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acrocyanosis
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
adverse drug reaction
affect, flat
agitation
algorithm
Alzheimer's disease
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
amyloid angiopathy, cerebral
amyloid beta protein
amyloid plaques
amyloid-related imaging abnormalities
amyotrophic lateral sclerosis
angiitis, granulomatous of CNS
angiography, cerebral
anomic aphasia
anticoagulant, treatment
antiphospholipid antibody syndrome
aphasia
aphasia, logopenic, progressive
aphasia, progressive
aphasia, progressive, non-fluent
aphasia, progressive, primary
apolipoprotein E
APP
APP gene
apraxia
arteritides
ataxia
ataxic gait
atypical
autoimmune disease
axonal spheroid
B 12 deficiency
B12
Balint's syndrome
basal ganglia, calcification of
behavioral disorder
biologic markers
bone biopsy
bone survey
bradykinesia
brain atrophy
brain biopsy
brain biopsy, negative
C9orf72
calcification, intracranial
CAT scan
CAT scan, abnormal
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, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, young adult
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 1
chromosome 14
chromosome 17
chromosome 20
chromosome 21
clindamycin
Clinical Pathologic Conference(C.P.C.)
cognition
comorbidities
compulsivity
confusion
corneal dystrophy
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
cortical ribbon sign
coumarin
COVID-19
crying, pathologic
cyst, bone
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, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, subcortical
dementia, transmissible
dementia, treatment of
depression
developmental retardation
diagnostic criteria
differential diagnosis
disease modifying agents
disorientation
dizziness
dysarthria
dysdiadochokinesia
dysphagia
dystonia
echolalia
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, focal delta activity
electromyogram
electron microscopy
encephalopathy
encephalopathy, progressive
enzyme, defect
epidemiology of neurology
executive dysfunction
exome sequencing
Fabry's disease
falling
false negative
familial
fasciculation
fever
fistula, arterio-venous, dural
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
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
genu of corpus callosum
Gerstmann-Straussler-Scheinker disease
gliadin antibodies
gliosis
grasp reflex
grasping
hallucination
hallucination, visual
handedness
head injury
headache
hearing loss
hemosiderosis of CNS, superficial
hepatomegaly
hepatosplenomegaly
heralding manifestation
Hodgkin's disease
human immunodeficiency virus type 1
Huntington's chorea
hydrocephalus
hydrocephalus, exvacuo
hydrocephalus, normal pressure
hyperreflexia
hypersomnia
hypertension
hypoglycorrhachia
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
jaundice
Kluver-Bucy syndrome
Lafora body
Lafora's disease
language disorder in adults
laughing, pathologic
lecanemab
leg weakness, bilateral
lethargy
leukodystrophy
leukoencephalopathy
leukoencephalopathy, adult onset, sporadic
Lewy body
life expectancy
lipid storage disorder of CNS
lipomembranous polycystic osteodysplasia
livedo reticularis
lobar atrophy
logopenia
loss of sympathy
lupus anticoagulant
lysosomal storage disease
manganese intoxication
memory, defect of recent
memory, impairment of
memory, impairment of, subjective
mental status, abnormal
microangiopathy, brain
microhemorrhage, intracerebral
miglustat
mild cognitive impairment
mimics
Mini Mental Status Examination
misdiagnosis
molecular genetics
monoclonal antibodies
mood change
mortality
motor neuron disease
movement disorder
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
multiple sclerosis, differential diagnosis of
muscle atrophy, progressive
mutism
myoclonic jerks
myoclonus
neologism
neuroaxonal dystrophy
neuroaxonal leukodystrophy
neurocutaneous disease
neurocutaneous melanosis
neurofibrillary degeneration
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuropathology
neuropathology, brain
neurosyphilis
Niemann-Pick disease
nutritional deficiency
nystagmus
obsessive-compulsive disorder
organomegaly
pain, increased response
paranoia
paraparesis, spastic
paraphasias
paratonia
Parkinson disease
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
pathologic reflex
perseveration
personality change
Pick bodies
Pick's disease
Pittsburgh Compound B
pleocytosis of cerebrospinal fluid
polycystic lipomembranous osteodysplasia
polymerase chain reaction
posterior cortical atrophy
practice guidelines
preclinical
presenilin-1 gene
presenilin-2 gene
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
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
reticulum antibodies
review article
roaming behavior
safety
salivation, excessive
schizophrenia
screening
seizure
seizure, children
seizure, diagnosis of
seizure, intractable
seizure, laughing as manifestation
seizure, teenager
semantic dementia
senile plaques
serologic testing
single photon emission computed tomography
skin, biopsy
skin, lesions in neurologic disorders
Sneddon's syndrome
somnolence
spasticity
speech disorder
splenomegaly
spongy degeneration of brain
startle myoclonus
stereotyped behavior
steroid therapy, CNS treatment and complications with
stuttering
stuttering following CVA
symmetric brain lesions
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
uremia
urinary incontinence
vanishing white matter
vasculopathy
vegetarianism
vertigo
vertigo, episodic
vitamin deficiency
walking, difficulty with
weight loss
wheelchair
Whipple's disease
white matter disease
whole genome sequencing
word-finding difficulty
Showing articles 50 to 100 of 2282 << Previous Next >>

