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acanthocytosis
acetazolamide
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome-related complex
Adies pupil
advances in neurology
adverse drug reaction
aggression
agitation
akathisia
alcohol
alcohol, neurologic complications with
algorithm
alien hand syndrome
alternating hemiplegia
alternating hemiplegia of childhood
alveolar hypoventilation
amimia
aminoacidopathies
aminoacidurias
AMPA receptor antibodies
amphiphysin antibodies
amyotrophic chorea-acanthocytosis
anemia
anti basal ganglia antibodies
anti GQ1b IgG antibody
anti IgLON5
anticonvulsants
anticonvulsants, blood level determination of
anticonvulsants, untoward effects of
antihistamines
anxiety
apraxia
apraxia of eye movements
apraxia, constructional
areflexia
arthralgia
asterixis
astrocytoma
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
athetosis
ATP1A3 gene
attention deficit disorder with hyperactivity
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autoimmune encephalopathy
autoimmune epilepsy
autonomic dysfunction
autonomic neuropathy
B 12 deficiency
Babinski sign
ballismus, bilateral
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery migraine
behavioral disorder
behavioral disorder, acute
benign essential tremor
beta adrenergic blocker
biotin
biotin deficiency
biotin deficiency, juvenile form
biotin-responsive basal ganglia disease
bladder dysfunction
blepharospasm
blinking, reduced
body odor
bone marrow biopsy
botulinum toxin
bradycardia
bradykinesia
brain biopsy
brainstem, atrophy
brainstem, lesion of
bruxism
burning skin
calcification, intracranial
calcium antagonist
carbamazepine
carbamazepine, toxicity
carbon monoxide poisoning
carcinoma
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, emission, abnormal
CAT scan, isodense lesion with acute hemorrhage
cataracts
catatonia
catecholamine
caudate nucleus, atrophy
central nervous system, infection of
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
cerebral edema
cerebral ischemia
cerebral palsy
cerebral palsy, adults
cerebral palsy, associated problems with
cerebral vasculature, calcification
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count, normal
cerebrovascular accident
cerebrovascular accident, complications with
cerebrovascular accident, young adult
ceruloplasmin, serum
channelopathy
children
chorea
chorea, familial
chorea, treatment of
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 1
chromosome 7
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clonazepam
cognition
cold intolerance
collapsin response mediator protein 5 IgG
coma
coma, causes of
coma, episodic
coma, unknown etiology
complications
compression fracture
computers, neurologic diagnosis and
confusion
conjugate gaze, forced
consanguinity
contactin associated protein like 2 antibodies
conversion reaction
copper metabolism, abnormal
cortical-basal ganglionic degeneration
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
dementia, rapidly progressive
dementia, reversible
dementia, treatment of
depression
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes insipidus
diabetes mellitus
diagnostic criteria
diarrhea
diet
differential diagnosis
dilantin
dilantin, toxicity
diphenhydramine
diplopia
disability, neurological
dopamine
dopamine antagonist
down-beat nystagmus
DPPX
DPPX, antibodies
DPPX, antibodies, encephalitis
drooling
dysarthria
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, drug induced
dyskinesia, facial
dysphagia
dyspnea
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, children
dystonia, delayed onset
dystonia, drug induced
dystonia, face
dystonia, focal
dystonia, infancy
dystonia, painful
dystonia, paroxysmal
dystonia, psychogenic
dystonia, treatment of
dystonic reaction, acute
DYT1 mutation
efficacy
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
ELISA
emergencies, neurologic
emotional lability
encephalitis
encephalitis lethargica
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, clinical picture and treatment of
encephalitis, etiology
encephalitis, focal
encephalitis, paraneoplastic
encephalitis, viral
encephalopathy
encephalopathy, neonatal
encephalopathy, post anoxic
enuresis
enzyme, defect
epileptic encephalopathy
episodic disorders
episodic neurologic deficits
epsilon sarcoglycan gene
exercise
exercise intolerance
exome sequencing
extralimbic encephalitis
eye color
eye movement, disorders of
face, contractions
facial nerve palsy
faciobrachial dystonic seizure
Fahr disease
falling
familial
fatigue
felbamate
fever
fluctuate
flunarizine
gait disorder
gamma amino butyric acid
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gaze deviation
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gender
gene
gene mutation
genetic neurologic disorders
genetic testing
Gilles de la Tourette syndrome
globus pallidus
globus pallidus, lesion of
GLUT1
GLUT1 deficiency syndrome
glutamic acid decarboxylase, antibody
glycine receptor antibodies
grimacing
Hallervorden Spatz disease
handedness
hands, fisted
head injury
head nodding
headache
hearing loss
heart block
hemiballismus
hemichorea
hemimyoclonic jerks
hemiparesis
hemiparesis, transient
hemiplegia
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
heralding manifestation
herpes simplex encephalitis
hippocampus
Hodgkin's disease
homovanillic acid
human immunodeficiency virus type 1
Huntington's chorea
Huntington's disease, children
hydrocephalus
hyperekplexia
hyperreflexia
hypertension
hypocalcemia
hypoglycorrhachia
hyponatremia
hypoparathyroidism
hyporeflexia
hyposmia
hypotension, systemic
hypotonia
hypotonia, infants
hypoxia, newborn
hypoxic encephalopathy
imbalance
immunologic disease
immunosuppression
immunosuppressive agents
immunotherapy
inappropriate antidiuretic(A.D.H.)hormone
inborn errors of metabolism
incidence
incoordination
infantile hemiplegia
insomnia
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
intracerebral hemorrhage
iron, brain
islet cell tumor
Jakob-Creutzfeldt disease
karyotyping
Kayser-Fleischer ring
Kearns-Sayre syndrome
ketogenic diet
lactic acidemia
lateropulsion
L-dopa
Leber's hereditary optic neuropathy
left handedness
Leigh's disease
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
