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Differential
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abdominal muscle paralysis
acetylcholine
acetylcholine in CNS
acid maltase deficiency
acid maltase deficiency, adult
acral sensory symptoms
acyl CoA dehydrogenase deficiency
adenosine deaminase deficiency
adrenoleukodystrophy
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
agalsidase alfa
alopecia
alpha galactosidase A deficiency
alpha glucosidase
Alzheimer's disease
aminoacidopathies
aminoacidurias
aminoacylase 1 deficiency
ammonia
amniocentesis
anemia
anemia, hemolytic
aneurysm
angiokeratoma
angiotensin-converting enzyme
anorexia nervosa
anterior horn cell disease
anticonvulsants
anticonvulsants, untoward effects of
apraxia
apraxia of eye movements
aromatic amino acid decarboxylase deficiency
arthropathy
arthropathy, neuropathic
arylsulfatase A
aspartate aminotransferase
aspartocyclase
asymptomatic
ataxia
ataxia, cerebellar
athetosis
autism
autonomic dysfunction
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
biotin deficiency
biotinidase deficiency
blindness
blood dyscrasias, neurologic findings with
bone marrow transplantation
brain atrophy
brain biopsy
brain purpura
brainstem
brainstem, infarction of
brainstem, lesion of
burning feet
burning feet, differential diagnosis of
burning hands
burning paresthesia
calcification, intracranial
calf hypertrophy
Canavan's disease
carbamyl phosphate synthetase-I deficiency
carbidopa
carbonic anhydrase II deficiency
cardiomegaly
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
caudate nucleus, lesion of
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemorrhage
cerebellar infarction
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebral infarction, hemorrhagic
cerebral ischemia
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, glycine
cerebrospinal fluid, protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, cryptogenic
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
cherry red spot
cherry red spot-myoclonus syndrome
children
cholesterol
choline acetyltransferase
choline chloride
choreoathetosis
chromosomal abnormality
chromosome 20
chromosome 6
cirrhosis
cirrhosis, infancy
Clinical Pathologic Conference(C.P.C.)
codfish vertebrae
coenzyme Q10 deficiency
coma
compression fracture
confusion
congestive heart failure
conjunctivitis
consanguinity
contractures, joint
coprolalia
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
cranial nerve enlargement
cranial nerve palsies
creatine phosphokinase(CPK)elevated
creatinine, elevated
cry, abnormal
crying
cultured skin fibroblasts
cystinuria
cytochrome c oxidase
cytochrome c oxidase, deficiency
deep gray nuclei
deficiency of ADA2
degenerative diseases of CNS
dementia
dementia, presenile
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
developmental milestones, loss of
developmental retardation
diaphragmatic paralysis
diet
distal muscle atrophy
distal muscle weakness
dopa responsive dystonia
dopamine
drooling
dropped head syndrome
dysarthria
dysmorphic
dysostosis multiplex
dysphagia
dyspnea
dyspraxia
dystonia
dystonia, children
dystonic reaction, acute
echolalia
efficacy
electrocardiogram, abnormal
electromyogram
electron microscopy
emergencies, neurologic
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
enzyme treatment
enzyme, defect
enzyme, muscle disease
epidemiology of neurology
exercise
exercise intolerance
eye movement, disorders of
Fabry's disease
facial anomalies
facial appearance, abnormal
facial hypoplasia
facial weakness
failure to thrive
familial
Farber's disease
fatigue
fatty acid, elevated plasma content
feeding disorder
fever
floppy infant
flow study, carotid artery
fornix, lesion of
fracture, pathologic
frontal bossing
frontal lobe, behavior with disease of
frontal lobe, lesion of
fucosidosis
fundus, abnormality of
gait disorder
galactocerebrosidase
galactorrhea
galactosemia
galactosidase
gangliosidosis GM1
gangliosidosis GM2
gangliosidosis GM2-AB variant
Gaucher's disease
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
Gilles de la Tourette syndrome
globoid cells
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glucocerebrosidase
glutamate dehydrogenase deficiency
glutaric acidemia
glutaric aciduria
glycine
glycogen debranching enzyme deficiency
glycogen storage disease
glycoprotein
growth retardation
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hallucination
hallucination, auditory
hand pain
hands, fisted
head lag
headache
headache, progressive
headache, thunderclap
headbanging
hearing loss
heart murmur
hematopoietic tissue, extramedullary
hemianopia, homonymous
hepatic failure
hepatomegaly
hepatosplenomegaly
heralding manifestation
herniated disc, thoracic
hexosaminidase-A
hexosaminidase-A and B
histochemistry
histochemistry of muscle
homocystinuria
Hurler's syndrome
hydrocephalus
hydrocephalus, normal pressure
hydroxytryptophan L-5(L-5 HTP)
hyperammonemic encephalopathy
hyperbilirubinemia
hyperglycinemia
hyperhomocysteinemia
hyperreflexia
hypertension
hypertonia
hypogammaglobulinemia
hypoglycemia
