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Differential
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abulia
acute disseminated encephalomyelitis
adverse drug reaction
agnosia, color
akathisia
akinetic mute
alexia without agraphia
Alzheimer's disease
ammonia
amnesia
amnesia, diencephalic
amnesic stroke
amnestic syndrome
anatomy of
angiography, cerebral
angiography, cerebral, false negative
angiography, cerebral, negative
anisocoria
anorexia
antibodies to measles
aphasia
apraxia
arbovirus
areflexia
arousal
aspirin
astrocytoma
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
audiogram
automobile accidents
autonomic dysfunction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery occlusion
behavioral disorder
Behcet's syndrome
benign essential tremor
bladder dysfunction
blood transfusion
bradykinesia
brain atrophy
brain biopsy
brain biopsy, stereotaxic
brainstem, lesion of
carbon monoxide poisoning
CAT scan
CAT scan, abnormal
CAT scan, angiography
CAT scan, angiography, false negative
CAT scan, venography
cavernous sinus, syndrome
central nervous system, infection of
central pontine myelinolysis
cerebellar lesion
cerebellar peduncle
cerebral arteries
cerebral cortex
cerebral edema, vasogenic
cerebral embolism
cerebral embolism, cardiac origin
cerebral infarction
cerebral peduncle
cerebral vasculature
cerebral venous infarction
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, etiology
cerebrovascular accident, mimics
cerebrovascular accident, nonvascular territory
cerebrovascular accident, prognosis in
cerebrovascular accident, women
chemosis
children
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 20
cingulate gyrus
Clinical Pathologic Conference(C.P.C.)
cognition
coma
concentration, impaired
confusion
corpus callosum
corpus callosum, lesion of
cranial nerve palsies
Creutzfeldt-Jakob disease, genetic
deafness
deafness, bilateral
deafness, sudden
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, cerebrovascular disease causing
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, subcortical
dementia, thalamic
dementia, treatment of
demyelinating disease
depression
diencephalon
differential diagnosis
diplopia
dopamine agonist
dural arteriovenous malformation
dural sinus thrombosis
dysarthria
dysdiadochokinesia
dyskinesia
dysmetria
dyspnea
dystonia
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
ELISA
embolism
encephalitis
encephalitis, Japanese
encephalitis, viral
encephalopathy
endovascular therapy
epidemiology of neurology
executive dysfunction
eye movement, disorders of
Fabry's disease
facial weakness
facial weakness, central
facial weakness, central, emotional
Fahr disease
failure to thrive
familial
fatal familial insomnia
fatigue
fever
fibrillations
finger nose finger test
fistula, arterio-venous
fistula, arterio-venous, dural
flaccid paralysis
flavivirus
frontal lobe, anatomy and physiology
frontal lobe, pathologic signs of
fundus, abnormality of
funduscopic exam
gait disorder
gammaglobulin therapy, intravenous
gangliosidosis GM2
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic linkage
genetic neurologic disorders
genital ulcerations
Gilles de la Tourette syndrome
glioma
gliomatosis cerebri
gliosis
gray matter
gyrus, abnormal
hallucination
handwriting
headache
hearing loss
hearing loss, bilateral
hearing loss, sudden, bilateral
hemiakathisia
hemianopia
hemianopia, homonymous
hemichorea
hemiparesis
hemiplegia
hemorrhage, thalamic
hepatolenticular degeneration(Wilson's disease)
heralding manifestation
hippocampus
hydrocephalus
hyperglycemia
hyperhidrosis
hyperphagia
hypersomnia
hypertension
hyperthermia
hypoglycemia
hyponatremia
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immunohistochemistry
immunosuppression
immunosuppressive agents
inattention
incidence
inclusion bodies
inclusion bodies, eosinophilic intranuclear
incoordination
insomnia
insular cortex
intellectual deficit
intellectual deterioration
internal capsule
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intracerebral hemorrhage
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
Korsakoff's psychosis
Krabbe's disease
lacunar infarction
L-dopa
L-dopa, drug interactions with and side effects of
Leigh's disease
lenticular nucleus, lesion of, bilateral
leukoencephalopathy
level of consciousness, decreased
limbic encephalitis
liver disease
logopenia
lumbar puncture, complications of
lymphoma
lymphoma involving CNS
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, dural
masked facies
MELAS syndrome
memory
memory enhancement
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
meningitis, neutrophilic
meningoencephalitis
mental status, abnormal
microangiopathy, brain
microangiopathy, retina
microhemorrhage, intracerebral
microsurgery
midbrain, infarction of
middle cerebellar peduncle, lesion
misdiagnosis
mitochondrial disease
molecular genetics
mortality
mosquito
movement disorder
MRI
MRI, abnormal
MRI, ADC maps
MRI, angiography
MRI, angiography, false negative
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, false positive
MRI, FLAIR
MRI, flow void, blood
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, indications for
MRI, negative
MRI, serial
MRI, spinal cord
MRI, sulcal hyperintensity
MRI, T1 weighted high signal foci
MRI, target sign
MRI, venography
MRS
multiple sclerosis
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle biopsy
muscle pain
myelinolysis, extrapontine
myelitis, longitudinal
myoclonic jerks
myoclonus
myotonia dystrophica
neoplasm, primary intracranial
neoplasm, primary of CNS
neoplasm, primary of CNS-treatment of
nerve conduction studies
neurofibromatosis 1
neurologic disease, diagnoses of
neurologic signs
neuroophthalmology
neuropathology
neuropathology, brain
neurotoxin
nystagmus
obsessive-compulsive disorder
optic atrophy
oral ulcerations
osmotic demyelination syndrome
overlap syndrome
owl's eye sign of spinal cord
pain, leg
palinopsia
paralysis, acute
paralysis, acute areflexic
paraparesis, spastic
Parkinson disease
Parkinson disease, diagnosis
Parkinson disease, early symptoms
Parkinson disease, fluctuations in
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinsonism syndrome
pergolide
personality change
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
polymerase chain reaction, false negative
pons, lesion of
positive sharp waves
posterior cerebral artery
posterior cerebral artery embolism
posterior cerebral artery territory infarction
posterior choroidal artery
postural abnormality
preclinical
pregnancy, neurologic complications in
prion disease
prognosis
progressive neurologic disorder
proptosis
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
pulvinar sign
pure sensory stroke
pursuit eye movements, abnormal
putamen, lesion of, bilateral
pyramidal tract dysfunction
radiation therapy, CNS treatment and complications with
radiation therapy, stereotactic
rapidly progressing neurologic illness
reading disorder, acquired
real-time quaking-induced conversion
remote effect of cancer on the nervous system
respiratory failure
retinal artery occlusion
retinal branch artery occlusion
retinal infarction
retinopathy
review article
risk factors
risk stratification
Romberg's sign
rubeola virus
saccadic eye movements, abnormal
Sandhoff's disease
seizure
sensorimotor stroke
sensorineural hearing loss
serologic testing
sleep pathology and physiology
snout reflex
spinal cord, lesion of
splenium of corpus callosum
square wave jerks
steroid therapy, CNS treatment and complications with
stimulation, deep brain
straight sinus
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
stuporous
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subacute sclerosing panencephalitis, adult onset
substantia nigra
Susac's syndrome
symmetric brain lesions
tachycardia
tau protein
Tay-Sachs disease
temporal lobe
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamic amnesia
thalamic aphasia
thalamic syndrome
thalamic tumors
thalamic tumors, bilateral
thalamus
thalamus, atrophy of
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine deficiency
tinnitus
tinnitus, pulsatile
tonsil biopsy
top of the basilar syndrome
treatment of neurologic disorder
tremor
tremor, thalamic stimulation for suppression of
urinary incontinence
vasculopathy
venous ectasia
venous engorgement
venous hypertension
venous ischemia
vertigo
viral infection
viral infection, CNS
vision, blurred
visual field defect
visual loss
visuospatial disturbance
walking, difficulty with
weakness
weakness, generalized
weight loss
Wernicke's encephalopathy
West Nile fever
wheelchair
white matter disease
wide based gait
Showing articles 0 to 50 of 2657 Next >>

