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abulia
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, infants and children
acute disseminated encephalomyelitis
adrenoleukodystrophy
adrenomyeloneuropathy
advances in neurology
Alexanders disease
algorithm
amnesia
amnesia, diencephalic
amnesic stroke
AMPA receptor antibodies
amyloid angiopathy, cerebral
amyloid angiopathy, cerebral, inflammatory type
angiitis, granulomatous of CNS
angiitis, isolated of CNS
angiography, cerebral
antibodies to measles
antiviral agents
anxiety
arteriopathy
asymptomatic
ataxia
ataxia, progressive
ataxic gait
autoantibodies
autoimmune basal ganglia encephalitis
autonomic dysfunction
azidodeoxythymidine
B 12 deficiency
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
behavioral disorder, acute
Behcet's syndrome
Binswanger disease
biologic markers
bladder dysfunction
blood pressure
bradyphrenia
brain atrophy
brain biopsy
brainstem, lesion of
calcification, intracranial
Canavan's disease
carbon monoxide poisoning
carcinoma
carotid angiogram
CAT scan
CAT scan, abnormal
CAT scan, cerebrovascular disease
catatonia
CD4 counts
central nervous system, infection of
central pontine myelinolysis
cerebellar vermis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral infarction
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral ischemia
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, multiple
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, recurrent
cerebrovascular accident, silent
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, risk factors in
chemotherapy, CNS treatment and complications with
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 17
chromosome 19
cognition
collapsin response mediator protein 5 IgG
coma
complications
concentration, impaired
confusion
corpus callosum, lesion of
cortical blindness
cortical ribbon sign
cyclophosphamide
cytokines
deep gray nuclei
delay in diagnosis
dementia
dementia, cerebrovascular disease causing
dementia, familial
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, subcortical
dementia, thalamic
demyelinating disease
depression
diabetes mellitus
diagnostic criteria
diarrhea
diencephalon
differential diagnosis
disability rating scale, neurological
disability, neurological
disinhibition-dementia-parkinsonism-amyotrophic complex
DPPX, antibodies, encephalitis
dysarthria
dyskinesia
dyskinesia, facial
dysmetria
dysphagia
dyspraxia
electroencephalogram, abnormalities of
electroencephalogram, pediatric patients
electroencephalogram, periodic complexes
electron microscopy
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, etiology
encephalitis, human immunodeficiency virus type 1
encephalitis, viral
exercise
Fabry's disease
faciobrachial dystonic seizure
falling
familial
familial hemiplegic migraine
fever
frontal lobe, behavior with disease of
frontal lobe, pathologic signs of
gait disorder
gait, apraxic
gamma amino butyric acid receptor antibody
gaze palsy, vertical
gender
gene
gene mutation
genetic neurologic disorders
genetic screening
genetic testing
genital ulcerations
gliomatosis cerebri
gliosis
granular osmiphilic material
grasp reflex
gray matter
hallucination
headache
hearing loss
hemosiderosis of CNS, superficial
herpes simplex encephalitis
highly active antiretroviral therapy
hip flexor weakness
human immunodeficiency virus type 1
Huntington's chorea
hydrocephalus
hydrocephalus, normal pressure
hyperekplexia
hypertension
hypertension, cerebrovascular disease with
hypertensive encephalopathy
hyponatremia
imbalance
imbalance, postural
immunosuppressive agents
immunotherapy
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
insomnia
intellectual deficit
intellectual deterioration
internal capsule
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intracerebral hemorrhage
intracerebral hemorrhage, lobar
jaw jerk, abnormal
judgement, impaired
Korsakoff's psychosis
Krabbe's disease
lacunar infarction
L-dopa
leg weakness, bilateral
leucine rich glioma inactivated 1 antibodies
leuko-araiosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
level of consciousness, decreased
limbic encephalitis
lobar atrophy
lupus anticoagulant
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
mania
manic-depressive
marche a petits pas
MELAS syndrome
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
meningitis, noninfectious
mesial temporal lobe
metachromatic leukodystrophy
microangiopathy, brain
microhemorrhage, intracerebral
migraine
migraine with aura
migraine, hemiplegic
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
monoclonal antibodies
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, FLAIR
MRI, gradient-echo
MRI, negative
multinucleated giant cell
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
myelitis, transverse, recurrent
myelopathy
myelopathy, vacuolar
myoclonus
neoplasm, primary of CNS
neurexin-3 alpha antibodies
neurologic disease, diagnoses of
neurologic examination, focal
neuronal cell surface antigen
neuronal intranuclear inclusion disease
neuropathology
neuropathology, brain
neuropathy
neurotoxic
next-generation sequencing
NMDA antagonists
NOTCH2NLC
Notch3 gene
old age, neurology of
oral ulcerations
pallido-ponto-nigral degeneration
paraparesis
paraparesis, spastic
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, dementia with
Parkinson disease, L-dopa nonresponsive
Parkinsonism syndrome
paroxysmal neurologic deficits
PAS positive material in the brain
Pelizaeus Merzbacher
persistent vegetative state
personality change
phenylketonuria
pleocytosis of cerebrospinal fluid
polymerase chain reaction
posterior leukoencephalopathy syndrome
precipitating factors
pregnancy, neurologic complications in
prevention of neurologic disorders
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive subcortical gliosis
progressive supranuclear palsy
pseudobulbar palsy
pseudoxanthoma elasticum
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
psychotic behavior
pyramidal tract
pyramidal tract dysfunction
quadriparesis
radiation therapy, CNS treatment and complications with
recurrent
release phenomena
review article
rigidity, axial
risk factors
rituximab
Romberg's sign
rubeola virus
sarcoidosis
sarcoidosis, CNS
screening
seizure
serologic testing
serologic testing, false negative
skin, biopsy
slow virus infection of CNS
small vessel disease
small vessel disease, cerebral
snout reflex
spinal cord, infarction of
steroid therapy, CNS treatment and complications with
striatal encephalitis
striatum, lesion of
striatum, lesion of, bilateral
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
subcortical hemorrhage
subcortical U fibers
symmetric brain lesions
syncope
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
tau protein
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
thalamic amnesia
thalamus
thalamus, infarction of
thalamus, lesion of
thalamus, lesion of-bilateral
thymoma
transient ischemic attack
transient ischemic attack, recurrent
treatment of neurologic disorder
tremor
trinucleotide repeats
urinary frequency
urinary incontinence
vasculitides
vasculopathy
vertigo
viral infection
viral infection, CNS
virus, slow
walking, difficulty with
weight loss
wheelchair
Whipple's disease
white matter disease
white matter disease, periventricular
white matter disease, subcortical
workup
Showing articles 400 to 450 of 2392 << Previous Next >>

