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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
caudate nucleus, 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
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
eye movement, disorders of
facial nerve palsy
falling
familial
forceps delivery
gait disorder
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gene
gene mutation
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)
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
infantile hemiplegia
insomnia
intellectual deficit
intellectual deterioration
internal cerebral vein
iron, brain
islet cell tumor
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
limbic encephalitis
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
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
nitroproprionic acid
NMDA antagonists
nystagmus
nystagmus, monocular
obsessive-compulsive disorder
oculogyric crisis
old age, neurology of
ophelia syndrome
optic atrophy
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
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
screening
seizure
seizure, adult onset
seizure, children
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
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
weakness, progressive
white matter disease
wide based gait
workup
writers cramp
Showing articles 400 to 450 of 1826 << Previous Next >>

Clincopathologic Conference,Graves Disease with Thyrotoxic Periodic Paralysis
NEJM 366:553-560, Case 4-2012, 2012

Incidence and Prevalence of Epilepsy Among Older US Medicare Beneficiaries
Neurol 78:448-453, Faught,E.,et al, 2012

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

Topographic Location of Acute Pontine Infarction is Associated with the Development of Progressive Motor Deficits
Stroke 43:708-713, Oh,S.,et al, 2012

Solitary Sclerosis
Neurol 78:540-544, Schmalstieg,W.F.,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

Clinicopathologic Conference,Necrotizing Noninflammatory Myopathy Consistent with Exposure to Statins
NEJM 36:944-954, Case 7-2012, 2012

Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012

Progressive Weakness with Respiratory Failure in a Patient with Sarcoidosis
Arch Neurol 69:534-537, Chaudhry,P.,et al, 2012

Clinical Reasoning: A Middle-Aged Woman with Progressive Symmetric Weakness and a CSF Pleocytosis
Neurol 78:e88-e92, Marks,D.,et al, 2012

Radiosurgery for Unruptured Cerebral Arteriovenous Malformations
Neurol 78:1292-1298, Yang,S.Y.,et al, 2012

A Case of Necrotizing Myopathy with Proximal Weakness and Cardiomayopathy
Neurol 78:1527-1532, Matthews,E.,et al, 2012

A Musicians Dystonia
Lancet 379:2116, Vecchio, M.,et al, 2012

Guillain-Barre Syndrome
NEJM 366:2294-2304, Yuki, N. & Hartung, H.P., 2012

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

Bilateral Foot Drop in Polyarteritis Nodosa
NEJM 367:e9, Souza Neves, F. & Lin, K., 2012

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

A Pragmatic Approach Using Magnetic Resonance Imaging to Treat Ischemic Strokes of Unknown Onset Time in a Thrombolytic Trial
Stroke 43:2331-2335, Song, S.S.,et al, 2012

Lifelong Management of Amyloid-Beta Metabolism to Prevent Alzheimers Disease
NEJM 367:864-866, Gandy, S., 2012

Clinical and Biomarker Changes in Dominantly Inherited Alzheimers Disease
NEJM 367:795-804,864, Bateman, R.J.,et al, 2012

Amnesic Disorders
Lancet 380:1429-1440, H. Markowitsch & A. Staniloiu, 2012

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

Advances in Treatment of Bacterial Meningitis
Lancet 380:1693-1702,1623, Van de Beek, D.,et al, 2012

Timing of Stroke in Patients Undergoing Total Hip Replacement and Matched Controls
Stroke 43:3225-3229, Lalmohamed, A.,et al, 2012

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

Dopa-Responsive Dystonia Revisited
Arch Neurol 69:1558-1562, Tadic, V.,et al, 2012

Central Nervous System Herpes Simplex Virus Infection in Afebrile Children with Seizures
J Child Neurol 27:445-450, Majumdar,L.,et al, 2012

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

PANDAS
www.medlink.com,Feb, Erfe,M.C.B., 2011

Role of Brain Imaging in Early Parkinsonism
BMJ 324:d638, Breen,D.P.,et al, 2011

Deep Brain Stimulation
JAMA 305:732, Pluta,R.,et al, 2011

Revascularization of Asymptomatic High-Grade Carotid Stenosis Is Still Indicated in Some Cases
Stroke 42:1152-1153, 1156, Markus,H., 2011

Revascularization of Asymptomatic High-Grade Stenosis Is Not Indicated With Contemporary Stroke Prevention Medical Therapy
Stroke 42:1154-1155, 1156, Ingall,T.J., 2011

Population-based study of wake-up strokes
Neurol 76:1662-1667, Mackey, J.,et al, 2011

Autoimmune encephalitis
BMJ 342:d1918, Irani, S.R.,et all, 2011

Helicopter Transport of Stroke Patients and Its Influence on Thrombolysis Rates
Stroke 42:1295-1300, Reiner-Deitemyer, V.,et al, 2011

Reliability of Prehospital Real-Time Cellular Video Phone in Assessing the Simplified National Institutes of Health Stroke Scale in Patients With Acute Stroke
Stroke 42:1522-1527, Gonzalez, M.A.,et al, 2011

Ischemic Stroke During Sleep Its Association with Worse Early Functional Outcome
Stroke 42:1901-1906, Kim, B.J.,et al, 2011

Changing Concepts of Alzheimer Disease
JAMA 35:2458-2459, McKhann, G.M., 2011

Movement Disorders Emergencies Part 2 Hyperkinetic Disorders
Arch Neurol 68:719-724, Robottom, B.J.,et al, 2011

Clinical Reasoning: A 34-year-old man with recurrent limb weakness
Neurol 77:e68-e72, Karam, C.,et al, 2011

GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
Neurol 77:1287-1294, Prust, M.,et al, 2011

Treat Alzheimer Disease Before It Is Symptomatic
Arch Neurol 68:1237-1238, , 2011

Longitudinal Change of Biomakers in Cognitive Decline
Arch Neurol 68:1257-1266,1237, Lo, R.Y.,et al, 2011

A Strange Case of Waitress Headache
Lancet 378:1824, Libera, D.D.,et al, 2011

Clinicopathologic Conference, Cystoisospora Belli Enteritis and HIV Infection
NEJM 365:2306-2316, Case 38-2011, 2011

Functional Weakness: Clues to Mechanism from the Nature of Onset
JNNP 83:67-69, Stone, J.,et al, 2011

Epstein-Barr Virus Infections of the Nervous System
www.medlink.com, Nov, Amlie-Lefond,C., 2011

Anti-N-Methyl-d-Aspartate Receptor Encephalitis: Characteristic Behavioral and Movement Disorder
Arch Neurol 67:250-251, Ferioli,S.,et al, 2010



Showing articles 400 to 450 of 1826 << Previous Next >>