leucine rich glioma inactivated 1 antibodies
leukodystrophy
level of consciousness, decreased
levitation
Lewy body disease, diffuse
limbic encephalitis
lipid storage disorder of CNS
liver disease
lobar atrophy
lumbar puncture
lysosomal storage disease
masked facies
mediastinum, mass of
medical-legal aspects of neurology
MELAS syndrome
memory
memory, defect of recent
memory, impairment of
meningitis, carcinomatous
mental retardation
mental status, abnormal
MERRF syndrome
mesial temporal lobe
metabolic disorder, primary
metabolic disorder, primary-screening tests
microcephaly
migraine
migraine, hemiplegic
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
monoamines
monoclonal antibodies
mortality
motor neuron disease
movement disorder
movement disorder, delayed onset
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, hyperkinetic
movement disorder, paroxysmal
movement disorder, psychogenic
movement disorder, treatment of
MRI
MRI pattern
MRI, abdomen
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, FLAIR
MRI, negative
MRI, paramagnetic effect
MRI, pelvis
MRS
multiple sclerosis
multiple sclerosis, paroxysmal symptoms in
muscle pain
muscle weakness
musicians
musician's dystonia
mutism
mycotoxin
myelitis, transverse, recurrent
myelopathy
myoclonic dystonia
myoclonic jerks
myoclonus
myoclonus, action
myoclonus, cortical
myoclonus, segmental
myokymia
myopathy
myopathy, mitochondrial
myorhythmia
mysoline
neoplasm, intracranial
neoplasm, primary intracerebral
neoplasm, primary of CNS
neurexin-3 alpha antibodies
neuroendocrinology
neuroleptic
neuroleptic malignant syndrome
neurologic complications
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, multifocal
neurologic signs
neurologic symptoms
neurologic testing
neuromyotonia
neuronal cell surface antigen
neuropathology
neuropathology, brain
neuropathy
neurotoxin
neurotransmitter
Niemann-Pick disease
nitroproprionic acid
NMDA antagonists
norepinephrine
nystagmus
nystagmus, monocular
nystagmus, periodic
nystagmus, vertical
occupational neurologic disorders
ocular motility, disorders of
oculogyric crisis
ophelia syndrome
ophthalmoplegia
opisthotonus
optic atrophy
optic neuropathy
optokinetic nystagmus, abnormal
pain
pancytopenia
PANK2 mutation
Parkinson disease
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, dystonia with
Parkinson disease, L-dopa nonresponsive
Parkinson disease, postencephalitic
Parkinson disease, psychogenic
Parkinson disease, tremor, absence of
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal exertion-induced dyskinesia
paroxysmal hemiplegia
paroxysmal hypnogenic dyskinesia
paroxysmal kinesigenic dyskinesia
paroxysmal neurologic deficits
paroxysmal neurologic disorder
paroxysmal nonkinesigenic dyskinesia
pathognomonic
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
penicillamine
peroxisomal disease
personality change
phencyclidine poisoning
phenylketonuria
pigmentary retinopathy
pitfalls
PLEDs
pleocytosis of cerebrospinal fluid
poison, neurologic problems with
polymyositis
pons, lesion of
potassium channel antibodies
practice guidelines
precipitating factors
primary episodic ataxia
primary familial brain calcification
prognosis
progressive neurologic disorder
propranolol
pseudohypoparathyroidism
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
psychotic behavior
ptosis
pulmonary edema
pupil, abnormality in neurologic disorders
pupil, tonic
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriplegia
ragged-red fibers
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rectal biopsy
recurrent
release phenomena
remote effect of cancer on the nervous system
respirator
respiratory failure
respiratory tract infection
retinitis pigmentosa
retinopathy
Rett's syndrome
reversible neurologic disorder
review article
rhabdomyolysis
rigidity
Riley-Day syndrome
rituximab
safety
salivation, excessive
Saudi Arabia
schizophrenia
screening
sea-blue histiocytes
sedimentation rate, elevated
seizure
seizure, adult onset
seizure, children
seizure, differential diagnosis of
seizure, dystonic
seizure, focal
seizure, neonatal
seizure, psychomotor-temporal lobe
seizure, stimulus sensitive
seizure, unknown origin
self harm
self-mutilation
semialdehyde dehydrogenase deficiency
sensorineural hearing loss
sensory loss
sensory loss, cortical
serologic testing
serologic testing, false negative
seronegative
sexual behavior, disorder of
short stature
sicca syndrome
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, lesions in neurologic disorders
sleep apnea, obstructive
sleep pathology and physiology
somnolence
spastic dysphonia
spasticity
speech disorder
speech disorder, childhood
spinal cord, lesion of
spinocerebellar ataxia type 16
splenomegaly
startle reaction
status dystonicus
status epilepticus
status epilepticus, intractable
stereotaxic surgery
stereotypy
steroid
steroid therapy, CNS treatment and complications with
stimulation, deep brain
stimulation, deep brain, bilateral
strabismus
striatal encephalitis
striatum, lesion of
striatum, lesion of, bilateral
striopallidodentate calcifications, familial idiopathic
subarachnoid hemorrhage
substantia nigra
sugarcane, mildewed
symmetric brain lesions
tardive dyskinesia
tardive dystonia
tauopathy
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
tetrahydrobiopterin
thalamic tumors
thalamotomy
thalamus, lesion of
thalamus, lesion of-bilateral
thymoma
tic
tonic foot response
tonic spasms
torticollis
toxic encephalopathy
toxins, nervous system
toxoplasmosis, CNS
transient neurologic deficit
transient paroxysmal dystonia in infancy
trauma
treatment of neurologic disorder
tremor
tremor, jaw
tremor, leg
tremor, postural
tremor, psychogenic
tremor, treatment of
trigeminal neuralgia
trinucleotide repeats
twitching, face
undiagnosed
urea-cycle enzymopathies
urine test for metabolic disorders
urine test in toxic screen
vasospasm, cerebral
vigabatrin
viral infection
viral infection, CNS
visual evoked response
visual impairment
visuospatial disturbance
walking, difficulty with
weight loss
wheelchair
Whipple's disease
white matter disease
white matter disease, subcortical
wide based gait
Wolfram syndrome
workup
xerophthalmia
xerostomia
Showing articles 350 to 400 of 4175 << Previous Next >>

