Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
acute ataxia of childhood
acute cerebellar ataxia
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
adverse drug reaction
affect, flat
agitation
akathisia
alcohol intolerance
alpha-synuclein
alternating rapid movement
alternating rapid movement, impaired
Alzheimer's disease, misdiagnosis
amphetamines
anemia
angiography, cerebral
animal exposure
ankle edema
anorexia
anosmia
anti IgLON5
anti Tr antibodies
anti Yo antibody
antidepressant
aphasia
aphonia
apnea
areflexia
ascites
ataxia
ataxia telangiectasia
ataxia, acute onset
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
atypical
autoantibodies
autoimmune cerebellar ataxia
autoimmune disease
autoimmune encephalopathy
automatic behavior
automobile accidents
autonomic dysfunction
axonal spheroid
B 12 deficiency
B12
Babinski sign
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
Benedikt's syndrome
biologic markers
bovine spongiform encephalopathy
bradykinesia
bradyphrenia
brain biopsy
brainstem, atrophy
brainstem, lesion of
brainstem, syndrome
bulbar palsy
burning paresthesia
CAG repeats
carbon monoxide poisoning
carcinoma
carcinoma of breast
CAT scan, abnormal
CAT scan, angiography
CAT scan, angiography, false negative
CAT scan, emission, abnormal
CAT scan, venography
catalepsy
cataplexy
cataracts
cauda equina, enhancement
caudate nucleus, lesion of, bilateral
central nervous system, infection of
cerebellar ataxia, autosomal recessive
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar cognitive affective syndrome
cerebellar degeneration
cerebellar lesion
cerebellitis
cerebellitis, autoimmune
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral edema
cerebrospinal fluid, abnormal
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident, mimics
ceruloplasmin, serum
chewing movements
chills
choking
chorea
choreoathetosis
chromosomal abnormality
cingulate island sign
Claude's syndrome
Clinical Pathologic Conference(C.P.C.)
clonus
cognition
cognition, slowed
cogwheel rigidty
coma
coma, episodic
complications
confabulation
confusion
constipation
controversies in neurology
conversion reaction
corpus callosum, lesion of
cough
cranial nerve enhancement
cranial neuropathy
cranial neuropathy, multiple
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, age at onset
dementia, familial
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, thalamic
dementia, transmissible
dementia, treatment of
depression
diabetes mellitus
diagnostic criteria
diarrhea
diet
difficulty climbing stairs
diplopia
disability, neurological
dizziness
DPPX
DPPX, antibodies, encephalitis
driving
drooling
drowsiness
dural arteriovenous malformation
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dystonia
dystonia, face
dystonia, focal
ear, pain in
edema, pedal
efficacy
electroencephalogram, periodic complexes
electromyogram
encephalitis
encephalitis, acanthamoeba
encephalitis, amebic
encephalitis, autoimmune
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, delayed
encephalopathy, progressive
enolase
epidemiology of neurology
episodic disorders
episodic neurologic deficits
episodic unconsciousness
Epstein-Barr virus
esophageal varices
executive dysfunction
exercise intolerance
eye movement, disorders of
facial expression abnormality
faciobrachial dystonic seizure
falling
false negative
familial
fasciculation
fatal familial insomnia
fatigue
fever
fine motor function, impaired
finger nose finger test
finger numbness
fingerprint bodies
Fisher C.M.
fistula, arterio-venous, dural
fluency
Friedreich's ataxia
frontal lobe, anatomy and physiology
gait disorder
gait, festinating
gamma amino butyric acid
gammaglobulin therapy, intravenous
gaze palsy, horizontal
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
genu of corpus callosum
granular osmiphilic material
growth hormone
gyrus, abnormal
hallucination
hallucination, hypnagogic
hallucination, visual
hand weakness
hands, fisted
handwriting
head nodding
headache
hearing loss
heel-knee-shin test
hemidystonia
hemimyoclonic jerks
hemiparesis
hemorrhage, thalamic
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
heralding manifestation
herniation syndromes, intracranial
HLA
hoarseness
hyperesthesia
hyperosmolality
hyperreflexia
hypersomnia
hypersomnia, idiopathic
hypoalbuminemia
hypocretin
hypoglycemia
hypometric saccades
hyponatremia
hypophonia
hyposmia
hypothalamus
hypotonia
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunohistochemistry
immunologic disease
immunomodulation
immunosuppression
immunotherapy
impulsivity
inattention
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incontinence, fecal
incoordination
infectious mononucleosis
infectious mononucleosis, neurologic findings with
inferior olivary nucleus
insight, loss
insomnia
intellectual deficit
intellectual deterioration
intracranial hypertension, benign
intracranial pressure, increased
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
Kayser-Fleischer ring
lactic acidemia
lateropulsion
leucine rich glioma inactivated 1 antibodies
leukodystrophy
leukoencephalopathy
leukoencephalopathy, adult onset, sporadic
leukopenia
Lewy body
Lewy body disease, diffuse
limbic encephalitis
liver disease
