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Differential
(Click to cross reference)
abducens nerve paralysis
abducens nerve paralysis, bilateral
abortion, spontaneous
abscess, intracranial
abscess, intracranial-fungal
acquired immunodeficiency syndrome
acute disseminated encephalomyelitis
Adies pupil
adverse drug reaction
affect, flat
aggression
agitation
Alexanders disease
Alexanders disease, adult onset
alien hand syndrome
altered states of consciousness
alternating hemiplegia
alternating hemiplegia of childhood
alveolar hypoventilation
amaurosis fugax
aminoacidopathies
aminoacidurias
AMPA receptor antibodies
amphetamines
anergy
angiography, cerebral
animal exposure
anorexia
anti IgLON5
anti MAG antibodies
anti Ri antibody
antibiotics
anticardiolipin antibodies
anticonvulsants
anticonvulsants, untoward effects of
antiphospholipid antibodies
aphasia
apnea
apraxia
apraxia of eye movements
areflexia
arrhythmia, cardiac
arteritides
arthralgia
arthritis
aspiration
astrogliopathy
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
athetosis
ATP1A3 gene
autoantibodies
autoimmune disease
autonomic dysfunction
autonomic neuropathy
Babinski sign
bacterial infection
bacterial infection, CNS
Balint's syndrome
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bat bite
behavioral disorder
Behcet's syndrome
bilirubin encephalopathy
body odor
Borrelia miyamotoi infection
bovine spongiform encephalopathy
bradykinesia
brain atrophy
brain biopsy
brain scan
brainstem, lesion of
breast feeding
bruxism
bulbar palsy
burning skin
burst suppression pattern, electroencephalogram
cachexia
calcification, intracranial
calcium antagonist
carbamazepine
carbamazepine, toxicity
carcinoma
carcinoma of breast
carcinoma of lung
carcinoma of prostate
cardiac arrest
cardiac arrest and resuscitation
CAT scan, abnormal
CAT scan, pelvis
cauda equina, enhancement
central nervous system, infection of
cerebellar atrophy, secondary
cerebellar disease, eye movement disorder in
cerebellar hypoplasia
cerebellar lesion
cerebellum
cerebellum, disease of
cerebral cortex
cerebral cortical encephaliis
cerebral edema
cerebral venous thrombosis
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gold sol.curve of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, mimics
chemosis
cherry red spot
cherry red spot-myoclonus syndrome
children
chlorpromazine
chorea
choreoathetosis
chromosomal abnormality
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clonazepam
cognition
coma
coma, episodic
coma, prognosis of
comorbidities
complications
confusion
congenital infection, CNS
conjugate gaze, forced
conjunctival injection
conjunctivitis
convergence
conversion reaction
cortical-basal ganglionic degeneration
cranial nerve enhancement
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, high-pitched
cyst, ovary
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, rapidly progressive
dementia, transmissible
depression
developmental milestones, loss of
developmental retardation
diabetes insipidus
diagnostic criteria
diarrhea
diet
differential diagnosis
dilantin
dilantin, toxicity
diplopia
dizziness
downward gaze, paralysis of
drooling
drowsiness
drug induced neurologic disorders
drug interactions
dysarthria
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dysmetria
dysphagia
dyspnea
dystonia
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, indications
electroencephalogram, periodic complexes
electroencephalogram, urgent
electromyogram
ELISA
emergencies, neurologic
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, focal
encephalitis, paraneoplastic
encephalomyelitis
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, parainfectious
encephalopathy, progressive
enzyme, defect
epidemiology of neurology
episodic disorders
episodic neurologic deficits
episodic unconsciousness
erythema migrans
exercise intolerance
exophthalmus, unilateral
eye color
eye movement, disorders of
eye movement, painful
eye, pain in
facial nerve palsy
facial nerve palsy, bilateral
facial weakness, bilateral
failure to thrive
falling
false negative
false positive
false positive VDRL
familial
fasciculation
fatigue
fever
fine motor function, impaired
finger nose finger test
flaccid paralysis
floaters
flunarizine
fluorescent treponema antibody absorption(FTA-ABS)
fluorescent treponema antibody absorption/false positive
flushing
frontal lobe, space occupying lesion of
fungal infection, CNS
gait disorder
gammaglobulin therapy, intravenous
gaze deviation
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gaze palsy, vertical
gender
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
GFAP gene
glaucoma
glaucoma, acute
glioma
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
GluD2
glutamic acid decarboxylase, antibody
granulomatous disease
grasp reflex
grimacing
growth hormone
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
guinea pig inoculation
hallucination, hypnagogic
hallucination, visual
handwriting
headache
headache, bifrontal
headache, severe
hearing loss
hemiparesis
hemiplegia
hepatic encephalopathy
hepatomegaly
hepatosplenomegaly
hoarseness
human immunodeficiency virus type 1
hydrocephalus
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
hypercalcemia
hyperreflexia
hypersomnia
hyperthermia
hypertonia
hypoglycemia
hypoglycorrhachia
hypoglycorrhachia, causes of
hyponatremia
hypophonia
hypothalamus, disturbance of
hypothermia
hypotonia
hypotonia, infants
hypoxic encephalopathy
iatrogenic neurologic disorders
idiopathic
IFA
imbalance
immunohistochemistry
immunosuppression
immunosuppressive agents
immunotherapy
impotence
impulsivity
inattention
inborn errors of metabolism
inclusion body myositis
incoordination
infantile bilateral striatal necrosis
infantile hemiplegia
infection
insomnia
intellectual deficit
intellectual deterioration
intestinal biopsy
intracranial hypertension, benign
intrauterine infection
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
jaundice
kernicterus
lactic acidemia
Leigh's disease
leukocytosis
level of consciousness
level of consciousness, decreased
levitation
limbic encephalitis
lupus anticoagulant
Lyme disease
