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adolescent medicine
advances in neurology
adverse drug reaction
akathisia
algorithm
alternating hemiplegia
alternating hemiplegia of childhood
AMPA receptor antibodies
amphiphysin antibodies
anti GQ1b IgG antibody
anti IgLON5
anticholinergic drugs
aphonia
areflexia
arylsulfatase A
ataxia
ataxia, cerebellar
athetosis
ATP1A3 gene
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autonomic dysfunction
basal ganglia
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
bent spine syndrome
benzodiazepine
blepharospasm
botulinum toxin
bradykinesia
brain damage
Brueghel's syndrome
camptocormia
carbon monoxide poisoning
cardiac arrest
cardiac arrest and resuscitation
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
CAT scan, muscle
catalepsy
cataplexy
caudate nucleus, atrophy
cerebellar degeneration
cerebral cortical atrophy
cerebral palsy
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrovascular accident
cerebrovascular accident, infancy and childhood
children
chorea
chorea, Sydenham's
choreoathetosis
chromosomal abnormality
chromosome 1
chromosome 19
chromosome 20
chromosome 6
Clinical Pathologic Conference(C.P.C.)
clonazepam
clozapine
cognition
collapsin response mediator protein 5 IgG
coma
complications
conversion reaction
creatine phosphokinase(CPK)elevated
cyanide poison
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, presenile
developmental milestones, loss of
developmental retardation
diagnostic criteria
diet
differential diagnosis
disease modifying agents
dopa responsive dystonia
dopamine agonist
dopamine depleting agents
DPPX
DPPX, antibodies
DPPX, antibodies, encephalitis
drug induced neurologic disorders
dysarthria
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, drug induced
dysphagia
dystonia
dystonia musculorum deformens
dystonia, classification
dystonia, delayed onset
dystonia, drug induced
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, treatment of
dystonia, truncal
dystonic reaction, acute
DYT1 mutation
efficacy
electroencephalogram, abnormalities of
electromyogram
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalopathy
encephalopathy, neonatal
encephalopathy, post anoxic
enzyme, defect
executive dysfunction
exome sequencing
eye movement, disorders of
facial nerve palsy
falling
familial
forceps delivery
gait disorder
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
gests antagoniste
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
GLUT1
GLUT1 deficiency syndrome
glutamic acid decarboxylase, antibody
glycine receptor antibodies
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
haloperidol
hand weakness
handedness
hands, fisted
head injury
head nodding
head tilt
hearing loss
hemidystonia
hemiplegia
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
Hodgkin's disease
Huntington's chorea
Huntington's disease, children
hyperreflexia
hypoglycorrhachia
hypotonia
hypotonia, infants
hypoxia
hypoxia, newborn
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunologic disease
immunotherapy
inborn errors of metabolism
inclusion bodies, intranuclear
incoordination
infantile hemiplegia
insomnia
intellectual deficit
intellectual deterioration
internal cerebral vein
iron, brain
islet cell tumor
jaundice
ketogenic diet
kyphosis
L-dopa
L-dopa, delayed treatment in Parkinsonism
L-dopa, drug interactions with and side effects of
left handedness
Leigh's disease
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
leucine rich glioma inactivated 1 antibodies
leukodystrophy
life expectancy
limbic encephalitis
lipid storage disorder of CNS
low back pain
lumbar puncture
