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addiction, heroin
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adverse drug reaction
akinetic mute
ammonia
amyloid angiopathy, cerebral
amyloid angiopathy, cerebral, inflammatory type
anasarca
anemia
angiitis, isolated of CNS
angiography, cerebral
angiography, cerebral, negative
anorexia
anterior cerebral artery territory infarction
anterior horn cell disease
aphasia
apnea
arbovirus
areflexia
arteriopathy
aspergillosis
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
Babinski sign
bacterial infection
bacterial infection, CNS
basal cistern
basilar artery occlusion
behavioral disorder
bradykinesia
brain biopsy
brainstem, infarction of
brainstem, lesion of
carotid artery stenosis, intracranial
carotid-siphon stenosis
CAT scan, angiography
CAT scan, angiography, false negative
CAT scan, dense artery sign
CAT scan, venography
cauda equina
central nervous system, infection of
cerebral cortex
cerebral embolism
cerebral embolism, mechanical extraction
cerebral infarction
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebrospinal fluid, culture negative
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, bilateral
cerebrovascular accident, multiple
cerebrovascular accident, nonvascular territory
cerebrovascular accident, young adult
cerebrovascular disease, rapidly progressive
children
chills
cingulate gyrus
Clinical Pathologic Conference(C.P.C.)
clot retrieval
coma
coma, sudden onset
complications
confusion
corpus callosum
corpus callosum, infarction of
corpus callosum, lesion of
cortical-basal ganglionic degeneration
cough
cranial nerve palsies
cyclophosphamide
decerebrate posture
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, frontotemporal
dementia, rapidly progressive
dementia, thalamic
dense basilar artery sign
dense middle cerebral artery sign
dexterity, impaired
diabetes mellitus
diagnostic criteria
differential diagnosis
difficulty climbing stairs
disorientation
doll's head maneuver
downward deviation of eyes
drug abuse
drug abuse, neurologic complications of
drug abuse, toxic screen In
drug overdose
dural arteriovenous malformation
dysarthria
dysmetria
dysphagia
dyspnea
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
ELISA
embolism, paradoxical
embolism, vertebral-basilar artery
emergencies, neurologic
encephalitis
encephalitis, brainstem
encephalitis, viral
encephalomyelitis
encephalopathy
encephalopathy, acute
encephalopathy, progressive
endovascular therapy
enterovirus
enterovirus infection of CNS
eosinophilia
epidemic
executive dysfunction
exome sequencing
falling
false negative
familial
fatigue
fever
fibrillations
fistula, arterio-venous, dural
flaccid paralysis
fungal infection
fungal infection, CNS
gait disorder
gammaglobulin therapy, intravenous
gastric partitioning
gaze palsy, vertical
gene mutation
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
globus pallidus, lesion of, bilateral
GM antigen test
grasp reflex
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
hand-foot-mouth disease
headache
headache, severe
hearing loss
hearing loss, sudden, bilateral
hemianopia, homonymous
hemiparesis, recurrent
hemiplegia
hemorrhage, thalamic
hemosiderosis of CNS, superficial
heralding manifestation
herniation syndromes, intracranial
HHH syndrome
hydrocephalus
hyperalimentation
hyperammonemic encephalopathy
hypercapnia
hypereosinophilic syndrome(HES)
hyperintense vessel sign
hypersomnia
hypoalbuminemia
hypogammaglobulinemia
hypoglycorrhachia
hypophosphatemia
hypoxia
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunocompetent
immunohistochemistry
immunosuppression
immunosuppressive agents
inattention
inborn errors of metabolism
infection
insular cortex
insular cortex, lesion
intellectual deterioration
intracerebral hemorrhage
intracerebral hemorrhage, lobar
intracranial pressure, increased
intravenous drug abuse
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
lactic acidemia
leg swelling
Legionnaires'disease
leukemia
leukemia, neurologic findings assoc.with
leukoencephalopathy
level of consciousness, decreased
life expectancy
limbic encephalitis
locked-in syndrome
logopenia
lumbar puncture, complications of
lymphoma
lymphoma involving CNS
masked facies
memory, impairment of
meningitis
meningitis, aseptic
meningitis, aspergillus
meningitis, basilar
meningitis, chronic
meningitis, fungal
meningitis, fungal-negative CSF culture
meningitis, granulomatous
meningitis, neutrophilic
meningitis, neutrophilic, persistent
meningitis, noninfectious
meningitis, spinal fluid smear and culture-negative
meningoencephalitis
mental status, abnormal
MERCI trial
microangiopathy, brain
microhemorrhage, intracerebral
mimics
misdiagnosis
mortality
mosquito
motor neuron disease
MRI
MRI, abnormal
MRI, angiography
MRI, angiography, false negative
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, FLAIR
MRI, FLAIR, hyperintense vessels
MRI, gradient-echo
MRI, negative
MRI, serial
MRI, spinal cord
MRI, sulcal hyperintensity
MRI, venography
multiple system atrophy
muscle pain
mutism
myelopathy
myoclonic jerks
myoclonus
nausea and vomiting
neck stiffness
neoplastic angioendotheliosis
nerve conduction studies
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic examination, focal
neurologic signs
neuropathology
neuropathology, brain
neuropathy, peripheral
numbness, generalized
nutritional deficiency
old age, neurology of
ophthalmoplegia
ophthalmoplegia, total
opiate
oral contraceptives
oral ulcerations
ornithine transcarbamylase deficiency
oxycodone
paralysis, acute
paralysis, acute areflexic
paraparesis
paraplegia
paresthesias
Parkinson disease, atypical
Parkinsonism syndrome
patent foramen ovale
Penumbra System
personality change
pituitary, adenoma
pituitary, apoplexy
pleocytosis of cerebrospinal fluid
pneumonia
polymerase chain reaction
polymerase chain reaction, false negative
pons, infarction of
positive sharp waves
prion disease
prion protein gene
prognosis
progressive neurologic disorder
progressive supranuclear palsy
protein 14-3-3, cerebrospinal fluid
psychomotor retardation
quadriparesis
quadriparesis, progressive
rapidly fatal neurologic illness
rapidly progressing neurologic illness
release phenomena
respiratory arrest
respiratory failure
reversible neurologic disorder
review article
rigidity, axial
risk factors
sedimentation rate
sedimentation rate, elevated
seizure
sensory level
serologic testing, false negative
small vessel disease
small vessel vasculitis
somnolence
speech, slowed
spinal cord
spinal cord, infarction of
spinal cord, lesion of
splenium of corpus callosum
steroid therapy, CNS treatment and complications with
stuporous
subcortical hemorrhage
synucleinopathy
tandem gait, ataxic
tau protein
tauopathy
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thrombectomy
thrombocytopenia
tonsillar herniation of cerebellum
treatment of neurologic disorder
tremor
tremulousness
ulcerative colitis
uncal herniation
urea-cycle enzymopathies
urine test in toxic screen
vasculitides
vasculopathy
venous hypertension
venous ischemia
very long chain fatty acids
viral infection
viral infection, CNS
vision, blurred
voriconazole
walking, difficulty with
watershed infarcts
weakness
weakness, generalized
weight loss
West Nile fever
wheelchair
white matter disease
zinc
Showing articles 150 to 200 of 3162 << Previous Next >>