lymphadenopathy
lymphadenopathy, hilar
lysosomal storage disease
macrocephaly
malignant papulosis
masked facies
MELAS syndrome
memory, defect of recent
memory, impairment of
meningeal enhancement
meningismus
meningitis
meningitis, aseptic
meningitis, carcinomatous
meningitis, neutrophilic
meningitis, TB
meningitis, treatment of
meningoencephalitis
mental retardation
mental status, abnormal
metabolic disorder, primary
metabolic disorder, primary-screening tests
microcephaly
micrographia
midbrain, atrophy
midbrain, lesion of
migraine
mimics
miosis
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
monoamine oxidase inhibitors
moro reflex
mortality
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, abnormal, seizure causing
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, negative
MRI, optic nerve
MRI, pelvis
MRI, spinal cord
MRI, sulcal hyperintensity
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle pain
muscle spasm, face
muscle weakness, proximal
mutism
myasthenia gravis
myelitis
myelitis, longitudinal
myelitis, transverse
myelopathy
myeloradiculopathy
myoclonic jerks
myoclonus
myoclonus, face
myoclonus, segmental
myopathy
myopathy, mitochondrial
myopia
myopia, sudden onset of
myxedema, neurologic manifestations of
N20 response
narcolepsy
nasopharyngeal carcinoma
nausea and vomiting
neck stiffness
nerve root enhancement
neuroblastoma
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neurologic examination, focal
neurologic signs
neuron specific enolase
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathy
neuropathy, peripheral
neurotoxin
neutropenia
New England
night sweats
NMDA antagonists
NMDA receptors
noncommunicative
nystagmus
nystagmus, epileptic
nystagmus, monocular
nystagmus, periodic
nystagmus, primary position of gaze
nystagmus, vertical
occipital lobe
occipital lobe, lesion of
ocular dipping
ocular flutter
ocular motility, disorders of
oculogyric crisis
olivary degeneration, hypertrophic
ophthalmoplegia
ophthalmoplegia, neonatal
ophthalmoplegia, progressive external
opisthotonus
opsoclonus
opsoclonus, differential diagnosis of
opsoclonus-myoclonus syndrome
optic atrophy
optic disc edema
optic neuritis
optic neuritis, bilateral
optic neuritis, recurrent
optic neuropathy
optical coherence tomography
orbit, injury of
orbitocranial injury, penetrating
oscillopsia
ovarian tumor
pacemaker, cardiac-transvenous
pain
palatal myoclonus
palpitations
papilledema
paramedian pontine reticular formation
paraparesis
Parkinson disease
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
partial thromboplastin time, prolonged
PAS positive
pericarditis
perineuritis
perineuritis, optic
peripheral nerve, lesion of
personality change
phenylketonuria
phonophobia
pituitary, hormones of
pituitary, lesion of
PLEDs
PLEDs, bilateral independent
pleocytosis of cerebrospinal fluid
pleural effusion
pleurisy
pneumoencephalogram(PEG)
pneumonia
polymerase chain reaction
polymyositis
polypharmacy
pons, lesion of
practice guidelines
precipitating factors
premature infant
prevention of neurologic disorders
prion disease
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
proptosis
protein 14-3-3, cerebrospinal fluid
proteinuria
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychotic behavior
ptosis
pupil
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, dilated, bilateral
pupil, light reflex, abnormal
pupil, tonic
Purkinje cell
Purkinje cell surface antibody
pursuit eye movements, abnormal
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis, progressive
quadriplegia
rabies, nervous system involvement with
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
real-time quaking-induced conversion
recurrent
Red flags
reflex, brainstem
REM sleep
REM sleep behavior disorder
remote effect of cancer on the nervous system
renal failure
renal stones
respiratory failure
retinal degeneration
retinal ischemia
retro-orbital pain
retropulsion
Rett's syndrome
review article
rigidity
risk factors
Romberg's sign
saccadic eye movements
saccadic eye movements, abnormal
salivation, excessive
sarcoidosis
sarcoidosis, CNS
schizophrenia
sedation
sedimentation rate, elevated
seizure
seizure, children
seizure, eye movement induced
seizure, nonconvulsive
seizure, occipital lobe
seizure, stimulus sensitive
selective serotonin reuptake inhibitors
self harm
sensorineural hearing loss
sensory loss
sensory loss, cortical
seroconversion
serologic testing
serotonin
serotonin syndrome
setting sun phenomena
short stature
sicca syndrome
simultanagnosia
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
skull x-ray
skull x-ray, abnormal
sleep
sleep pathology and physiology
somnolence
sonophobia
speech disorder, childhood
speech, delayed development of
spinal cord, lesion of
spirochete infection
spongy degeneration of brain
sporotrichum
square wave jerks
stare
staring spells
status epilepticus
status epilepticus, nonconvulsive
steroid therapy, CNS treatment and complications with
strabismus
striatum, lesion of
strokelike episodes
suck, poor
sweating
symmetric brain lesions
tandem gait, ataxic
tau protein
temporal lobe, lesion
temporal lobe, lesion, bilateral
temporalis muscle wasting
teratoma
teratoma, ovarian
thalamus, lesion of-bilateral
thrombocytopenia
titubation
topiramate
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
triangle of Guillain and Mollaret
trigeminal neuralgia
tuberculosis
tuberculous meningoencephalitis
ultrasonography
unconsciousness
unconsciousness, episodic
unconsciousness, transient
upgaze
upgaze, paralysis of
urinary incontinence
urine test for metabolic disorders
uveitis
vasospasm, cerebral
Venereal Disease Research Laboratory test
ventricular enlargement
vertical gaze
vertigo
viral infection, CNS
vision, blurred
vision, blurred, monocular
visual acuity, decreased
visual fields, constricted
visual impairment
visual loss
visual loss, sudden
vitreous opacities
vocalizations
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weight loss
Whipple's disease
white matter disease
wide based gait
word-finding difficulty
xerophthalmia
xerostomia
Showing articles 150 to 200 of 5788 << Previous Next >>

