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abscess, intracerebral
abscess, intracranial
abscess, retropharyngeal
abscess, sphenoid sinus
acetazolamide
aciduria
acrocyanosis
adolescent medicine
advances in neurology
adverse drug reaction
agitation
Aicardi-Goutieres syndrome
algorithm
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
alveolar hypoventilation
ammonia
AMPA receptor antibodies
aneurysm
aneurysm, intracranial
angiography, cerebral
angiography, posterior fossa
anorexia
anti basal ganglia antibodies
anti GQ1b IgG antibody
anticholinergic drugs
anti-dopamine 2 receptor antibody
anxiety
aortic valve, lesion of
apraxia of eye movements
areflexia
arteriovenous malformation
arteriovenous malformation, brainstem
arteriovenous malformation, cerebral
arylsulfatase A
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, truncal
athetosis
athetosis, causes of
atlanto-axial subluxation
ATP1A3 gene
atypical
auditory evoked brainstem potentials
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autonomic dysfunction
Babinski sign
bacterial infection
basal ganglia
basal ganglia, calcification of
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
benign essential tremor
biopterin deficiency
biotin
biotin deficiency
biotin deficiency, juvenile form
biotin-responsive basal ganglia disease
birth injury
blepharospasm
bone marrow biopsy
bradykinesia
brain atrophy
brainstem, hemorrhage, primary
brainstem, lesion of
brainstem, vascular malformation of
Brueghel's syndrome
bruit
bruit, cranial
CAG repeats
calcification, intracranial
carcinoembryonic antigen
carcinoma
cardiomyopathy
cardiopulmonary bypass
carotid artery occlusion, neck
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, isodense lesion with acute hemorrhage
cataracts
catatonia
caudate nucleus, atrophy
cavernous hemangioma
cavernous sinus, syndrome
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebellar edema
cerebellar hemorrhage
cerebellar lesion
cerebellar pontine angle
cerebellar pontine angle tumor
cerebral cortex
cerebral cortical atrophy
cerebral palsy
cerebral vasculature, calcification
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, young adult
cervical spine
channelopathy
chilbran skin lesions
children
chiropractic manipulation
chiropractic manipulation, neurologic complications with
chorea
chorea, causes of
chorea, treatment of
choreoathetosis
chromosomal abnormality
chromosome 1
chromosome 11
chromosome 14
chromosome 7
chronic progressive external ophthalmoplegia
cisterna magna
Clinical Pathologic Conference(C.P.C.)
cognition
Collier's sign
coma
coma, episodic
compression fracture
consanguinity
contractures, joint
cornea, opacity of
cranial nerve palsies
cranial neuropathy, multiple
C-reactive protein, elevated
crying
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
demyelinating disease
dentate nuclei, lesion of
depression
developmental milestones, loss of
developmental retardation
diabetes mellitus
diagnostic criteria
diet
differential diagnosis
diurnal variation
donut sign
dopa responsive dystonia
dopamine receptor, D2
down-beat nystagmus
drooling
drug induced neurologic disorders
drug overdose
drug overdose, accidental
dural sinus thrombosis
dying
dysarthria
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, causes of
dyskinesia, drug induced
dysphagia
dysphasia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, children
dystonia, delayed onset
dystonia, drug induced
dystonia, etiology of
dystonia, evaluation of
dystonia, focal
dystonia, painful
dystonia, symptomatic
dystonia, treatment of
dystonic reaction, acute
DYT1 mutation
ear, pain in
echocardiogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
ELISA
emotional lability
employment
empyema, epidural
empyema, subdural
encephalitis
encephalitis lethargica
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, etiology
encephalitis, paraneoplastic
encephalitis, viral
encephalopathy
encephalopathy, metabolic
encephalopathy, neonatal
encephalopathy, progressive
endocarditis
enuresis
enzyme, defect
ependymoma
episodic disorders
episodic neurologic deficits
epsilon sarcoglycan gene
equinovarus
ethics in neurology
evoked potentials
exercise
exercise-induced neurologic dysfunction
exome sequencing
extrapyramidal
eye movement, disorders of
Fahr disease
falling
familial
feeding disorder
fever
fluctuate
foot deformity
fourth ventricle, enlargement of
fourth ventricle, neoplasm of
frontal lobe, pathologic signs of
fungal infection, CNS
gait disorder
galactorrhea
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
GAMT gene
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
Gilles de la Tourette syndrome
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
GLUT1
GLUT1 deficiency syndrome
glutamic acid decarboxylase, antibody
growth retardation
Hallervorden Spatz disease
hands, fisted
head injury
head injury, pediatric
head lag
head nodding
head tilt
headache
health insurance
hearing loss
heart block
hemiballismus
hemidystonia
hemifacial spasm
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
hippocampus
Hodgkin's disease
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's disease, children
hydrocephalus
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hypertonia
hypocalcemia
hypoglycorrhachia
hypoparathyroidism
hyporeflexia
hypotonia
hypotonia, infants
hypoxia
iatrogenic neurologic disorders
imbalance
immunodeficiency
immunosuppression
immunosuppressive agents
immunotherapy
inborn errors of metabolism
inclusion bodies, intranuclear
incoordination
infantile hemiplegia
infection
insomnia
intellectual deficit
intellectual deterioration
interferon alpha
internal cerebral vein
