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Differential
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acanthocytosis
adult polyglucosan body disease
adult-onset leukodystrophy, with neuroaxonal spheroids
alternating hemiplegia
alternating hemiplegia of childhood
amimia
ammonia
amyloid angiopathy, cerebral
amyloid angiopathy, cerebral, Dutch type
anterior tibial muscle weakness
antiviral agents
aphasia
areflexia
arthrogryposis multiplex
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
ataxic-dystonia syndromes
ATP1A3 gene
attention deficit disorder with hyperactivity
atypical
autonomic dysfunction
Babinski sign
basal ganglia, lesion, bilateral
behavioral disorder
beta-D-glucon
bladder dysfunction
brain atrophy
brain biopsy
brainstem, atrophy
bronchoscopy
bulbar palsy
calcification, gyral
calcification, intracranial
candida albicans
cardiomyopathy
CAT scan, abnormal
CAT scan, emission, abnormal
catalepsy
cataplexy
cerebellar ataxia, children
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral palsy
cerebral palsy, etiology
cerebral palsy, work up
cerebrospinal fluid, beta-D-glucan
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular accident, cryptogenic
cerebrovascular accident, nonvascular territory
cerebrovascular accident, young adult
chest x-ray, abnormal
children
chorea
choreoathetosis
chromosomal abnormality
cingulate gyrus
Clinical Pathologic Conference(C.P.C.)
clonus
clubfoot as related to neurologic disease
Coats plus
cobalamin C deficiency
coma
coma, sudden onset
complications
confusion
congenital myasthenic syndromes
consanguinity
corpus callosum
corpus callosum, hypoplastic
corpus callosum, lesion of
corpus callosum, thinning
cortical ribbon sign
cranial nerve enhancement
creatine phosphokinase(CPK)elevated
cyst
cyst, benign intracranial
cyst, cortical parenchyma
cyst, parenchymal
deafness
delay in diagnosis
dementia
dementia, presenile
developmental disability
developmental retardation
diabetes mellitus
diagnostic criteria
diet
differential diagnosis
difficulty climbing stairs
difficulty going down stairs
disease modifying agents
distal muscle atrophy
distal muscle weakness
DNA sequencing
double-cortex syndrome
dysarthria
dysmetria
dysmorphic
dysphagia
dystonia
electromyogram
encephalopathy
encephalopathy, acute
eosinophilia
executive dysfunction
exome sequencing
Fabry's disease
facial appearance, abnormal
facial weakness
falling
false negative
familial
fatal familial insomnia
fatigue
feeding disorder
fever
fish
floppy infant
fourth ventricle, compression
fungal infection
fungal infection, CNS
gait disorder
gait speed
gait, spastic
GAMT gene
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
globus pallidus, lesion of, bilateral
gram positive cocci
gray hair
hammertoes
headache
headache, awakening with
headache, positional
headache, progressive
hearing loss
helminthic infection of CNS
hemianopia, homonymous
hemiparesis, transient
hemophagocytic lymphohistiocytosis
hepatomegaly
hepatosplenomegaly
heterotopia
HHH syndrome
high arched feet
high arched palate
human genome
hydrocephalus
hydrocephalus, non-communicating(obstructive)
hyperammonemic encephalopathy
hyperhomocysteinemia
hyperreflexia
hypoglycorrhachia
hypogonadism
hypogonadism, hypogonadotropic
hyporeflexia
hypotonia
hypotonia, causes of
hypotonia, infants
imbalance
immunotherapy
inborn errors of metabolism
inclusion bodies, intranuclear
incoordination
India
infection
insomnia
insular cortex
insular cortex, lesion
intellectual deficit
interstitial pulmonary fibrosis
intracerebral hemorrhage
intravenous drug abuse
intrinsic hand muscles, wasting of
jaundice
Jewish
Krabbe's disease
lactic acidemia
Leber's hereditary optic neuropathy
leg weakness, bilateral
leukodystrophy
leukoencephalopathy
leukoencephalopathy with calcification and cysts
level of consciousness, decreased
lid
lid abnormalities
life expectancy
linear lesion
lipid storage disorder of CNS
lung nodule
lung-brain syndromes
lysosomal storage disease
malformation, CNS, congenital
McLeod syndrome
megalencephaly
MELAS syndrome
memory, impairment of
meningeal enhancement
meningeal sarcomatosis
meningitis
meningitis, basilar
meningitis, candida
meningitis, chronic
meningitis, fungal
meningitis, neutrophilic
mental retardation
mestinon
metabolic acidosis
methylmalonic acidemia
microcephaly
microhemorrhage, intracerebral
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
miglustat
mimics
mineralization
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
movement disorder
moyamoya
moyamoya, adult
MRI, abnormal
MRI, blooming effect
MRI, contrast enhanced
MRI, diffusion weighted
MRI, mass effect on
MRI, muscle
MRI, negative
MRI, nodular enhancement
MRI, spinal cord
muscle biopsy
muscle weakness, proximal
mutism
myelomalacia
myeloneuropathy
myelopathy
myoclonus
myopathy
nasal speech
nausea and vomiting
needle tracks
neonatal intensive care unit
neonatal screening, genetic neurologic disorders
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neuronal intranuclear inclusion disease
neuroophthalmology
neuropathy
neuropathy, demyelinating
newborn, evaluation of
next-generation sequencing
Niemann-Pick disease
night blindness
normal
NOTCH2NLC
nystagmus
occipital lobe
ocular motility, disorders of
opened mouth
ophthalmoplegia
organomegaly
ornithine transcarbamylase deficiency
ovarian dysgenesis
pachygyria
papilledema
paragonimiasis
paraparesis, familial spastic
paraparesis, spastic
parasitic infection, CNS
Parkinsonism syndrome
paroxysmal neurologic deficits
peripheral blood smear
Perrault syndrome
pes cavus
philtrum, tented
phonophobia
photophobia
PICU
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
polyglucosan body disease
polymicrogyria
pons, lesion of
precipitating factors
prion disease
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
psychotic behavior
ptosis
ptosis, bilateral
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriplegia
ragged-red fibers
recurrent
ReNU syndrome
respiratory tract infection
retinopathy
review article
risk factors
Romberg's sign
salivation, excessive
schizophrenia
scissors gait
scotoma
screening
sedimentation rate, elevated
seizure
seizure, focal
seizure, laughing as manifestation
sensorineural hearing loss
short stature
shunt procedure, ventricular
shunt procedure, ventricular-complications of
sleep pathology and physiology
small vessel disease
spastic ataxia
spastic paraplegia, type 7
spasticity
speech disorder
speech, absence of
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 28
spinocerebellar degeneration
splenomegaly
strokelike episodes
symmetric brain lesions
systemic illness
tandem gait, ataxic
telangiectases, retinal
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, lesion of-bilateral
tinnitus
toe walking
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
tripping
tumefactive lesion
urea-cycle enzymopathies
urinary urgency
vasculitides
vasculopathy
vegetarianism
vestibular migraine
vision loss, sequential
vision, blurred
visual loss
visual loss, transient
visual obscurations, transient
visuospatial disturbance
walking, delayed
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weakness, proximal
weight loss
wheelchair
white matter disease
white matter disease, unilateral
whole genome sequencing
wide based gait
workup
x-linked intellectual deficit
x-linked mental retardation
Showing articles 100 to 150 of 305 << Previous Next >>

