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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 800 to 850 of 13273 << Previous Next >>

Chronic Meningitis
NEJM 385:930-936, Aksamit, A.J., 2021

Clinical and Radiologic Features, Pathology, and Treatment of Balo Concentric Sclerosis
Neurol 97:e414-e422, Jolliffe, E.A.,et al, 2021

A 68-Year-Old Man with Proximal Weakness and Seizures
Neurol 97:e423-e428, Chen, T., 2021

Controversy and Progress in Alzheimers Disease - FDA Approval of Aducanumab
NEJM 385:doi:10.1056/NEJMp2111320, Rabinovici, G.D., 2021

A 47-Year-Old With Headache, Vertigo, and Double Vision
Neurol 97:e535-e539, Frey, J.,et al, 2021

Wilson Disease Presenting with Catatonia
Neurol 96:e2781-e2782, Patel, R.A. & Bailey, M., 2021

Pain in Right Buttock after Carbon Monoxide Poisoning
BMJ 373:n1233, Hu, H. & Sun, Q., 2021

Pembrolizumab-Induced Migrating Cortico-Subcortical Brain Lesions
Ann Neurol 89:1255-1256, Lambert, N.,et al, 2021

Cocaine and Levamisole Cerebral Toxicity
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Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

A 71-Year-Old Man with Horizontal Gaze Palsy, Anarthria, and Quadriparesis
Neurol 96:1146-1150, Cheema, I.,et al, 2021

An Unusual Presentation of Prolonged Delirium
BMJ 373:N1423, Bume, R.,et al, 2021

US Case Reports of Cerebral Venous Sinus Thrombosis with Thrombocytopenia after Ad26.COV2.S Vaccination, March 2 to April 21, 2021
JAMA 325:2448-2456,2445, See, I.,et al, 2021

Clinicopathologic Conference, Delayed Postthypoxic Leukoencephalopathy
NEJM 384:2438-2445, Case 19-2021, 2021

Cerebral Venous Thrombosis
NEJM 385:59-64, Ropper, A.H. & Kline, J.P., 2021

A Brewing Back Pain
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Cerebral Microbleeds
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A 29-Year-Old Man with Fevers and Rapidly Progressive Cranial Neuropathies
Neurol 97:95-98, Dessy, A.,et al, 2021

A 64-Year-Old Man with Multiple Cranial Neuropathies
Neurol 97:e215-e221, Lefland, A.,et al, 2021

Encephalitis Induced by Immune Checkpoint Inhibitors
JAMA Neurol 78:864-873, Velasco, R.,et al, 2021

Lumbar Spinal Stenosis
BMJ 373:m1581, Kruger Jensen, R.,et al, 2021

A 13-Year-Old Boy with Subacute-Onset Spastic Gait
JAMA Neurol 78:e1-e2, Xie, N.,et al, 2021

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

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
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Clinical Presentation and Management of SMART Syndrome
Neurol 97:118-120, Winter, S.F.,et al, 2021

Clinicopathologic Conference, Cerebral Amyloid Angiopatny-Related Inflammation
NEJM 385:358-368, Case 22-2021, 2021

Mechanisms of Ischemic Stroke in Patients with Cancer
Ann Neurol 90:159-169, Navi, B.B.,et al, 2021

Asymmetrical Facial Flushing and Sweating Associated with Anisocoria
BMJ 373:m796, Michonidou, A. & Atan, D., 2021

Alzheimers Disease
Lancet 397:1577-1590, Scheltens, P.,et al, 2021

Bilateral Superior Ophthalmic Vein Thrombosis, Ischaemic Stroke, and Immune Thrombocytopenia After ChAdOx1 nCoV-19 Vaccination
Lancet 397:e11, Bayas, A.,et al, 2021

Occipital Cortical Calcifications in Cerebral Amyloid Angiopathy
Stroke 52:1851-1855, Rasing, I.,et al, 2021

National Institute of Neurological Disorders and Stroke Consensus Diagnostic Criteria for Traumatic Encephalopathy Syndrome
Neurol 96:848-863, Katz, D.I.,et al, 2021

A Teenager with Shortness of Breath and Difficulty Walking
Neurol 96:e2346-e2350, Liu, S.C.,et al, 2021

Cervical Spondylotic Myelopathy Secondary to Ochronotic Vertebral Arthropathy
Neurol 96:627-628, Pinto, W.,et al, 2021

A Triad of Tremor, Ataxia, and Cognitive Impairment
Neurol 96:e1802-e1803, Au, L.W.C.,et al, 2021

Decreased Visual Acuity After a Cat Scratch
BMJ 372:n552, Zhou, L. & Kong, X., 2021

Clinicopathologic Conference, Normal Pressure Hydrocephalus
NEJM 384:1350-1358, Case 10-2021, 2021

Adults with Cerebral Palsy Require Ongoing Neurologic Care
Ann Neurol 89:860-871, Smith, S.E.,et al, 2021

Development and Validation of a Deep Learning-Based Model to Distinguish Glioblastoma from Solitary Brain Metastasis Using Conventional MR Images
AJNR 42:838-844, Shin, I.,et al, 2021

Neurologic Involvement in Children and Adolescents Hospitalized in the United States for Covid-19 or Multisystem Inflammatory Syndrome
JAMA Neurol 78:536-547, LaRovere, K.L.,et al, 2021

Headache, Cognitive Decline, and a Curious Rim-Enhancing Lesion
JAMA Neurol 78:613-614, Beaman, C.B.,et al, 2021

Radiation-Induced Bilateral Oculomotor Nerve Palsy 20 Years After Radiation Treatment
Neurol 96:955-957, Grassmeyer, J.J.,et al, 2021

Teaching Video NeuroImages: Jaw Clonus in Amyotrophic Lateral Sclerosis
Neurol 96:e2563, Goel, A.,et al, 2021

Lesion Age Imaging in Acute Stroke: Water Uptake in CT Versus DWI-FLAIR Mismatch
Ann Neurol 88:1144-1152, Broocks, G.,et al, 2020

Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral Sclerosis
J Clin Med 9:1-12, Rizzo, G.,et al, 2020

Immunoglobulin G4-related Hypertrophic Pachymeningitis Mimicking Temporal Arteritis
Neurol 94:(15 suppl), Han, J.Y.,et al, 2020

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

A Case of Monocytic Pleocytosis in West Nile Virus Encephalitis and Review of the Literature
Case Reports 23:687-688, Villafuerte, B.J.,et al, 2020

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

Clinicopathologic conference, Cryptococcal meningoencephalitis and advanced HIV infection
NEJM 383:2572-2580, Case 40-2020, 2020



Showing articles 800 to 850 of 13273 << Previous Next >>