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abscess, intracerebral
abscess, intracerebral, multiple
achilles tendon, enlarged
acute ataxia of childhood
acute cerebellar ataxia
adolescent medicine
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
adverse drug reaction
affect, flat
agitation
akathisia
alcohol intolerance
alpha-synuclein
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
alternating rapid movement, impaired
Alzheimer's disease, misdiagnosis
amphetamines
amyotrophic lateral sclerosis
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
ATP1A3 gene
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 atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
brainstem, syndrome
bulbar palsy
burning paresthesia
C0ORF72
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
children
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
crying, pathologic
cystatin C mutation
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, age at onset
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, thalamic
dementia, transmissible
dementia, treatment of
depression
developmental retardation
diabetes mellitus
diagnostic criteria
diarrhea
diet
differential diagnosis
difficulty climbing stairs
diplopia
disability, neurological
dizziness
dopa responsive dystonia
down-beat nystagmus
DPPX
DPPX, antibodies, encephalitis
driving
drooling
drowsiness
dural arteriovenous malformation
dysarthria
dysdiadochokinesia
dyskinesia
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
Erdheim-Chester disease
escherichia coli
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
foam cells
foot numbness
Friedreich's ataxia
frontal lobe, anatomy and physiology
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
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 swelling
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
histiocytosis
HLA
hoarseness
hyperesthesia
hyperosmolality
hyperreflexia
hypersomnia
hypersomnia, idiopathic
hypoalbuminemia
hypocretin
hypoglycemia
hypometric saccades
hyponatremia
hypophonia
hyposmia
hypothalamus
hypotonia
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunocompetent
immunohistochemistry
immunologic disease
immunomodulation
immunosuppression
immunotherapy
impulsivity
inattention
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intranuclear
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
laughing, pathologic
L-dopa
leg weakness, bilateral
lesions too numerous to count
leucine rich glioma inactivated 1 antibodies
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, adult onset, sporadic
leukopenia
Lewy body
Lewy body disease, diffuse
limbic encephalitis
liver disease
liver function enzymes
lobar atrophy
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
meningitis
meningitis, acinetobacter calcoaceticus var.antitratus
meningitis, carcinomatous
meningoencephalitis
meningoencephalitis, amoebic
mental status, abnormal
microcephaly
microhemorrhage, intracerebral
midbrain
midbrain, atrophy
midbrain, infarction of
midbrain, lesion of
middle cerebellar peduncle, lesion
migraine
mild cognitive impairment
mimics
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
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, angiography
MRI, angiography, false negative
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, fast
MRI, negative
MRI, perfusion
MRI, punctate pattern
MRI, venography
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple sleep latency test
multiple system atrophy
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 intranuclear inclusion disease
neuronal loss
neuronopathy, sensory
neuropathology
neuropathology, brain
neuropathy
neuropathy, sensory
next-generation sequencing
night sweats
Nothnagel's syndrome
numbness, generalized
nutritional deficiency
nystagmus
nystagmus, monocular
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, dystonia with
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, nonmotor problems of
Parkinson disease, presymptomatic detection
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
pathologic reflex
penicillamine
perseveration
personality change
pituitary, hormones of
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
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
precipitating factors
pregnancy, neurologic complications in
prion disease
PRKN gene
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
pseudobulbar palsy
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
recurrent
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
RFC1 gene
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
sensory loss, leg
sexual intercourse
short stature
sinemet
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
status epilepticus
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, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
third nerve palsy
third nerve palsy, bilateral
thrombocytopenia
titubation
tongue, fasciculations of
tonic foot response
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
tremor, postural
trientine dihydrochloride
trinucleotide repeats
uncal herniation
unconsciousness
unconsciousness, episodic
unconsciousness, transient
undiagnosed
upgaze, paralysis of
urinary incontinence
vegetarianism
venous hypertension
venous ischemia
vertigo
vestibular areflexia
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
walking, difficulty with in dark
weakness
weakness, generalized
weakness, progressive
weight gain
weight loss
wheelchair
white matter disease
wide based gait
work loss
workup
zinc
Showing articles 150 to 200 of 1850 << Previous Next >>

Intravenous Alteplase for Stroke with Unknown Time of Onset Guided by Advanced Imaging:Systematic Review and Meta-Analysis of Individual Patient Data
Lancet 396:1574-1585, Thomalla,G.,et al, 2020

Multimodal CT or MRI for IV thrombolysis in ischemic stroke with unknown time of onset
Neurol 95:e2954-e2964, Macha, K.,et al, 2020

Clinical features, prognostic factors, and antibody effects in anti-mGluR1 encephalitis
Neurol 95:e3012-e3025, Spatola, M.,et al, 2020

Recent Administration of Iodinated Contrast Renders Core Infarct Estimation Inaccurate Using RAPID Software
AJNR 41:2235-2242, Copelan, A.Z.,et al, 2020

A Young Generalized Dystonia Patient with Globus-Pallidus-Specific Lesion
Ann Neurol 88:637-638, Wu, H.,et al, 2020

Muscle Stiffness, Gait Instability, and Liver Cirrhosis in Wilsons Disease
Lancet 396:990, Kronlage, C.,et al, 2020

