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activated protein C resistance
advances in neurology
agitation
agnosia
algorithm
aluminum
Alzheimer's disease
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Alzheimer's disease, conjugal
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Alzheimer's disease, familial
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Alzheimer's disease, heterogeneity of
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Alzheimer's disease, pathogenesis
Alzheimer's disease, preclinical
Alzheimer's disease, risk factors in
Alzheimer's disease, treatment of
amnesia
amyloid angiopathy, cerebral
amyloid beta protein
amyloid imaging
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
aneuploidy
aneurysm, intracranial, familial
anomic aphasia
anticholinesterase
antiphospholipid antibodies
antithrombin III deficiency
aphasia
aphasia, progressive
aphasia, progressive, primary
apolipoprotein E
APP
APP gene
apraxia
apraxia, constructional
arthrogryposis multiplex
aspiration
asymptomatic
ataxia
attention span
behavioral disorder
benign essential tremor
biologic markers
blood dyscrasias, neurologic findings with
blood transfusion
brain transplantation
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataplexy
cell fusion test
central core disease
central nervous system, infection of
cerebellar plaques, amyloid
cerebral cortical atrophy
cerebral edema, vasogenic
cerebral glucose metabolism
cerebral infarction
cerebral venous thrombosis
cerebral venous thrombosis, etiology
cerebrospinal fluid, biochemical markers of CNS disease
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, recurrent
cerebrovascular accident, women
cerebrovascular accident, work up for
cerebrovascular accident, young adult
cerebrovascular disease, risk factors in
Charcot-Marie-Tooth
children
choline acetyltransferase
chromosomal abnormality
chromosome 1
chromosome 12
chromosome 14
chromosome 21
chromosome 9
cigarette smoking
clindamycin
coagulopathy
cognition
cost
crying, pathologic
cultured skin fibroblasts
D-dimer
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dementia, familial
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depression
developmental milestones, loss of
diagnostic criteria
differential diagnosis
DNA probes
donepezil
dural sinus thrombosis
dysarthria
dysnomia
dysphagia
dystonia
echolalia
epidemiology of neurology
ethics in neurology
executive dysfunction
Factor V Leiden
false negative
familial
Fazio-Londe's disease
fluency
foam cells
Friedreich's ataxia
frontotemporal dementia, behavioral variant
gaze palsy
gaze palsy, supranuclear
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genetic counselling
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genetic neurologic disorders
genetic screening
genetic testing
Gilles de la Tourette syndrome
hallucination
head injury
headache
headache, persistent
headache, severe
heavy metal intoxication
hemiparesis
hemoglobin abnormality, neurologic complications of
hepatic failure
hepatosplenomegaly
hippocampus
human genome
Huntington's chorea
hyperpyrexia, CNS disorder causing
hyperreflexia
inattention
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incoordination
infantile hemiplegia
inflexibility, mental
intellectual deficit
intracerebral hemorrhage
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, medical precaution with
jaundice
Kugelberg-Welander syndrome
language disorder in adults
lipid storage disorder of CNS
lobar atrophy
lupus anticoagulant
lymphoma involving CNS
manic-depressive
medical-legal aspects of neurology
memory, impairment of
middle cerebral artery territory infarction
middle cerebral artery, occlusion of
mild cognitive impairment
misdiagnosis
molecular genetics
mongolism
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, false negative
MRI, functional
MRI, negative
MRI, serial
muscular dystrophy
muscular dystrophy, Duchenne
mutism
myasthenia gravis
myoclonic jerks
myoclonus
myotonia dystrophica
nausea and vomiting
neurofibrillary degeneration
neurofibromatosis 1
neurofibromatosis 2
neurologic disease, diagnoses of
neurologic signs
neuropathology
neuropathology, brain
neuropathy, amyloid
neurotransmitter
nicotine
Niemann-Pick disease
obsessive-compulsive disorder
pain, increased response
paranoia
paraparesis, spastic
paratonia
Parkinson disease
Parkinson disease, familial
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinsonism syndrome
PAS positive material in the brain
personality change
Pittsburgh Compound B
poison, mercury
poison, neurologic problems with
practice guidelines
preclinical
presenilin-1 gene
presenilin-2 gene
prethrombotic state
prognosis
progressive neurologic disorder
protein C deficiency
protein S deficiency
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
pulmonary embolism
recombinant DNA
release phenomena
research
review article
RFLPs
risk factors
seizure
senile plaques
single photon emission computed tomography
slow virus infection of CNS
spinal muscular atrophy
spinocerebellar ataxia
splenomegaly
spongy degeneration of brain
stereotyped behavior
stimulation, deep brain
straight sinus
subarachnoid hemorrhage
subdural hematoma
superior sagittal sinus thrombosis
tau protein
thrombophlebitis
treatment of neurologic disorder
tremor
tricresylphosphate
trinucleotide repeats
twins
ubiquilin 1
viral infection, CNS
visuospatial disturbance
Werdnig-Hoffman disease
Wernicke's aphasia
word-finding difficulty
Showing articles 400 to 450 of 2374 << Previous Next >>

LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
Disease Models & Mechanisms 4:562-568, Lu,J.T., et al, 2011

Longitudinal Change of Biomakers in Cognitive Decline
Arch Neurol 68:1257-1266,1237, Lo, R.Y.,et al, 2011

Computerized Visual Field Defects in Posterior Cortical Atrophy
Neurol 77:2119-2122, Pelak, V.S.,et al, 2011

Thrombolytic Treatment of Patients with Acute Ischemic Stroke Related to Underlying Arterial Dissection in the United States
Arch Neurol 68:1536-1542, Qureshi, A.I.,et al, 2011

