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acetazolamide
advances in neurology
agitation
amnesia
AMPA receptor antibodies
amphiphysin antibodies
anti GQ1b IgG antibody
anti IgLON5
antibodies to voltage-gated calcium channels
arrhythmia, cardiac
ataxia
ataxia, cerebellar
ataxia, paroxysmal
atypical
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autoimmune encephalopathy
autoimmune epilepsy
autonomic dysfunction
autonomic neuropathy
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
behavioral disorder, acute
bradykinesia
brain atrophy
brain biopsy
burning feet
calcium channel dysfunction
carcinoma
carcinoma of lung
CAT scan, emission, abnormal
catatonia
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
central core disease
cerebellar degeneration
cerebral cortex
cerebral cortical atrophy
cerebrospinal fluid, abnormal
cerebrospinal fluid, childhood
cerebrospinal fluid, oligoclonal IgG in
children
chloride channel dysfunction
chorea
chorea, senile
choreoathetosis
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
cold hands sign
collapsin response mediator protein 5 IgG
coma
complications
confabulation
confusion
constipation
contactin associated protein like 2 antibodies
controversies in neurology
cortical ribbon sign
cytochrome c oxidase
deep gray nuclei
dementia
dementia, rapidly progressive
dementia, reversible
dementia, treatment of
depression
dermatomyositis
diagnostic criteria
diarrhea
dichlorphenamide
differential diagnosis
disability, neurological
DPPX
DPPX, antibodies
DPPX, antibodies, encephalitis
dyskinesia
dyskinesia, facial
dystonia
efficacy
electroencephalogram, abnormalities of
electromyogram
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, clinical picture and treatment of
encephalitis, etiology
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis
encephalopathy
episodic neurologic deficits
faciobrachial dystonic seizure
false negative
familial hemiplegic migraine
fasciculation
fever
flu-like illness
gait disorder
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gastrointestinal disease, neurologic complications
gender
gene
gene mutation
genetic neurologic disorders
glutamic acid decarboxylase, antibody
glycine receptor antibodies
hallucination
hallucination, olfactory
headache
hemimyoclonic jerks
heralding manifestation
herpes simplex encephalitis
hippocampus
Hodgkin's disease
hyperekplexia
hyperhidrosis
hyperkalemic periodic paralysis
hypersomnia
hypertension
hypokalemic periodic paralysis
hyponatremia
hyponatremia with cerebral disorders
immunologic disease
immunology and the nervous system
immunomodulation
immunosuppressive agents
immunotherapy
inappropriate antidiuretic(A.D.H.)hormone
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
insomnia
intellectual deficit
intellectual deterioration
Jakob-Creutzfeldt disease
lateropulsion
leucine rich glioma inactivated 1 antibodies
leukemia, neurologic findings assoc.with
level of consciousness, decreased
limbic encephalitis
limbic system
malignancy screen
malignancy, occult
malignant hyperpyrexia
masked facies
memory
memory, defect of recent
memory, impairment of
meningeal enhancement
mental status, abnormal
mesial temporal lobe
mesial temporal sclerosis
mexiletine
migraine
mild cognitive impairment
mimics
misdiagnosis
molecular genetics
monoclonal antibodies
mood change
mortality
Morvan's fibrillary chorea
movement disorder
movement disorder, extrapyramidal
MRI
MRI pattern
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, FLAIR
MRI, negative
muscle diseases, characteristics of
muscle spasm
muscle stiffness
muscle twitching
myasthenia gravis, paraneoplastic
myasthenic syndrome
myelitis, transverse, recurrent
myoclonic jerks
myoclonus
myokymia
myotonia
myotonia congenita
near syncope
negative
neurexin-3 alpha antibodies
neurologic disease, diagnoses of
neurologic disease, multifocal
neuromuscular junction
neuromyotonia
neuronal cell surface antigen
neuronopathy, sensory
neuropathy, paraneoplastic
night sweats
NMDA antagonists
old age, neurology of
onconeural antibodies
ophelia syndrome
opsoclonus-myoclonus syndrome
pain
paralysis
paramyotonia congenita
paraneoplastic cerebellar degeneration
paresthesias
Parkinsonism syndrome
paroxysmal neurologic deficits
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
periodic paralysis
peripheral nerve, lesion of
personality change
plasmapheresis
pleocytosis of cerebrospinal fluid
potassium channel antibodies
potassium channel dysfunction
practice guidelines
precipitating factors
prognosis
progressive neurologic disorder
pruritus
psychiatric problems in neurologic disorders
psychological testing
psychosis
psychosis, acute
rapidly progressing neurologic illness
recurrent
Red flags
remote effect of cancer on the nervous system
retinopathy
reversible neurologic disorder
review article
rippling muscle disease
rituximab
safety
screening
seizure
seizure, adult onset
seizure, drug resistance
seizure, focal
seizure, intractable
seizure, intractable, treatment of
seizure, psychomotor-temporal lobe
seizure, treatment of
seizure, unknown origin
serologic testing
serologic testing, false negative
seronegative
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
sleep pathology and physiology
sodium channel dysfunction
spinocerebellar ataxia
spinocerebellar ataxia type 6
status epilepticus
steroid
steroid therapy, CNS treatment and complications with
striatal encephalitis
striatum, lesion of
striatum, lesion of, bilateral
symmetric brain lesions
tangential
temporal lobe
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
thiazide diuretic
thymoma
transient neurologic deficit
treatment of neurologic disorder
treatment, empirical
tremor
unconsciousness
undiagnosed
visual loss
weight loss
wheelchair
white matter disease
white matter disease, subcortical
wide based gait
workup
Showing articles 900 to 950 of 4410 << Previous Next >>

