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Differential
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abducens nerve paralysis
agitation
agnosia, color
akathisia
alexia without agraphia
alien hand syndrome
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
alveolar hypoventilation
amaurosis fugax
amnesia
amnesic stroke
anatomy of
anemia
aneurysm
anorexia
anti basal ganglia antibodies
antibiotics
anticonvulsants, untoward effects of
aphasia
apraxia
apraxia of eye movements
apraxia of eyelid opening
areflexia
arrhythmia, cardiac
arteritides
arteritis, temporal
arthralgia
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic gait
athetosis
ATP1A3 gene
autoantibodies
autoimmune disease
autoimmune encephalopathy
autonomic dysfunction
Babinski sign
bacterial infection
Balint's syndrome
basal ganglia, degeneration
basal ganglia, lesion of
basilar artery
basilar artery occlusion
behavioral disorder
bilirubin encephalopathy
biologic markers
bradykinesia
bradyphrenia
brain damage
brainstem
brainstem, hemorrhage, primary
brainstem, infarction of
brainstem, lesion of
bruxism
calcium antagonist
carcinoembryonic antigen
carcinoma
carcinoma of breast
carcinoma of lung
cardiomyopathy
CAT scan, abnormal
CAT scan, pelvis
ceftriaxone
central nervous system, infection of
central retinal artery occlusion
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebellar disease, eye movement disorder in
cerebellar lesion
cerebellitis, autoimmune
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral infarction
cerebral peduncle
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, agitated delirium following
cerebrovascular accident, prognosis in
children
chills
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 20
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clonazepam
cognition
collagen vascular disease
Collier's sign
confusion
conjugate gaze, forced
convergence, impaired
cortical blindness
cortical-basal ganglionic degeneration
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
cyst, ovary
deafness
deafness, unilateral
degenerative diseases of CNS
delirium
dementia
dementia, presenile
dementia, rapidly progressive
developmental retardation
diabetes mellitus
diagnostic criteria
differential diagnosis
diplopia
dizziness
DPPX
DPPX, antibodies, encephalitis
drooling
dysarthria
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dysphagia
dyspnea
dyspraxia
dystonia
electroencephalogram, abnormalities of
embolism
embolism, vertebral-basilar artery
encephalitis
encephalitis lethargica
encephalitis, autoimmune
encephalitis, paraneoplastic
encephalomyelitis
encephalopathy
encephalopathy, neonatal
encephalopathy, parainfectious
epidemiology of neurology
epistaxis
exercise intolerance
eye movement, disorders of
face, numbness of
facial movement disorder
facial weakness
falling
familial
fever
flunarizine
fluorescent treponema antibody absorption/false positive
fundus, abnormality of
gait disorder
gammaglobulin therapy, intravenous
gastrointestinal bleeding
gaze deviation
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gender
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
geniculate body, lateral
glabellar sign
globus pallidus, lesion of
gram positive rod
grimacing
growth retardation
Guillain Barre syndrome
hallucination
hallucination, visual
headache
headache, positional
hearing loss
hemiakathisia
hemianopia
hemianopia, homonymous
hemichorea
hemiparesis
hemiplegia
hemisensory loss
hepatic failure
hepatomegaly
hepatosplenomegaly
heralding manifestation
Horner's syndrome
human immunodeficiency virus type 1
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
hyperesthesia
hyperpigmentation of skin
hyperreflexia
hypertension
hyperthermia
hypertonia
hypotonia
idiopathic
imbalance
imbalance, postural
immune reconstitution inflammatory syndrome
immunodeficiency
immunosuppression
immunosuppressive agents
inborn errors of metabolism
incoordination
infantile bilateral striatal necrosis
infection
intellectual deficit
intestinal biopsy
intracerebral hemorrhage
intracranial hypertension, benign
intracranial pressure, increased
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, young adult
jaundice
kernicterus
lacunar infarction
leukemia
level of consciousness
level of consciousness, decreased
levitation
limbic encephalitis
lipid storage disorder of CNS
lymphadenopathy
lymphoma
masked facies
mastoiditis
memory, defect of recent
memory, impairment of
meningismus
meningitis