An unusual cause of stroke and hypoxia
BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011

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

A Randomized, Double-Blind, Placebo Controlled Trial of Simvastatin to Treat Alzheimer Disease
Neurol 77:556-563, Sano, M.,et al, 2011

Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
UpToDate, Feb, Shovlin, C., 2011

Evidence-based guideline update: Treatment of Essential Tremor
Neurol 77:1752-1755, Zesiewicz, T.A.,et al, 2011

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Classification of Primary Progressive Aphasia and Its Variants
Neurol 76:1009-1014, Gorno-Tempini,M.L.,et al, 2011

Effectiveness of Adding Memantine to an Alzheimer Dementia Treatment Regimen Which Already Includes Stable Donepezil Therapy: A Critically Appraised Topic
The Neurologist 17:121-123, Riordan,K.C.,et al, 2011

Deep Brain Stimulation
JAMA 305:732, Pluta,R.,et al, 2011

Longitudinal Assessment of A-beta and Cognition in Aging and Alzheimer Disease
Ann Neurol 69:181-192, Villemagne,V.L.,et al, 2011

Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus
RadioGraphics 31:5-30, Hegde,A.N.,et al, 2011

Family Paralysis
Lancet 377:352, Sung,C.-C.,et al, 2011

Diagnosis and Management of Cerebral Venous Thrombosis: A Statement for Healthcare Professionals From the American Heart Association/American Stroke Association
Stroke 42:1158-1192, Saposnik,G.,et al, 2011

CSF biomarkers in posterior cortical atrophy
Neurol 76:1782-1788, Seguin, J.et al, 2011

Cerebral microhemorrhage and brain B-amyloid in aging and Alzheimer disease
Neurol 77:48-54, Yates, P.A.,et al, 2011

Changing Concepts of Alzheimer Disease
JAMA 35:2458-2459, McKhann, G.M., 2011

Mild Cognitive Impairment
NEJM 362:2227-2234, Peterson, R.C., 2011

Sleep-Disordered Breathing, Hypoxia, and Risk of Mild Cognitive Impairment and Dementia in Older Women
JAMA 306(6):613-619, Yaffe, K.,et al, 2011

Spinal Muscular Atrophy A Timely Review
Arch Neurol 68:979-984, Kolb, S.J.,et al, 2011

Lack of Evidence for the Efficacy of Memantine in Mild Alzheimer Disease
Arch Neurol 68:991-998, Schneider, L.S.,et al, 2011

Antidepressant Treatment in Alzheimers Disease
Lancet 378:375-378, Brodaty, H., 2011

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

Comparison of Clinical, Familial, and MRI Features of CADASIL and NOTCH3-Negative Patients
Neurol 74:57-63, Pantoni,L.,et al, 2010

Clinical Reasoning: A 34-Year-Old Woman with Recurrent Bouts of Acral Paresthesias
Neurol 74:775-778, Karam,C. &Scelsa,S., 2010

Genetic Susceptibility to Stuttering
NEJM 362:750-752, Fisher,S.E. &Phil,D., 2010

Familial Versus Sporadic Cavernous Malformations: Differences in Developmental Venous Anomaly Association and Lesion Phenotype
AJNR 31:377-382, Petersen,T.A.,et al, 2010

Use of Angiotension Receptor Blockers and Risk of Dementia in a Predominantly Male Population: Prospective Cohort Analysis
BMJ 340:141-147, 111, Li,N.-C.,et al, 2010

Alzheimers Disease
NEJM 362:329-344, Querfurth,H.W. &LaFerla,F.M., 2010

Familial Mediterranean Fever and Central Nervous System Involvement: A Case Series
Medicine 89:75-84, Kalyoncu,U.,et al, 2010

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

The Older Adult Driver with Cognitive Impairment: "Its a Very Frustrating Life"
JAMA 303:1632-1641, 1642, 1660, Carr,D.B. &Ott,B.R., 2010

Practice Parameter Update: Evaluation and Management of Driving Risk in Dementia: Report of the Quality Standards Subcommittee of the American Academy of Neurology
Neurol 74:1316-1324, Iverson,D.J., et al, 2010

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

Absence Epilepsies With Widely Variable Onset are a Key Feature of Familial GLUT1 Deficiency
Neurol 75:432-440, Mullen,S.A., et al, 2010

Familial Neuromyelitis Optica
Neurol 75:310-315, Matiello,M., et al, 2010

A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
Neurol 75:259-264, Herv�,D., et al, 2010

Serial MRI and CSF Biomarkers in Normal Aging, MCI, and AD
Neurol 75:143-151, Vemuri,P., et al, 2010

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

Early Alzheimers Disease
NEJM 362:2194-2201, Mayeux,R., 2010

Huntingtons Disease
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010

Association Between Familial Atrial Fibrillation and Risk of New-Onset Atrial Fibrillation
JAMA 304:2263-2269, Lubitz,S.A.,et al, 2010

Update on the Natural History of Cavernous Malformations and Factors Predicting Aggressive Clinical Presentation
Neurosurg Focus 29:E7, Washington,C.W.,et al, 2010

Dysexecutive Syndrome: Diagnostic Criteria and Validation Study
Ann Neurol 68:855-864, Godefroy,O.,et al, 2010

Optimal Screening Strategy for Familial Intracranial Aneurysms: A Cost-Effectiveness Analysis
Neurol 74:1671-1679, Bor,A.S.E., 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

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



Showing articles 400 to 450 of 2374 << Previous Next >>