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Differential
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acquired immunodeficiency syndrome
acquired immunodeficiency syndrome-related complex
akathisia
alcohol
alien hand syndrome
altered states of consciousness
anemia
anorexia
anti basal ganglia antibodies
anti IgLON5
anticholinergic drugs
anxiety
apraxia
apraxia of eye movements
apraxia, constructional
astrocytoma
asymptomatic
ataxia
athetosis
autoantibodies
B 12 deficiency
ballismus, bilateral
basal ganglia
basal ganglia, calcification of
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
benign essential tremor
beta adrenergic blocker
blepharospasm
blinking, reduced
bradykinesia
brain biopsy
bruxism
carbon monoxide poisoning
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, emission, abnormal
cataracts
central nervous system, infection of
cerebral cortical atrophy
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gold sol.curve of
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, complications with
cerebrovascular accident, young adult
ceruloplasmin, serum
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 7
chronic progressive external ophthalmoplegia
cisternogram, radionuclide
Clinical Pathologic Conference(C.P.C.)
coccidioidomycosis
cold intolerance
conjugate gaze, forced
consanguinity
conversion reaction
copper metabolism, abnormal
cortical-basal ganglionic degeneration
crying
delay in diagnosis
dementia
depression
developmental retardation
dexterity, impaired
diabetes mellitus
differential diagnosis
disability, neurological
drooling
dysarthria
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, drug induced
dysphagia
dyspraxia
dystonia
dystonia, delayed onset
dystonia, face
dystonia, focal
dystonia, psychogenic
dystonic reaction, acute
electroencephalogram
electromyogram
emergencies, neurologic
encephalitis
encephalitis lethargica
encephalitis, paraneoplastic
encephalitis, viral
encephalopathy
encephalopathy, post anoxic
epileptic encephalopathy
epsilon sarcoglycan gene
extralimbic encephalitis
face, contractions
faciobrachial dystonic seizure
familial
frontal lobe, pathologic signs of
gait disorder
gamma amino butyric acid receptor antibody
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic neurologic disorders
granuloma, pulmonary
grasp reflex
handedness
head injury
head lag
head nodding
headache
hearing loss
heart block
hemiballismus
hemichorea
hemiparesis
hepatic failure
hepatolenticular degeneration(Wilson's disease)
heralding manifestation
human immunodeficiency virus type 1
hydrocephalus
hydrocephalus, normal pressure
hyperreflexia
hypoglycorrhachia
hypotonia
hypotonia, infants
hypoxia, newborn
hypoxic encephalopathy
imbalance
immunotherapy
intellectual deficit
intestinal pseudoobstruction
intracerebral hemorrhage
irritability
Kayser-Fleischer ring
Kearns-Sayre syndrome
L-dopa
Leber's hereditary optic neuropathy
left handedness
Leigh's disease
leucine rich glioma inactivated 1 antibodies
levitation
Lewy body disease, diffuse
liver disease
lobar atrophy
masked facies
mediastinum, mass of
medical-legal aspects of neurology
MELAS syndrome
memory, defect of recent
memory, impairment of
meningismus
meningitis
meningitis, fungal
meningitis, syphilitic
meningitis, TB
MERRF syndrome
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
mortality
movement disorder
movement disorder, delayed onset
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, paroxysmal
movement disorder, psychogenic
movement disorder, treatment of
MRI
MRI, abnormal
myelopathy
myoclonic dystonia
myoclonic jerks
myoclonus
myoclonus, action
myoclonus, cortical
myoclonus, segmental
myopathy
myopathy, mitochondrial
myorhythmia
mysoline
neoplasm, intracranial
neoplasm, primary intracerebral
neoplasm, primary of CNS
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, multifocal
neurologic signs
neurologic symptoms
neuropathology
neuropathy
oculogyric crisis
ophthalmoplegia
optic neuropathy
pancytopenia
Parkinson disease
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, L-dopa nonresponsive
Parkinson disease, postencephalitic
Parkinson disease, psychogenic
Parkinson disease, tremor, absence of
Parkinsonism syndrome
paroxysmal nonkinesigenic dyskinesia
pathognomonic
penicillamine
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
prognosis
progressive neurologic disorder
propranolol
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
ragged-red fibers
remote effect of cancer on the nervous system
retinopathy
Rett's syndrome
review article
rigidity
salivation, excessive
seizure
seizure, dystonic
sensorineural hearing loss
sensory loss
sensory loss, cortical
short stature
sleep apnea, obstructive
sleep pathology and physiology
somnolence
spastic dysphonia
speech disorder
spinocerebellar ataxia type 16
spongy degeneration of brain
startle reaction
status dystonicus
status epilepticus, intractable
stereotypy
steroid therapy, CNS treatment and complications with
subarachnoid hemorrhage
suck, poor
tardive dyskinesia
tardive dystonia
tauopathy
term infant
thalamic tumors
thalamus, lesion of
thymoma
tic
tonic spasms
torticollis
toxoplasmosis, CNS
treatment of neurologic disorder
tremor
tremor, jaw
tremor, leg
tremor, psychogenic
tremor, treatment of
tremor, writing
viral infection
viral infection, CNS
visuospatial disturbance
weight loss
Whipple's disease
wrist drop
writers cramp
writing
Showing articles 150 to 200 of 791 << Previous Next >>

