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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 50 to 100 of 5788 << Previous Next >>

Case Records of MGH
NEJM 288:674, Cerebral Abscess-Bacterial1973., , 1973

Encephalomyelopathy of Leigh
Editorial BMJ 238, 1971, May., , 1971

Behcets Syndrome
NEJM 390:640-651, Saadoun,D.,et al, 2024

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

Primary Central Nervous System Lymphoma:Clinical Features, Diagnosis, and Extent of Disease Evaluation
www.UptoDate.com, Jan, Nayak,L & Batchelor,T., 2024

Ocular Myasthenia Gravis, Central Ocular Motor Signs and Unilateral Visual Loss Caused by the Great Neuro-Ophthalmologic Impersonator
Neurol 102:e209260, Young,A. & Johnston,J.L., 2024

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024

Clinicopathologic Conference, Thyrotoxic Periodic Paralysis Associated with Graves Disease
NEJM 390:1514-1522, Case 13-2024, 2024

Wall-Eyed Bilateral Internuclear Ophthalmoplegia Variant Syndrome Caused by Isolated Left Thalamic Infarction
Neurol 102:e209475, Wu,B.P.,et al, 2024

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

Paraneoplastic Calmodulin Kinase-Like Vesicle-Associated Protein (CAMKV) Autoimmune Encephalitis
Ann Neurol 96:21-33, Gilligan,M.,et al, 2024

The "Chameleon Eyes Sign" in Myasthenia Gravis
Neurol 103:e209756, Zara,P.,et al, 2024

Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
Neurol 103:e209844, Dhawan,A.,et al, 2024

Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
Neurol 101:e1884-e1892, van der Veen,S.,et al, 2023

Clinicopathologic Conference, Functional Seiaures
NEJM 388:1210-1218, Case 10-2023, 2023

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
UptoDate.com, March, Flanagan,E.P. & Tillema,J-M, 2023

A Teenager with Chronic Meningitis-Does Occams Razor Apply?
Neurol 100:828-835, Havuluri,H.,et al, 2023

Clinicopathologic Conference, Factitious Disorder
NEJM 388:1609-1615, Case 13-2023, 2023

A 25-Year-Old Woman With Eye Swelling and HEadache
Neurol 100:879-883, Hehir,A.,et al, 2023

A Young Man with Daily Episodes of Altered Awareness
Neurol 98:e1197-e1203, Villamar, M.F.,et al, 2022

A Dizzy Architect
Neurol 98:543-549, Scutelnic, A.,et al, 2022

A 48-Year-Old Woman Presenting with Vertigo, Ptosis, and Red Eyes
Neurol 98:678-683, Kim, K.T.,et al, 2022

A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

Bilateral Complete Ophthalmoplegia in a 50-Year-Old Man
JAMA Neurol 79:724-725, Arora, N.,et al, 2022

A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
Neurol 99:26-30, Cao, T.Q.,et al, 2022

Neuroimaging Biomarkers in a Patient with Probable Psychiatric-Onset Prodromal Dementia with Lewy Bodies
Neurol 99:654-657, Urso, D.,et al, 2022

Functional Neurological Disorders
Neurologist 27:276-289, Mishra, A. & Pandey, S., 2022

Sturge-Weber Syndrome
www.UptoDate.com,Dec, Patterson,M.C., 2022

A 56-Year-Old Man with Unusual Presentation of Subacute Encephalopathy and Seizure
Neurol 98:e95-e102, Wang, T.,et al, 2022

Choreoathetosis and Focal Dystonia in Vitamin B12 Deficiency
Neurol 97:e1545, Ng, C.F.,et al, 2021

A Teenager with Shortness of Breath and Difficulty Walking
Neurol 96:e2346-e2350, Liu, S.C.,et al, 2021

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

Rapidly Progressive Thalamic Dementia
Neurol 96:e809-e813, Rizzo, A.C.,et al, 2021

A 48-Year-Old Man Presenting With Diplopia
Neurol 96:399-405, Pehere,N.K.,& Gofer,K., 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020

A 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
Neurol 94:713-717, Silverman, A.,et al, 2020

Sensory Ganglionopathy
NEJM 383:1657-1662, Amato, A.A. & Ropper, A.H., 2020

Clinicopathologic Conference, LGI1 autoimmune encephalitis
NEJM 382:1943-1950, Case 15-2020, 2020

Progressive Ataxia and Palatal Tremor
Neurol 94:e1445-e1447, Pradeep, S.,et al, 2020

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

Characteristic Head Jerks in Congenital Oculomotor Apraxia due to Joubert Syndrome
Neurol 93:e1125-e1126, Borngraber, F.,et al, 2019

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
Neurol 92:e274-e281, Chen, Z. & Neo, S., 2019

Recurrent Involuntary Contractions of the Face, Arm, and Leg in an Elderly Man
JAMA Neurol 76:728-729, Kim, D.D.,et al, 2019

Behcet Disease
emedicine.medscape.com Dec, Davey-Ranasinghe, N. & Diamond, H.S., 2018

Clinicopathological Conference, Insulinoma
NEJM 379:376-384, Case 23-2018, 2018



Showing articles 50 to 100 of 5788 << Previous Next >>