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abdominal protrusion
abdominal x-ray
abducens nerve paralysis
abiotrophy
achilles tendon, enlarged
adult polyglucosan body disease
advance directives
advances in neurology
adverse drug reaction
agnosia
agnosia, visual
akinesia of eyelid function
algorithm
alpha coma
Alzheimer's disease
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis-like syndrome
anisocoria
anomic aphasia
anti GQ1b IgG antibody
anti IgLON5
anti Ri antibody
antitoxin
aphasia
aphasia, progressive, primary
apnea
applause sign
apraxia
apraxia of eyelid opening
areflexia
arm swing, reduced
arm weakness
arthralgia
aspiration
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
autoantibodies
autonomic dysfunction
autonomic dysfunction, acute
autonomic neuropathy
axonal degeneration
Babinski sign
basal ganglia, lesion of
behavioral disorder
Bickerstaff's brainstem encephalitis
biologic markers
BiPAP
bismuth
bladder dysfunction
blepharospasm
botulinum toxin
botulism
botulism antitoxin
botulism immune globulin
botulism, infant
brain atrophy
brainstem
brainstem, dysfunction
brainstem, lesion of
bulbar dysfunction
bulbar palsy
bulbar palsy, acute
bulbar palsy, childhood
bulbar palsy, juvenile
bulbar palsy, progressive
C0ORF72
CAG repeats
calcification, intracranial
camptocormia
carcinoma
carcinoma of bladder
carotid angiogram
CAT scan, abnormal
CAT scan, emission, abnormal
central hypoventilation
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral infarction, subcortical
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
Charcot's sign
chewing, impaired
choking
chorea
clam poisoning
Clinical Pathologic Conference(C.P.C.)
clonus
cognition
cogwheel rigidty
coma
coma, episodic
compulsivity
confusion
corpus callosum, lesion of
corpus callosum, thinning
cough
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
crying
crying, pathologic
cystatin C mutation
deafness
deafness, bilateral progressive vs.unilateral acute
deafness, unilateral
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
depression
diabetes mellitus
diaphragmatic paralysis
differential diagnosis
difficulty climbing stairs
diplopia
disorientation
distal muscle weakness
DNA probes
downward gaze
drooling
drowsiness
dying
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dysphonia
dyspnea
dystonia
dystonia, cervical
ears of the Lynx MR sign
electromyogram
electromyogram, decremental response
emergencies, neurologic
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalomyelitis
encephalopathy
enterovirus
epidemiology of neurology
episodic disorders
episodic neurologic deficits
episodic unconsciousness
Erdheim-Chester disease
executive dysfunction
extrapyramidal movement disorder, progressive
eye movement, disorders of
Fabry's disease
facial nerve palsy
facial nerve palsy, bilateral
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatigable chewing
fatigue
feeding disorder
fever
fibrillations
fine motor function, impaired
fish poisoning
Fisher's syndrome
flaccid paralysis
flail arm syndrome
foam cells
food poisoning
food-borne infection
foot drop
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gag reflex, depressed
gait disorder
gait, apraxic
gait, spastic
gastroparesis
gastrostomy
gastrostomy, percutaneous endoscopic
gaze palsy
gaze palsy, horizontal
gaze palsy, horizontal-bilateral
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic neurologic disorders
genetic testing
glabellar sign
glycogen storage disease
granulomatosis with polyangiitis
granulomatous disease
grasp reflex
Guillain Barre syndrome
Guillain Barre syndrome, axonal form
Guillain Barre syndrome, variant forms of
gynecomastia
hand weakness
head bobbing
headache
hearing loss
heel swelling
hemianopia
hemifacial spasm
hemiparesis
heralding manifestation
histiocytosis
histochemistry of muscle
HLA
hoarseness
honey
hospice
hyperreflexia
hypersomnia
hypertension
hypometric saccades
hypophonia
hyporeflexia
hypotension, systemic
hypotonia
hypotonia, infants
ideomotor apraxia
imbalance
immunotherapy
impulsivity
inclusion bodies
inclusion bodies, intracytopasmic
infant, evaluation of
insomnia
intellectual deficit
intellectual deterioration
internal capsule
intracerebral hemorrhage
intrinsic hand muscles, wasting of
irritability
irritable baby
jaw clonus
jaw jerk, abnormal
Jewish
Kugelberg-Welander syndrome
lacunar infarction
language disorder in adults
laughing
laughing, pathologic
L-dopa
leg weakness, bilateral
leg weakness, unilateral
lethargy
leukoencephalopathy
leukopenia
lid closure, weakness of
life expectancy
lip, biting
lobar atrophy
loss of sympathy
lymphoma involving CNS
lymphomatoid granulomatosis