meningitis, aseptic
meningitis, carcinomatous
mental retardation
mesencephalic artery syndrome
metamorphopsia
microcephaly
midbrain, atrophy
midbrain, infarction of
migraine
migraine, children
migraine, visual symptoms in
mimics
miosis
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
molecular genetics
mononeuropathy
mononeuropathy multiplex
mortality
movement disorder
movement disorder, delayed onset
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, negative
multiple system atrophy
muscle biopsy
muscle pain
myasthenia gravis
myelitis
myoclonic jerks
myoclonus
myopathy
myositis
nasal septum, perforation of
nausea and vomiting
neurocutaneous disease
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neuropathy, vasculitic, systemic
neurotoxic
neurotoxin
Niemann-Pick disease
night sweats
NMDA antagonists
NMDA receptors
noncommunicative
nystagmus
nystagmus, cerebellar
nystagmus, monocular
nystagmus, pendular
occipital lobe, infarction
occipital lobe, infarction, bilateral
ocular bobbing
ocular dipping
ocular dyskinesia
ocular dysmetria
ocular flutter
ocular motility, disorders of
oculogyric crisis
oculomasticatory myorhythmia
ophthalmoplegia
ophthalmoplegia, progressive external
opsoclonus
opsoclonus, differential diagnosis of
opsoclonus-myoclonus syndrome
optic atrophy
optic neuritis
optic neuropathy
optic neuropathy, ischemic
optokinetic nystagmus, abnormal
oscillopsia
otitis, neurologic complications with
pain
pain, abdominal
pain, testicular
palinopsia
papilledema
Parkinson disease
Parkinson disease, atypical
Parkinson disease, dystonia with
Parkinson disease, postencephalitic
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
pathology
peduncular hallucinosis
periarteritis nodosa
pericarditis
personality change
phenothiazine
phenothiazine, dyskinesia associated with
pleocytosis of cerebrospinal fluid
POLG1 gene
polymerase chain reaction
polyneuropathy
pontine hemorrhage
posterior cerebral artery
posterior cerebral artery embolism
posterior cerebral artery territory infarction
posterior choroidal artery
posterior inferior cerebellar artery syndrome
postural abnormality
precipitating factors
preclinical
premature infant
prevention of neurologic disorders
prion disease
progeria
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
pseudoabducens palsy
psychiatric problems in neurologic disorders
psychosis
psychotic behavior
ptosis
pulmonary infiltrates
pupil
pupil, abnormality in neurologic disorders
pupil, ectopic-acquired
pure sensory stroke
quadrantanopsia, homonymous
quadriparesis
quadriplegia
radiation hypersensitivity
radiculopathy
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
reading disorder, acquired
reading problem, causes of
recurrent
release phenomena
remote effect of cancer on the nervous system
respirations in CNS disease
retinal artery occlusion
retinal infarction
retinopathy
Rett's syndrome
review article
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rhinorrhea
rigidity
rigidity, axial
saccadic eye movements
saccadic eye movements, abnormal
salivation, excessive
schizophrenia
scotoma
sedimentation rate, elevated
seizure
sensorineural hearing loss
sensory loss
sensory loss, cortical
seroconversion
simultanagnosia
sinusitis
skew deviation
skin, lesions in neurologic disorders
somnolence
speech disorder
spinal muscular atrophy
splenomegaly
status epilepticus
steroid therapy, CNS treatment and complications with
striatum, lesion of
strokelike episodes
subarachnoid hemorrhage
subthalamic nucleus
suck reflex
sweating
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
tachycardia
tardive dyskinesia
tardive dyskinesia, treatment of
tardive dystonia
tau protein
tauopathy
telangiectases
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
term infant
testicular biopsy
tetrabenazine
thalamoperforating arteries
thalamus, infarction of
thalamus, lesion of
thalamus, lesion of-bilateral
third nerve palsy
tinnitus
titubation
tonic spasms
top of the basilar syndrome
toxic encephalopathy
transient ischemic attack
treatment of neurologic disorder
tremor
trigeminal neuropathy
trigeminal neuropathy, sensory
upgaze, paralysis of
uremia
urinary incontinence
vertigo
viral infection
vision, blurred
visual field defect
visual impairment
visual loss
visual obscurations, transient
walking, difficulty with
weakness, generalized
web sites
weight loss
wheelchair
Whipple's disease
wide based gait
workup
Showing articles 350 to 400 of 1797 << Previous Next >>