Sustained Downgaze as the only remained sign after regaining consciousness in hepatic encephalopathy
Neurol Asia 19:105-106, Park, D.G.,et al, 2014

A 75-year-old man with 3 years of Visual Difficulties
Neurol 83:e160-e165, Berkowitz, A.L.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Encephalitis Lethargica (non Economo Disease, sleeping sickness)
Adams & Victors Principles of Neurology, Chp 33, pg 768, Ropper, A.H.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
Adams & Victors Principles of Neurology, Chp 32, pg 710, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Galactosemia
Adams & Victors Principles of Neurology, Chp 37, pg 951, Ropper, A.H.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Subdural Empyema
Adams & Victors Principles of Neurology, Chp 32, pg 711, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Infantile Gaucher Disease
Adams & Victors Principles of Neurology, Chp 37, pg 958, Ropper, A.H.,et al, 2014

Limbic Encephalitis Associated with Anti-Voltage-Gated Potassium Channel Complex Antibodies Mimicking Creutzfeldt-Jakob Disease
JAMA Neurol 71:79-82, Yoo,J.Y. & Hirsch, L.J., 2014

The Clinical Features of Psychogenic Movement Disorders Resembling Tics
JNNP 85:573-575, Baizabal-Carvallo, J.F. & Jankovic, J., 2014

Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
NEJM 370:1830-1841, Case 14-2014, 2014

Actionable Diagnosis of Neuroleptospirosis by Next-Generation Sequencing
NEJM 370:Doi:10.1056/NEJMoal1401268, Wilson, M.R.,et al, 2014

Pathognomonic Seizures in Limbic Encephalitis Associated with Anti-LGl1 antibodies
Lancet 383:2018, Sen, A.,et al, 2014

A 72-year-old Man with Rapid Cognitive Decline and Unilateral Muscle Jerks
Neurol 82:e194-e197, Duncan, M.,et al, 2014

Effect of Rituximab in Patients with Leucine-Rich, Glioma-Inactivated 1 Antibody-Associated Encephalopathy
JAMA Neurol 71:896-900, Irani, S.R.,et al, 2014

Long-Term Improvement of Musicians Dystonia after Stereotactic Ventro-Oral Thalamotomy
Ann Neurol 74:648-654,627, Horisawa, S.,et al, 2013

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

Clinical Reasoning: A 45-year-old Woman with Reversible Bilateral Hearing Loss
Neurol 80:e23-e26, Woo, P.,et al, 2013

