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Differential
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abducens nerve
abducens nerve paralysis
abducens nerve paralysis, bilateral
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, heralded by neurologic invol
acute ataxia of childhood
acute disseminated encephalomyelitis
Adies pupil
ageusia
algorithm
altered states of consciousness
AMSAN
anal wink response
anemia
angiotensin-converting enzyme
anisocoria
anosmia
antecedent illness
anterior horn cell disease
anti GQ1b IgG antibody
anti GT1aIgG antibody
antibiotics
antiganglioside antibodies
antineurofascin antibodies
aphasia
arbovirus
areflexia
arm weakness
arrhythmia, cardiac
arsenic
arthritis
ascending paralysis
ataxia
ataxia, acute onset
ataxia, cerebellar
ataxia, sensory
ataxic gait
atypical
auditory evoked brainstem potentials
autoantibodies
autoimmune disease
autonomic dysfunction
autonomic dysfunction, acute
autonomic neuropathy
autonomic neuropathy, idiopathic
axonal degeneration
Babinski sign
bacterial infection
bacterial infection, CNS
BAL
basophilic stippling of red blood cells
behavioral disorder
Bickerstaff's brainstem encephalitis
biologic markers
bone marrow suppression
Borrelia burgdorferi infection
botulism
brachial neuritis
brachial plexus neuropathy
brainstem
brainstem, lesion of
brainstem, neoplasms of
Brazil
bulbar palsy
bulbar palsy, acute
burning feet
burning hands
burning paresthesia
campylobacter infection
cardiomegaly
cardiomyopathy
case studies
CAT scan
CAT scan, abnormal
cauda equina, enhancement
cavernous sinus, syndrome
central nervous system, infection of
cerebellar lesion
cerebellar peduncle
cerebral edema
cerebral edema, vasogenic
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
chest x-ray, abnormal
children
Clinical Pathologic Conference(C.P.C.)
coinfection
coma
comorbidities
complications
conduction block
congenital infection, viral
constipation
contactin associated protein like 1 antibodies
corneal reflex, abnormal
coronavirus
cough
COVID-19
Coxiella burnetti
cranial nerve enhancement
cranial nerve palsies
cranial nerve palsies, bilateral
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
critical care unit
deep tendon reflexes
delay in diagnosis
depression
dermatitis
descending paralysis
diagnostic criteria
diarrhea
differential diagnosis
dilantin
diphtheria
diplegia, brachial
diplopia
disability, neurological
distal muscle weakness
dog bite
drowsiness
dysarthria
dysphagia
edema, pedal
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electroencephalogram, triphasic delta waves
electromyogram
electromyogram, decremental response
ELISA
emergencies, medical
emergencies, neurologic
encephalitis
encephalitis, brainstem
encephalitis, viral
encephalomyelitis
encephalopathy
endemic area
enteritis
eosinophilia
epidemiology of neurology
Epstein-Barr virus
erythema migrans
erythrocyte
evoked potentials
eye movement, disorders of
facial nerve
facial nerve palsy
facial nerve palsy, bilateral
facial nerve palsy, causes of
facial nerve palsy, recurrent
facial weakness
facial weakness, bilateral
false negative
fatigue
fever
fibrillations
fingernails, abnormal
fish poisoning
Fisher C.M.
Fisher's syndrome
Fisher's syndrome, atypical
flaccid paralysis
flavivirus
flu-like illness
F-wave response
gadolinium
gait disorder
gammaglobulin therapy, intravenous
gammaglobulin therapy, intravenous, refractory
ganglionitis
gangliosides
gastroenteritis
geographic location
glutamic acid decarboxylase, antibody
GM1 ganglioside
GM1 ganglioside antibodies
gram negative rod
granulomatous disease
Guillain Barre syndrome
Guillain Barre syndrome, ataxic form
Guillain Barre syndrome, axonal form
Guillain Barre syndrome, complications
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, etiology of
Guillain Barre syndrome, infantile and childhood form
Guillain Barre syndrome, neuropathology of inflammatory lesion of
Guillain Barre syndrome, ophthalmoplegia in
Guillain Barre syndrome, pharyngeal-cervical-brachial variant
Guillain Barre syndrome, prognosis of
Guillain Barre syndrome, recurrent
Guillain Barre syndrome, sensory
Guillain Barre syndrome, variant forms of
hallucination
hand weakness
headache
heavy metal intoxication
hemoglobinuria
hepatitis
hepatitis E virus
heralding manifestation
herpes virus
hippocampus
HLA
hoarseness
H-reflex testing
human immunodeficiency virus type 1
hydrocephalus
hyperamylasemia
hypercoagulable state
hyperkalemia
hyperkeratosis
hyperreflexia
hypertension
hypoglossal nerve
hypohidrosis
hyporeflexia
hyposmia
hypothalamus
hypothalamus, disturbance of
iatrogenic neurologic disorders
idiopathic cranial polyneuropathy
IgG4-related disease
ileus, paralytic
imbalance
immunotherapy
India
infection
infectious mononucleosis
infectious mononucleosis, neurologic findings with
influenza immunization
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intracranial hypertension, benign
intraneural hemorrhage
intubation
iridoplegia
irritability
leg weakness, bilateral
lethargy
leukoencephalitis
leukopenia
level of consciousness, decreased
light-near dissociation, causes of
liver disease
liver function enzymes
lumbosacral plexopathy
lumbosacral plexus
lumbosacral plexus, neuritis
lumbosacral radiculopathy
Lyme disease
lymphocytic meningoradiculitis
lymphoma
lymphoma involving CNS
Mees lines
memory, impairment of
meningismus
meningitis
meningitis, aseptic
meningitis, carcinomatous
meningoencephalitis
mental status, abnormal
microcephaly
midbrain, infarction of
midbrain, lesion of
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
mimics
misdiagnosis
Moebius syndrome