liver function enzymes
logopenia
lumbar puncture, complications of
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
masked facies
MELAS syndrome
memory, defect of recent
memory, impairment of
meningeal enhancement
meningoencephalitis
meningoencephalitis, amoebic
mental status, abnormal
microhemorrhage, intracerebral
midbrain
midbrain, atrophy
midbrain, infarction of
midbrain, lesion of
migraine
mild cognitive impairment
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
modafinil
molecular genetics
monoclonal antibodies
mood change
mortality
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, angiography
MRI, angiography, false negative
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, negative
MRI, perfusion
MRI, punctate pattern
MRI, venography
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple sleep latency test
muscle biopsy
muscle weakness, proximal
mutism
myasthenia gravis
myelinolysis, extrapontine
myelomalacia
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopathy, mitochondrial
myxedema, neurologic manifestations of
narcolepsy
nausea and vomiting
negative
nerve conduction studies
nerve root biopsy
neuroaxonal dystrophy
neuroaxonal leukodystrophy
neuroleptic
neuroleptic sensitivity
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuron specific enolase
neuronal ceroid-lipofuscinosis
neuronal loss
neuronopathy, sensory
neuropathology
neuropathology, brain
neuropathy
neuropathy, sensory
next-generation sequencing
night sweats
Nothnagel's syndrome
numbness, generalized
nutritional deficiency
nystagmus
nystagmus, primary position of gaze
old age, neurology of
olivary degeneration, hypertrophic
ophthalmoplegia
ophthalmoplegia, progressive external
opportunistic infection
opportunistic infection, CNS
optic atrophy
orthostatic hypotension
osmotic demyelination syndrome
otitis, neurologic complications with
palatal myoclonus
paraneoplastic cerebellar degeneration
parasitic infection
parasitic infection, CNS
paresthesias
paresthesias, hands
parietal lobe, atrophy
Parkinson disease
Parkinson disease, dementia with
Parkinson disease, L-dopa nonresponsive
Parkinson disease, nonmotor problems of
Parkinson disease, presymptomatic detection
Parkinsonism syndrome
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
penicillamine
perseveration
personality change
pituitary, hormones of
pleocytosis of cerebrospinal fluid
POLG1 gene
polymerase chain reaction
polyneuropathy, chronic inflammatory demyelinating
polysomnogram
pons, lesion of
positional head-hanging test
post infectious cerebellar ataxia
posterior cortical atrophy
postinfectious
postural abnormality
potassium channel antibodies
practice guidelines
pregnancy, neurologic complications in
prion disease
prognosis
progressive ataxia and palatal tremor
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
proteinuria
protozoan infection
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
ptosis
ptosis, bilateral
pull test
pupil, dilated and fixed, bilateral
pursuit eye movements, abnormal
rapid onset dystonia parkinsonism
rapidly fatal neurologic illness
rapidly progressing neurologic illness
reading disorder, acquired
real-time quaking-induced conversion
regional cerebral blood flow
rehabilitation for neurologic disorders
release phenomena
REM sleep
REM sleep behavior disorder
remote effect of cancer on the nervous system
renal failure
renal stones
retropulsion
review article
rigidity
ritalin
rituximab
Romberg's sign
saccadic eye movements, abnormal
safety
salivation, excessive
sarcoidosis
schizophrenia
seizure
seizure, psychomotor-temporal lobe
selective serotonin reuptake inhibitors
sensorineural hearing loss
sexual intercourse
short stature
single photon emission computed tomography
sleep
sleep apnea
sleep offset paralysis
sleep onset paralysis
sleep paralysis
sleep pathology and physiology
slit lamp examination
slurred speech
smell
snoring
somnolence
spasticity
speech disorder
speech disorder, non aphasic
spinocerebellar ataxia
spinocerebellar ataxia type 7
splenomegaly
spongy degeneration of brain
spontaneous remission
square wave jerks
staggering
startle myoclonus
startle reaction
stimulant drugs
storage disease of CNS
strokelike episodes
stuttering
suicide
swallow evaluation
sweating
symmetric brain lesions
synucleinopathy
systemic illness
tandem gait, ataxic
tau protein
tauopathy
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
third nerve palsy
third nerve palsy, bilateral
thrombocytopenia
titubation
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trientine dihydrochloride
trinucleotide repeats
uncal herniation
unconsciousness
unconsciousness, episodic
unconsciousness, transient
undiagnosed
upgaze, paralysis of
urinary incontinence
vegetarianism
venous hypertension
venous ischemia
vertigo
vestibulopathy
vibratory sensation, abnormal
viral infection
viral infection, CNS
vision, blurred
visual acuity, decreased
visuospatial disturbance
vitamin deficiency
vitamin E deficiency
vitiligo
vocalizations
voice, abnormality of
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weight gain
weight loss
wheelchair
white matter disease
wide based gait
work loss
workup
zinc
Showing articles 0 to 50 of 1814 Next >>