A 35-Year-Old Woman with Acute Seizures and Behavior Change
Neurol 81:e55-e59, Rejeski, J.J.,et al, 2013

Clinical Presentation of Chronic Traumatic Encephalopathy
Neurol 81:1122-1129, Stern, R.A.,et al, 2013

Clinicopathologic Conference, Acute Infectious Mononucleosis due to Epstein-Barr Virus Infection, Complicated by Acute Otitis Media and Postinfectious Cerebellitis
NEJM 369:1253-1261, Case 30-2013, 2013

Is There a Link Between Open-Angle Glaucoma and Dementia?: The Three-City-Alienor Cohort
Ann Neurol 74:171-179, Helmer, C.,et al, 2013

Mystery Case: A Young Boy with Myoclonic Jerks
Neurol 81:e130-e134, Musleh, C.,et al, 2013

Central Nervous System Involvement in Whipple Disease
Medicine 92:324-330, Compain, C.,et al, 2013

An Expanded Role for Neuroimaging in the Evaluation of Memory Impairment
AJNR 34:2075-2082, Desikan, R.S.,et al, 2013

New Insights into the Dementia Epidemic
NEJM 369:2275-2277, Larson, E.B.et al, 2013

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

Should Patients with Dementia who Wander be Electronically Tagged? Yes
BMJ 346:f3603, McShane, R., 2013

Incidence and Pathology of Synucleinopathies and Tauopathies Related to Parkinsonism
JAMA Neurol 70:859-866, Savica, R.,et al, 2013

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

Limbic Encephalitis as the Presenting Feature of Sj�gren Syndrome
Neurol Clin Pract 3:165-167, Finelli, P. & Inoa, V., 2013

Clinicopathologic Conferences, Celiac Disease, Addisons Disease, and Major Depression Disorder
NEJM 368:2015-2024, Case 16-2013, 2013

Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
NEJM 368:1992-2003, Margolin, D.,et al, 2013

Sturge-Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ
NEJM 368:1971-1979, Shirley, M.,et al, 2013

Severe Carotid Stenosis and Impaired Cerebral Hemodynamics can Influence Cognitive Deterioration
Neurol 80:2145-2150, Balestrini, S.,et al, 2013

