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Differential
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aminoacidurias
ammonia
anatomy of
anorexia
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ataxia, truncal
ataxic gait
Babinski sign
basal ganglia
basal ganglia, calcification of
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basal ganglia, lesion of
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basilar artery occlusion
Behcet's syndrome
beriberi
beriberi, infantile
blood dyscrasias, neurologic findings with
brain atrophy
brainstem
brainstem, lesion of
bulimia
calcification, intracranial
Canavan's disease
carbon monoxide poisoning
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, false negative
cataracts
caudate nucleus
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
central nervous system, infection of
central pontine myelinolysis
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar atrophy, secondary
cerebellar lesion
cerebral cortex
cerebral infarction
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cerebrospinal fluid, lactic acid concentration
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cerebrovascular accident, young adult
children
chorea
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
coenzyme Q10 deficiency
cognition
color vision, impaired
crying
cultured skin fibroblasts
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafness
deafness, congenital
deep gray nuclei
degenerative diseases of CNS
dementia
dentate nuclei
dentate nuclei, lesion of
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
differential diagnosis
dizziness
dysarthria
dystonia
electron microscopy
encephalitis
encephalitis, Japanese
encephalitis, viral
encephalopathy
encephalopathy, neonatal
enkephalins
enzyme, defect
eye movement, disorders of
Fabry's disease
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failure to thrive
familial
flavivirus
fontanel, bulging
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gadolinium
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glutaric acidemia
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head injury
head lag
headache
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histochemistry
histochemistry of muscle
hyperglycemia
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hypotonia
hypotonia, infants
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iatrogenic neurologic disorders
inborn errors of metabolism
infant and newborn with distress, neurologic prognosis in
infant, evaluation of
intellectual deterioration
internuclear ophthalmoplegia
internuclear ophthalmoplegia, unilateral
intestinal pseudoobstruction
intraventricular hemorrhage
iron, brain
irritability
Jakob-Creutzfeldt disease
Kearns-Sayre syndrome
lactic acidemia
Leber's hereditary optic neuropathy
leg numbness
leg weakness, bilateral
Leigh's disease
Leigh's disease, adult variety
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
lethargy
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
lipid storage disorder of CNS
liver disease
magnetic susceptibility
maple syrup urine disease
Marinesco-Sjogren syndrome
MELAS syndrome
mental retardation
MERRF syndrome
metabolic disorder, primary
metabolic disorder, primary-screening tests
metronidazole
microhemorrhage, intracerebral
midbrain, lesion of
mitochondrial disease
mitochondrial encephalomyopathy
mitochondrial recessive ataxic syndrome
MNGIE syndrome
molecular genetics
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
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MRI, complications with
MRI, contrast enhanced
MRI, diffusion weighted
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MRI, serial
MRI, spinal cord
MRI, T1 weighted high signal foci
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MRS
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle pain
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myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
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myopathy, mitochondrial
neoplasm, primary of CNS
neurofibromatosis 1
neurologic complications of, systemic cancer
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neuropathology
neuropathology, brain
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neuropathy, peripheral
neurotoxin
nutritional deficiency
nystagmus
nystagmus, rotary
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic atrophy, hereditary
optic neuropathy
osmotic demyelination syndrome
overlap syndrome
owl's eye sign of spinal cord
pancytopenia
paraparesis, spastic
Parkinson disease
pes cavus
pigmentary retinopathy
POLG1 gene
polyneuropathy
pons, lesion of
progressive infantile poliodystrophy
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
ragged-red fibers
remote effect of cancer on the nervous system
respiratory failure
restless leg syndrome
retinopathy
review article
Romberg's sign
seizure
seizure, children
sensorineural hearing loss
sensory loss
short stature
spasticity
speech, loss of
spinal cord
spinal cord, lesion of
spinocerebellar degeneration
spongy degeneration of brain
status epilepticus
striatonigral degeneration
striatonigral degeneration, infantile
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
substantia nigra
suck, poor
symmetric brain lesions
term infant
thalamic tumors
thalamic tumors, bilateral
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine deficiency
titubation
tonic spasms
treatment of neurologic disorder
tremor
tremor, intention
urine test for metabolic disorders
visual acuity, decreased
vitamin deficiency
Von Hippel Lindau
weakness
weakness, progressive
weight loss
Wernicke's encephalopathy
white matter disease
white matter disease, periventricular
wide based gait
workup
Showing articles 200 to 250 of 751 << Previous Next >>

