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advances in neurology
akinetic mute
animal exposure
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anxiety
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ataxia
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ataxia, truncal
atypical
Balint's syndrome
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basal ganglia, lesion of
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behavioral disorder
blood transfusion
bovine spongiform encephalopathy
brain biopsy
central nervous system, infection of
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cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, enzymes in
cerebrospinal fluid, protein of
children
choreoathetosis
Clinical Pathologic Conference(C.P.C.)
concentration, impaired
cortical blindness
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, diagnostic evaluation of
dementia, familial
dementia, prevention of
dementia, rapidly progressive
dementia, transmissible
denial of blindness(Antons syndrome)
depression
diagnostic criteria
diet
differential diagnosis
diplopia
dysarthria
dysdiadochokinesia
dysmetria
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electrophoretic pattern, CSF
encephalopathy
endoscopy
enolase
epidemic
epidemiology of neurology
episodic disorders
eye movement, disorders of
familial
farmer
fatal familial insomnia
finger nose finger test
genetic counselling
genetic neurologic disorders
Gerstmann-Straussler-Scheinker disease
gliosis
growth hormone
hallucination
hallucination, visual
handwriting
headache
headache, episodic
heralding manifestation
hockey stick sign
hyperosmia
hypogeusia
iatrogenic neurologic disorders
imbalance
immunohistochemistry
incidence
incoordination
incubation period
insomnia
intellectual deterioration
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, Heidenhain variant
Jakob-Creutzfeldt disease, medical precaution with
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
kuru
life expectancy
limbic encephalitis
lymphoma
lymphoma involving CNS
memory, defect of recent
memory, impairment of
mental status, abnormal
misdiagnosis
mortality
movement disorder
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, false negative
MRI, false positive
MRI, FLAIR
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, negative
myoclonic jerks
myoclonus
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic signs
neuron specific enolase
neuropathology
neuropathology, brain
occipital lobe
occipital lobe, lesion of
occupational neurologic disorders
old age, neurology of
pain
pain, leg
Parkinson disease
Parkinsonism plus syndrome
Parkinsonism syndrome
personality change
pituitary, hormones of
preclinical
prevention of neurologic disorders
prion disease
prognosis
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
psychiatric disorder
psychiatric problems in neurologic disorders
psychosis
pulvinar sign
pursuit eye movements, abnormal
rapidly progressing neurologic illness
real-time quaking-induced conversion
remote effect of cancer on the nervous system
review article
risk factors
Romberg's sign
saccadic eye movements, abnormal
scrapie
senile plaques
sensory symptoms
single photon emission computed tomography
smell
spongy degeneration of brain
square wave jerks
symmetric brain lesions
taste
tau protein
thalamus, lesion of
thalamus, lesion of-bilateral
tonsil biopsy
treatment of neurologic disorder
vertigo
vertigo, episodic
vision, blurred
visual cortex
visual impairment
walking, difficulty with
weight loss
wide based gait
Showing articles 100 to 150 of 2384 << Previous Next >>

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

Open Biopsy in Patients With Acute Progressive Neurologic Decline and Absence of Mass Lesion
Neurol 75:419-424, Schuette,A.J., et al, 2010

Sporadic Creutzfeldt-Jakob Disease Mimicking Nonconvulsive Status Epilepticus
Neurol 74:1995-1999, Lapergue,B., et al, 2010

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

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

Pathologic Correlates of Diffusion MRI Changes in Creutzfeldt-Jakob Disease
Neurol 72:1425-1431, Manners,D.N.,et al, 2009

A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
Neurol 72:1262-1276, DiMauro,S.,et al, 2009

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

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Rapidly Progressive Dementia
Ann Neurol 64:97-108, Geschwind,M.D.,et al., 2008

Isolated Cortical Signal Increase on MR Imaging as a Frequent Lesion Pattern in Sporadic Creutzfeldt-Jakob Disease
AJNR 29:1519-1524, Meissner,B.,et al., 2008

Voltage-Gated Potassium Channel Autoimmunity Mimicking Creutzfeldt-Jakob Disease
Arch Neurol 65:1341-1346, Geschwind,M.D.,et al, 2008

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

Clinicopath Conf., Leighs syndrome, Intraventricular Hemorrhage and Periventricular Leukomalacia
NEJM 359:1156-1166, Case 28-2008, 2008

Differential Diagnosis of Restricted Diffusion Confined to the Cerebral Cortex
Clin Radiol 63:1245-1253, Sheerin,F.,et al, 2008