internet
intestinal pseudoobstruction
intracerebral hemorrhage
intracerebral hemorrhage, recurrent
intracranial hemorrhage
intracranial pressure, increased
intrauterine
iron, brain
irritability
islet cell tumor
jugular foramen syndrome
Kearns-Sayre syndrome
ketogenic diet
L-dopa
Leber's hereditary optic neuropathy
leg spasms
leg spasms, painful
Leigh's disease
lenticular nucleus, lesion of, bilateral
leucine rich glioma inactivated 1 antibodies
leukemia
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
limbic encephalitis
linear lesion
lipid storage disorder of CNS
liver disease
lumbar puncture
lymphoma
malformation, vascular
malformation, vascular, cerebral
masked facies
mastoiditis
MELAS syndrome
memory, impairment of
meningismus
meningitis
meningitis, carcinomatous
mental retardation
mental status, abnormal
MERRF syndrome
metabolic acidosis
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
methylmalonic acidemia
microcephaly
migraine
migraine, children
mimics
mineralization
miosis
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
monoclonal antibodies
morphine
mortality
movement disorder
movement disorder, delayed onset
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, extrapyramidal-treatment of
movement disorder, hyperkinetic
movement disorder, treatment of
MRI
MRI pattern
MRI, abdomen
MRI, abnormal
MRI, blooming effect
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, FLAIR
MRI, paramagnetic effect
MRI, pelvis
MRI, serial
MRI, spinal cord
MRS
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple system atrophy
mycoplasma
mycoplasma pneumoniae
myelopathy
myoclonic dystonia
myoclonic jerks
myoclonus
myoclonus, action
myokymia
myopathy
myopathy, mitochondrial
nasal stuffiness
neck pain
neoplasm, posterior fossa
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neoplasm, primary of CNS-infants
nerve biopsy
nerve conduction studies
neurocutaneous disease
neuroendocrinology
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuromyotonia
neuronal intranuclear inclusion disease
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neurotomy
neurotoxic
neurotoxin
next-generation sequencing
Niemann-Pick disease
NMDA antagonists
nystagmus
nystagmus, congenital
nystagmus, dissociated
nystagmus, infancy
nystagmus, monocular
nystagmus, vertical
obsessive-compulsive disorder
occipital lobe, lesion of
ocular motility, disorders of
ophelia syndrome
ophthalmoplegia
opiate
optic atrophy
optic neuropathy
osteomyelitis
osteomyelitis, skull
otitis, neurologic complications with
pain
pancytopenia
PANK2 mutation
Parkinson disease
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinson disease, treatment of
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
pathology
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
pediatric opioid use associated neurotoxicity
personality change
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
pleural effusion
poison, neurologic problems with
POLG1 gene
poliomyelitis
polycythemia, primary
pons, lesion of
pontine glioma
posterior fossa, arteriovenous malformation
posterior fossa, lesion of
posterior fossa, signs of
potassium channel antibodies
practice guidelines
precipitating factors
prenatal
primary episodic ataxia
primary familial brain calcification
PRKN gene
procyclidine
progeria
prognosis
progressive neurologic disorder
prolactin, elevated
proptosis
proptosis, unilateral
pseudohypoparathyroidism
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
radiation hypersensitivity
ragged-red fibers
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rectal biopsy
recurrent
Red flags
release phenomena
remote effect of cancer on the nervous system
respirator
restless leg syndrome
retinitis pigmentosa
retinopathy
reversible neurologic disorder
review article
rhabdomyolysis
rigidity
rituximab
running
Saudi Arabia
scoliosis
screening
sea-blue histiocytes
seizure
seizure, children
seizure, neonatal
sensorineural hearing loss
serologic testing
serologic testing, false negative
seronegative
sexual behavior, disorder of
short stature
sinemet
sinusitis
skin, lesions in neurologic disorders
sleep pathology and physiology
spasmus nutans
spastic dysphonia
spasticity
speech disorder
speech disorder, childhood
spinal cord, neoplasm
spinal cord, neoplasm, infants and children
spinal muscular atrophy
splenomegaly
spongy degeneration of brain
startle reaction
status epilepticus
stereotaxic surgery
steroid
steroid therapy, CNS treatment and complications with
stimulation, deep brain
stimulation, deep brain, bilateral
striatal encephalitis
striatum, lesion of
striatum, lesion of, bilateral
striopallidodentate calcifications, familial idiopathic
subarachnoid hemorrhage
substantia nigra
subtraction of x-rays
suck, poor
suicide
sural nerve
symmetric brain lesions
syringomyelia
tardive dyskinesia
tardive dyskinesia, treatment of
tardive dystonia
telangiectases
teratoma
teratoma, ovarian
term infant
tetrabenazine
tetrahydrobiopterin
thalamotomy
thalamus, infarction of
thalamus, lesion of-bilateral
titubation
toe walking
tonic foot response
tonic spasms
torticollis
torticollis, acute infectious
torticollis, benign paroxysmal
torticollis, familial
torticollis, infants and children
torticollis, ocular
toxins, nervous system
treatment of neurologic disorder
tremor
tremor, postural
trigeminal neuralgia
trinucleotide repeats
tripping
tyrosine hydroxylase deficiency
valvulopathy
viral infection
viral infection, CNS
visual evoked response
visual impairment
walking
walking frame
walking, difficulty with
weight loss
wheelchair
white matter disease
workup
writers cramp
Showing articles 500 to 550 of 3081 << Previous Next >>