lysosomal storage disease
masked facies
mellaril
memory
memory, impairment of
meningitis, carcinomatous
mental retardation
mental status, abnormal
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metoclopramide
microcephaly
miglustat
migraine
migraine, children
mimics
misdiagnosis
mitochondrial disease
monoclonal antibodies
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, abnormal
MRI, CAT scan compared to
MRI, eye of tiger sign
MRI, negative
MRI, paramagnetic effect
muscle biopsy
muscle weakness
muscular dystrophy
myasthenia gravis
mycotoxin
myoclonus
myopathy
myopathy, metabolic
neuroleptic
neuroleptic, atypical
neurologic disease, diagnoses of
neurologic signs
neuronal intranuclear inclusion disease
neuropathology
neurotoxin
Niemann-Pick disease
nitroproprionic acid
NMDA antagonists
nystagmus
nystagmus, monocular
obsessive-compulsive disorder
oculogyric crisis
old age, neurology of
ophelia syndrome
optic atrophy
organomegaly
pain
pain, genital
palilalia
PANK2 mutation
paraspinal muscle
paraspinal muscle weakness
Parkinson disease
Parkinson disease, drug induced
Parkinson disease, dystonia with
Parkinson disease, fluctuations in
Parkinson disease, freezing phenomena in
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, mode of onset
Parkinson disease, on-off phenomena in
Parkinson disease, prognosis of
Parkinson disease, rapid onset
Parkinson disease, treatment of
Parkinson disease, unilateral
Parkinson disease, young onset
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
phenothiazine
phenothiazine, dyskinesia associated with
pigmentary retinopathy
Pisa syndrome
pleocytosis of cerebrospinal fluid
postural abnormality
potassium channel antibodies
practice guidelines
precipitating factors
prevention of neurologic disorders
PRKN gene
prognosis
progressive neurologic disorder
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychotic behavior
pull test
putamen, lesion of
putamen, lesion of, bilateral
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quality of life
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
recurrent
remote effect of cancer on the nervous system
reserpine treatment in movement disorder
retinal degeneration
retinitis pigmentosa
retinopathy
retrocollis
review article
rigidity
rituximab
safety
salivation, excessive
schizophrenia
screening
seizure
seizure, adult onset
seizure, children
seizure, laughing as manifestation
seizure, neonatal
seizure, unknown origin
sensorineural hearing loss
sensory tricks
serologic testing
serologic testing, false negative
seronegative
sinemet
sleep pathology and physiology
spasticity
speech disorder
splenomegaly
status epilepticus
stem cell transplantation
steroid
steroid therapy, CNS treatment and complications with
stimulation, deep brain
stooped posture
streptococcal infection
streptococcus pyogens
striatal encephalitis
striatum, lesion of
sugarcane, mildewed
swallow evaluation
tardive akathisia
tardive dyskinesia
tardive dyskinesia, treatment of
tardive dystonia
tardive pain syndrome
tetrabenazine
tetrahydrobiopterin
thalamus, infarction of
thalamus, lesion of-bilateral
tonic foot response
torticollis
torticollis, benign paroxysmal
torticollis, familial
torticollis, infants and children
toxic encephalopathy
toxins, nervous system
treatment of neurologic disorder
tremor
tremor, postural
tremor, resting
tremor, thalamic
tricyclic antidepressant
trinucleotide repeats
urinary sulfatidase excretion
walking, difficulty with
weakness, progressive
white matter disease
whole genome sequencing
wide based gait
workup
writers cramp
Showing articles 150 to 200 of 1853 << Previous Next >>