malignancy screen
masked facies
memory, defect of recent
memory, impairment of
meningitis, aseptic
mental status, abnormal
microhemorrhage, intracerebral
midbrain
midbrain, atrophy
middle cerebellar peduncle, lesion
migraine
Mills syndrome
mimics
misdiagnosis
mitochondrial disease
monoclonal gammopathy
mood change
mortality
motor neuron disease
motor neuron disease, misdiagnosis
MRI
MRI, abnormal
MRI, mouse ears
MRI, negative
MRI, serial
multiple sclerosis, differential diagnosis of
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle spasm, face
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
mutism
myasthenia gravis
myasthenia gravis, presenting manifestations
myasthenic syndrome
myelitis
myelomalacia
myeloneuropathy
myoclonic jerks
myoclonus
myokymia
myokymia, facial
myopathy
myopathy, mitochondrial
myorhythmia
nasal speech
nausea and vomiting
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
nerve conduction studies
nerve injury
neurogenic bladder
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction
neuromuscular junction, abnormality of
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neuroprotective agents
neurotoxic
neurotoxin
next-generation sequencing
nystagmus
nystagmus, dissociated
nystagmus, vertical
obsessive-compulsive disorder
ocular myopathy
ocular myopathy, differential diagnosis
oculocephalic reflex
opened mouth
ophthalmoplegia
ophthalmoplegia, acute
ophthalmoplegia, bilateral, acute
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic atrophy
pain
pain, abdominal
pain, management of chronic
palate, paralysis
palliative care
paralysis
paralysis, acute
paralysis, acute areflexic
paraneoplastic brainstem encephalitis
paraparesis
paraparesis, familial spastic
paraparesis, spastic
parasomnia
paraspinal muscle
paraspinal muscle weakness
Parkinson disease
Parkinson disease, axial symptoms
Parkinson disease, tremor, absence of
Parkinsonism syndrome
pathologic reflex
penguin silhouette sign
Pick bodies
Pick's disease
pleocytosis of cerebrospinal fluid
poliomyelitis
poliomyelitis vaccine
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymyositis
post infectious polyneuropathy
post polio syndrome
postural abnormality
practice guidelines
prevention of neurologic disorders
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
progressive supranuclear palsy
proximal muscle atrophy
pseudobulbar palsy
pseudoxanthoma elasticum
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
ptosis, bilateral
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, oval
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
quality of life
radiation therapy, CNS treatment and complications with
radiculopathy
ragged-red fibers
rapidly progressing neurologic illness
rash
release phenomena
REM sleep behavior disorder
remote effect of cancer on the nervous system
repetitive nerve stimulation
respirations in CNS disease
respirator
respiratory failure
respiratory tract infection
retrocollis
retropulsion
review article
rigidity
rigidity, axial
riluzole
risk factors
saccadic eye movements, abnormal
salivation, excessive
saxitoxin
seizure
semantic dementia
sequencing difficulty
shell fish poisoning
sinemet
skin, lesions in neurologic disorders
sleep
sleep apnea, obstructive
sleep pathology and physiology
small vessel disease
small vessel disease, cerebral
spastic paraplegia, type 11
spasticity
speech disorder
speech, loss of
spinal cord, lesion of
spinal cord, pathologic exam of
spinal muscular atrophy
splenomegaly
standing difficulty
startle reaction
stem cell transplantation
steroid therapy, CNS treatment and complications with
stooped posture
subarachnoid hemorrhage
suck, poor
systemic illness
tachycardia
tandem gait, ataxic
tau protein
tauopathy
temporal lobe
temporal lobe, atrophy
temporalis muscle wasting
thrombocytopenia
tinnitus
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, weakness
toxins, nervous system
transverse smile
trauma
treatment of neurologic disorder
tremor
tremor, jaw
tremor, postural
trinucleotide repeats
tripping
unconsciousness
unconsciousness, episodic
unconsciousness, transient
urinary incontinence
urinary retention
vertigo
vestibular function, tests of
viral infection
viral infection, CNS
vision, blurred
visual symptoms
vocal cord paralysis
vocalizations
walking, difficulty with
weakness
weakness, acute
weakness, fatiguable
weakness, focal
weakness, generalized
weakness, infant
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weight loss
West Nile fever
wheelchair
white matter disease
white matter disease, subcortical
word-finding difficulty
X-linked bulbospinal neuronopathy
Showing articles 100 to 150 of 3938 << Previous Next >>

