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abscess, intracranial
achilles tendon, enlarged
aciduria
acute disseminated encephalomyelitis
adult polyglucosan body disease
adult-onset leukodystrophy, with neuroaxonal spheroids
adverse drug reaction
akathisia
algorithm
alternating hemiplegia
alternating hemiplegia of childhood
amimia
aneurysm
anterior tibial muscle weakness
antiviral agents
areflexia
arthrogryposis multiplex
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic-dystonia syndromes
ATP1A3 gene
attention deficit disorder with hyperactivity
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autoimmune meningitis
autonomic dysfunction
axonal degeneration
axonal spheroid
Babinski sign
basal ganglia, lesion, bilateral
beta-D-glucon
bladder dysfunction
brain biopsy
brain biopsy, false negative
brain biopsy, indication
brainstem, atrophy
brainstem, lesion of
bronchoscopy
bruising
bulbar palsy
calcification, intracranial
candida albicans
cane
CAT scan, abnormal
CAT scan, disappearing lesion on
central nervous system, infection of
cerebellar ataxia, children
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral infarction, subcortical
cerebral palsy
cerebral palsy, etiology
cerebral palsy, work up
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, beta-D-glucan
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular accident, mimics
chemical meningitis
chest x-ray, abnormal
chewing movements
children
chorea
choreoathetosis
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
clonus
clubfoot as related to neurologic disease
Coats plus
cobalamin C deficiency
cognition
coinfection
cold intolerance
collagen vascular disease
complications
confabulation
congenital myasthenic syndromes
consanguinity
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
cranial nerve enhancement
cranial neuropathy
creatine phosphokinase(CPK)elevated
crying, pathologic
cryptococcal meningitis
cyst
cyst, benign intracranial
cyst, cortical parenchyma
cyst, parenchymal
cystatin C mutation
deafness
degenerative diseases of CNS
delay in diagnosis
delayed muscle relaxation
dementia
dementia, presenile
dementia, rapidly progressive
dental infection
developmental disability
developmental retardation
diagnostic criteria
diet
differential diagnosis
difficulty going down stairs
diplopia
distal muscle atrophy
distal muscle weakness
DNA sequencing
dopa responsive dystonia
double-cortex syndrome
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
DYSF gene
dysferlinopathy
dysmetria
dysphagia
dystonia
dystonia, children
Ehlers-Danlos syndrome
Ehlers-Danlos syndrome, classification
electromyogram
empyema, subdural
encephalitis
encephalitis, acute
encephalitis, autoimmune
encephalitis, diagnosis of
encephalitis, etiology
encephalitis, Japanese
encephalitis, viral-causes of
encephalopathy
eosinophilia
Erdheim-Chester disease
exome sequencing
Fabry's disease
facial weakness
falling
false negative
familial
fasciculation
fatal familial insomnia
fatigue
fever
fibrillations
fine motor function, impaired
fish
floppy infant
foam cells
fourth ventricle, compression
fungal infection
fungal infection, CNS
gait disorder
gait, spastic
GAMT gene
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
geographic location
globus pallidus, lesion of, bilateral
GLUT1 deficiency syndrome
glycogen storage disease
gram positive cocci
gray hair
hammertoes
headache
headache, awakening with
headache, positional
headache, progressive
hearing loss
heel swelling
helminthic infection of CNS
hemianopia, homonymous
hemiparesis, transient
hemophagocytic lymphohistiocytosis
heralding manifestation
herpes simplex encephalitis
heterotopia
high arched feet
high arched palate
histiocytosis
human genome
hydrocephalus
hydrocephalus, non-communicating(obstructive)
hyperhomocysteinemia
hyperreflexia
hypoglycorrhachia
hypogonadism
hypogonadism, hypogonadotropic
hyporeflexia
hypotonia
hypotonia, causes of
hypotonia, infants
imbalance
immunocompetent
immunomodulation
immunosuppression
immunosuppressive agents
inattention
inborn errors of metabolism
inclusion bodies, intranuclear
incoordination
India
infection
insight, loss
insomnia
intellectual deficit
interstitial pulmonary fibrosis
intracerebral hemorrhage
intravenous drug abuse
intrinsic hand muscles, wasting of
Jewish
joint hypermobility
Krabbe's disease
lactate
lactic acidemia
lacunar infarction
laughing, pathologic
Leber's hereditary optic neuropathy
leg weakness, bilateral
leukodystrophy
leukoencephalopathy
leukoencephalopathy with calcification and cysts
level of consciousness, decreased
limb-girdle weakness
linear lesion
lung nodule
lung-brain syndromes
lysosomal storage disease
malformation, CNS, congenital
malignancy screen
megalencephaly
MELAS syndrome
memory, defect of recent
memory, impairment of
meningeal enhancement
meningeal sarcomatosis
meningitis
meningitis, aseptic
meningitis, bacterial
meningitis, basilar
meningitis, candida
meningitis, carcinomatous
meningitis, chronic
meningitis, diagnosis
meningitis, fungal
meningitis, helminthic
meningitis, neutrophilic
meningitis, noninfectious
meningitis, parameningeal
meningitis, parasitic
meningitis, TB
meningitis, treatment of
meningitis, treatment of, empirical
meningitis, viral
meningitis, viral etiology in
meningitis-encephalitis PCR panel
mental retardation
mental status, abnormal
mestinon
metabolic acidosis
methylmalonic acidemia
microhemorrhage, intracerebral
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
mimics
mineralization
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
mortality
motor neuron disease
movement disorder
MRI, abnormal
MRI, blooming effect
MRI, contrast enhanced
MRI, diffusion weighted
MRI, mass effect on
MRI, nodular enhancement
MRI, spinal cord
muscle atrophy, progressive
muscle biopsy
muscle stiffness
muscle twitching
muscle wasting, diffuse
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, limb-girdle
mutism
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, misdiagnosis of