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Effect of Cannabidiol on Drop Seizures in the Lennox-Gastaut Syndrome
NEJM 378:1888-1897, Devinsky, O.,et al, 2018

Transient swelling in the globus pallidus and substantia nigra in childhood suggests SENDA/BPAN
Neurol 90:974-976, Ishiyama, A.,et al, 2018

Cost-Effectiveness of Left Atrial Appendage Closure With the WATCHMAN Device Compared with Warfarin or Non-Vitamin K Antagonist Oral Anticoagulants for Secondary Prevention in Nonvalvular Atrial Fibrillation
Stroke 49:1464-1470, Reddy, V.Y.,et al, 2018

Encephalitis with mGluR5 antibodies
Neurol 90:e1964-e1972, Spatola, M.,et al, 2018

An 18-year-old man with progressive headache and visual loss
Neurol 90:1076-1081, Jiang, N.,et al, 2018

Teaching NeuroImages: Acute Necrotizing Encephalopathy of Childhood
Neurol 90:e177-e178, Biswas, A.,et al, 2018

Seizures and Encephalitis in Myelin Oligodendrocyte Glycoprotein IgG Disease vs Aquaporin 4 IgG Disease
JAMA Neurol 75:65-71, Hamid, S.H.M.,et al, 2018

Clinical Reasoning: A 66-year-old Woman with Seizures and Progressive Right-Sided Weakness
Neurol 90:e435-e439, St-Pierre, B.D.,et al, 2018

Five and 10 Minute Apgar Scores and Risks of Cerebral Palsy and Epilepsy: Population Based Cohort Study in Sweden
BMJ 360:k207, Persson, M.,et al, 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
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Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
Clin Microbiol Reviews 31:1-17, Olijve, L.,et al, 2018

Behcet Disease
emedicine.medscape.com Dec, Davey-Ranasinghe, N. & Diamond, H.S., 2018