monoclonal antibodies
monoclonal gammopathy
monoclonal gammopathy of uncertain significance
mononeuritis multiplex
mononeuropathy
mononeuropathy multiplex
mortality
mosquito
motor neuron disease
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, cranial nerves
MRI, disappearing lesion on
MRI, lumbosacral plexus
MRI, negative
MRI, serial
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, spine
mucormycosis
muscle pain
muscle weakness
muscle weakness, proximal
myasthenia gravis
mycoplasma
mycoplasma pneumoniae
myelitis
myelitis, transverse
myelopathy
myeloradiculitis
myopathy
myopathy, proximal
nasal speech
nasopharyngeal carcinoma
nausea and vomiting
neck weakness
neoplasm, metastatic to base of skull
nephrotic syndrome
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
nerve root enhancement
nerve root hypertrophy
neuritis, heavy metals causing
neurologic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic evaluation
neurologic examination
neurologic signs
neurologic symptoms
neurologic testing
neurological intensive care
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronopathy
neuronopathy, sensory
neuropathology
neuropathy
neuropathy, acute
neuropathy, ataxic
neuropathy, autoimmune
neuropathy, diphtheritic
neuropathy, motor, multifocal
neuropathy, painful
neuropathy, paraneoplastic
neuropathy, peripheral
neuropathy, recurrent
neuropathy, sensory
neuropathy, small-fiber
neuropathy, small-fiber, painful sensory
neuropathy, toxic
neurotoxin
node of Ranvier
nodopathy, autoimmune
nonresponsive
numbness, ascending
numbness, extremity
nystagmus
nystagmus, dissociated
one and a half syndrome
ophthalmoplegia
ophthalmoplegia, acute
ophthalmoplegia, bilateral, acute
ophthalmoplegia, cause of
ophthalmoplegia, postinfectious
ophthalmoplegia, progressive external
ophthalmoplegia, recurrent
ophthalmoplegia, total
optic atrophy
optic disc edema
optic nerve
optic neuritis
optic neuropathy
oropharyngeal weakness
orthostatic hypotension
overlap syndrome
pain
pain, abdominal
pain, back
pain, flank
pain, leg
pancreatitis
pancytopenia
papilledema
papillitis
paralysis, acute
paralysis, acute areflexic
paralysis, asymmetric
paraparesis
paraplegia
paresthesias
paresthesias, feet
paresthesias, hands
pembrolizumab
pericardial effusion
perioral numbness
peripheral blood smear
peripheral blood smear, abnormal
personality change
photophobia
pituitary, apoplexy
plasmapheresis
pleocytosis of cerebrospinal fluid
pleural effusion
pneumonia
poliomyelitis
poliomyelitis-like illness
polymerase chain reaction
polymerase chain reaction, false negative
polymyositis
polyneuritis
polyneuritis, acute sensory
polyneuropathy
polyneuropathy, acute sensory
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic inflammatory demyelinating, variant form
polyneuropathy, chronic inflammatory demyelinating-pure motor syn
polyneuropathy, chronic inflammatory demyelinating-sens atax var
polyneuropathy, chronic inflammatory demyelinating-variant forms
polyneuropathy, chronic relapsing
polyneuropathy, critically ill
polyneuropathy, subacute idiopathic demyelinating
pons, lesion of
pontine glioma
position sensation, abnormal
post infectious polyneuropathy
postinfectious
precipitating factors
pregnancy, neurologic complications in
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
proprioception, abnormal
protein 14-3-3, cerebrospinal fluid
pseudointernuclear ophthalmoplegia
psychiatric problems in neurologic disorders
ptosis
ptosis, acute onset
ptosis, bilateral
ptosis, unilateral
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, dilated, bilateral
pupil, light reflex, abnormal
pupil, tonic
Q fever
quadriparesis
quadriplegia
rabies, nervous system involvement with
radicular pain
radiculoneuritis
radiculopathy
rapidly progressing neurologic illness
rash
recurrent
Refsum's disease
remote effect of cancer on the nervous system
repetitive nerve stimulation
respirator
respiratory distress syndrome, neurologic status with
respiratory failure
respiratory tract infection
reversible neurologic disorder
review article
rhabdomyolysis
rheumatoid arthritis
rhinorrhea
rickettsial organism
risk factors
sarcoidosis
sarcoidosis, CNS
screening
seizure
sensory loss
sensory nerve action potentials
sensory polyneuropathy
serologic testing
serologic testing of cerebrospinal fluid
seronegative
serum alanine aminotransferase
severe acute respiratory syndrome
sexually transmitted disease
shunt procedure, ventricular
skin, biopsy
skin, lesions in neurologic disorders
slurred speech
smell
somatosensory evoked potentials
spinal accessory nerve
spinal cord
spinal cord, lesion of
spirochete infection
steroid
steroid therapy, CNS treatment and complications with
stool culture
strabismus
sweating, abnormality of
syncope
syncope, recurrent
syphilis, diagnosis and treatment
syphilis, neurologic complications with
systemic illness
third nerve
third nerve palsy
thrombocytopenia
tick bite
tongue, impaired movements of
tongue, weakness
tracheostomy
travel, foreign
treatment of neurologic disorder
tremor
trigeminal nerve
trigeminal neuropathy
upgaze, paralysis of
uremia
urinary retention
urine test in toxic screen
vaccination, neurologic complications with
vectors of infection
vestibulopathy
viral infection
viral infection, CNS
viral infection, transmission
viral isolation
vision, blurred
visual acuity, decreased
vital capacity
vocal cord paralysis
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
Wernicke's encephalopathy
Western immunoblot test
white matter disease
workup
yersinia enterocolitica
Zika virus infection
Showing articles 1750 to 1800 of 2212 << Previous Next >>