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

Sudden, Unexpected Death in Epilepsy
NEJM 365:2902-11, Devinsky, O., 2011

Internal Carotid Artery Dissection Heralded by an Oculomotor Nerve Palsy
Neurologist 17:333-337, Nizam, A.,et al, 2011

Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
Acta Radiologica 52:336-339, Talbott,S.D.,et al, 2011

Cerebral Amyloid Angiopathy Related Inflammation: Three Case Reports and a Review
JNNP 82:20-26, Chung,K.K.,et al, 2011

Patterns and Trends in Antipsychotic Prescribing for Parkinson Disease Psychosis
Arch Neurol 68:899-904, Weintraub, D.,et al, 2011

A Case of Hashimoto Encephalopathy Clinical Manifestation, Imaging, Pathology, Treatment, and Prognosis
The Neurologist 17:141-143, Zhao, W.,et al, 2011

Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease
Neurol 76:1372-1376, Sone, J.,et al, 2011

Post-acute care and secondary prevention after ischaemic stroke
BMJ 342:d2083, McArthur, K.S.,et al, 2011

Redefining the Guillain-Barre Spectrum in Children: Neuroimaging Findings of Cranial Nerve Involvement
AJNR 32:639-42, Zuccoli, G.,et al, 2011

Transition to Adult Care for Children with Chronic Neurological Disorders
Ann Neurol 69:437-444, Camfiled, P. & Camfield, C., 2011

From Jekyll to Hydeafter limbic subthalamic nucleus infarction
Neurol 77:82-84, Park, H.K.,et al, 2011

Rhombencephalitis A Series of 97 Patients
Medicine 90:256-261, Moragas, M.,et al, 2011

Late onset autism and anti-NMDA-receptor encephalitis
Lancet 378:98;378, Creten, C.,et al, 2011

Trigger Factors and Their Attributable Risk for Rupture of Intracranial Aneurysms A Case-Crossover Study
Stroke 42:1878-1882, Vlak, M.H.M.,et al, 2011

Presentation, Diagnosis, Pathophysiology, and Treatment of the Neurological Features of Sturge-Weber Syndrome
The Neurologist 17:179-184, Comi, A.M., 2011

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

Mild Cognitive Impairment
NEJM 362:2227-2234, Peterson, R.C., 2011

The Evaluation of Rapidly Progressive Dementia
The Neurologist 17:67-74, Rosenbloom,M.H. &Atri,A., 2011

Anti-Ab Autoantibodies in the CSF of a Patient With CAA-Related Inflammation: A Case Report
Neurol 76:842-844, DiFrancesco,J.C.,et al, 2011

Clinical and Functional Outcome and Factors Predicting Prognosis in Osmotic Demyelination Syndrome (Central Pontine and/or Extrapontine Myelinolysis) in 25 Patients
JNNP 82:326-331, Kallakatta,R.N.,et al, 2011