Treat Alzheimer Disease Before It Is Symptomatic
Arch Neurol 68:1237-1238, , 2011

Longitudinal Change of Biomakers in Cognitive Decline
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Positron Emission Tomography-Computed Tomography in Paraneoplastic Neurologic Disorders: Systematic Analysis and Review
Arch Neurol 67:322-329, McKeon,A.,et al, 2010

Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
NEJM 362:1181-1191, Lupski,J.R., et al, 2010

Pediatric Moyamoya Disease: An Analysis of 410 Consecutive Cases
Ann Neurol 68:92-101, Kim,S.-K., et al, 2010

Imaging Manifestations of Progressive Multifocal Leukoencephalopathy
Clinical Radiol 65:431-439, Shah,R.,et al, 2010

Combining MR Imaging, Positron-Emission Tomography, and CSF Biomarkers in the Diagnosis and Prognosis of Alzheimers Disease
AJNR 31:347-354, Walhovd, K.B.,et al, 2010

Acute Limbic Encephalitis and Glutamic Acid Decarboxylase Antibodies:A Reality?
J Neurosci 287:69-71, Blanc,F.,et al, 2009

In Vivo Mapping of Amyloid Toxicity in Alzheimer Disease
Neurol 72:1504-1511, Frisoni,B.G.,et al, 2009

Genomewide Association Studies of Stroke
NEJM 360:1718-1728, Ikram,M.A.,et al, 2009

Positron Emission Tomography in Diagnosis of Visual Variant Alzheimer Disease
J Neuro-Ophthalmol 29:149-150, Finelli,P.F., 2009

Conversion of Amyloid Positive and Negative MCI to AD over 3 Years: An 11C-PIB PET Study
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Pittsburg Compound B Imaging and Prediction of Progression From Cognitive Normality to Symptomatic Alzheimer Disease
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Anti-Ma and Anti-Ta Associated Paraneoplastic Neurological Syndromes: 22 Newly Diagnosed Patients and Review of Previous Cases
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Assessment of �-Amyloid in a Frontal Cortical Brain Biopsy Specimen and by Positron Emission Tomography with Carbon 11-Labeled Pittsburgh Compound B
Arch Neurol 65:1304-1309,1281, Leinonen,V.,et al, 2008

A 60-Year-Old Woman with Mild Memory Impairment: Review of Mild Cognitive Impairment
JAMA 300:1566-1574,1598, Ellison,J.M., 2008