The Value of Interphase Cytogenetics in Cytology for the Diagnosis of Leptomeningeal Metastases
Neurol 51:906-908, Van Oostengrugge,R.J.,et al, 1998

Cerebral Amyloid Angiopathy:Propsects for Clinical Diagnosis and Treatment
Neurol 52:690-694, Greenberg,S.M., 1998

Genetic Analysis Enables Definite and Rapid Diagnosis of Cerebrotendinous Xanthomatosis
Neurol 51:865-867, Chen,W.,et al, 1998

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

Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
AJR 171:1131-1137, Antunez, E.,et al, 1998

Flail Arm Syndrome: A Distinctive Variant of Amyotrophic Lateral Sclerosis
JNNP 65:950-951, Hu, M.T.M.,et al, 1998

Alzheimers Disease with Asymmetric Parietal Lobe Atrophy: A Case Report
J Neurol Sci 160:96-99, Kaida,K.-I.,et al, 1998

Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
Neurol 49:1026-1030, Saiz,A.,et al, 1997

Cryptic Vascular Malformations:Controversies in Terminology, Diagnosis, Pathophysiology, and Treatment
AJNR 18:1839-1846, Dillon,W.P., 1997

Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
Neurol 49:1598-1604, Brandmann,O.,et al, 1997

Multifocal Motor Neuropathy, Serum IgM Anti-GM1 Ganglioside Antibodies Detected Using Linkage of GM1 to ELISA Plates
Neurol 49:1289-1292, Pestronk,A.&Choksi,R., 1997

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

Laboratory Evaluation in the Diagnosis of Lyme Disease
Ann Int Med 127:1109-1123, 1106-11081997., Tugwell,P.,et al, 1997