A 72-year-old Man with Rapid Cognitive Decline and Unilateral Muscle Jerks
Neurol 82:e194-e197, Duncan, M.,et al, 2014

Clinicopathologic Conference, Dermatomyositis. Malignant Atrophic Papulosis (Degoss Disease), Involving the Skin and Gastrointestinal Tract
NEJM 370:2327-2337, Case 18-2014, 2014

Palliative Care and Neurology
Neurol 83:561-567, Boersma, I.,et al, 2014

Clinicopathologic Conference, Infective Endocarditis and Infectious Aortitis due to Staphylococcus Aureus
NEJM 370:651-660, Case 5-2014, 2014

IgG4-Related Leptomeningitis: A Reversible Cause of Rapidly Progressive Cognitive Decline
Neurol 82:540-542, Mehta, S.H.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Ischemic-Hypoxic Encephalopathy
Adams & Victors Principles of Neurology Chp 40, pg 1133, Ropper, A.H.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Carbon Monoxide Poisoning
Adams & Victors Principles of Neurology Chp 40, pg 1138, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Acute Anterior Poliomyelitis
Adams & Victors Principles of Neurology, Chp 33, pg 763, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Creutzfeldt-Jakob Disease (Subacute Spongiform Encephalopathy)
Adams & Victors Principles of Neurology, Chp 33, pg 769, Ropper, A.H.,et al, 2014

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

A 62-Yeal-Old Man with Fluctuating Neurological Deficits and Skin Lesions
JAMA Neurol 70:120-124, Konikkara, J.,et al, 2013

