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Differential
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abdominal distention
adrenoleukodystrophy
alternating rapid movement
Alzheimer's disease
Alzheimer's disease, familial
anemia
anomic aphasia
anorexia
antibiotics
aphasia
apraxia
arteriopathy
arthralgia
arthritis
ataxia
ataxia, cerebellar
ataxic gait
Babinski sign
bacterial infection
bacterial infection, CNS
basal ganglia, infarction
behavioral disorder
Bing-Neel syndrome
blindness
bradyphrenia
brain biopsy
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, demyelinating disease
central nervous system, infection of
cephalosporins
cerebellar atrophy, primary
cerebellar lesion
cerebellar plaques, amyloid
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral embolism
cerebral infarction
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, multiple
cerebrovascular accident, recurrent
children
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
coma
confusion
cry, abnormal
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, cerebrovascular disease causing
dementia, presenile
dementia, rapidly progressive
dementia, transmissible
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
developmental milestones, loss of
developmental retardation
diarrhea
diplopia
disorientation
dizziness
downward gaze, paralysis of
dysarthria
electroencephalogram, abnormalities of
electroencephalogram, triphasic delta waves
electron microscopy
electrophoretic pattern, serum
electroretinograph
encephalopathy
encephalopathy, progressive
endocarditis, marantic
enzyme, defect
epistaxis
eye movement, disorders of
facial movement disorder
false negative
familial
feeding disorder
fever
fingerprint bodies
frontal lobe, pathologic signs of
fundus, abnormality of
gait disorder
gangliosidosis GM2
gangliosidosis GM2-AB variant
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene mutation
genetic neurologic disorders
genetic testing
globoid cells
gram positive rod
granular osmiphilic material
granulomatous disease
hallucination
hallucination, visual
hands, fisted
head lag
hemiparesis
hemiplegia
hemorrhagic diathesis
hepatomegaly
hippocampus
hippocampus, hyperintense
hydrocephalus
hydrocephalus, normal pressure
hyperphagia
hyperpigmentation of skin
hypertonia
hyperviscosity
hypoalbuminemia
hypothalamus, damage to
hypothalamus, disturbance of
immunofluorescence
impotence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intracytopasmic
infection
insomnia
intellectual deficit
intellectual deterioration
intestinal biopsy
intracerebral hemorrhage
irritability
Jakob-Creutzfeldt disease
Krabbe's disease
kuru
kuru plaques
Lafora body
Lafora's disease
lethargy
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
limbic encephalitis
lymph node biopsy
lymphadenopathy
macroglobulinemia
malaise
meconium staining
memory, defect of recent
memory, impairment of
meningitis, aseptic
mental status, abnormal
migraine
misdiagnosis
mitral valve vegetation
mononeuritis multiplex
mononeuropathy
mortality
movement disorder
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, hypointense signal foci on
MRI, spinal cord
MRS
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
myelopathy
myoclonus
myoclonus, epilepsy
narcolepsy
negative
nerve conduction studies
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neurologic signs
neuronal ceroid-lipofuscinosis
neuropathology
neuropathy
night sweats
Notch3 gene
nystagmus
nystagmus, vertical
ocular motility, disorders of
oculomasticatory myorhythmia
ophthalmoplegia
ophthalmoplegia, total
opisthotonus
optic atrophy
optic chiasm, enlarged
optic nerve, enlarged
pain, abdominal
papilledema
PAS positive
PAS positive material in the brain
pericarditis
personality change
pleocytosis of cerebrospinal fluid
pleurisy
pneumonia
polydipsia
polymerase chain reaction
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
psychiatric disorder
psychiatric problems in neurologic disorders
pyramidal tract
Red flags
retinal hemorrhages
retinopathy
review article
sea-blue histiocytes
sedimentation rate, elevated
seizure
seizure, children
seizure, intractable
seizure, teenager
senile plaques
skin, biopsy
skin, darkening of
sleep pathology and physiology
slow virus infection of CNS
small vessel disease
somnolence
spasticity
sphingolipodoses
spinal cord, lesion of
splenomegaly
spongy degeneration of brain
startle myoclonus
startle reaction
steatorrhea
storage disease of CNS
stuttering
subarachnoid hemorrhage
symmetric brain lesions
systemic illness
tapetoretinal degeneration
temporal lobe, lesion
temporal lobe, lesion, bilateral
testicular biopsy
thalamus, lesion of-bilateral
tinnitus
treatment of neurologic disorder
tremor
tremor, intention
trimethoprim-sulfamethoxazole
upgaze
upgaze, paralysis of
urinary incontinence
uveitis
vasculopathy
vertical gaze
viral infection, CNS
vision, blurred
visual acuity, decreased
visual loss
visual loss, slow
vitreous opacities
Waldenstrom's macroglobulinemia
walking, difficulty with
weakness
weakness, progressive
weight loss
wheelchair
Whipple's disease
white matter disease
Showing articles 100 to 150 of 16194 << Previous Next >>

