum

corpus callosum, lesion of

corpus callosum, thinning

degenerative diseases of CNS

delusion

dementia

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, clinical diagnosis

dementia, diagnostic evaluation of

dementia, differential diagnosis of

dementia, early detection

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, prevention of

dementia, rapidly progressive

dementia, reversible

dementia, screening for

dementia, subcortical

dementia, transmissible

dementia, treatment of

depression

developmental retardation

diagnostic criteria

differential diagnosis

disease modifying agents

electroencephalogram, abnormalities of

electroencephalogram, focal delta activity

electromyogram

electron microscopy

encephalopathy

encephalopathy, progressive

enzyme, defect

epidemiology of neurology

ethics in neurology

evidence-based research

executive dysfunction

fistula, arterio-venous, dural

florbetapir

fluency

fracture, pathologic

frontal lobe, anatomy and physiology

frontal lobe, atrophy

frontal lobe, lesion of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

gait disorder

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

Gerstmann-Straussler-Scheinker disease

hallucination, visual

hemosiderosis of CNS, superficial

hepatomegaly

hepatosplenomegaly

heralding manifestation

hippocampal atrophy

hippocampus

Hodgkin's disease

human immunodeficiency virus type 1

Huntington's chorea

hydrocephalus

hydrocephalus, exvacuo

hydrocephalus, normal pressure

hypotension, systemic

imbalance

impulsivity

inappropriate behavior

inclusion bodies

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incoordination

inflexibility, mental

intellectual deficit

intellectual deterioration

intestinal biopsy

intracerebral hemorrhage

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, young adult

language disorder in adults

laughing, pathologic

L-dopa

L-dopa, drug interactions with and side effects of

lecanemab

leg weakness, bilateral

lethargy

leukodystrophy

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

Lewy body

Lewy body disease, diffuse

life expectancy

lipid storage disorder of CNS

lipomembranous polycystic osteodysplasia

lysosomal storage disease

manganese intoxication

memory

Memory Impairment Screen

memory, defect of recent

memory, evaluation of

memory, impairment of

memory, impairment of, subjective

mental status, abnormal

microangiopathy, brain

microhemorrhage, intracerebral

miglustat

mild cognitive impairment

mild cognitive impairment converting to Alzheimer's disease

mimics

Mini Mental Status Examination

misdiagnosis

molecular genetics

monoclonal antibodies

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, functional

MRI, intravascular enhancement

MRI, linear enhancement

MRI, negative

MRI, serial

MRI, T1 weighted high signal foci

MRI, volumetry

multiple sclerosis, differential diagnosis of

muscle atrophy, progressive

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neurocutaneous disease

neurocutaneous melanosis

neurofibrillary degeneration

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic signs

neuropathology

neuropathology, brain

neuroprotective agents

neurosyphilis

Niemann-Pick disease

nonsteroidal anti-inflammatory drug

normal

nutritional deficiency

nystagmus

obsessive-compulsive disorder

old age, neurology of

organomegaly

orthostatic hypotension

pain, increased response

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, early symptoms

Parkinson disease, familial

Parkinson disease, fluctuations in

Parkinson disease, nonmotor problems of

Parkinson disease, presymptomatic detection

Parkinson disease, rapid progression

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, young onset

Parkinsonism syndrome

Parkinsonism-dementia complex

PAS positive

PAS positive material in the brain

pathologic reflex

patient information and support

Pittsburgh Compound B

pleocytosis of cerebrospinal fluid

polycystic lipomembranous osteodysplasia

polymerase chain reaction

posterior cortical atrophy

prevention of neurologic disorders

prion disease

prognosis