Acute Silent Cerebral Ischemic Events in Children with Sickle Cell Anemia
JAMA Neurol 70:58-65, Quinn, C.,et al, 2013

Clinical Reasoning: A 12-year-old Boy with Ascending Weakness
Neurol 80:e110-ee114, French, K.F.,et al, 2013

Pediatric Intracerebral Hemorrhage
JAMA Neurol 70:448-454,437, Beslow, L.et al, 2013

Evidence-based Guideline: Treatment of Parenchymal Neurocysticercosis
Neurol 80:1424-1429, Baird, R.,et al, 2013

Parkin Disease
JAMA Neurol 70:571-579, Doherty, K.,et al, 2013

Association Between Childhood Migraine and History of Infantile Colic
JAMA 309:1607-1612,1636, Romanello, S.,et al, 2013

Clinicopathologic Conferences, Celiac Disease, Addisons Disease, and Major Depression Disorder
NEJM 368:2015-2024, Case 16-2013, 2013

Sturge-Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ
NEJM 368:1971-1979, Shirley, M.,et al, 2013

Diagnosis of Lambert-Eaton Myasthenic Syndrome in Children
Neurol 80:e220-e222, Morgan-Followell,B.& de los Reyes,E., 2013

Facial Bradykinesia
JNNP 84:681-685, Bologna, M.,et al, 2013

Autoimmune Limbic Encephalopathy and Anti-Hu Antibodies in Children without Cancer
Neurol 80:2226-2232, Honnorat, J.,et al, 2013

Paediatric Autoimmune Encephalopathies: Clinical Features, Laboratory Investigations and Outcomes in Patients with or without Antibodies to known Central Nervous System Autoantigens
JNNP 84:748-755, Hacohen, Y.,et al, 2013

The Myositis Autoantibody Phenotypes of the Juvenile Idiopathic Inflammatory Myopathies
Medicine 92:223-243, Rider, L.,et al, 2013

Clinicopathologic Conference, Blind and Confused, Neuromyelitis Optica Spectrum Disorder
JAMA Neurol 70:932-936, Sharma, V.,et al, 2013

Current Concept of Neuromyelitis Optica (NMO) and NMO Spectrum Disorders
JNNP doi:10.1136/JNNP-2012-302310, Jacob, A.,et al, 2012

Progressive Gait Deterioration in Adolescents with Dravet Syndrome
Arch Neurol 69:873-878, Rodda, J.M.,et al, 2012

Utility of MRI in Spinal Arteriovenous Fistula
Neruol 79:25-30,15, Toossi, S.,et al, 2012

Comorbidity of Migraine in Children Presenting with Epilepsy to a Tertiary Care Center
Neurol 79:468-473, Kelly, S.A.,et al, 2012

Stroke Recurrence in Children with Congenital Heart Disease
Ann Neurol 72:103-111, Rodan, L.,et al, 2012