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

Evidence-Based Guideline Update: Determining Brain Death in Adults: Report of the Quality Standards Subcommittee of the American Academy of Neurology
Neurol 74:1911-1918, Wijdicks,E.F.M., et al, 2010

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

Clinicopath Conf., Brain Abscess, Pulmonary Arteriovenous Malformation Due to Hereditary Hemorrhagic Telangiectasia
NEJM 362:1326-1333, Case 10-2010, 2010

Diagnosis and Management of the Antiphospholipid Syndrome
BMJ 340:1125-1132, Cohen,D., et al, 2010

The Case Against Confirmatory Tests for Determining Brain Death in Adults
Neurol 75:77-83, Wijdicks,E.F.M., 2010

Reversible Paraneoplpastic Limbic Encephalitis Associated with Antibodies to the AMPA Receptor
Neurol 74:265-267, Bataller,L.,et al, 2010

Spinal Cord Sarcoidosis: Clinical and Laboratory Profile and Outcome of 31 Patients in a Case-Control Study
Medicine 89:133-140, Cohen-Aubart,F.,et al, 2010

Clinicopath Conf, Intravascular Large-B-Cell Lympoma
NEJM 362:1129-1138, Case 9-2010, 2010

Case 38-2009: A 16-Year-Old Boy with Paroxysmal Headaches and Visual Changes
NEJM 361:2367-2378, Brass,S.,et al, 2009

Clinicopath Conf, Neurosarcoidosis
NEJM 360:802-809, Case 6-2009, 2009

Multiple Bilateral Non-Hemorrhagic Cerebral Infarctions Associated with Microscopic Polyangiitis
Clin Neurol Neurosurg 111:904-906, Ku, B. & Shin, H., 2009

Microscopic Polyangiitis Presenting with Capsular Warning Syndrome and Subsequent Stroke
J Neurol Sci 277:174-175, Tang, C.,et al, 2009

Hyperdense or Pseudohyperdense MCA Sign, A Damocles Sword?
Neurol 72:116-117, Jha,B. & Kothari,M., 2009

Endarterectomy for Mild Cervical Carotid Artery Stenosis in Patients with Ischemic Stroke Events Refractory to Medical Treatment
Neurol Med Chir 48:211-215, Kobayashi,M.,et al, 2008

Clinicopath Conf, Giant-Cell Arteritis
NEJM 359:2267-2278, Case 36-2008, 2008

Clinicopath Conf., Anti-MNDAR Antibody Mediated Paraneoplastic Limbic Encephalitis Associated With Ovarian Teratoma
NEJM 359:842-853, Case 26-2008, 2008

Clinicopath Conf, Giant-Cell Arteritis
NEJM 359:2267-2278,1153, Case 36-2008, 2008

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts & Leukoencephalopathy (CADASIL)
UpToDate (www.uptodate.com) Aug 21, Dichgans,M.,et al., 2007

Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
J Neurol 254:1609-1611, Collison,K. and Rees,J., 2007

Behcets Disease Presented with Isolated Peduncular Hallucinosis: A Case Report
Internet J Neurol 9, Celik, Y.,et al, 2007

Posterior Reversible Encephalopathy Syndrome in Infection, Sepsis, and Shock
AJNR 27:2179-2190, Bartynski,W.S.,et al, 2006

Poststroke C-Reactive Protein Is a Powerful Prognostic Tool Among Candidates for Thrombolysis
Stroke 37:1205-1210, Montaner,J.,et al, 2006