progressive myoclonic epilepsy

progressive neurologic disorder

progressive subcortical gliosis

protein 14-3-3, cerebrospinal fluid

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis

psychotic behavior

radiation therapy, CNS treatment and complications with

rapidly progressing neurologic illness

real-time quaking-induced conversion

Red flags

release phenomena

REM sleep

REM sleep behavior disorder

reticulum antibodies

review article

risk factors

risk factors, modification

roaming behavior

safety

salivation, excessive

seizure, diagnosis of

seizure, intractable

seizure, laughing as manifestation

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

sleep pathology and physiology

smell

Smell Identification Test

spongy degeneration of brain

startle myoclonus

stereotyped behavior

steroid therapy, CNS treatment and complications with

stimulation, deep brain

stuttering

stuttering following CVA

symmetric brain lesions

syncope

synucleinopathy

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

tau protein

tauopathy

temporal lobe, atrophy

thalamus, lesion of

thalamus, lesion of-bilateral

tinnitus

tissue plasminogen activator, intravenous

tongue, fasciculations of

transient neurologic deficit

treatment of neurologic disorder

tremor, thalamic stimulation for suppression of

uremia

urinary incontinence

vanishing white matter

walking, difficulty with

whole genome sequencing

word-finding difficulty

workup

Showing articles 250 to 300 of 3759 << Previous Next >>

The Epidemiology of Parkinson's Disease, A Case-Control Study of Young-Onset and Old-Onset Patients
Arch Neurol 48:903-907, Stern,M.,et al, 1991

Preclinical Detection of Parkinson's Disease
Neurology Suppl 2, 41:5-921991., Koller,W.C.&Langston,J.W., 1991

Single Photon Emission Computed Tomography in Cerebrovascular Disease
Stroke 22:950-954, Fayad,P.B.&Brass,L.M., 1991

Young-Onset Parkinson's Disease:A Clinical Review
Neurol 41:168-173, Golbe,L.I., 1991

Early Development of Levodopa-Induced Dyskinesias and Response Fluctuations in Young-Onset Parkinson's Disease
Neurol 41:202-205, Kostic,V., 1991

A Follow-up Study of Intractable Seizures in Childhood
Ann Neurol 28:699-705, Huttenlocher,P.R.&Hapke,R.J., 1990

Multiple Sclerosis in Adolescents:CT and MR Findings
AJR 155:385-390, Osborn,A.G.,et al, 1990

Advanced Alzheimer's Disease is a Risk Factor for Late-Onset Seizures
Arch Neurol 47:847-850, Romanelli,M.F.,et al, 1990

A Large Kindred with Autosomal Dominant Parkinson's Disease
Ann Neurol 27:276-282, Golbe,L.I.,et al, 1990

Adult-Onset Adrenoleukodystrophy Manifesting as Dementia
Am J Med 87:481-483, Panegyres,P.K.,et al, 1989

Effect of Age at Onset on Progression and Mortality in Parkinson's Disease
Neurol 39:1187-1190, Diamond,S.G.,et al, 1989

New-Onset Seizures Associated with Human Immunodeficiency Virus Infection: Causation and Clinical Features in 100 Cases
Am J Med 87:173-177, Holtzman, D.M.,et al, 1989

Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
Ann Neurol 24:692-694, Sethi,K.D.,et al, 1988

A Comparison of Clinical and Pathological Features of Young-and Old-Onset Parkinson's Disease
Neurol 38:1402-1406, Gibb,W.R.G.&Lees,A.J., 1988

Multiple Sclerosis in Childhood:Clinical Profile in 125 Patients
J Pediatr 111:359-363, Duquette,P.,et al, 1987

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

The Role of Nuclear Magnetic Resonance Imaging in the Diagnosis of MS in Childhood
Neurol 37:689-693, Golden,G.S.,et al, 1987

Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism
Neurol 35:227-234, Jankovic,J.,et al, 1985

Metachromatic Leukodystrophy Manifesting as a Schizophrenic Disorder:Computed Tomographic Correlation
Ann Neurol 18:94-95, Finelli,P.F., 1985

Onset of Multiple Sclerosis in a 24-Month Old Child
Arch Neurol 41:881-882, Bejar,J.M.,et al, 1984

Metachromatic Leukodystrophy (MLD) , XV. Adult MLD with Focal Lesions by Computed Tomography
Arch Neurol 40:354-355, Skomer,C.,et al, 1983

Childhood Multiple Sclerosis:Clinical Features & Demonstration of Changes in T Cell Subsets with Disease Act
Ann Neurol 11:463-468, Hauser,S.L.,et al, 1982