TREM2 Variants in Alzheimers Disease
NEJM 368:117-127, Guerreiro, R.,et al, 2013

Variant of TREM2 Associated with the Risk of Alzheimers Disease
NEJM 368:107-116, Jonsson, T.,et al, 2013

Variant TREM2 as Risk Factor for Alzheimers Disease
NEJM 368:182-184, Neumann, H. & Daly, M., 2013

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

Parkinsonism is a Late, Not Rare, Feature of CADASIL
Stroke 44:1147-1149, Ragno, M.,et al, 2013

PET Imaging for Alzheimer Disease: Are Its Benefits Worth the Cost?
JAMA 309:1099-1100, Mitka, M., 2013

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

Misdiagnosis of Treatable Stroke Mimic: The Case for HIV Screening in Practice Guidelines
Neurohosp 3:125-130, Finelli, P.F., 2013

Predicting Alzheimer Disease with �-Amyloid Imaging: Results from the Australian Imaging, Biomarkers, and Lifestyle Study of Ageing
Ann Neurol 74:905-913, Rowe, C.C.,et al, 2013

Neurological Disorders in Primary Sjogrens Syndrome
Autoimmune Dis: DOI: ID.1152012/645967, Tobon, G.J.,et al, 2012

Clinico-Radiological Spectrum of Bilateral Temporal Lobe Hyperintensity: A Retrospective Review
Br J Radiol 85:e782-e792, Sureka, J. & Jakkani, R.K., 2012

Neurodegenerative causes of death among retired National Football League Players
Neurol 79:1970-1974, Lehman, E.,et al, 2012

Neurosyphilis presenting as mesial temporal encephalitis
Neurol 79:e206-e209, AbdeleRahman, K.,et al, 2012

Brain Atrophy is Related to Lacunar Lesions and Tissue Microstructural Changes in CADASIL
Stroke 38:1786-1790, Jouvent, E.,et al, 2012

Differential Diagnosis of Jakob-Creutzfeldt Disease
Arch Neurol 69:1578-1582,1554, Paterson, R.,et al, 2012

Cerebral Amyloid Angiopathy
eMedicine, Jan, Menon, R.S., 2012

Sporadic Cerebral Amyloid Angiopathy Revisited: Recent Insights Into Pathophysiology and Clinical Spectrum
JNNP 83:124-137, Charidimou,A.,et al, 2012

Memantine for Dementia in Adults Older than 40 years with Downs Syndrome (MEADOWS): a Randomised,double-blind,placebo-controlled Trial
Lancet 379:528-536, Hanney,M.,et al, 2012

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

Subjective Cognition and Amyloid Deposition Imaging
Arch Neurol 69:223-229, Perrotin,A.,et al, 2012

The Types of Neurological Deficits Might Not Justify Withholding Treatment in Patients with Low Total National Institutes of Health Stroke Scale Scores
Stroke 43:782-786,625, Leira,E.C.,et al, 2012

Donepezil and Memantine for Moderate-to Severe Alzheimers Disease
NEJM 366:893-903,957, Howard,R.,et al, 2012

Inverse Association between Cancer and Alzheimers Disease: Results from the Framingham Heart Study
BMJ 344:e1442, Driver,J.A.,et al, 2012

Autoimmune Epilepsy
Arch Neurol 69:582-593,565, Quek, A.M.L.,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

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

Clinical Reasoning: Encephalopathy in a 10-year-old boy
Neurol 79:e12-e18, Rodan, L. & Tein, I., 2012

A Comparison of Tau and 14-3-3 Protein in the Diagosis of Creutzfeldt-Jakob Disease
Neurol 79:547-552, Hamlin, C.,et al, 2012

Visuospatial deficits in posterior cortical atrophy: structural and functional correlates
JNNP 83:860-863,855, Andrade, K.,et al, 2012

A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy
Neurol 79:e63, Komatsuzaki, S.,et al, 2012

Anti-Glutamic Acid Decarboxylase Limbic Encephalitis Without Epilepsy Evolving Into Dementia with Cerebellar Ataxia
Arch Neurol 69:1064-1066, Mirabelli-Badenier, M.,et al, 2012

Lifelong Management of Amyloid-Beta Metabolism to Prevent Alzheimers Disease
NEJM 367:864-866, Gandy, S., 2012

Clinical and Biomarker Changes in Dominantly Inherited Alzheimers Disease
NEJM 367:795-804,864, Bateman, R.J.,et al, 2012



Showing articles 400 to 450 of 2392 << Previous Next >>