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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 300 to 350 of 1853 << Previous Next >>

A Young Man with Progressive Language Difficulty and Early-Onset Dementia
JAMA Neurol 73:595-599, Botha, H.,et al, 2016

Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease
JAMA Neurol 73:668-674, Martikainen, M.H.,et al, 2016

And Why Not Thrombolysis in the Ambulance (At Least for Some)?
Neurol 87:214-219, Rosenberg, G. & Steiner, I., 2016

Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
JAMA Neurol 73:888-890, Kawarai, T.,et al, 2016

Acute Flaccid Myelitis; A Clinical Review of US Cases 2012-2015
Ann Neurol 80:326-338, Messacar, K.,et al, 2016

Endovascular Thrombectomy of Ischemic Stroke
JAMA 316:1265-1266, Warach, S. & Johnston, C., 2016

A 2-year-old Child with Acute Flaccid Paralysis
Neurol 87:e149-e154, Al-Ghamdi, F. & Ghosh, P.S., 2016

An Unusual Cause of Hypokalemic Paralysis
Neurol 87:e174-e177, Shree, R.,et al, 2016

Facial Grimacing and Sensorineural Hearing Loss in a Woman with Cirrhosis of the Liver
Neurol 87:e239, Sgobbi de Souza, P.V.,et al, 2016

A 30-year-old Man with Progressive Weakness and Atrophy
Neurol 87:e227-e230, Quinn, C.,et al, 2016

Rapidly Progressive Quadriplegia and Encephalopathy
JAMA Neurol 73:1363-1366, Wynn, D.,et al, 2016

Trial of Amitriptyline, Topiramate, and Placebo for Pediatric Migraine
NEJM 376:115-124, Powers, S.W.,et al, 2016

Myasthenia Gravis after Botulinum Toxin Type A Injection
Turk J Neurol 22:143-144, Tekce, H.D.,et al, 2016

Paroxysmal Kinesigenic Dyskinesia
Neurol 85:1546-1553, Huang, X.J.,et al, 2015

Hippocampal Foci of Restricted Diffusion in Transient Global Amnesia
Neurol 85:e145, Oderiz, C.C.,et al, 2015

Demyelinating Encephalopathy in Adult Onset Stills Disease: Case Report and Review of the Literatures
Clin Neurol Neurosurg 115:2213-2216, Jie, W., et al, 2015

Acute Flaccid Myelitis of Unknown Etiology in California 2012-2015
JAMA 314:2663-2671, Van Haren, K.,et al, 2015

Molybdenum Cofactor Deficiency
Neurol 85:e175-e178, Nagappa, M.,et al, 2015

Prevalence of Cerebral Amyloid Pathology in Persons without Dementia
JAMA 313-1924-1938,1913, Jansen, W.J.,et al, 2015

Clinicopathologic Conference, CAT Scratch Disease (Encephalopathy Associated with Bartonella Henselae)
NEJM 372:2050-2058, Case 16-2015, 2015

Paroxysmal Dystonia as a Manifestation of Multiple Sclerosis
Neurologist 19:132-134, Machado, C.,et al, 2015

Stent-Retriever Thrombectomy after Intravenous t-PA vs. t-PA Alone in Stroke
NEJM 372:2285-2295,2347, Saver, J.L.,et al, 2015

Thrombectomy within 8 hours after Symptom Onset in Ischemic Stroke
NEJM 372:2296-2306,2347, Jovin, T.G.,et al, 2015

Screening with MRI for Accurate and Rapid Stroke Treatment
Neurol 84:2438-2444, 2394, Shah, S.,et al, 2015

Parkinsons Disease Beyond 20 Years
JNNP 86:849-855, Cilia, R.,et al, 2015

A 44-year-old Woman with Rapidly Progressive Weakness and Ophthalmoplegia
Neurol 85:e22-e27, Schreck, K.C.,et al, 2015

Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
JNNP 86:774-781, Van Egmond, M.E.,et al, 2015

Treatment Concepts for Wake-Up Stroke and Stroke with Unknown Time of Symptom Onset
Stroke 46:2707-2713, Thomalla, G. & Gerloff, C., 2015

A 27-Year Old Man with Rapidly Progressive Coma
Neurol 85:e74-e78, Wong,J.M.,et al, 2015

Seizing the Clinical Presentation in Adult Onset Stills Disease
Autoimmun Rev 14:472-477, Narula, N.,et al, 2015

Acute Headache Diagnosis in Pregnant Women
Neurol 85:1024-1030, Robbins, M.S.,et al, 2015

A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
Neurol 85:e116-e122, Baker, J.M.,et al, 2015

Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015

Non-Alzheimers Dementia 2 Lewy Body Dementias
Lancet 386:1683-1697, Walker, Z.,et al, 2015

Autopsy Case of Severe Generalized Dystonia and Static Ataxia with Marked Cerebellar Atrophy
Neurol 85:1522-1524, Miyamoto, R.,et al, 2015

MRI Findings in Children with Acute Flaccid Paralysis and Cranial Nerve Dysfunction Occurring during the 2014 Enterovirus D68 Outbreak
AJNR 36:245-250, Maloney, J.A.,et al, 2015

Plasma Levels of Apolipoprotein E and Risk of Dementia in the General Population
Ann Neurol 77:301-311, Rasmussen, K.L.,et al, 2015

"Noncognitive" Symptoms of Early Alzheimer Disease
Neurol 84:617-622, Masters, M.C.,et al, 2015

Implementing a Mobile Stroke Unit Program in the United States
JAMA Neurol 72:229-234, Rajan, S.,et al, 2015

Pisa Syndrome
Neurol 84: e12-e14, Malhotra, H.S. & Garg, R.K., 2015

Effects of Golden Hour Thrombolysis
JAMA Neurol 72:25-30,9, Ebinger, M.,et al, 2015

MRI in X-Linked Adrenoleukodystrophy
Neurol 84:211, Siddiqui, S.,et al, 2015

When it is Safe to Return to Driving Following First-Ever Seizure?
JNNP 86:60-64, Brown, J.W.L.,et al, 2015

Differentiation Between Traumatic Tap and Aneurysmal Subarachnoid Hemorrhage: Prospective Cohort Study
BMJ 350:h568, Perry, J.J.,et al, 2015

Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
NEJM 372:1151-1162, Miller, B.L.,et al, 2015

Rates of Ischemic Stroke During Warfarin Treatment for Atrial Fibrillation
Stroke 46:1120-1122, Tung, J.M.,et al, 2015

Significant Period Between Presentation and Diagnosis in Basilar Artery Occlusion
Stroke 46:e79-e81, Organek, N.,et al, 2015

Clinicopathologic Conference, Invasive Neisseria Meningitidis Infection and Primary C8 Deficiency
NEJM 372:1454-1462, Case 11-2015, 2015

Evidence-Based Guideline: Management of an Unprovoked First Seizure in Adults
Neurol 84:1705-1713, Krumholz, A.,et al, 2015

Stent-Retriever Thrombectomy after Intravenous t-PA vs. t-PA Alone in Stroke
NEJM 372:DOI:10.1056/NEJMoa1415061, DOI:10.1056 NEJM e1503217, Saver, J.L.,et al, 2015



Showing articles 300 to 350 of 1853 << Previous Next >>