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

Automated Brain Perfusion Imaging in Acute Ischemic Stroke: Interpretation Pearls and Pitfalls
Stroke 52:3728-3738, Nicolas-Jilwan, M. & Wintermark, M., 2021

Clinicopathologic Conference, Seizure from Neurocysticercosis
NEJM 385:1894-1902, Case 34-2021, 2021

A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
Neurol 97:958-963, Davalos, L.,et al, 2021

Antiseizure Medication Withdrawal in Seizure-Free Patients: Practice Advisory Update Summary
Neurol 97:1072-1081, Gloss, D.,et al, 2021

Choreoathetosis and Focal Dystonia in Vitamin B12 Deficiency
Neurol 97:e1545, Ng, C.F.,et al, 2021

Which Imaging Approach Should be Used for Stroke of Unknown Time of Onset?
Stroke 52:373-380, Simonsen, C.Z.,et al, 2021

A 71-Year-Old Man Presenting with Acute Onset Dysarthria and Dysphagia
Neurol 96:180-184, Spagni, G.,et al, 2021

Acute Flaccid Myelitis: Cause, Diagnosis, and Management
Lancet 394:334-397, Murphy, O.C.,et al, 2021

Clinicopathologic Conference, Disseminated Mycobacterium Bovis Infection
NEJM 384:651-662, Case 5-2021, 2021

Bilateral Temporal Pole Involvement in Adult-Onset X-Linked Adrenoleukodystrophy
JAMA Neurol 78:367-368, Liu, M.,et al, 2021

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

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

Vagus Nerve Stimulation and Seizure Outcomes in Pediatric Refractory Epilepsy
Neurol 96:1041-1051, Jain, P. & Arya, R., 2021

Initial Management of Seizure in Adults
NEJM 385:251-263, Smith, P.E.M., 2021

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

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

Vitamin B12 Deficiency in a 29-Year-Old Woman
Neurol 97:e643-e646, Huddar, A.,et al, 2021

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

Efficacy and Safety of Adjunctive Lacosamide in the Treatment of Primary Generalised Tonic-Clonic Seizures: A Double-Blind, Randomised, Placebo-Controlled Trial
JNNP 91:1067-1075, Vossler, D.G.,et al, 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

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

Clinical and Radiological Characteristics and Outcome of Wake-Up Intracerebral Hemorrhage
www.nature.com/scienticreports 10:18749, Marti-Fabregas, J.,et al, 2020

Cyclic Vomiting Syndrome in Children
AJGH 2:doi:10.33552/AJGH.2020, Al-Ansari, N., 2020

An Underrecognized Etiology of New Daily Persistent Headache
Neurol 94:e114-e120, Duvall, J.R.,et al, 2020

Hashimoto Encephalopathy in the 21st Century
Neurol 94:e217-e224, Mattozzi, S.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Melbourne Mobile Stroke Unit and Reperfusion Therapy
Stroke 51:922-930, Zhao, H.,et al, 2020

Machine Learning Approach to Identify Stroke Within 4.5 Hours
Stroke 51:860-866, Lee, H.,et al, 2020

Epilepsy in Older People
Lancet 395:735-748, Sen, A.,et al, 2020

Mobile Stroke Unit Computed Tomography Angiography Substantially Shortens Door-to-Puncture Time
Stroke 51:1613-1615, Czap, A.L.,et al, 2020

Clinical and Radiologic Features of Pedicatric Opioid Use-Associated Neurotoxicity with Cerebellar Edema (POUNCE) Syndrome
Neurol 94:710-712, Kim, D.D. & Prasad, A.N., 2020

Isolated Oculomotor Nerve Palsy due to Pituitary Apoplexy Missed on CT scan
Neurol 94:e1774-e1777, Marzoughi, S.,et al, 2020

Thrombolysis for Acute Ischemic Stroke in the Unwitnessed or Extended Therapeutic Time Window
Neurol 94:e1241-e1248, Tsivgoulis, G.,et al, 2020

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

When the Temporal Artery Biopsy is Negative
Neurologist 25:70-72, Ford, E. & Smith, J.H., 2020

Association of Pediatric Acute-Onset Neuropsychiatric Syndrome with Microstructural Differences in Brain Regions Detected via Diffusion-Weighted Magnetic Resonance Imaging
JAMA Network Open 3:doi:10.1001/JAMANETWORKOPEN.2020.4063, Zheng, J.,et al, 2020

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

Implementation of a Prehospital Stroke Triage System Using Symptom Severity and Teleconsultation in the Stockholm Stroke Triage Study
JAMA Neurol 77:691-699, Mazya, M.V.,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

Diffusion-Weighted MRI in Transient Global Amnesia and its Diagnositc Implications
Neurol 95:e206-e212, Szabo, K.,et al, 2020

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

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

Spinal Cord Involvement in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia
JAMA Neurol 77:1169-1170, Li, S.,et al, 2020

Migraine
NEJM 383:1866-1876, Ashina, M., 2020

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

Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
Neurol 95:933-938, Paul,P.,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

An 11-year-old girl with focal seizures, fevers, and unilateral, enhancing cortical lesions
Neurol 95:e3153-e3159, Russ, J.B.,et al, 2020



Showing articles 150 to 200 of 1853 << Previous Next >>