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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 1100 to 1150 of 1853 << Previous Next >>

Clinicopath Conf
Small Cell CA (of lung) with Lambert-Eaton Myasthenic Syndr, Case 32-1994, NEJM 331:528-5354., , 1994

Brief Report:Organic Osmolytes in the Brain of an Infant with Hypernatremia
NEJM 331:439-442, Lee,J.H.,et al, 1994

Dopa-Responsive Dystonia:Pathological and Biochemical Observations in a Case
Ann Neurol 35:396-402, 3811994., Rajput,A.H.,et al, 1994

Parkinson's Disease
JNNP 57:672-681, Marsden,C.D., 1994

Discontinuing Antiepileptic Drugs in Children with Epilepsy
NEJM 330:1407-1410, Tennison,M.,et al, 1994

Relapse Following Discontinuation of Antiepileptic Drugs:A Meta-Analysis
Neurol 44:601-608, Berg,A.T.&Shinnar,S., 1994

Discontinuing Antiepileptic Drugs in Children with Epilepsy:A Prospective Study
Ann Neurol 35:534-545, 5091994., Shinnar,S.,et al, 1994

Video Game Induced Seizures
JNNP 57:925-931, Ferrie,C.D.,et al, 1994

Efficacy of Felbamate in Therapy for Partial Epilepsy in Children
J Pediatr 125:481-486, Carmant,L.,et al, 1994

Early Presentation of Hemispheric Intracerebral Hemorrhage:Prediction of Outcome and Guidelines for Treatment Allocation
Neurol 44:133-139, Lisk,D.R.,et al, 1994

Long-Term Risk of Recurrent Stroke After a First-Ever Stroke:The Oxfordshire Community Stroke Project
Stroke 25:333-337, Burn,J.,et al, 1994

Involuntary Tonic Spasms of a Limb Due to a Brain Stem Lacunar Infarction
Stroke 25:217-219, Kaufman,D.K.,et al, 1994

Electroencephalography as an Aid in the Exclusion of Alzheimer's Disease
Arch Neurol 51:280-284, Robinson,D.J.,et al, 1994

Aspartame Has no Effect on Seizures or Epileptiform Discharged in Epileptic Children
Ann Neurol 35:98-103, Shaywitz,B.A.,et al, 1994

Long-Term Botulinum Toxin Treatment of Focal Hand Dystonia
Neurol 44:70-76, Karp,B.I.,et al, 1994

Video Game-Related Seizures:A Report on 10 Patients and a Review of the Literature
Pediatrics 93:551-556, Graf,W.D.,et al, 1994

Characteristics of the Dementia in Late-Onset Metachromatic Leukodystrophy
Neurol 44:662-665, Shapiro,E.G.,et al, 1994

Prognostic Factors for Seizure Recurrence after Withdrawal of Antiepileptic Drugs in Patients with Neurocysticercosis
Neurol 44:1706-1709, DelBrutto,O.H., 1994

Delayed Symptoms and Death After Minor Head Trauma with Occult Vertebral Artery Injury
JNNP 57:500-502, Auer,R.N.,et al, 1994

Prospective Study of Sentinel Headache in Aneurysmal Subarachnoid Haemorrhage
Lancet 344:590-593, Linn,F.H.,et al, 1994

Delayed Sequelae of Vertebral Artery Dissection and Occult Cervical Fractures
Neurol 44:1397-1399, Tulyapronchote,R.,et al, 1994

Prospective Study of Endogenous Tissue Plasminogen Activator and Risk of Stroke
Lancet 343:940-943, Ridker,P.M.,et al, 1994

Cocaine-Induced Choreoathetoid Movements ('Crack Dancing')
Neurol 44:751-752, Daras,M.,et al, 1994

The Relationship of Essential Tremor to Other Movement Disorders:Report on 678 Patients
Ann Neurol 35, 717-7231994., Koller,W.C.,et al, 1994

Prolonged MRI T2 Times of the Lentiform Nucleus in Idiopathic Spasmodic Torticollis
Neurol 44:846-850, Schneider,S.,et al, 1994

Dystonia after Head Trauma
Neurol 44:1374-1378, Lee,M.S.,et al, 1994

Levodopa Failure in Chronic Manganism
Neurol 44:1600-1602, 15831994., Lu,C-S.,et al, 1994

Familial Alzheimer's Disease
Ann Neurol 36:335-336, Bird,T.D., 1994

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Chromosome 14-Encoded Alzheimer's Disease:Genetic and Clinicopathological Description
Ann Neurol 36:362-367, Haltia,M.,et al, 1994

Familial Progressive Subcortical Gliosis
Neurol 44:1633-1643, Lanska,D.J.,et al, 1994

Isolated Sphenoid Sinusitis: The Tornoto Hospital for Sick Children Experience and Review of the Literature
J Otolaryngol 23:36-41, Hnatuk,L.A.P.,et al, 1994

Acquired Cerebral Achromatopsia
Neuro Ophthalmol 14:31-36, Setala, K. & Vesti, E., 1994

Headache Caused by a Single Lesion of Multiple Sclerosis in the Periaqueductal Gray Area
Headache 33:452-455, Haas,D.C.,et al, 1993

Essential Tremor and Dystonia
Neurol 43:2382-2384, Dubinsky,R.M.,et al, 1993

Myositis-Specific Autoantibodies, Touchstones for Understanding the Inflammatory Myopathies
JAMA 270:1846-1849, Miller,F.W., 1993

Benign Exertional Headache
Lance, J. W. In Mechanism and Management of Headache, 5th Ed, Butterworth-Heinemann, Boston, p. 193, , 1993

Coital Cerebral Hemorrhage
Neurol 43:2683-2685, Finelli,P.F., 1993

Evaluation Times for Patients with In-Hospital Strokes
Stroke 24:1817-1822, Alberts,M.J.,et al, 1993

Time of Hospital Presentation in Patients with Acute Stroke
Arch Int Med 153:2558-2560, Barsan,W.G.,et al, 1993

Factors Associated with Early Presentation of Acute Stroke
Stroke 24:1805-1810, Feldmann,E.,et al, 1993

Clinicopath Conf
progressive Supranuclear Palsy, Case 46-1993, NEJM 329:1560-1567993., , 1993

Clinicopath Conf
Acquired Demyelinating Neuropathy, ? CIDP, ? Motor Neuropathy with Multifocal Conduction Blocks, Cas, 41-1EJM 329:1182-1190,1993., 1993

Intractable Seizures in Infancy and Early Childhood
Neurol 43 (suppl-5) :S2-S37993., Moshe,S.L.&Dulac,O., 1993

Hippocampal Sclerosis in Epilepsy and Childhood Febrile Seizures
Lancet 342:1391-1394, Kuks,J.B.M.,et al, 1993

Hippocampal Sclerosis in Children with Intractable Temporal Lobe Epilepsy:Detection with MR Imaging
AJR 161:1045-1048, Grattan-Smith,J.D.,et al, 1993

Transient Epileptic Amnesia-A Clinical Update and a Reformulation
JNNP 56:1884-1190, Kapur,N., 1993

Risk Factors for Parkinson's Disease
Neurol 43:1693-1697, 16411993., Hubble,J.P.,et al, 1993

Environmental Antecedents of Young-Onset Parkinson's Disease
Neurol 43:1150-1158, Butterfield,P.G.,et al, 1993

Prognostic Significance of the Onset Mode in Parkinsonism
Neurol 43:829-830, Rajput,A.H.,et al, 1993



Showing articles 1100 to 1150 of 1853 << Previous Next >>