hypomyelination
hyponatremia
hyporeflexia
hypothermia
hypotonia
hypotonia, infants
ileus, paralytic
imbalance
immunosuppression
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies, intracytopasmic
infection
infection, recurrent
insulin resistance
intellectual deficit
intellectual deterioration
intelligence quotient
internal capsule
internuclear ophthalmoplegia
internuclear ophthalmoplegia, unilateral
intrauterine
iron, brain
irritability
ischemic exercise test
jaundice
Jewish
Kearns-Sayre syndrome
Korsakoff's psychosis
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactate
lacunar infarction
L-dopa
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
Leigh's disease, adult variety
lens, dislocation of
lens, ectopic
Lesch-Nyhan syndrome
lethargy
leukocyte enzyme abnormality
leukodystrophy
life expectancy
lipid storage disorder of CNS
livedo reticularis
liver disease
lysosomal storage disease
lysosomes, abnoral
macrocephaly
marihuana
McArdle's disease
meconium staining
melanomatosis, primary malignant
MELAS syndrome
memory, defect of recent
mental retardation
mental status, abnormal
MERRF syndrome
mesial temporal lobe
metabolic acidosis
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
microspherophakia
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, demyelinating disease
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, eye of tiger sign
MRI, hypointense signal foci on
MRI, paramagnetic effect
MRI, vessel wall
MRI, vessel wall enhancement
MRS
mucopolysaccharidoses
multiple sclerosis, differential diagnosis of
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle spasm
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, neonatal screening
myelopathy
myoclonic jerks
myoclonus
myoglobinuria
myopathy
myopathy, distal, vacuolar
myopathy, metabolic
myopathy, mitochondrial
myopathy, necrotizing
myopathy, vacuolar
myopia
nausea and vomiting
neck weakness
neonatal screening, genetic neurologic disorders
nerve biopsy
nerve conduction studies
neuraminidase deficiency
neurologic disease, diagnoses of
neurologic examination
neurologic signs
neuropathology
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, painful
neuropathy, peripheral
neurotransmitter
nystagmus
oculogyric crisis
ophthalmoplegia
ophthalmoplegia, progressive external
opisthotonus
optic atrophy
optic chiasm, enlarged
optic nerve
optic nerve, enlarged
ornithine transcarbamylase deficiency
orthopnea
osteoporosis
pain
palilalia
PANK2 mutation
paraparesis, spastic
paraspinal muscle
paraspinal muscle weakness
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
pectus excavatum
pediatric neurology
peroxisomal disease
peroxisomes
phenylketonuria
phosphorylase b kinase deficiency
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
polymerase chain reaction
polyneuropathy
Pompe's disease of glycogen storage
porphyria
postpartum
postpartum coma
postural abnormality
precipitating factors
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognathism
prognosis
progressive neurologic disorder
prolactin, elevated
proteinuria
pseudomyotonia
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
putamen, lesion of
pyramidal tract
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
pyruvate-kinase deficiency anemia
rash
recurrent
renal failure
renal tubular acidosis
respiratory failure
respiratory tract infection
retinal degeneration
retinopathy
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
Reye's syndrome
rigidity
Sandhoff's disease
Sanfilippo syndrome
schizophrenia
scoliosis
scoliosis, neurologic association with
screaming
screening
second wind phenomena
seizure
seizure, children
seizure, neonatal
seizure, psychomotor-temporal lobe
self-mutilation
semialdehyde dehydrogenase deficiency
short stature
skin, biopsy
skin, lesions in neurologic disorders
small vessel disease
sodium valproate
sodium valproate, toxicity
somnolence
spasticity
speech disorder
speech disorder, childhood
sphingolipodoses
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinocerebellar ataxia type 1
spinocerebellar degeneration
splenomegaly
spongy degeneration of brain
startle reaction
stem cell transplantation
strabismus
striatum, lesion of
stuporous
stuttering
subarachnoid hemorrhage
subarachnoid hemorrhage, cerebral convexity
substantia nigra
suck, poor
symmetric brain lesions
systemic illness
Tay-Sachs disease
temporal lobe, lesion
term infant
tetrahydrobiopterin
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine
tinnitus
tone, muscle, increased
tongue, enlarged
tongue, weakness
transketolase
treatment of neurologic disorder
tyrosine
tyrosine hydroxylase deficiency
tyrosinemia
umbilical-cord blood transplantation
urea
urea-cycle enzymopathies
uremia
urinary incontinence
urine test for metabolic disorders
urine, dark
vasculitides
vasculopathy
vertebral-basilar insufficiency
vertigo
vertigo, episodic
visual loss
vital capacity
vitamin deficiency
weakness
weakness, progressive
weakness, proximal
Wernicke's encephalopathy
wheelchair
white matter disease
winging of scapula
Showing articles 950 to 1000 of 13273 << Previous Next >>

