Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
accommodation
accomodation, abnormal
acquired immunodeficiency syndrome
acrocyanosis
advances in neurology
aggression
agitation
agnosia
agnosia, visual
Aicardi-Goutieres syndrome
algorithm
alternating rapid movement
aluminum
alveolar hypoventilation
Alzheimer's disease
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
Angelman syndrome
anomic aphasia
aphasia
aphasia, classification of
aphasia, conduction
aphasia, global
aphasia, global-without hemiparesis
aphasia, progressive, primary
aphasia, references
aphasia, rehabilitation
aphasia, sign language
aphasia, testing
aphasia, transcortical
aphasia, transcortical-motor
aphasia, transcortical-sensory
aphonia
apraxia
areflexia
arm drift
artificial intelligence
arylsulfatase A
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
attention span
atypical
autism
autoantibodies
autoimmune disease
autoimmune encephalopathy
autonomic dysfunction
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
behavior, combative
behavioral disorder
benchmark
billing
black box
blepharospasm
blinking
blinking, reduced
brachycephaly
bradykinesia
brain atrophy
Broca's aphasia
bruit
bruxism
bulbar palsy
bulbar palsy, progressive
calcification, intracranial
calculations
carcinoma
carotid artery occlusion, bilateral
carotid artery occlusion, intracranial
carotid artery occlusion, neck
carotid siphon
carotid-siphon occlusion
CAT scan, abnormal
CAT scan, emission, abnormal
catatonia
celiac disease, adult
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar disease, eye movement disorder in
cerebellar hypoplasia
cerebellitis, autoimmune
cerebellum, disease of
cerebral cortical atrophy
cerebrospinal fluid, abnormal
cerebrovascular accident
cerebrovascular accident, clinical diagnosis
cerebrovascular accident, mimics
cerebrovascular accident, thrombolytic agents in treatment
cerebrovascular disease
chilbran skin lesions
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 15
Clinical Pathologic Conference(C.P.C.)
cogwheel rigidty
complications
comprehension, impaired
computers, medicine and
computers, neurologic diagnosis and
confusion
consanguinity
consciousness
contractures, joint
convergence
convergence, impaired
conversion reaction
coronavirus
cortical-basal ganglionic degeneration
cough
COVID-19
crying, pathologic
decision aids
decision analysis
deep learning
degenerative diseases of CNS
dementia
dementia, childhood
dementia, differential diagnosis of
dementia, frontotemporal
dementia, presenile
dentate nuclei, lesion of
developmental retardation
diagnosis, difficult
diagnostic criteria
dialysis
dialysis dementia
diarrhea
differential diagnosis
differential diagnosis generators
digital health
digital health, wearable technology
diplopia
disability, neurological
DPPX
DPPX, antibodies, encephalitis
drooling
dysarthria
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dysmorphic
dysnomia
dysphagia
dysphonia
dyspraxia
dystonia
dystonia, children
efficacy
electroencephalogram, abnormalities of
electromyogram
electronic differential diagnosis
electronic health records
ELISA
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, etiology
encephalitis, viral
encephalopathy
encephalopathy, metabolic
enuresis
EPIC electronic medical record
epidemiology of neurology
ethics in neurology
executive dysfunction
expert opinion
eye movement, disorders of
face arm speech test
facial appearance, abnormal
facial expression abnormality
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatigue
feeding disorder
fever
fish
Fisher C.M.
fluorescene in situ hybridization
frontal lobe, atrophy
fundus, abnormality of
funduscopic exam
gait analysis technology
gait disorder
gait, apraxic
gait, festinating
gaze palsy, vertical
gene
gene mutation
Generative Pretrained Transformer 4
genetic diagnosis, prenatal
genetic neurologic disorders
Gilles de la Tourette syndrome
give-way weakness
glabellar sign
globus pallidus
globus pallidus, lesion of
growth retardation
Hallervorden Spatz disease
hallucination
handwriting
head lag
headache
heel-knee-shin test
hemianopia, homonymous
hemiparesis