West Nile Virus: Review of the Literature
JAMA 310:308-315,267, Petersen, L.R.,et al, 2013

Cortical and Cerebellar Hypometabolism After Bilateral Antero-Inferior Cerebellar Artery Infarct
Neurol 78:69-70, Ayrignac, X.,et al, 2012

Clincopathologic Conference,Graves Disease with Thyrotoxic Periodic Paralysis
NEJM 366:553-560, Case 4-2012, 2012

Acute Unilateral Hearing Loss as an Early Symptom of Lateral Cerebral Sinus Venous Thrombosis
Arch Neurol 69:1508-1511, Gattringer, T.,et al, 2012

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

Evidence-based Guideline: Diagnostic accuracy of CSF 14-3-3 Protein in Sporadic Creutzfeldt-Jakob Disease
Neurol 79:1499-1506, Muayqil, T.,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

Monosymptomatic Clinically Isolated Syndrome with Sudden Sensorineural Hearing Loss
The Neurologist 18:302-305, Anagnostouli, M.C.,et al, 2012

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

Clinicopathologic Conference,Necrotizing Noninflammatory Myopathy Consistent with Exposure to Statins
NEJM 36:944-954, Case 7-2012, 2012

Progressive Weakness with Respiratory Failure in a Patient with Sarcoidosis
Arch Neurol 69:534-537, Chaudhry,P.,et al, 2012

Clinical Reasoning: A Middle-Aged Woman with Progressive Symmetric Weakness and a CSF Pleocytosis
Neurol 78:e88-e92, Marks,D.,et al, 2012

Clinicopathologic Conference, Cystoisospora Belli Enteritis and HIV Infection
NEJM 365:2306-2316, Case 38-2011, 2011

Functional Weakness: Clues to Mechanism from the Nature of Onset
JNNP 83:67-69, Stone, J.,et al, 2011

Rhombencephalitis A Series of 97 Patients
Medicine 90:256-261, Moragas, M.,et al, 2011

Rapidly Progressive Alzheimer Disease
Arch Neurol 68:1124-1130, Schmidt, C.,et al, 2011

Treatable Neurological Disorders Misdiagnosed as Creutzfeldt-Jakob Disease
Ann Neurol 70:437-444, Chitravas, N.,et al, 2011

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

The Evaluation of Rapidly Progressive Dementia
The Neurologist 17:67-74, Rosenbloom,M.H. &Atri,A., 2011

Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias
Neurol 76:1711-1719, Vitali, P.,et al, 2011

A Case of Hashimoto Encephalopathy Clinical Manifestation, Imaging, Pathology, Treatment, and Prognosis
The Neurologist 17:141-143, Zhao, W.,et al, 2011

Oral vs Intratympanic Corticosteroid Therapy for Idiopathic Sudden Sensorineural Hearing Loss
JAMA 305(20):2071-2079,2114, Rauch, S.D.,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

Autoimmune Encephalopathy
Semin Neurol 31:144-157, Flanagan, E.,et al, 2011

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

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

Sudden Sensorineural Hearing Loss
The Lancet 375:1203-1211, Schreiber,B.E., et al, 2010

Delirious Deficiency
Lancet 376:1362, Olsen,R.Q &Regis,J.T., 2010

Atypical Dementia
Lancet 376:656, Cohen-Bittan,J. et al, 2010

Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
NEJM 362:929-940, Case 7-2010, 2010

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

Intravascular Lymphoma Masquerading as Multiembolic Stroke Developing After Coronary Artery By-Pass Surgery
The Neurologist 15:98-101, Sumer,M.,et al, 2009

Rapidly Progressive Neurodegenerative Dementias
Arch Neurol 66:201-207, Josephs,K.A.,et al, 2009

Hypokalemia
eMedicine Sept, Verive,M.J., 2009

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

The Floppy Infant: Evaluation of Hypotonia
Pediatrics in Review 30:e66-e76, Peredo, D. & Hannibal M., 2009

Neurologic Manifestations of von Hippel-Lindau Disease
JAMA 300:1334-1342, Butman,J.A.,et al, 2008

Trapped in Bed (After 32 Years of a Blocked Nose)
Lancet 372:1606, Imtiaz,K.E.,et al, 2008

Spinal Muscular Atrophy
Lancet 371:2120-2133, Lunn,M.R. &Wang,C.H., 2008



Showing articles 150 to 200 of 3162 << Previous Next >>