An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
Neurol 95:e1760-e1763, Brigham, E.,et al, 2020

Clinicopathologic Conference, Borrelia Miyamotoi Infection
NEJM 383:1578-1586, Case 32-2020, 2020

Bornavirus Encephalitis Shows a Characteristic Magnetic Resonance Phenotype in Humans
Ann Neurol 88:723-735, Finck, T.,et al, 2020

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

Dressing Apraxia as Initial Manifestation of Creutzfeldt-Jakob Disease
Tremor and Other Hyperkinetic Movements 10:1-3, Heckmann, J.G.,et al, 2020

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

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

Carotid-Cavernous Fistula Presenting with Bilateral Abducens Palsy
Stroke 51:e107-e110, Peng, T.J.,et al, 2020

Functional Gait Disorders
Neurol 94:1093-1099, Nonnekes, J.,et al, 2020

Psychogenic Paroxysmal Hemifacial Spasm
Ann Neurol 88:14-15, Park, J.E., 2020

Involuntary Hand-Shaking: Transient Ischemic Attack, Seizure, or Psychogenic?
Ann Neurol 88:12-13, Sharma, V.K. & Sinha, A.K., 2020

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

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020

Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
Neurol 94:273-275, Macaron, G.,et al, 2020

Tardive Diaphragmatic Tremor
Neurol 94:e656, Gupta, H.V., 2020

A Rare Presentation of Whipple Disease
Neurol 94:e758-e761, Koek, A.T.,et al, 2020

Questionnaire-Based Diagnosis of Benign Paroxysmal Positional Vertigo
Neurol 94:e942-e949, Kim, H.J.,et al, 2020

Homonymous Hemianopia with Normal Magnetic Resonance Imaging
JAMA Ophthalmol doi:10.1001/JAMAOphthalmol.2020.0447, Cai, S.,et al, 2020

Anti-NMDAR Encephalitis with Overlapping Demyelinating Syndrome
Neurol 94:e1866-e1869, Kim, H.W., et al, 2020

Three-year Follow-up of Prospective Trial of Focused Ultrasound Thalamotomy for Essential Tremor
Neurol 93:e2284-e2293, Halpern, C.H.,et al, 2019

Orofacial Dyskinesia in a Young Man
JAMA Neurol 76:1517-1518, Tian, X.,et al, 2019

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

Automated ASPECTS in Acute Ischmeic Stroke: A Comparative Analysis with CT Perfusion
AJNR 40:2033-2038, Sundaram, V.K.,et al, 2019

Rapidly Progressive Vision Loss in a Patient with Breast Cancer
JAMA 322:1098-1099, Izzo, M.C.,et al, 2019

Clinicopathologic Conference, Adenovirus Meningoencephalitis
NEJM 381:1459-1470, Case 31-2019, 2019

Tics and Functional Tic-Like Movements
Neurol 93:750-758, Ganos, C.,et al, 2019

Chronic Dengue Virus Panencephalitis in a Patient with Progressive Dementia with Extrapyramidal Features
Ann Neurol 86:695-703, Johnson, T.P.,et al, 2019

Acute Rheumatic Fever: Clinical Manifestations and Diagnosis
www.UptoDate.com, Oct, Steer, A. & Gibofsky, A., 2019

Sydenham Chorea
www.UptoDate.com, Oct, Gilbert, D.L., 2019

Automated CT Perfusion Imaging for Acute Ischemic Stroke
Neurol 93:888-898, Vagal, A.,et al, 2019

No-Cutoff Large Vessel Occlusion Stroke
Neurol 93;1014-1015, Atchaneeyasakul, K.,et al, 2019

Childhood Primary Angiitis of the Central Nervous System
www.UptoDate.com, Dec, Twilt, M. & Benseler, S., 2019

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

A 47-year-old Man with Diffuse White Matter Disease and Rapidly Progressive Dementia
Neurol 92:e2832-e2837, Di Luca, D.G.,et al, 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

Extending Thrombolysis to 4.5-9 h and Wake-Up Stroke Using Perfusion Imaging: A Systematic Review and Meta-Analysis of Individual Patient Data
Lancet 394:139-147,97, Campbell, B.C.V.,et al, 2019

A Misdiagnosis of Atypical Trigeminal Neuralgia
Neurol 93:124-131, Duvall, J.R. & Robertson, C.E., 2019

Thrombolysis Guided by Perfusion Imaging up to 9 Hours after Onset of Stroke
NEJM 380:1795-1803,1865, Ma, H.,et al, 2019

A 68-year-old Man with Rapid Cognitive Decline
Neurol 93:315-318, Berth, S.H.,et al, 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

MR Imaging of the Brain in Neurologic Wilson Disease
AJNR 40:178-183, Yu, X.-E.,et al, 2019

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

A 61-Year-Old Woman with Acute Onset Dysgraphia
Neurol 92:e386-e391, Smith, L.R.,et al, 2019

Bobblehead-Doll Syndrome
NEJM 380:e5, Sacks, C.A., 2019



Showing articles 150 to 200 of 1850 << Previous Next >>