Frequent Amyloid Deposition Without Significant Cognitive Impairment Among the Elderly
Arch Neurol 65:1509-1517, Aizenstein,H.J.,et al, 2008

Prognosis of Children With Partial Epilepsy: MRI and Serial 18FDG-Pet
Neurol 68:665-659, Gaillard,W.D.,et al, 2007

Brain Glucose Supply and The Syndrome of Infantile Neuroglycopenia
Arch Neurol 64:507-513, Pascual,J.M.,et al, 2007

Imaging of Amyloid Burden and Distribution in Cerebral Amyloid Angiopathy
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The Woman Who Needed a Pet
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Detection of Unknown Primary Tumor in a Patient with Cerebellar Metastasis Using FDG PET-CT: Case Report
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Whole-Body MRI and PET-CT in the Management of Cancer Patients
Eur Radiol 16:1216-1225, Schmidt,G.P.,et al, 2006

Multiple Diagnostic Tests Are Needed to Assess Multiple Causes of Dementia
Arch Neurol 63:144-146,146, Rikkert,M.G.M.O.,et al, 2006

Chronic Disorders of Consciousness
Lancet 367:1181-1192, Bernat,J.L., 2006

Episodic Neurologic Dysfunction with Migraine and Reversible Imaging Findings After RadiationRRH
Neurol 67:676-678, Pruitt,A.,et al, 2006

Diagnosis of Neurolymphomatosis with FDG PET
Neurol 67:722-723, Rosso,S.M.,et al, 2006

PET of Brain Amyloid and Tau in Mild Cognitive Impairment
NEJM 355:2652-2663, Small,G.W.,et al, 2006

Tuberculosis Meningitis Mimics Malignancy Like Lesion in Fluroine-18-FDG PET Scan and Gallium Scan
Ann Nucl Med Sci 19:275-278, Chang,W.-D.,et al, 2006

The role of radiotracer imaging in Parkinson disease
Neurol 64:208-215, Ravina, B., et al, 2005

Metabolic Patterns Associated with the Clinical Response to Galantamine Therapy
Arch Neurol 62:721-728, Mega,M.S.,et al, 2005

A Positron Emission Tomographic Study in Spontaneous Migraine
Arch Neurol 62:1270-1275, Afridi,S.K.,et al, 2005

Diagnostic Evaluation of Patients with a Brain Mass as the Presenting Manifestation of Cancer
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Unknown Primary Tumors: Detection with Dual-Modality PET/CT--Initial Experience
Radiology 234:227-234, Gutzeit,A.,et al, 2005

A New Cause of Limbic Encephalopathy
Brain 128:1745-1746, Darnell,R.B., et al, 2005

Neuroprotection in Parkinson Disease, Mysteries, Myths, and Misconceptions
JAMA 291:358-364, Schapira,A.H.V.&Olanow,C.W., 2004

Serial 18F-fluoro-2-deoxy-D-glucose Positron Emmission Tomography and Magnetic Resonance Imaging of Paraneoplastic Limbic Encephalitis
Arch Neurol 61:1785-1789, Scheid,R.,et al, 2004

Neuroimaging and Early Diagnosis of Alzheimer Disease: A Look to the Future
Radiology 226:315-336, Petrella,J.R.,et al, 2003

A Study of Persistent Post-Concussion Symptoms in Mild Head Trauma Using Positron Emission Tomogrophy
JNNP 74:326-332, Chen,S.H.A.,et al, 2003

Alzheimer's Disease and Parkinson's Disease
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Best Measure of Ischemic Penumbra: Positron Emission Tomography
Stroke 34:2534-2535, Heiss,W.-D., 2003

The Topography of Metabolic Deficits in Posterior Cortical Atrophy (the Visual Variant of Alzheimers Disease) with FDG-PET
JNNP 74:1521-1529, Nestor,P.J.,et al, 2003

Functional Brain Mapping of Psychopathology
JNNP 72:432-439, Honey,G.D.,et al, 2002

Severe Neurologic Complications After Hematopoietic Stem Cell Transplantation in Children
Neurol 59:1895-1904,E13, Farci,M.,et al, 2002

The Effect of Brain Atrophy on Cerebral Hypometabolism in the Visual Variant of Alzheimer Disease
Arch Neurol 58:480-486, Bokde,A.L.W.,et al, 2001

Chorea and Antiphospholipid Antibodies: Treatment with Methotrexate
Neurol 56:137-138, Paus,S.,et al, 2001

Functional Correlates of Pallidal Stimulation for Parkinson's Disease
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Effect of Donepezil on Brain Acetylcholineserase Activity in Patients with AD Measured by PET
Neurol 56:408-410, Shinotoh,H.,et al, 2001

Transplantation of Embryonic Dopamine Neurons for Severe Parkinson's Disease
NEJM 344:710-719,763, Freed,C.R.,et al, 2001

Impact of the Human Genome Projects and Identification of a Stroke Gene
Stroke 32:1239-1241, Alberts,M.J., 2001



Showing articles 100 to 150 of 305 << Previous Next >>