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Mystery Case: A 48-year-old Woman with Bizarre Behavior, Neurologic Symptoms, and Progressive Decline
Neurol 90:242-247, Kesari, N.K.,et al, 2018

Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018

A Man with Rapidly Progressive Weakness and Respiratory Failure
Neurol 91:e686-e691, Xu,D.,et al, 2018

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
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A Child with Arthrogryposis
Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
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Orbital Apex Syndrome
NEJM 378:18, Sacks. C.A., 2018

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
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Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
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Intracranial Dural Arteriovenous Fistulae
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

Cranial Nerve Hypertrophy in IgG4 Anti-Neurofascin 155 Antibody-Positive Polyneuropathy
Neurol 88:e52, Franques, J.,et al, 2017

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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An 11-year-old Boy with Language Disorder and Epilepsy
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Rapid Multifocal Neurologic Decline in an Immunocompromised Patient
JAMA Neurol 73:226-231, Kromm, J.A.,et al, 2016

A 37-Year-Old Man with Multiple Cranial Neuropathies
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Acute Bulbar Palsy as a Variant of Guillain-Barre Syndrome
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Leptomeningeal Enhancement in a Patient with Progressive Cranial Neuropathies and Lumbosacral Radiculopathies
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Clinical Manifestations of Myasthenia Gravis
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A 30-year-old Man with Progressive Weakness and Atrophy
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Rapidly Progressive Quadriplegia and Encephalopathy
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Myasthenia Gravis
NEJM 375:2570-2581, Gilhus, N.E.,et al, 2016

Acute Flaccid Myelitis; A Clinical Review of US Cases 2012-2015
Ann Neurol 80:326-338, Messacar, K.,et al, 2016

Ocular Manifestations in Systemic Lupus Erythematosus
Br J Ophthalmol 100:135-144, Silpa-Archa,S.,et al, 2016

Paraneoplastic Cerebellar Degeneration with Anti-Yo Antibodies - A Review
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MRI Findings in Children with Acute Flaccid Paralysis and Cranial Nerve Dysfunction Occurring during the 2014 Enterovirus D68 Outbreak
AJNR 36:245-250, Maloney, J.A.,et al, 2015

Tonic Eye Deviation in Stiff-Person Syndrome
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A 44-year-old Woman with Rapidly Progressive Weakness and Ophthalmoplegia
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The Acquired Metabolic Disorders of the Nervous System, Central Pontine Myelinolysis and other Patterns of Osmotic Demyelination
Adams & Victors Principles of Neurology Chp 40, pg 1149, Ropper, A.H.,et al, 2014

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

Intracranial Neoplasms and Paraneoplastic Disorders, Gliomatosis Cerebri
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Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
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Progressive Parkinsonism, Balance Difficulties, and Supranuclear Gaze Palsy
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Brugada Syndrome in Spinal and Bulbar Muscular Atrophy
Neurol 82:1813-1821, Araki, A.,et al, 2014

The Limbic-Girdle Muscular Dystrophies
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Juvenile Myasthenia Gravis: Recommendations for Diagnostic Approaches and Treatment
Neuropediatrics 45:75-83, Marina, A.D.,et al, 2014

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

Functional Impairment in Progressive Supranuclear Palsy
Neurol 80:380-384, Duff, K.,et al, 2013

Peripheral Neuropathy - Lead Astray?
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Facial Bradykinesia
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Incidence and Pathology of Synucleinopathies and Tauopathies Related to Parkinsonism
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Brain Abnormalities as an Initial Manifestation of Neuromyelitis Optica Spectrum Disorder
MSJ 17:1107-1112, Kim, W.,et al, 2013

Bilirubin-Induced Neurologic Damage - Mechanisms and Management Approaches
NEJM 369:2021-2030, Watchko, J.F.,et al, 2013



Showing articles 100 to 150 of 3938 << Previous Next >>