hepatolenticular degeneration(Wilson's disease)
hip abductor sign
hippocampus
Hoover's sign
human immunodeficiency virus type 1
hydrocephalus
hyperactivity
hyperesthesia
hyperlipoproteinemia
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hypophonia
hypopigmentation of skin
hypotonia
hypotonia, infants
imbalance
immunosuppression
immunosuppressive agents
inclusion bodies
inclusion bodies, intracytopasmic
incoordination
informatics
information technology
intellectual deficit
interferon alpha
intestinal biopsy
intrauterine
iron, brain
irritability
jaw jerk, abnormal
Kayser-Fleischer ring
kinesia paradoxica
Kluver-Bucy syndrome
language disorder in adults
language disorders in children
laughing, pathologic
left-right orientation
leg dragging
leg weakness, unilateral
lenticular nucleus, lesion of, bilateral
leukocyte alkaline phosphotase
leukocytosis
leukodystrophy
leukoencephalopathy
liver disease
lobar atrophy
locked-in syndrome
machine learning
macrognathia
malabsorption syndrome
marche a petits pas
masked facies
medical information
memory, defect of recent
memory, impairment of
mental retardation
mental status, abnormal
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
microcephaly
micrographia
midbrain, atrophy
mimics
misdiagnosis
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
moyamoya
MRI
MRI, abdomen
MRI, abnormal
MRI, disappearing lesion on
MRI, pelvis
MRI, serial
multiple sclerosis, differential diagnosis of
muscle atrophy, progressive
muscle weakness
mutism
myoclonus
neoplasm, metastatic to CNS
nerve biopsy
nerve conduction studies
neurologic complications
neurologic consultation
neurologic disease
neurologic disease, burden
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic examination
neurologic history
neurologic signs
neurologic symptoms
NeurologicDx
neurologist
neuropathology
neuropathology, brain
neuropathy
neuropathy, sensory
NMDA antagonists
nystagmus
ocular fundus photography
ocular motility, disorders of
optic atrophy
oversight
palatal myoclonus
palmomental response
pandemic
papilledema
paranoia
paraparesis
paraparesis, spastic
paraplegia, in flexion
Parkinson disease
Parkinson disease, diagnosis
Parkinsonism syndrome
pathologic reflex
personality change
Pick bodies
Pick's disease
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
polycythemia, primary
positional head-hanging test
postural abnormality
posturography
prenatal
primary lateral sclerosis
prognathism
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
reading disorder, acquired
real-world case
release phenomena
remote effect of cancer on the nervous system
repetition, impaired
respirations in CNS disease
respirator
retinitis pigmentosa
retropulsion
Rett's syndrome
review article
rhabdomyolysis
rigidity
risk factors
roaming behavior
robotic therapy
rocking
saccadic eye movements, abnormal
safety
scoliosis
sea-blue histiocytes
seizure
semantic dementia
sensory loss
sentience
sexual behavior, disorder of
shared decision making
sign language
skin, lesions in neurologic disorders
sleep pathology and physiology
slit lamp examination
smiling
spasticity
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech, delayed development of
speech, loss of
stare
startle reaction
stooped posture
stuttering
stuttering following CVA
substantia nigra
suck reflex
tachycardia
tandem gait, ataxic
tauopathy
teeth, wide-spaced
telemedicine
teleneurology
temporal lobe
temporal lobe, atrophy
teratoma
teratoma, ovarian
thrombocytosis
thrombosis, cerebral
tissue plasminogen activator, intravenous
titubation
tongue, fasciculations of
tongue, impaired movements of
tongue, protrusion of
transient ischemic attack
treatment of neurologic disorder
tremor
tremor, intention
tremor, resting
upgaze
upgaze, paralysis of
validation
verification
vestibulopathy
vibratory sensation, abnormal
virtual learning
visual evoked response
voice, abnormality of
walking frame
walking, difficulty with
weakness, functional
weight loss
Wernicke's aphasia
wheelchair
white matter disease
wide based gait
word-finding difficulty
workup
Zeroth Law
Showing articles 1400 to 1450 of 2508 << Previous Next >>