Nivolumab-Induced Autoimmune Encephalitis in Two Patients with Lung Adenocarcinoma
Case Rep Neurol Med 2018;doi:10.1155/2018/2548528, Shah, S.,et al, 2018

Autoimmune Encephalitis: Pathophysiology and Imaging Review of an Overlooked Diagnosis
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Is it Necessary to Alter Anticoagulation Therapy for Tooth Extraction in Patients Taking Direct Oral Anticoagulants?
Med Oral Patol Oral Cir Bucal 22:e767-e773, Caliskan, M.,et al, 2017

Powassan Virus-A New Reemerging Tick-Borne Disease
Front Public Health 5:342, Fatmi,S.S., et al, 2017

Maternal Use of antiepileptic Agents During Pregnancy and Major Congenital Malformations in Children
JAMA 318:1700-1701, Bromley, R.L.,et al, 2017

A Patient with a History of Encephalomyelitis and Recurrent Optic Neuritis
Neurol 89:e231-e234, Gutman, J.M.,et al, 2017

Adult-Onset Leukoencephalopathy with Intracranial Calcifications and Cysts (Labrune Syndrome)
Neurol 88:e113-e114, Villar-Quiles, R.et al, 2017

A Woman in her 40s with Headache and New-Onset Seizures
JAMA Neurol 74:476-480, Graham, M.S.,et al, 2017

Neurological Autoantibody Prevalence in Epilepsy on Unknown Etiology
JAMA Neurol 74:397-402,384, Dubey, D.,et al, 2017

Primary Angiitis of the Central Nervous System
Stroke 48:1248-1255, Boulouis, G.,et al, 2017

Anticoagulant-Associated Intracranial Hemorrhage in the Era of Reversal Agents
Stroke 48:1432-1437, Steiner, T.,et al, 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Clinicopathologic Conference, Copper Deficiency Myelopathy
NEJM 377:1977-1984, Case 35-2017, 2017

Should Patients with Ischemic Stroke or Transient Ischemic Attack with Atrial Fibrillation and Microbleeds be Anticoagulated?
Stroke 48:3408-3412, Shoamanesh, A.,et al, 2017

Treatment of Cryptogenic Stroke with Active Cancer with a New Oral Anticoagulant
J Stroke Cerebrovasc Dis 26:2976-2980, Nam, K.W.,et al, 2017

Oral Anticoagulants for Prevention of Stroke in Atrial Fibrillation: Systematic Review, Network Meta-Analysis, and Cost Effectiveness Analysis
BMJ 359:J5058, Lopez-Lopez, J.A.,et al, 2017

Clinical Decision-Making in Functional and Hyperkinetic Movement Disorders
Neurol 88:118-123,114, van der Salm, S.M.A.,et al, 2017

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

Association of Antithrombotic Drug Use with Subdural Hematoma Risk
JAMA 317:836-846, Gaist, D.,et al, 2017

Investigations in GABA? Receptor Antibody-Associated Encephalitis
Neurol 88:1012-1020,1010, Spatola, M.,et al, 2017

Recurrence Risk of Ictal Asystole in Epilepsy
Neurol 89:785-791, Hampel, K.G.,et al, 2017

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
Neurol 89:e182-e187, Tabuas-Pereira, M.,et al, 2017

Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
Lancet 390:1758-1768, Ory, D.S.,et al, 2017

A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
Neurol 89:e193-e196, Lamb, C.J.,et al, 2017

Off-Label use of Direct Oral Anticoagulants in Intracerebral Hemorrhage Patients with Prosthetic Valves
Stroke 48:3183-3186, Chaturvedi, S.,et al, 2017

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
NEJM 377:1648-1656, Blumcke, I.,et al, 2017

Surgery for Drug-Resistant Epilepsy in Children
NEJM 377:1639-1647, Dwivedi, R.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

A Returning Traveler with Epilepsy
BMJ 359:J4664, Bandi, H.,et al, 2017

Carotid Artery Web and Ischemic Stroke
Neurol 88:65-69, Coutinho, J.M.,et al, 2017

Pregnancy, Hormonal Treatments for Infertility, Contraception, and Menopause in Women After Ischemic Stroke
Stroke 48:501-506, Caso, V.,et al, 2017

Successful Management of Super-Refractory Status Epilepticus with Thalamic Deep Brain Stimulation
Ann Neurol 81:142-146, Lehtimaki, K.,et al, 2017

Arteriovenous Malformations of the Brain
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Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017

Outcome of Intracerebral Hemorrhage Associated with Different Oral Anticoagulants
Neurol 88:1693-1700,1686, Wilson, D.,et al, 2017

Lithium-Induced Reversible Pisa Syndrome
Neurol 88:e184, Kumar, N.,et al, 2017



Showing articles 350 to 400 of 4175 << Previous Next >>