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

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

Epidemiology and Clinical Outcomes of Infective Endocarditis in Hemodialysis Patients
Ann Thorac Surg 83:2081-2086, 2086, Kamalakannan,D.,et al, 2007

MR Imaging, Diffusion-Weighted Imaging and MR Spectroscopy Findings in Acute Rapidly Progressive Subacute Sclerosing Panencephalitis
Brain Dev 29:306-311, Oguz, K.K.,et al, 2007

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

Neurologic Complications of Gastric Bypass Surgery for Morbid Obesity
Neurol 68:1843-1850, Juhasz-Pocsine,K.,et al, 2007

Neuroimaging Findings in Human Prion Disease
JNNP 78:664-670, Macfarlane,R.G.,et al, 2007

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

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

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

Risk Factors for Variant Creutzfeldt-Jakob Disease: A Case-Control Study
Ann Neurol 59:111-120, Ward,H.J.T.,et al, 2006

Adult Onset Subacute Sclerosing Panencephalitis: Clinical Profile of 39 Patients From a Tertiary Care Centre
JNNP 77:630-633, Prashanth,L.K.,et al, 2006

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

Kuru in the 21st Century--An Acquired Human Prion Disease With Very Long Incubation Periods
Lancet 367:2068-2074, Collinge,J.,et al, 2006

Neurological Outcome of Septic Cardioembolic Stroke After Infective Endocarditis
Stroke 37:2094-2099, Ruttmann,E.,et al, 2006

Recurrent Ibuprofen-Induced Aseptic Meningitis: Evidence Against an Antigen-Specific Immune Response
Neurol 67:539-540, Periard,D.,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

Infective Endocarditis
BMJ 333:334-339, Beynon,R.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

Spinal Epidural Abscess
NEJM 355:2012-2020, Darouiche,R.O., 2006

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

Post-operative aspergillosis
Clin Microbiol Infect 12:1060-1076, Pasqualotto, A.C. & Denning, D.W., 2006

Neurological presentation of intravascular lymphoma: report of two cases and discussion of diagnostic challenges
Eur J Neurol 12:710-714, Lozsadi, D.A.,et al, 2005

Clinicopath Conf, Acute Myelogenous Leukemia Presenting as Meningitis
NEJM 352:274-283, Case 2-2005, 2005

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

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

Folate, Vitamin B12, and Risk of Ischemic and Hemorrhagic Stroke
Stroke 36:1426-1431, Guelpen,B.V.,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

Transmissible Spongiform Encephalopathies
Lancet 363:51-61, Collins,S.J.,et al, 2004

Stroke as the First Manifestation of a Concealed Pancreatic Neoplasia
Rev Neurol 38:332-335, Perez-Lazaro,C.,et al, 2004

Tissue Distribution of Bovine Spongiform Encephalopathy Agent in Primates after Intravenous or Oral Infection
Lancet 363:422-428,411, Herzog,C.,et al, 2004

Possible Transmission of Variant Creutzfeldt-Jakob Disease by Blood Transfusion
Lancet 363:417-421,411, Llewelyn,C.A.,et al, 2004

Recipients of Blood or Blood Products "at vCJD risk"
BMJ 328:118-119, Bird,S.M., 2004

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

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

Subacute Sclerosing Panencephalitis Findings at MR Imaging, Diffusion MR Imaging, and Proton MR Spectroscopy
AJNR 25:892-894, Sener,R.N., 2004

Recurrent Meningitis of Unknown Aetiology
Lancet 363:1772, Ellerin,T.B.,et al, 2004

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

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

Novel Methods for Disinfection of Prion-Contaminated Medical Devices
Lancet 364:521-526, Fichet,G.,et al, 2004



Showing articles 200 to 250 of 751 << Previous Next >>