Clinicopath Conf
Demyelinating Process Consistent with Multiple Sclerosis, Case 26-1998, NEJM 339:542-549998., , 1998

Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Susac Syndrome
Medicine 77:3-11, Papo,T.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

Persistent MR Contrast Enhancement of Calcified Neurocysticercosis Lesions
AJNR 19:79-82, Sheth,T.N.,et al, 1998

Respiratory Management in Acute Neurologic Illness
Neurol 50:11-20, Wijdicks,E.F.M.&Borel,C.O., 1998

Assisted Suicide
Euthanasia, and the Neurologist, The Ethics and Humanities Subcom of AAN, Neurol 50:596-59898., , 1998

Taste and Smell Losses in Normal Aging and Disease
JAMA 278:1357-1362, Schiffman,S.S., 1997

Granulomatous Angiitis of the Nervous System
In Vasculitis & The Nervous System, Neurol Clin 15:821-83497., Younger,D.S.,et al, 1997

Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Diagnosis and Treatment of Alzheimer Disease and Related Disorders
JAMA 278:1363-1371, Small,G.W.,et al, 1997

Patients'Awareness of Stroke Signs, Symptoms & Risk Factors
Stroke 28:1871-1875, Kothari,R.,et al, 1997

CIDP:Clinical Features & Responses to Trtm in 67 Consecutive Pts with/without a Monoclonal Gammopathy
Neurol 48:321-328, Gorson,K.G.,et al, 1997

Ataxia and Slurred Speech after Artesunate Treatment for Falciparum Malaria
NEJM 336:1328, Miller,L.G.&Panosian,C.B., 1997

Clinical and Neuroradiographic Manifestations of Eastern Equine Encephalitis
NEJM 336:1867-1874, Deresiewicz,R.L.,et al, 1997

A Case of Acute Monocytic Ehrlichiosis with Prominent Neurologic Signs
Neurol 48:1619-1623, Grant,A.C.,et al, 1997

Clinicopath Conf
Hodgkin's Disease, Paraneoplastic Cerebellar Degeneration, Case 21-1997, NEJM 337:115-12297., , 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

The Variable MR Appearance of Primary Lymphoma of the Central Nervous System:Comparison with Histopathologic Features
AJNR 18:563-572, Johnson,B.A.,et al, 1997

Neurological Signs and Frontal White Matter Lesions in Vascular Parkinsonism
Stroke 28:965-969, Yamanouchi,H.&Nagura,H., 1997

Neurodevelopmental Dysfunction Among Nonreferred Children with Idiopathic Megalencephaly
J Pediatr 131:320-324, Sandler,A.D.,et al, 1997

"Pseudoocclusion"of the Internal Carotid Artery:A Pitfall on Intracranial MRA
J Comput Assist Tomogr 21:831-833, Okamoto,K.,et al, 1997

Diagnosing Syncope
Ann Int Med 126:989-996, Linzer,M.,et al, 1997

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

Causes and Mechanisms of Cerebellar Infarction in Young Patients
Stroke 28:2400-2404, Barinagarrementeria,F.,et al, 1997

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997

Cerebral Tuberculosis in Pts with AIDS, Report of 6 Cases & Review
Medicine 76:423-431, Lesprit,P.,et al, 1997

Patterns of Sensory Dysfunction in Lateral Medullary Infarction, Clinical-MRI Correlation
Neurol 49:1557-1563, Kim,J.S.,et al, 1997

Melatonin"A Clinical Perspective
Ann Neurol 42:545-553, Penev,P.D.,et al, 1997

Evaluation of Malignancy in Ring Enhancing Brain Lesions on CT by Thallium-201 SPECT
JNNP 63:569-574, Kallen,K.,et al, 1997

Measuring Quality of Care in Neurology
Arch Neurol 54:1329-1332, 13271997., Ringel,S.P.&Vickrey,B.G., 1997

Predictors of Intracranial Path Findings in Pts Who Seek ER Care Because of Headache
Arch Neurol 54:1506-1509, Ramirez-Lassepas,M.,et al, 1997

Herpes Simplex Encephalitis Treated with Acyclovir:Diagnosis and Long Term Outcome
JNNP 63:321-326, McGrath,N.,et al, 1997

Ocular Findings in Ramsay Hunt Syndrome
J Neuro-Ophthalmol 17:199-201, Mansour,A.M.&Bailey,B.J., 1997

CSF Findings in Children with Lyme Disease-Associated Facial Nerve Palsy
Arch Pediatr Adolesc Med 151:1224-1228, 11831997., Belman,A.L.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Identification of Brain Region for Coordianting Speech Articulation
Lancet 394:221-222, Donnan,G.A.,et al, 1997

Epidemiology, Pathophysiology, & Management of Hyponatremic Encephalopathy
Am J Med 102:67-77, Fraser,C.L.,et al, 1997

Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,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

Tremor Caused by Trimethoprim-Sulfamethoxazole in a Patient with AIDS
Neurol 48:537-538, VanGerpen,J.A., 1997

Is There a Gulf War Syndrome? Searching for Syndromes by Factor Analysis of Symptoms
JAMA 227:215-222, 2591997., Haley,R.W.,et al, 1997

Self-Reported Exposure to Neurotoxic Chemical Combinations in the Gulf War:A Cross-Sectional Epidemiologic Study
JAMA 227:231-237, 2591997., Haley,R.W.&Kurt,T.L., 1997



Showing articles 1400 to 1450 of 2508 << Previous Next >>