Longitudinal Assessment of A-beta and Cognition in Aging and Alzheimer Disease
Ann Neurol 69:181-192, Villemagne,V.L.,et al, 2011

Child Development Following In Utero Exposure: Levetiracetam vs Sodium Valproate
Neurol 76:383-389, Shallcross,R.,et al, 2011

Family Paralysis
Lancet 377:352, Sung,C.-C.,et al, 2011

Clinicopathologic Conference, Sjogrens syndrome with dorsal-root ganglionitis
NEJM 364:1856-1865, Case 14-2011, 2011

CSF Complements Serum for Evaluating Paraneoplastic Antibodies and NMO-IgG
Neurol 76:1108-1110, McKeon,A.,et al, 2011

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Diagnosing variant Creutzfeldt-Jakob disease: a retrospective analysis of the first 150 cases in the UK
JNNP 82:646-651, Heath, C.A.,et al, 2011

Autoimmune Encephalopathy
Semin Neurol 31:144-157, Flanagan, E.,et al, 2011

Subacute sclerosing panencephalitis: An Update
Dev Med Child Neurol 52:901-907, Guitierrez, J.,et al, 2010

Clinical Reasoning: A 9-year-old Girl With Seizures and Encephalopathy
Neurol 74:e97-e100, Nguyen,T.P. &El-Hakam,L.M., 2010

Cerebral Amyloid Angiopathy
UpToDate: May 2010, Greenberg,S.M.,et al, 2010

Vitamin B12-Responsive Severe Leukoencephalopathy and Autonomic Dysfunction in a Patient With "Normal" Serum B12 Levels
JNNP 81:1369-1371, Graber,J.J.,et al, 2010

Brain Biopsy in Children With Primary Small-Vessel Central Nervous System Vasculitis
Ann Neurol 68:602-610, 573, Elbers,J.,et al, 2010

Dysexecutive Syndrome: Diagnostic Criteria and Validation Study
Ann Neurol 68:855-864, Godefroy,O.,et al, 2010

Atypical Dementia
Lancet 376:656, Cohen-Bittan,J. et al, 2010

Hemichorea-Hemiballism after Diabetic Ketoacidosis
NEJM 363:e27, Duker,A.P. &Epsay,A.J., 2010

Tourettes Syndrome
NEJM 363:2332-2338, Kurlan,R., 2010

Validation of the Coin Rotation Test: A Simple, Inexpensive, and Convenient Screening Tool for Impaired Psychomotor Processing Speed
Neurologist 16:249-253, Hill,B.D., et al, 2010

Bilateral Facial Nerve Palsy Associated With Epstein-Barr Virus Infection
JNNP 81:1155-1156, Coddington,C.T.,et al, 2010

3-Methylglutaconic Aciduria Type I Redefined: A Syndrome With Late-Onset Leukoencephalopathy
Neurol 75:1079-1083, Wortmann,S.B.,et al, 2010

Huntingtons Disease
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010

Delirious Deficiency
Lancet 376:1362, Olsen,R.Q &Regis,J.T., 2010

Profound Deafness in Childhood
NEJM 363:1438-1450, Kral,A.,et al, 2010

A Horse Bite to Remember
Lancet 376:1194, Brouwer,M.C.,et al, 2010

What Predicts Mortality in Parkinson Disease? A Prospective Population-Based Long-Term Study
Neurol 75:1270-1276, Forsaa,E.B.,et al, 2010

Traumatic Brain Injury - Football, Warfare, and Long-Term Effects
NEJM 363:1293-1296, DeKosky,S.T.,et al, 2010

Cognitive Impairment and Dementia in Neurocysticercosis: A Cross-Sectional Controlled Study
Neurol 74:1288-1295, Ciampi de Andrade,D., et al, 2010

Practice Parameter Update: Evaluation and Management of Driving Risk in Dementia: Report of the Quality Standards Subcommittee of the American Academy of Neurology
Neurol 74:1316-1324, Iverson,D.J., et al, 2010

Clinicopath Conf., Progressive Multifocal Leukoencephalopathy
NEJM 362:1431-1437, Case 11-2010, 2010



Showing articles 900 to 950 of 4410 << Previous Next >>