An Expedited Code Stroke Protocol Is Feasible and Safe
Stroke 37:2935-2939,2863, Sattin,J.A.,et al, 2006

Identification of Embolic Stroke Patterns by Diffusion-Weighted MRI in Clinically Defined Lacunar Stroke Syndromes
Stroke 36:757-761, Wessels,T.,et al, 2005

Spinal MR Findings in Continuous Epidural Analgesia Without Infection
AJNR 26:991-995,987, Ikushima,I.,et al, 2005

Screening for Obstructive Sleep Apnea in Stroke Patients
Stroke 36:1291-1294, Brown,D.L.,et al, 2005

Pseudo-Subarachnoid Hemorrhage:A CT-Finding in Spontaneous Intracranial Hypotension
Neurol 65:135-137, Schievink,W.I.,et al, 2005

Carbamazepine Encephalopathy Masquerading as Creutzfeldt-Jakob Disease
Neurol 65:650-651, Horvath,J.,et al, 2005

Evaluation of C-Reactive Protein Measurement for Assessing the Risk and Prognosis in Ischemic Stroke
Stroke 36:1316-1329, Di Napoli,M.,et al, 2005

The Ependymal "Dot-Dash" Sign: An MR Imaging Finding of Early Multiple Sclerosis
AJNR 26:2033-2036, Lisanti, C.J.,et al, 2005

CJD--A Case of Mistaken Identity
Lancet 364:2068, Campbell,S.,et al, 2004

False-Positive Pulvinar Sign on MRI in Sporadic Creutzfeldt-Jakob Disease
Neurol 62:1235-1236, Petzold,G.C.,et al, 2004

The Redefinition of TIA, The Uses and Limitations of DWI in Acute Ischemic Cerebrovascular Syndromes
Neurol 62:359-360, Warach,S.&Kidwell,C.S., 2004

Systemic Inflammatory Response Depends on Initial Stroke Severity but is Attenuated by Successful Thrombolysis
Stroke 35:2128, Audebert,H.J.,et al, 2004

Sensitivity of 14-3-3 Protein Test Varies in Subtypes of Sporadic Creutzfeldt-Jakob Disease
Neurol 63:436-442,410, Castellani,R.J.,et al, 2004

Intramedulary Tuberculoma Mimicking Primary CNS Lymphoma
JNNP 75:1636-1638, Mohit,A.A.,et al, 2004

Clinicopath Conf., Giant-Cell Arteritis
NEJM 349:170-180, Case 21-2003, 2003

Dementia with Lewy Bodies
Lancet 362:1689-1690, Wilcock,G.K., 2003

Pseudo-Subarachnoid Hemorrhage: A Potential Imaging Pitfall Associated with Diffuse Cerebral Edema
AJNR 24:254-256, Given,C.A. II,et al, 2003

Antivonvulsants for Creutzfeldt-Jakob Disease?
Lancet 361:224, Fioel,A.,et al, 2003

Clinicopath Conf., Brain Abscess Due to Infection with Streptococcus milleri and Haemophilus aphrophilus
NEJM 348:2125-2132, Case 16:2003, 2003

Neurologic Complications of Anthrax
Arch Neurol 60:483-488, Meyer,M.A., 2003

Challenging the Clinical Utility of the 14-3-3 Protein for the Diagnosis of Sporadic Creutzfeldt-Jakob Disease
Arch Neurol 60:813-816,803, Geschwind,M.D.,et al, 2003

14-3-3 Protein in the CSF of Patients with Rapidly Progressive Dementia
Neurol 61:354-357, Huang,N.,et al, 2003

Diagnostic Strategies in CADASIL
Neurol 59:1134-1138, Markus,H.S.,et al, 2002

Anthrax meningoencephalitis
Neurol 59:327-334,300, Lanska,D.J., 2002

Polymyalgia Rheumatica and Giant-Cell Arteritis
NEJM 347:261-271, Salvarani,C.,et al, 2002

Polycythemia Mimicking Venous Sinus Thrombosis
AJNR 23:1402-1403, Healy,J.F.&Nichols,C., 2002

Intraarterial Thrombolysis: Ready for Prime Time?
AJNR 22:55-58, Executive Committee of the ASITN, 2001



Showing articles 100 to 150 of 16194 << Previous Next >>