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

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

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,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

Vitamin B12 Deficiency in a 29-Year-Old Woman
Neurol 97:e643-e646, Huddar, A.,et al, 2021

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

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

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

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

A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
Neurol 94:e1664-e1669, Han, F.,et al, 2020

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

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

A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
Neurol 89:e182-e187, Tabuas-Pereira, M.,et al, 2017

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

Clinicopathologic Conference, Granulomatous Amebic Encephalitis and Sarcoidosis (Inactive)
NEJM 376:368-379, Case 3-2017, 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

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

Diagnosis and Management of Dementia with Lewy Bodies
Neurol 89:88-100, McKeith, I.G.,et al, 2017

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

Non-Alzheimers Dementia 2 Lewy Body Dementias
Lancet 386:1683-1697, Walker, Z.,et al, 2015

Progressive Neuropsychiatric Symptoms and Motor Impairment
JAMA Neurol 71:794-798, Ghadiri, M.,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

Clinicopathologic Conference, Acute Infectious Mononucleosis due to Epstein-Barr Virus Infection, Complicated by Acute Otitis Media and Postinfectious Cerebellitis
NEJM 369:1253-1261, Case 30-2013, 2013

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

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

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

Clinicopath conf., Human Prion Disease, Sporadic CJD
Neurol 69:1881-1887, Geschwind,M.D., et al, 2007

A 75-Year-Old Man With Cognitive Impairment and Gait Changes, Lewy Body Disease
Neurol 69:1183-1189, Lippa,C.F.,et al, 2007

Clinicopath Conf., Paraneoplastic Cerebellar Degeneration Due to Anti-Yo Antibodies From Breast Cancer
NEJM 356:612-620, Case 4-2007, 2007

Narcolepsy With Cataplexy
Lancet 369:499-511, Dauvilliers,Y.,et al, 2007

The Parkinsons Complex: Parkinsonism Is Just the Tip of the Iceberg
Ann Neurol 59:591-596, Langston,J.W., 2006

The Neurobiology, Diagnosis, and Treatment of Narcolepsy
Ann Neurol 53:154-166, Scammell,T.E., 2003

Clinicopath Conf, Primary Lymphoma of CNS
NEJM 346:1009-1015, Case 10-2002, 2002

Diagnostic Aspects of Narcolepsy
Neurol 50:S2-S7, Aldrich,M.S., 1998

Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998

Delayed Emergence of a Park Dis in 38% of 29 Older Men Initially Dx with Idiop REM Sleep Behavior Disorder
Neurol 46:388-393, Schenck,C.H.,et al, 1996

The Narcolpetic Syndrome
JNNP 59:221-224, Parkes,J.D.,et al, 1995

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Midbrain Syndromes of Benedikt, Claude, and Nothnagel:Setting the Record Straight
Neurol 42:1820-1822, Liu,G.T.,et al, 1992

Neurological and Neuropsychiatric Spectrum of Wilson's Disease:A Prospective Study of 45 Cases
J Neurol 238:281-287, Oder,W.,et al, 1991

Narcolspey
NEJM 323:389-394, Aldrich,M.S., 1990

Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
Arch Neurol 44:365-370, Starosta-Rubinstein,S.,et al, 1987

Narcolepsy-Cataplexy
Arch Neurol 39:164-168, Kales,A.,et al, 1982

Narcolepsy:Regional Cerebral Blood Flow During Sleep & Wakefulness
Neurol 29:61-67, Sakai,F.,et al, 1979

Narcolepsy
NEJM 288:1156, Zarcone,V., 1973

A Simple Test of Cordination in the Fingers
Neurol 10:745, Fisher,C.M., 1960

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024



Showing articles 0 to 50 of 1814 Next >>