myasthenia gravis, seronegative
myasthenia gravis, treatment of
myelomalacia
myeloneuropathy
myelopathy
myoclonic jerks
myopathy
myopathy, vacuolar
nasal speech
nausea and vomiting
neck weakness
needle tracks
neonatal intensive care unit
neonatal screening, genetic neurologic disorders
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination, focal
neuromyotonia
neuromyotonia and axonal neuropathy
neuronal intranuclear inclusion disease
neuronopathy, sensory
neuroophthalmology
neuropathy
neuropathy, demyelinating
neurotomy
newborn, evaluation of
next-generation sequencing
night blindness
normal
NOTCH2NLC
nystagmus
nystagmus, gaze-evoked
ocular motility, disorders of
opened mouth
ophthalmoplegia
opportunistic infection
opportunistic infection, CNS
ovarian dysgenesis
pachygyria
papilledema
paragonimiasis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
parasitic infection, CNS
Parkinsonism syndrome
paroxysmal neurologic deficits
pathologic reflex
Perrault syndrome
pes cavus
phonophobia
photophobia
PICU
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
POLG1 gene
polyglucosan body disease
polymerase chain reaction
polymicrogyria
Pompe's disease of glycogen storage
pons, lesion of
precipitating factors
prion disease
prognosis
progressive neurologic disorder
proximal muscle atrophy
pseudobulbar palsy
pseudoxanthoma elasticum
psychiatric problems in neurologic disorders
psychosis
ptosis
ptosis, bilateral
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriplegia
recurrent
release phenomena
respiratory tract infection
retinopathy
review article
risk factors
Romberg's sign
salivation, excessive
sarcoidosis, CNS
scissors gait
scotoma
screening
sedimentation rate, elevated
seizure
seizure, focal
sensorineural hearing loss
seronegative
shunt procedure, ventricular
shunt procedure, ventricular-complications of
skin, biopsy
skin, hyperextensible
skin, lesions in neurologic disorders
skin, thin
skin, translucent
sleep pathology and physiology
small vessel disease
small vessel disease, cerebral
spastic ataxia
spastic paraplegia, type 7
spasticity
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 28
spinocerebellar degeneration
standing difficulty
status epilepticus
striatal encephalitis
strokelike episodes
subarachnoid hemorrhage
symmetric brain lesions
systemic illness
tandem gait, ataxic
telangiectases, retinal
thalamus, lesion of
thalamus, lesion of-bilateral
tinnitus
toe walking
tone, muscle, increased
tongue, enlarged
treatment of neurologic disorder
treatment, empirical
tremor
tremor, intention
trinucleotide repeats
tripping
tumefactive lesion
urinary incontinence
urinary urgency
vasculitides
vasculopathy
vegetarianism
viral infection
viral infection, CNS
vision loss, sequential
vision, blurred
visual field defect
visual loss
visual loss, progressive
visual loss, transient
visual obscurations, transient
walking, delayed
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
wheelchair
white matter disease
white matter disease, subcortical
white matter disease, unilateral
wide based gait
winging of scapula
workup
wound healing, poor
x-linked intellectual deficit
x-linked mental retardation
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Application of Deep Learning to Predict Standardized Uptake Value Ratio and Amyloid Status on 18F-Florbetapir PET Using ADNI Data
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A Woman with Monocular Vision Loss
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Diagnostic Tools for Immune Causes of Encephalitis
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A 23-Year-Old Man with Headaches, Confusion, and Lower Extremity Weakness
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Links in the Chain of Chronic Traumatic Encephalopathy
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Florbetapir Imaging in Cerebral Amyloid Angiopathy-Related Hemorrhages
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EULAR Recommendations for the Use of Imaging in Large Vessel Vasculitis in Clinical Practice
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Autopsy Validation of ���I-FP-CIT Dopaminergic Neuroimaging for the Diagnosis of DLB
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Paraneoplastic Neurological Syndromes and Glutamic Acid Decarboxylase Antibodies
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Prevalence of Cerebral Amyloid Pathology in Persons without Dementia
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Prevalence of Amyloid PET Positivity in Dementia Syndromes
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Hypometabolism of the Primary Motor Cortex in Primary Lateral Sclerosis
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Progressive Cerebellar Ataxia and New-Onset Diabetes
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PET Imaging for Alzheimer Disease: Are Its Benefits Worth the Cost?
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Is It All Cerebral Toxoplasmosis?
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Cortical and Cerebellar Hypometabolism After Bilateral Antero-Inferior Cerebellar Artery Infarct
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�-Amyloid Burden in Healthy Aging
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Subjective Cognition and Amyloid Deposition Imaging
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Central Nervous System Neuronal Surface Antibody Associated Syndromes: Review and Guidelines for Recognition
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Predicting sites of New Hemorrhage with Amyloid Imaging in Cerebral Amyloid Angiopathy
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Cancer Risk Among Patients with Myotonic Muscular Dystrophy
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Role of Brain Imaging in Early Parkinsonism
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Showing articles 50 to 100 of 282 << Previous Next >>