Transmissible Spongiform Encephalopathies
NEJM 337:1821-1828, Haywood,A.M., 1997

A 56-Year-Old Woman with Chronic Fatigue Syndrome
JAMA 278:1179-1185, Komaroff,A.L., 1997

Brain magnetic Resonance Diffusion Abnormalities in Creutzfeldt-Jakob Disease
Arch Neurol 54:1411-1415, Bahn,M.M.,et al, 1997

Frontotemporal Degeneration, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1425-1427, 14291997., Neary,D., 1997

Frontotemporal Dementia, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1427-1429, Kertesz,A., 1997

Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997

Genetic Testing of Children at Risk for Huntington's Disease
Neurol 49:1048-1053, Nance,M.A.,et al, 1997

The Effect of Different Diagnostic Criteria on the Prevalence of Dementia
NEJM 337:1667-1674, Erkinjuntti,T.,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

Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
Arch Neurol 54:1226-1229, Roses,A.D., 1997

Criteria for Alzheimer's Disease and the Nosology of Dementia with Lewy Bodies
Neurol 48:126-132, Hansen,L.A.&Samuel,W., 1997

Small-Vessel Vasculitis
NEJM 337:1512-1523, Jennette,J.C.&Falk,R.J., 1997

Polymerase Chain Reaction-Based Detection of Tropheryma Whippelii in Central Nervous System Whipple's Disease
Ann Neurol 42:120-124, Lynch,T.,et al, 1997

Diagnostic Value of CSF Exam in Children with Peripheral Facial Palsy & Suspected Lyme Borreliosis
Neurol 49:817-824, Albisetti,M.,et al, 1997

Magnetic Resonance Imaging of the Forearm as a Diagnostic Aid in Pts with Sporadic Inclusion Body Myositis
Neurol 48:863-866, Sekul,E.A.,et al, 1997

X-Linked Emery-Dreifuss Muscular Dystrophy Can Be Diagnosed from Skin Biopsy or Blood Sample
Ann Neurol 42:249-253, Mora,M.,et al, 1997

ALS Standard of Care Consensus
Neurol 48 (Suppl 4) :S33-S37997., Miller,R.G.,et al, 1997

Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
Neurol 49:568-572, Parboosingh,J.S.,et al, 1997

The Clinical Limits of Myasthenia Gravis and Differential Diagnosis
Neurol 48 (Suppl 5) :S36-S39997., Lisak,R.P., 1997

Spinal Epidural Metastasis as the Initial Manifestation of Malignancy:Clinical Features and Diagnostic Approach
Neurol 49:452-456, Schiff,D.,et al, 1997

What is the Accuracy of the Clinical Diagnosis of Multiple System Atrophy
Arch Neurol 54:937-944, Litvan,I.,et al, 1997

Distinction of Idiopathic Parkinson's Dis from Multi-Syst Atrophy by Stim of Growth-Hormone Release w Clonidine
Lancet 349:1877-1881, Kimber,J.R.,et al, 1997

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

Diagnosing Syncope, Part 2:Unexplained Syncope
Ann Int Med 127:76-86, Linzer,M.,et al, 1997

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

New Variant Creutzfeldt-Jakob Disease:Psychiatric Features
Lancet 350:908-910, Zeidler,M.,et al, 1997

Lumbar Puncture Still Has an Important Role in Diagnosing Subarachnoid Heemorrhage
BMJ 315:1598-1599, Wasserberg,J.&Barlow,P., 1997

Color Duplex Ultrasonography in the Diagnosis of Temporal Arteritis
NEJM 337:1336-1386, 13851997., Schmidt,W.A.,et al, 1997

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

Sympathetic Cardioneuropathy in Dysautonomias
NEJM 336:696-702, 7211997., Goldstein,D.S.,et al, 1997

The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
JAMA 277:832-836, Post,S.G.,et al, 1997

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,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

Frontotemporal Dementia is on the MAP
Ann Neurol 41:139-140, Wilhelmsen,K.C., 1997

Alteration of White Matter MR Signal Intensity in Frontotemporal Dementia
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Assessment of CSF Levels of Tau Protein in Mildly Demented Patients with Alzheimer's Disese
Neurol 48:632-635, Galasko,D.,et al, 1997

Diagnosis of AIDS-Related Focal Brain Lesions
Neurol 48:687-694, Antinori,A.,et al, 1997



Showing articles 1750 to 1800 of 2212 << Previous Next >>