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

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

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

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

Demonstration of CSF Gamma-globulin Banding in Presenile Dementia
Neurol 30:882-884, Williams,A.,et al, 1980

Decreased Computerized Tomography Numbers in Patients With Presenile Dementia
Arch Neurol 37:401-409, Naeser,M.A.,et al, 1980

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

Presenile Dementia With Motor Neuron Disease in Japan, A New Entity
Arch Neurol 36:592-593, Mitsuyama,Y.,et al, 1979

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

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

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Neurological Stuttering-A Clinical Entity
et al. , JNNP 40:699977., Quinn,P.T., 1977

Granulomatous Angiitis of the Brain:A Successfully-treated Case
Neurol 27:588, Rajjoub,R.K.,et al, 1977

Presenile Dementia Presenting as Aphasia
JNNP 40:303, Wechsler,A.F., 1977

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

Myoclonus in Alzheimer Disease
Arch Neurol 33:278-280, Faden,A.I.,et al, 1976

Clinical Neuropathological Conference
(Ed) , Dis Ner Sys 34:124, 1973, Pick's Disease., Aronson,S.&Aronson,B., 1973

Alzheimer's disease, Diffuse Parenchymatous Diseases of the CNS, In Dementia
F. A. Davis Co. , Phila. , 1971, p. 165., Wells,C.E., 1971

Encephalopathy in Whipple's Disease
Neurol 12:65, Lampert,P.,et al, 1962

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

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

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

Autoimmune Encephalitis as Treatment-Responsive Cause of Rapidly Progressive Dementia
Neurol 106:e214933, van Steenhoven,R.W.,et al, 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

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

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

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

Melas Syndrome
Stat PearlsPubl Jan 25, Pia,S. & Lui,F., 2025

Wildfire Smoke Exposure and Incident Dementia
JAMA Neurol 82:40-48, Elser,H.,et al, 2025

Amyloid-Related Imaging Abnormalities (ARIA) in Clinical Trials of Gantenerumab in Early Alzheimer Disease
JAMA Neurol 92:19-29, Salloway,S.,et al, 2025

A 68-YEar-Old Man with Progressive Numbness, Vertigo, and Cognitive Decline
Neurol 104:e213437, Regan,S.M. & Davalos,L.F., 2025

Unveiling the Clinical and Imaging Signatures of Intravascular Lymphoma of the Central Nervous System:A Multicentric Cohort Study
Ann Neurol 97:435-448, Berthet,E.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

A 56-Year-Old Woman with New-Onset Hoarsement and Dysphagia
Neurol 104:e213363, McAree,M. & Frontera, J.A., 2025

Teaching NeuroImage: The House Soign in Behavioral Varianht Frontotemporal Dementia
Neurol 104:e213519, Ioannidis,S.,et al, 2025

Risk of Dementia in Individuals with Emergency Department Visits or Hospitalizations Due to Cannabis
JAMA Neurol 82:570-579, Myran,D.T.,et al, 2025

Real-World Evidence of Brexpiprazole Use and 6-Month Mortality, Hospitalization, and Emergency Department Visits Among Persons with Dementia
Neurol 105: e213717, Zissimopoulos, J.,et al, 2025

Neuropathologic Changes in People with Essential Tremor With Dementia
Neurol 105:e214310, Wainman,E.,et al, 2025



Showing articles 50 to 100 of 2282 << Previous Next >>