Familial Psychosis & Diverse Neurologic Abnormalities in Adult-Onset Gaucher's Disease
Arch Neurol 36:95-99, Neil,J.F.,et al, 1979

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Normocalcemic Tetany
Neurol 26:825, Isgreen,W.P., 1976

Pathogenesis & Natural History of Transient Global Amnesia
Stroke 5:303, Mathew,N.T.,et al, 1974

Organic Disease Presenting as a Psychiatric Syndrome
Postgrad Med 54:78, , 1973

Huntington's Disease in Children
Neurol 23:561, Byers,R.,et al, 1973

Neuro CPC of MGH
Acute Multiple Sclerosis, NEJM 273:760-7671965., , 1965

Reversible Leukoencephalopathy and Parkinsonism Due to CNS Involvement in Cryoglobulinemia
Neurol 106:e214622, German,A.,et al, 2026

Intravenous Thrombolysis Use in the Late Time Window Before Interhospital Transfer for Thrombectomy
JAMA Neurol 83:60-67, Seners,P.,et al, 2026

Neurosyphilis with Abnormal in the Bilateral Pons and Multifocal Cranial Nerve Enhancement
Ann Neurol 99:283-284, Zhang,Y.,et al, 2026

Treating Hearing Loss with Hearing Aids for the Prevention of Cognitive Decline and Dementia
Neurol 106:e214572, Cribb,L.,et al, 2026

Tenecteplase for Acute Non-Large Vessel Occlusion 4.5 to 24 Hours After IschemicStroke, The OPTION Randomized Clinical Trial
JAMA doi:10.1001/JAMA.2026.0210, Ma,G.,et al, 2026

A Randomized Trial of Tenecteplase in Acute Central Retinal Artery Occlusion
NEJM 394:442-450, Ryan,S.J.,et al, 2026

Mucormycosis
NEJM 394:684-698, Kontoyiannia,D.P. & Walsh, T.J., 2026

A 69-Year Old Man With Rapid Cognitive Decline and Abnormal Movements
Neurol 106:e214686;2026, Lim,G.Z.,et al, 2026

Creutzfeldt-Jakob-Like Presentation in Anti-AMPAR Encephalitis
Ann Neurol 99:1466-1467, Durbano,K.et al, 2026

Late-Onset Seizures, Etiology and Demographics in US Tertiary Care Epilepsy Centers
Neurol 106:e214948, Blank,L.J.,et al, 2026

Cerebral Syphilitic Vasculitis Presenting with Recurrent Stroke
Stroke 57:e197-e198, Yilmaz,E.,et al, 2026

Using Susceptibility-Based Imaging in Highly Active Late-Onset Multiple Sclerosis
Neurol 106:e214794, Sosa,S.M.,et al, 2026

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

Syphilis as an Important Modern-Day Risk Factor for Intracranial Vasculopathy and Ischemic Stroke:A Teaching Case
Stroke 57:e108-e111, Higham-Kessler,C.,et al, 2026

Clinicopathologic Conference, non-islet-Cell Tumor hypoglycemia Due to a Benign Cellular Smooth-Muscle Tumor of the Abdomen
NEJM 394:1216-1225, Case 9-2026, 2026

A 67-Year-Old Man with Exercise Intolerance nd Progressive Weakness
Neurol 106:e214830, Gosset,A.,et al, 2026

Using Susceptibility-Based Imaging in highly ctive Late-Onset Multiple Sclerosis
Neurol 106:e214794, Sosa,S.M.,et al, 2026

Deep Venous Dural Arteriovenous Fistula Mimicking Progressive Dementia
Stroke 57:e180-181, Langlois-Therien,T.,et al, 2026

Syphilitic Aortitis Presenting as Aortic Arch Thrombus and Acute Ischemic Stroke
Neurol 106:e214868, Ferro,J.,et al, 2026

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

A 35-Year-Old Patient with Rapidly Progressive Ascending Weakness Leading to Loss of Brainstem Reflexes
Neurol 106:e218059, Lyons,H.J.,et al, 2026

Showing articles 250 to 300 of 3759 << Previous Next >>