Radiation Exposure from CT Scans in Childhood and Subsequent Risk of Leukemia and Brain Tumors: A Retrospective Cohort Study
Lancet 380:499-505, Pearce, M.S.,et al, 2012

Evidence-Based Guideline: Pharmacologic Treatment of Chorea in Huntington Disease
Neurol 79:597-603, Armstrong, M.J. & Miyasaki, J.M., 2012

Seizure risk with AVM Treatment or Conservative Management
Neurol 79:500-507, Josephson, C.B.,et al, 2012

Multimodal Imaging of Reversible Cerebral Vasoconstriction Syndrome: A Series of 6 Cases
AJNR 33:1403-1410, Marder, C.P.,et al, 2012

A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy
Neurol 79:e63, Komatsuzaki, S.,et al, 2012

Heterogeneity of Coenzyme Q10 Deficiency
Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012

Painful Tonic Spasm in Neuromyelitis Optica
Arch Neurol 69:1026-1031, Kim, S.M.,et al, 2012

Anti-Glutamic Acid Decarboxylase Limbic Encephalitis Without Epilepsy Evolving Into Dementia with Cerebellar Ataxia
Arch Neurol 69:1064-1066, Mirabelli-Badenier, M.,et al, 2012

MRI Abnormalities Follwing Febrile Status Epilepticus in Children
Neurol 79:871-877, Shinnar, S.,et al, 2012

Clinicopathologic Conference, Acute Ischemic Stroke due to Basilar Artery Embolism. Patent Foramen Ovale
NEJM 367:1450-1460, Case 31-2012, 2012

Range of Genetic Mutations Associated with Severe Non-Syndromic Sporadic Intellectual Disability: An Exome Sequencing Study
Lancet 380:1674-1682, Rauch, A.,et al, 2012

Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

Neurologic Complications of Influenza A (H1N1)pdm09
Neurol 79:1474-1481, Khandaker,G.,et al, 2012

Silent Ischemic Lesions in Young Adults with First Stroke are Associated with Recurrent Stroke
Neurol 79:1208-1214, Gioia, L.C.,et al, 2012

The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
Stroke 43:2871-2876, Pescini, F.,et al, 2012

Clinical Reasoning: A Case of Acute Onset Bilateral Ptosis in a Young Child
Neurol 79:e155-e160, Das, D.,et al, 2012

Antithrombotic Therapy and Bleeding Risk in a Prospective Cohort Study of Patients with Cerebral Cavernous Malformations
Stroke 43:3196-3199, Schneble, H.,et al, 2012

Efficacy and Safety of Ketamine in Refractory Status Epilepticus in Children
Neurol 79:2355-2358, Rosati, A.,et al, 2012

Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
Stroke 43:72-78, Bharatha, A.,et al, 2012

Risk Factors for Spinal Cord Lesions in Dystonic Cerebral Palsy and Generalised Dystonia
JNNP 83:159-163, Guettard,E.,et al, 2012

Intramuscular Versus Intravenous Therapy for Prehospital Status Epilepticus
NEJM 366:591-600,659, Silbergleit,R.,et al, 2012

Variable Presentations of Postpartum Angiopathy
Stroke 43:670-676, Fugate,J.E.,et al, 2012

Epileptic Seizures at Initial Presentation in Patients with Brain Arteriovenous Malformation
Neurol 78:626-631, Garcin,B.,et al, 2012

CAG Repeat Expansion in Huntington Disease Determines Age at Onset in a Fully Dominant Fashion
Neurol 78:690-695, Lee,J.M.,et al, 2012

Cogan Syndrome An Analysis of Reported Neurological Manifestations
The Neurologist 18:55-63, Antonios,N. and Silliman,S., 2012

Restricted Diffusion in Vanishing White Matter
Arch Neurol 69:723-727, Van de Lei, H.D.W.,et al, 2012

Endoscopic Treatment of Hydrocephalus
Arch Neurol 69:664, Walcott, B.P.,et al, 2012

Clinical Reasoning: Encephalopathy in a 10-year-old boy
Neurol 79:e12-e18, Rodan, L. & Tein, I., 2012

Effects of Fetal Antiepileptic Drug Exposure
Neurol 78:1207-1214, Meador,K.J.,et al, 2012

Susceptibility-Weighted MR Imaging for Diagnosis of Capillary Telangiectasia of the Brain
AJNR 33:715-720, El-Koussy,M.,et al, 2012

CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
Neurol 78:1150-1156, Deiva,K.,et al, 2012



Showing articles 500 to 550 of 3081 << Previous Next >>