Dural Anteriovenous Fistulas Presenting as Symmetric Lesions in the Internal Capsule on Imaging Studies, A Case Report and Literature REview
Neurologist 28:304-309, Zhang,D.,et al, 2023

Rapidly Progressive Thalamic Dementia
Neurol 96:e809-e813, Rizzo, A.C.,et al, 2021

Bithalamic Lesions
Stroke 51:e355-e358, Chen, P.M.,et al, 2020

Pediatric Leigh Syndrome
Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020

A 68-year-old Man with Rapid Cognitive Decline
Neurol 93:315-318, Berth, S.H.,et al, 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Clinical Pathologic Conference, West Nile Virus Encephalitis
NEJM 377:1878-1886, Case 34-2017, 2017

Intracranial Dural Arteriovenous Fistulae
Stroke 48:1424-1431, Reynolds, M.R.,et al, 2017

Clinical Reasoning: An Unusual Case of Subacute Encephalopathy
Neurol 84:e33-e37, Parikh, N.,et al, 2015

Serial Magnetic Resonance Imaging Changes in Sporadic Creutzfeldt-Jakob Disease with Valine Homozygosity at Codon 129 of the Prion Protein Gene
JAMA Neurol 71:1186-1187, Furukawa, F.,et al, 2014

Deep-Brain Stimulation - Entering the Era of Human Neural-Network Modulation
NEJM 371:1369-1373, Okun, M.S., 2014

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

Memory Enhancement and Deep-Brain Stimulation of the Entorhinal Area
NEJM 366:502-510, Suthana,N.,et al, 2012

Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus
RadioGraphics 31:5-30, Hegde,A.N.,et al, 2011

The Use of Neuroimaging in the Diagnosis of Mitochondrial Disease
Dev Disabil Res Rev 16:129-135, Friedman, S.D.,et al, 2010

Bilateral Thalamic Lesions
AJR 192:W53-W62, Smith,A.B.,et al, 2009

MRI Lesion Profiles in Sporadic Creutzfeldt-Jakob Disease
Neurol 72:1994-2001, Meissner,B.,et al, 2009

MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
AJNR 29:1638-1643, Fulbright,R.K.,et al, 2008

Pattern of Cortical Changes in Sporadic Creutzfeldt-Jakob Disease
AJNR 28:1114-1118, Tschampa,H.J.,et al, 2007

Differential Diagnosis of Bilateral Thalamic Lesions
Clin Neuroradiol 17:3-22, Linn,J.,et al, 2007

Clinical Presentation and Pre-Mortem Diagnosis of Variant Creutzfeldt-Jakob Disease Associated With Blood Transfusion: A Case Report
Lancet 368:2061-2067, Wroe,S.J.,et al, 2006

The "Pulvinar Sign" in a Case of Paraneoplastic Limbic Encephalitis Associated with Non-Hodgkins Lymphoma
JNNP 76:882-884, Mihara,M.,et al, 2005

Vascular Syndromes of the Thalamus
Stroke 34:2264-2278, Schumahmann,J.D., 2003

Thalamic Involvement in Sporadic Creutzfeldt-Jakob Disease: A Diffusion-Weighted MR Imaging Study
AJNR 24:908-915, Tschampa,H.J.,et al, 2003

Sporadic CJD Clinically Mimicking Variant CJD With Bilateral Increased Signal in the Pulvinar
Neurol 58:148-149, Haik,S.,et al, 2002

Thalamic Venous Infarction as a Cause of Subacute Dementia
Neurol 58:1689-1691, Krolak-Salmon,P.,et al, 2002

The Pulvinar Sign on Magnetic Resonance Imaging in Variant Creutzfeldt-Jakob Disease
Lancet 355:1412-1418,1384, Zeidler,M.,et al, 2000

Progressive Dementia and Gait Disorder in a 78 Year Old Woman
JNNP 68:526-531, Tagliati,M.,et al, 2000

Leigh Syndrome: Serial MR Imaging and Clinical Follow-Up
AJNR 21:1502-1509, Arii,J. & Tanabe,Y., 2000

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Posterior Cerebral Artery Syndromes
, Caplan,L.R. &Bogousslavsky,J., 1998

Adult-Onset Subacute Sclerosing Panecephalitis:Case Reports and Review of the Literature
Mov Dis 12:342-353, Singer,C.,et al, 1997

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

Fatal Insomnia in a Case of Familial Creutzfeldt-Jakob Disease with the Codon 200Lys Mutation
Neurol 46:758-761, Chapman,J.,et al, 1996

Clinical and Genetic Studies of Fatal Familial Insomnia
Neurol 45:1068-1075, Reder,A.T.,et al, 1995

Parkinson's Disease
JNNP 57:672-681, Marsden,C.D., 1994

Analysis of the Prion Protein Gene in Thalamic Dementia
Neurol 42:1859-1863, Petersen,R.B.,et al, 1992

Bilateral Thalamic Glioma-Review of Eight Cases with Personality Change and Mental Deterioration
AJNR 13:1225-1230, Partlow,G.D.,et al, 1992

Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
NEJM 326:444-449, Medori,R.,et al, 1992

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992

Reversibility of CT and MR Findings in Neuro-Bechet Disease
J Comput Assist Tomogr 13:669-673, Patel,D.V.,et al, 1989

Thalamic Infarcts:Clinical Syndromes, Etiology, and Prognosis
Neurol 38:837-848, Bogousslavsky,J.,et al, 1988

Dementia Following Strokes in the Mesencephalon & Diencephalon
Arch Neurol 44:1127-1133, Katz,D.I.,et al, 1987

Familial Myoclonic Dementia Masquerading as Creutzfeldt-Jakob Disease
Ann Neurol 20:231-239, Little,B.W.,et al, 1986

Familial Multisystem Atrophy with Possible Thalamic Dementia
Neurol 34:1213-1217, Katz,D.A.,et al, 1984

The Syndrome of Bilateral Paramedian Thalamic Infarction
Neurol 33:540-546, Guberman,A.,et al, 1983

Thalmic Neuronal Inclusion Disease
Neurol 22, 3961972., Segarra,J., 1972

Thalamic Tumors
J Neurosurg 24:505, Cheek,W.R.,et al, 1966

Extensive Brainstem and Striatal Involvement in Neuropsychiatric Systemic Lupus Erythematosus
Neurol 102:e209153, Branch, A.,et al, 2024



Showing articles 0 to 50 of 2657 Next >>