A Woman with Monocular Vision Loss
Neurol 95:e1105-e1109, Danish, H.,et al, 2020

Clinicopathologic Conference, HIV Type 2 Infection & Cerebral Toxoplasmosis
NEJM 383:859-866, Case 27-2020, 2020

A 14-Year-Old Boy with Acute Weakness, Parethesias, and Headache
Neurol 95:e1285-e1289, Seese, R.R.,et al, 2020

Polymyalgia Rheumatica and Giant Cell Arteritis
JAMA 324:993-994, Buttgereit, F.,et al, 2020

Radiologically Isolated Syndrome: A Review for Neuroradiologists
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Bilateral Globus Pallidus Lesions in a Patients with COVID-19
Neurol 95:454-457, Kulick-Soper, C.V.,et al, 2020

Leukoencephalopathy Associated with Severe COVID-19
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A Young Generalized Dystonia Patient with Globus-Pallidus-Specific Lesion
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Spinal Cord Involvement in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia
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Tattoo Reaction - A Diagnostic Clue in Neurosarcoidosis
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Encephalomyelitis and Lymphadenopathy in a Man in His Early 40s
JAMA Neurol 77:1171-1172, Bakirtzis, C.,et al, 2020

Spinal Xanthomatosis
Neurol 95:e1615-e1616, Valencia-Sanchez, C.,et al, 2020

Clinical Features of Trousseau Syndrome with Cerebral Infarction as the Initial Manifestation
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Diffusion-Weighted Imaging-Documented Bilateral Small Embolic Stroke Involving Multiple Vascular Territories May Indicate Occult Cancer: A Retrospective Case Series and a Brief Review of the Literature
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Delayed Nonischemic Cerebral Enhancing Lesions Post Endovascular Coil Embolization
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Neuropathy, Encephalopathy, Status Epilepticus, and Acute Intermittent Porphyria
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CASPR2 Autoimmunity in Children Expanding to Mild Encephalopathy with Hypertension
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A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
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MR Target Sign in Cerebral Aspergillosis
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Contrast-Induced Encephalopathy Following Coronary Angiography
Neurol 94:e2491-e2494, Harada, Y.,et al, 2020

Application of Deep Learning to Predict Standardized Uptake Value Ratio and Amyloid Status on 18F-Florbetapir PET Using ADNI Data
AJNR 41:980-986, Reith, F.,et al, 2020

High Prevalence of Spinal Cord Cavernous Malformations in the Familial Cerebral Cavernous Malformations
AJNR 41:1126-1130, Mabray, M.C.,et al, 2020

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

A 53-year-old Woman with Lower Extremity Paresthesias
Neurol 94:1105-1108, Dehbashi, S.,et al, 2020

Early Evidence of Pronounced Brain Involvement in Fatal COVID-19 outcomes
Lancet 395:e109, von Weyhern, C.H.,et al, 2020

Severe Neurological Toxicity of Immune Checkpoint Inhibitors: Growing Spectrum
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COVID-19: A Global Threat to the Nervous System
Ann Neurol 88:1-11, Koralnik, I.J. & Tyler, K.L., 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
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The Incidence of Central Neurological Disorders Among Patients with Isolated Dizziness and the Diagnostic Yield of Neuroimaging Studies
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CT Scanning in Suspected Stroke or Head Trauma: Is It Worth Going the Extra Mile and Including the Chest to Screen for COVID-19 Infection?
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Surprise Diagnosis of COVID-19 following Neuroimaging Evaluation for Unrelated Reasons during the Pandemic in Hot Spots
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Paraneoplastic Encephalomyelitis with Glutamic Acid Decarboxylase Antibodies Presenting as Longitudinal Pyramidal Tract Hyperintensity
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Long Survival Sporadic Creutzfeldt-Jakob Disease
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Diffusion-Weighted MRI in Transient Global Amnesia and its Diagnositc Implications
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The Face of Myasthenia Gravis
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Clinical Characteristics, Risk Factors, and Outcomes of POEMS Syndrome
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Complex Ataxia
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Burning Pain in the Legs
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Childhood Multisystem Inflammatory Syndrome
NEJM 383:393-395, Levin, M., 2020

MRI-EEG Correlation for Outcome Prediction in Postanoxic Myoclonus
Neurol 95:e335-e341, Beuchat, I.,et al, 2020

Artificial Intelligence Applications in Stroke
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COVID-19 Presenting with Ophthalmoparesis from Cranial Nerve Palsy
Neurol 95:221-223, Dinkin, M.,et al, 2020

Bilateral Transient Olfactory Bulb Edema During COVID-19-Related Anosmia
Neurol 95:224-225, Laurendon, T.,et al, 2020

A 10-Year-Old Girl with Muscle Stiffness
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Magnetic Resonance Imaging Alteration of the Brain in a Patient with Coronavirus Disease 2019 (COVID-19) and Anosmia
JAMA Neurol 77:1028-1029, Politi, L.S.,et al, 2020

Long-Term Outcome of Patients with Spinal Dural Arteriovenous Fistula: The Dilemma of Delayed Diagnosis
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An Atypical Presentation of Creutzfeldt-Jakob Disease with a Heidenhain Variant and Balints Syndrome
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"Motor Band Sign" in Susceptibility-Weighted Imaging in Motor Neuron Disease
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Cerebrospinal Fluid Hypovolemia and Posterior Reversible Encephalopathy Syndrome
Front Neurol 11:591, Zheng,Y-y, et al, 2020



Showing articles 950 to 1000 of 13273 << Previous Next >>