Sporadic Creutzfeldt-Jakob Disease in Two Adolescents
JNNP 79:14-18, Murray,K.,et al, 2008

Transmissible Spongiform Encephalopathy in the 21st Century: Neuroscience for the Clinical Neurologist
Neurol 70:713-722, Brown,P., 2008

Clinical Features and Diagnosis of Dura Mater Graft-Associated Creutzfeldt-Jakob Disease
Neuorl 69:360-367, Noguchi-Shinohara,M.,et al, 2007

Clinicopath conf., Human Prion Disease, Sporadic CJD
Neurol 69:1881-1887, Geschwind,M.D., et al, 2007

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

CSF Analysis in Patients With Sporadic CJD and Other Transmissible Spongiform Encephalopathies
Eur J Neurol 14:121-124, Green,A.,et al, 2007

Pyramidal Tract Degeneration in Sporadic Creutzfeldt-Jakob Disease
Neuropathology 27:434-441, Iwasaki,Y.,et al, 2007

Early Clinical Signs and Imaging Findings in Gerstmann-Straussler-Scheinker Syndrome (Pro102Leu)
Neurol 66:1672-1678, Arata,H.,et al, 2006

Sleep-wake Disturbances in Sporadic Creutzfeldt-Jakob Disease
Neurol 66:1418-1424, Landolt,H.-P.,et al, 2006

Onset of Creutzfeldt-Jakob Disease Mimicking an Acute Cerebrovascular Event
Neurol 67:538-539, Hohler,A.D. &Flynn,F.G., 2006

Iatrogenic Creutzfeldt-Jakob Disease: The Waning of an Era
Neurol 67:389-393, Brown,P.,et al, 2006

CSF Tests in the Differential Diagnosis of Cretuzfeldt-Jakob Disease
Neurol 67:637-643, Sanchez-Juan,P.,et al, 2006

Creutzfeldt-Jakob Disease: Comparative Analysis of MR Imaging Sequences
AJNR 27:1459-1462, Kallenberg,K.,et al, 2006

First Symptom in Sporadic Creutzfeldt-Jakob Disease
Neurol 66:286-287, Rabinovici,G.D.,et al, 2006

Diffusion-Weighted and Fluid-Attenuated Inversion Recovery Imaging in Creutzfeldt-Jakob Disease:High Sensitivity and Specificity for Diagnosis
AJNR 26:1551-1562, Young,G.S.,et al, 2005

Creutzfeldt-Jakob Disease Mimicking Radiologic Posterior Reversible Leukoencephalopathy
Neurol 65:329, Sibon,I.,et al, 2005

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

Clinicopath Conf, Prion Disease (Sporadic Creutzfeldt-Jakob Disease)
NEJM 353:1042-1050, Case 27-2005, 2005

Psychiatric Manifestations of Creutzfeldt-Jakob Disease: A 25-Year Analysis
J Neuropsychiatry Clin Neurosci 17:489-495, Wall,C.A.,et al, 2005

Diffusion-Weighted MRI Abnormalities as an Early Diagnostic Marker for Creutzfeldt-Jakob Disease
Neurol 63:443-449,410, Shiga,Y.,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

Sporadic Creutzfeldt-Jakob Disease
Neurol 63:450-456,410, Meissner,B.,et al, 2004

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

Balint Syndrome Due to Creutzfeldt-Jakob Disease
Neurol 63:395, Ances,B.M.,et al, 2004

Familial Multiple Sclerosis and Other Inherited Disorders of the White Matter
The Neurologist 10:201-215, Kalman,B. &Leist,T.P., 2004

White Matter Lesions in Panencephalopathic Type of Creutzfeldt-Jakob Disease: MR Imaging and Pathologic Correlation
AJNR 25:910-918,905, Matsusue,E.,et al, 2004

Prion Deposition in Olfactory Biopsy of Sporadic Creutzfeldt-Jakob Disease
Ann Neurol 55:294-296, Tabaton,M.,et al, 2004

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

Extraneural Pathologic Prion Protein in Sporadic Creutzfeldt-Jakob Disease
NEJM 349:1812-1820, Glatzel,M.,et al, 2003

Detection of Pathologic Prion Protein in the Olfactory Epithelium in Sporadic Creutzfeldt-Jakob Disease
NEJM 348:711-719,681, Zanusso,G.,et al, 2003

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

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



Showing articles 100 to 150 of 2384 << Previous Next >>