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

Basal Ganglia Involvement in Facio-Brachial Dystonic Seizures Associated with LGI1 Antibodies
Neurol 80:e183-184, Plantone, D.,et al, 2013

Paediatric Autoimmune Encephalopathies: Clinical Features, Laboratory Investigations and Outcomes in Patients with or without Antibodies to known Central Nervous System Autoantigens
JNNP 84:748-755, Hacohen, Y.,et al, 2013

The Eye of the Beholder: Inter-rater Agreement among Experts on Psychogenic Jerky Movement Disorders
JNNP 84:742-747, Van de Salm, S.,et al, 2013

Clinicopathologic Conference, West Nile Virus Infection, Case 15-2013
NEJM 368:1919-1927, Vyas, J.,et al, 2013

Subacute Sclerosing Panencephalitis
www.MedLink.com, February, Auwaeter,P.G.&Johnson,R.T., 2013

Clinicopathologic Conference, Dissection of the left vertebral artery and cerebellar infarction
NEJM 369:1736-1748, Case 34-2013, 2013

Miller Fisher Syndrome with Positivity of Anti-GAD Antibodies
Clin Neurol Neurosurg 115:1479-1481, Pietrini, V.,et al, 2013

Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

Development of a Suspicion Index to Aid Diagnosis of Niemann-Pick Disease Type C
Neurol 78:1560-1567,1546, Wijburg, F.A.,et al, 2012

Intracranial Dural Arteriovenous Fistulas: Classification, Imaging Findings, and Treatment
AJNR 33:1007-1013, Gandhi, D.,et al, 2012

Immunotherapy-Responsive Chorea as the Presenting Feature of LGI1-Antibody Encephalitis
Neurol 79:195-196, Tofaris,G.K.,et al, 2012

Migraine in the Borderland of Epilepsy: "Migralepsy" an overlapping syndrome of children and adults?
Epilepsia 53 (Suppl:7):20-25, Kasteleyn-Nolst Trenite, D. & Parisi, P., 2012

Acquired Neurosyphilis Presenting as Movement Disorders
Mov Disord 27:690-695, Shah, B.B. & Lang, A.E., 2012

The Frequency of Autoimmune N-Methyl-D-Aspartate Receptor Encephalitis Surpasses That of Individual Viral Etiologies in Young Individuals Enrolled in the California Encephalitis Project
Clin Inf Dis 54:899-904, Gable, M.S.,et al, 2012

Epstein-Barr Virus Infections of the Nervous System
www.medlink.com, Nov, Amlie-Lefond,C., 2011

Paraneoplastic Upbeat Nystagmus
Neurol 77:691-693, Wray, S.H.,et al, 2011

Movement Disorders Emergencies Part 2 Hyperkinetic Disorders
Arch Neurol 68:719-724, Robottom, B.J.,et al, 2011

Treatment of Severe Neurological Deficits with IgG Depletion through Immunoadsorption in Patients with Escherichia coli O104:H4-Associated Haemolytic Uraemic Syndrome: A Prospective Trial
Lancet 378:1166-1173,1120, Greinacher, A.,et al, 2011

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Presentation, Diagnosis, Pathophysiology, and Treatment of the Neurological Features of Sturge-Weber Syndrome
The Neurologist 17:179-184, Comi, A.M., 2011

Ipsilateral Stroke in a Patient with Horizontal Gaze Palsy with Progressive Scoliosis and a Subcortical Infarct
Stroke 42:e1-e3, Ng, A.S.L.,et al, 2011

Anti-N-Methyl-d-Aspartate Receptor Encephalitis: Characteristic Behavioral and Movement Disorder
Arch Neurol 67:250-251, Ferioli,S.,et al, 2010

Retrospective Analysis of NMDA Receptor Antibodies in Encephalitis of Unknown Origin
Neurol 75:1735-1739, Pr�ss,H.,et al, 2010

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

The Expanding Phenotype of GLUT1-Deficiency Syndrome
Brain & Dev 31:545-552, Brockmann,K., 2009

Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
AJNR 30:1971-1976, Uggetti,C.,et al, 2009

N-Methyl-D-Aspartate Receptor Antibodies in Pediatric Dyskinetic Encephalitis Lethargica
Ann Neurol 66:704-709, Dale,R.,et al, 2009

Medial Medullary Infarction: Clinical, Imaging, and Outcome Study in 86 Consecutive Patients
Stroke 40:3221-3225, Kim,J. &Han,Y., 2009

The Neurologic Manifestations of Systemic Lupus Erythematosus
The Neurologist 15:115-121, Greenberg,B.M., 2009

Neurologic Prognosis After Cardiac Arrest
NEJM 361:605-611, Young,G.B., 2009

Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
Ann Neurol 66:11-18,1, Florance,N.R.,et al, 2009



Showing articles 150 to 200 of 5788 << Previous Next >>