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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 950 to 1000 of 1826 << Previous Next >>

Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
Arch Neurol 54:539-544, Basun,H.,et al, 1997

Sumatriptan for Migraine Attacks in Children:A Randomized Placebo-Controlled Study
Neurol 48:1100-1103, Hamalainen,M.L.,et al, 1997

Seizures in Medically Complex Patients
Epilepsia 38:S55-S59, Boggs,J.G., 1997

Arterial Injuries in Transsphenoidal Surgery for Pituitary Adenoma:The Role of Angiography and Endovascular Treatment
ANJR 18:655-665, Raymond,J.,et al, 1997

If First AED Fails to Control Child's Epilepsy, What Are the Chances of Success with Next Drug
J Pediatr 131:821-824, 7941997., Camfield,P.R.,et al, 1997

Epilepsy in Childhood
BMJ 315:924-930, Neville,B.G.R., 1997

A Meta-Analytic Review of the Preventive Treatment of Recurrences of Febrile Seizures
J Pediatr 131:922-925, Rantala,H.,et al, 1997

Tongue Protrusion Dystonia:Treatment with Botulinum Toxin
South Med J 90:522-525, Charles,P.D.,et al, 1997

Treatment of First Tonic-Clonic Seizure Does Not Improve the Prognosis of Epilepsy
Neurol 49:991-998, Musicco,M.,et al, 1997

Movement Disorders Associated with the Serotonin Selective Reuptake Inhibitors
J Clin Psychiatry 57:449-454, Leo,R.J., 1996

Status Epilepticus in Children with Epilepsy:The Role of Antiepileptic Drug Levels in Prevention
Pediatrics 98:1119-1121, Maytal,J.,et al, 1996

Early Treatment of a Single Generalized Tonic-Clonic Seizure to Prevent Recurrence
Arch Neurol 53:1149-1152, Gilad,R.,et al, 1996

Post-Traumatic Movement Disorders in Survivors of Severe Head Injury
Neurol 47:1488-1492, Krauss,J.K.,et al, 1996

Neurocysticercosis:Report of Unusual Pediatric Cases
Pediatrics 98:974-977, Stamos,J.K.,et al, 1996

Precipitants of Brain Infarction:Roles of Preceding Infection/Inflammation & Recent Psychological Stress
Stroke 27:1999-2004, Macko,R.F.,et al, 1996

Diagnosis of Patients Presenting to a Huntington Disease (HD) Clinic without a Family History of HD
Neurol 47:1578-1580, Nance,M.A.,et al, 1996

Clinical Genetic Analysis of Parkinson's Disease in the Contursi Kindred
Ann Neurol 40:767-775, Golbe,L.I.,et al, 1996

Factors Delaying Hospital Admission After Acute Stroke
Stroke 27:398-400, Fogelholm,R.,et al, 1996

Striatopallidal and Thalamic Dystonia, A Magnetic Resonance Imaging Anatomoclinical Study
Arch Neurol 53:241-250, Lehericy,S.,et al, 1996

Clinical Heterogeneity of Adhalin Deficiency
Ann Neurol 39:196-202, Morandi,L.,et al, 1996

High-Dose Corticotropin (ACTH) vs. Prednisone for Infantile Spasms:A Prospective, Randomized, Blinded Study
Pediatrics 97:375-379, Baram,T.Z.,et al, 1996

An Increased Frequency of Patent Foramen Ovale in Patients with Transient Global Amnesia
Arch Neurol 53:504-508, Klotzsch,C.,et al, 1996

Is Stroke Incidence Related to Season or Temperature
Lancet 347:934-936, Rothwell,P.M.,et al, 1996

Weekend and Holiday Increase in the Onset of Ischemic Stroke in Young Women
Stroke 27:1023-1027, Haapaniemi,H.,et al, 1996

Factors Delaying Hospital Admission in Acute Stroke:The Copenhagen Stroke Study
Neurol 47:383-387, Jorgensen,H.S.,et al, 1996

The Syndrome of Posterior Choroidal Artery Territory Infarction
Ann Neurol 39:779-788, Neau,J.&Bogousslavsky,J., 1996

Neurologic Presentation of Wilson Disease without Kayser-Fleischer Rings
Neurol 46:1040-1043, Demirkiran,M.,et al, 1996

Delayed-Onset Cerebellar Syndrome
Arch Neurol 53:450-454, Louis,E.D.,et al, 1996

Antiepileptic Drugs
NEJM 334:168-175, Brodie,M.J.&Dichter,M.A., 1996

Discontinuation of Antiepileptic Drug Treatment after Two Seizure-Free Yrs in Children with Cerebral Palsy
Pediatr 97:192-197, Delgado,M.R.,et al, 1996

High Apolipoprotein E e4 Allele Frequency in Age-Related Memory Decline
Ann Neurol 39:548-551, Blesa,R.,et al, 1996

Botulinum Toxin Versus Trihexphenidyl in Cervical Dystonia:A Prospective, Randomized, Double-Blind Controlled Study
Neurol 46:1066-1072, Brans,J.W.M.,et al, 1996

Dementia and Adult-Onset Unprovoked Seizures
Neurol 46:727-730, Hesdorffer,D.C.,et al, 1996

Celiac Disease with Cerebral Calcium and Silica Deposits:X-ray Spectroscopic Findings, An Autopsy Study
Neurol 46:1088-1092, Toti,P.,et al, 1996

Reversible Dementia and Chorea in a Young Woman with the Lupus Anticoagulant
Neurol 46:1599-1603, Van Horn,G.,et al, 1996

Cough, Exertional, and Sexual Headaches:An Analysis of 72 Benign and Symptomatic Cases
Neurol 46:1520-1524, Pascual,J.,et al, 1996

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

Varicalla-Zoster Virus DNA in CSF & Arteries in Delayed Contralat Hemiplegia:Evid for Viral Invasion of Cerebr Art
Neurol 47:569-570, Melanson,M.,et al, 1996

Chorea-Ballismus with Nonketotic Hyperglycemia in Primary Diabetes Mellitus
AJNR 17:1057-1064, Lai,P.,et al, 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Blepharospasm:Report of a Workshop
Neurol 46:1213-1218, Hallett,M.&Daroff,R.B., 1996

Multifocal Motor Neuropathy
JNNP 60:599-603, Nobile-Orazio,E., 1996

Preclinical Evidence of Alzheimer's Disease in Persons Homozygous for the e4Allele for Apolipoprotein E
NEJM 334:752-758, 7911996., Reiman,E.M.,et al, 1996

Subcortical Heterotopia:A Distinct Clinicoradiologic Entity
AJNR 17:1315-1322, Barkovich,A.J., 1996

Discontinuation of Anticonvulsant Therapy in Children Free of Seizures for 1 Year:A Prospective Study
Neurol 46:969-974, Dooley,J.,et al, 1996

Simple Partial Status Epilepticus:Causes, Treatment and Outcome in 47 Patients
JNNP 61:90-92, Scholtes,F.B.,et al, 1996

Non-Convulsive Status Epilepticus:Causes, Treatment, and Outcome in 65 Patients
JNNP 61:93-95, Scholtes,F.B.,et al, 1996

Random Comp Monother Trial of Phenobarb, Phenytoin, Carbamazepine, or Sod Valp for Newly Dx Child Epilep
Lancet 347:709-713, deSilva,M.,et al, 1996

Startle Provoked Epileptic Seizures:Features in 19 Patients
JNNP 61:151-156, Manford,M.R.A.,et al, 1996



Showing articles 950 to 1000 of 1826 << Previous Next >>