Painful Ophthalmoplegia Following Dental Procedure
Neuroophthalmol 37:165-168, Simsek, I.,et al, 2013

IgG4-Related Orbital Disease and Enlargement of the Trigeminal Nerve Branches
Neurol 81:e117-e118, Deschamps, R.,et al, 2013

Clinicopathologic Conference, Dissection of the left vertebral artery and cerebellar infarction
NEJM 369:1736-1748, Case 34-2013, 2013

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

Clinicopathologic Conference, Squamous- Cell Carcinoma of the Tongue with Metastasis to Lungs, Liver, Bone of Skull, Trigeminal Nerve, Base of Skull, Pituitary Gland and Dura Matter. Infarcts of Cerebellum and Right Frontal Lobe.
NEJM 367:1136-1145, Case 29-2012, 2012

Conjugate Eye Deviation in Acute Intracerebral Hemorrhage
Stroke 43:2898-2903, Sato, S.,et al, 2012

Immunotherapy-Responsive Chorea as the Presenting Feature of LGI1-Antibody Encephalitis
Neurol 79:195-196, Tofaris,G.K.,et al, 2012

A Man with Anxiety, Confusion, and Red Eyes
BMJ 345:e4443, Ali, S.N.,et al, 2012

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

Morvan Syndrome: Clinical and Serological Observations in 29 Cases
Ann Neurol 72:241-255, Irani, S.R.,et al, 2012

Deep-Brain Stimulation for Parkinsons Disease
NEJM 367:1529-1538, Okon, M.S., 2012

MELAS
MedLink.com, August, Klopstock, T., 2012

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

Cogan Syndrome An Analysis of Reported Neurological Manifestations
The Neurologist 18:55-63, Antonios,N. and Silliman,S., 2012

Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012

Cluster Headache
BMJ 344:e2407, Nesbitt,A.D.,et al, 2012

Oculomotor Nerve Enhancement after Mild Head Trauma
AJNR 33:E78, Anagnostou, E.,et al, 2012

Development of a Suspicion Index to Aid Diagnosis of Niemann-Pick Disease Type C
Neurol 78:1560-1567,1546, Wijburg, F.A.,et al, 2012

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

The Frequency of Autoimmune N-Methyl-D-Aspartate Receptor Encephalitis Surpasses That of Individual Viral Etiologies in Young Individuals Enrolled in the California Encephalitis Project
Clin Inf Dis 54:899-904, Gable, M.S.,et al, 2012

Neuro-Sweets Disease
Pract Neurol 12:126-130, Maxwel,G.,et al, 2012

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

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

A Rare Cause of Gait Ataxia
Lancet 378:1274, Rous, C.,et al, 2011

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

Clinicopathologic Conference, Limbic Encephaitis with Antibodies to Leucine - Rich Glioma - inactivated 1 (LGI 1).
NEJM 365:1825-1833, Case 34-2011, 2011

Evidence-based guideline update: Treatment of Essential Tremor
Neurol 77:1752-1755, Zesiewicz, T.A.,et al, 2011

Vertebral Artery Dissection Leading to Stroke Caused by Violent Neck Tics of Tourette Syndrome
Neurol 77:1706-1707, Lehman, L.L.,et al, 2011

Movement Disorders Emergencies Part 1
, Robottom, B.J., et al, 2011

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

Movement Disorders Emergencies Part 2 Hyperkinetic Disorders
Arch Neurol 68:719-724, Robottom, B.J.,et al, 2011

Paraneoplastic Upbeat Nystagmus
Neurol 77:691-693, Wray, S.H.,et al, 2011

Ipsilateral Stroke in a Patient with Horizontal Gaze Palsy with Progressive Scoliosis and a Subcortical Infarct
Stroke 42:e1-e3, Ng, A.S.L.,et al, 2011

PANDAS
www.medlink.com,Feb, Erfe,M.C.B., 2011

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

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

Clinical Presentation, Pathologic Features, and Diagnosis of Primary Central Nervous System Lymphoma
Up to Date Sept 2010, Hochberg,F.H.,et al, 2010

Cogan Syndrome
www.medlink.com, Feb, Ramachandran, T.S., 2010

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

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

Essential Palatal Myoclonus
NEJM 362:e64, Scozzafava,J. &Yager,J., 2010

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

Absence Epilepsies With Widely Variable Onset are a Key Feature of Familial GLUT1 Deficiency
Neurol 75:432-440, Mullen,S.A., et al, 2010

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

A 64-Year-Old Man With Painful, Unilateral External Opthalmoplegia
Neurol 75:e35-e39, Bhatti,M.T., 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

Retrospective Analysis of NMDA Receptor Antibodies in Encephalitis of Unknown Origin
Neurol 75:1735-1739, Pr�ss,H.,et al, 2010

Clincopath Conference, Endogenous Endophthalmitis Due to Aspergillus Niger
NEJM 363:1749-1758, Case 33-2010, 2010



Showing articles 350 to 400 of 1797 << Previous Next >>