Bilirubin-Induced Neurologic Damage - Mechanisms and Management Approaches
NEJM 369:2021-2030, Watchko, J.F.,et al, 2013

Long-Term Improvement of Musicians Dystonia after Stereotactic Ventro-Oral Thalamotomy
Ann Neurol 74:648-654,627, Horisawa, S.,et al, 2013

Subacute Sclerosing Panencephalitis
www.MedLink.com, February, Auwaeter,P.G.&Johnson,R.T., 2013

Delayed Onset of Progressive Chorea After Acute Basal Ganglia Injury
Mov Disord 28:585-587, Virmani, T.,et al, 2013

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

Parkin Disease
JAMA Neurol 70:571-579, Doherty, K.,et al, 2013

Basal Ganglia Involvement in Facio-Brachial Dystonic Seizures Associated with LGI1 Antibodies
Neurol 80:e183-184, Plantone, D.,et al, 2013

Clinicopathologic Conference, West Nile Virus Infection, Case 15-2013
NEJM 368:1919-1927, Vyas, J.,et al, 2013

Facial Bradykinesia
JNNP 84:681-685, Bologna, M.,et al, 2013

The Eye of the Beholder: Inter-rater Agreement among Experts on Psychogenic Jerky Movement Disorders
JNNP 84:742-747, Van de Salm, S.,et al, 2013

Clinicopathologic Conference, Blind and Confused, Neuromyelitis Optica Spectrum Disorder
JAMA Neurol 70:932-936, Sharma, V.,et al, 2013

Risk Factors for Spinal Cord Lesions in Dystonic Cerebral Palsy and Generalised Dystonia
JNNP 83:159-163, Guettard,E.,et al, 2012

Hashimoto Encephalopathy
Neurol 78:e134, Afshari, M.,et al, 2012

A Musicians Dystonia
Lancet 379:2116, Vecchio, M.,et al, 2012

Progressive Gait Deterioration in Adolescents with Dravet Syndrome
Arch Neurol 69:873-878, Rodda, J.M.,et al, 2012

Comorbidity of Migraine in Children Presenting with Epilepsy to a Tertiary Care Center
Neurol 79:468-473, Kelly, S.A.,et al, 2012

Painful Tonic Spasm in Neuromyelitis Optica
Arch Neurol 69:1026-1031, Kim, S.M.,et al, 2012

Dopa-Responsive Dystonia Revisited
Arch Neurol 69:1558-1562, Tadic, V.,et al, 2012

Adult-Onset Opsoclonus-Myoclonus Syndrome
Arch Neurol 69:1598-1607, Klaas, J.,et al, 2012

Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study
Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012

Acquired Neurosyphilis Presenting as Movement Disorders
Mov Disord 27:690-695, Shah, B.B. & Lang, A.E., 2012

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011

Progressive Encephalomyelitis with Rigidity and Myoclonus Gycine and NMDA Receptor Antibodies
Neurol 77:439-443,414, Turner, M.R.,et al, 2011

Treatment of Severe Neurological Deficits with IgG Depletion through Immunoadsorption in Patients with Escherichia coli O104:H4-Associated Haemolytic Uraemic Syndrome: A Prospective Trial
Lancet 378:1166-1173,1120, Greinacher, 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

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

Deep Brain Stimulation
JAMA 305:732, Pluta,R.,et al, 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 encephalitis
BMJ 342:d1918, Irani, S.R.,et all, 2011

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

Predictors of Neurologic Outcome in Hypothermia After Cardiac Arrest
Ann Neurol 68:907-914, Fugate,J.E.,et al, 2010

Anti-N-Methyl-d-Aspartate Receptor Encephalitis: Characteristic Behavioral and Movement Disorder
Arch Neurol 67:250-251, Ferioli,S.,et al, 2010

MRI in Methylmalonic Acidemia
Neurol 74:e14, Bindu, P.S.,et al, 2010

Pneumonias Link With the Head and Neck
Lancet 376:388, Mariotti,P., et al, 2010

Transverse Myelitis
NEJM 363:564-572, Frohman,E.M. &Wingerchuk,D.M., 2010

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

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

Sjogren Syndrome: Neurologic Complications
www.Medlink.com,Jan, Roman,G.C., 2010

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

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

The Expanding Phenotype of GLUT1-Deficiency Syndrome
Brain & Dev 31:545-552, Brockmann,K., 2009

N-Methyl-D-Aspartate Receptor Antibodies in Pediatric Dyskinetic Encephalitis Lethargica
Ann Neurol 66:704-709, Dale,R.,et al, 2009

High Doses of Deferiprone May Be Associated with Cerebellar Syndrome
BMJ 338:653, Beau-Salinas,F.,et al, 2009

Deep Brain Stimulation for Primary Generalized Dystonia: Long-Term Outcomes
Arch Neurol 66:465-470, Isaias,I.U.,et al, 2009

Diffusion Abnormalities in the Primary Sensorimotor Pathways in Writers Cramp
Arch Neurol 66:502-508, Delmaire,C.,et al, 2009

Long-Term Effects of Pallidal Deep Brain Stimulation in Tradive Dystonia
Neurol 73:53-58, Gruber,D.,et al, 2009

Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
Neurol 73:430-437, Verhagen,M.M.M.,et al, 2009

Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
Ann Neurol 66:11-18,1, Florance,N.R.,et al, 2009

A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009



Showing articles 150 to 200 of 791 << Previous Next >>