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activated protein C resistance
advances in neurology
agitation
agnosia
algorithm
aluminum
Alzheimer's disease
Alzheimer's disease, age of onset
Alzheimer's disease, conjugal
Alzheimer's disease, diagnosis of
Alzheimer's disease, early onset
Alzheimer's disease, familial
Alzheimer's disease, familial, late onset
Alzheimer's disease, heterogeneity of
Alzheimer's disease, incidence
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
degenerative diseases of CNS
delusion
dementia
dementia, age at onset
dementia, differential diagnosis of
dementia, familial
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
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dementia, transmissible
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
gene
gene mutation
genetic counselling
genetic linkage
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 350 to 400 of 2374 << Previous Next >>

Red Papules on the Tongue of a Patient with Hemiparesis
JAMA 312:741-742, Chiu, H.Y. & Lin, S.J., 2014

Somatic Mutations in Cerebral Cortical Malformations
NEJM 371:733-743, Jamuar, S.S.,et al, 2014

Benzodiazepine Use and Risk of Alzheimers Disease: Case-Control Study
BMJ 349:g5205, Billioti deGage, S.,et al, 2014

A 52-year-old Woman with Progressive Proximal Weakness
Neurol 83:e106-e109, Enduri, S.,et al, 2014

The Limbic-Girdle Muscular Dystrophies
Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014

Clinical Manifestations and Diagnosis of Bicuspid Aortic Valve in Adults
UpToDate Nov, Braverman, D.C., 2014

Psychosis in an Adolescent Girl: A Common Manifestation in Niemann-Pick Type C Disease
Child Adolesc Pych Ment Health 8:20, Wouters,S.,et al, 2014

Predicting Alzheimer Disease with �-Amyloid Imaging: Results from the Australian Imaging, Biomarkers, and Lifestyle Study of Ageing
Ann Neurol 74:905-913, Rowe, C.C.,et al, 2013

TREM2 Variants in Alzheimers Disease
NEJM 368:117-127, Guerreiro, R.,et al, 2013

Variant of TREM2 Associated with the Risk of Alzheimers Disease
NEJM 368:107-116, Jonsson, T.,et al, 2013

Variant TREM2 as Risk Factor for Alzheimers Disease
NEJM 368:182-184, Neumann, H. & Daly, M., 2013

Efficacy and Safety of Everolimus for Subependymal Giant Cell Astrocytomas Associated with Tuberous Sclerosis Complex (EXIST-1): A Multicenter, Randomized, Placebo-Controlled Phase 3 Trial
Lancet 381:125-132, Franz, D.,et al, 2013

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

PET Imaging for Alzheimer Disease: Are Its Benefits Worth the Cost?
JAMA 309:1099-1100, Mitka, M., 2013

Should Patients with Dementia who Wander be Electronically Tagged? Yes
BMJ 346:f3603, McShane, R., 2013

A Pilot Study of Focused Ultrasound Thalamotomy for Essential Tremor
NEJM 369:640-648, Elias, W.J.,et al, 2013

Frontotemporal Dementia
BMJ 347:f4827, Warren, J.D.,et al, 2013

Is There a Link Between Open-Angle Glaucoma and Dementia?: The Three-City-Alienor Cohort
Ann Neurol 74:171-179, Helmer, C.,et al, 2013

Mystery Case: A Young Boy with Myoclonic Jerks
Neurol 81:e130-e134, Musleh, C.,et al, 2013

Longitudinally Extensive Transverse Myelitis in Neuro-Beh�et Disease
Neurol 80:e189-e190, Graham, D.,et al, 2013

Chediak-Higashi Syndrome: Pathognomonic Feature
Lancet 382:1514, Antunes, H.,et al, 2013

Extending the KCNQ2 encephalopathy Spectrum
Neurol 81:1697-1703, Weckhuysen, S.,et al, 2013

An Expanded Role for Neuroimaging in the Evaluation of Memory Impairment
AJNR 34:2075-2082, Desikan, R.S.,et al, 2013

Intracranial Lesions with High Signal Intensity on T1-weighted MR images - Review of Pathologies
Pol J Radiol 78:36-46, Zimmy, Anna.,et al, 2013

Sturge-Weber Syndrome
MedLink Neurology, July, Comi, A.M., 2013

Clinical Reasoning: A Case of Treatable Spastic Paraparesis
Neurol 79: e50-e53, McKinnon, J.H. & Bosch E.P., 2012

Visuospatial deficits in posterior cortical atrophy: structural and functional correlates
JNNP 83:860-863,855, Andrade, K.,et al, 2012

A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy
Neurol 79:e63, Komatsuzaki, S.,et al, 2012

Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
Neurol 79: e70-e72, Zhong, L.,et al, 2012

Lifelong Management of Amyloid-Beta Metabolism to Prevent Alzheimers Disease
NEJM 367:864-866, Gandy, S., 2012

Screening Patients with a Family History of Subarachnoid Haemorrhage for Intracranial Aneurysms: Screening Uptake, Patient Characteristics and Outcome
JNNP 83:86-88, Miller, T.D.,et al, 2012

Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
Stroke 43:72-78, Bharatha, A.,et al, 2012

Cerebral Amyloid Angiopathy
eMedicine, Jan, Menon, R.S., 2012

Relapse Risk after Discontinuation of Risperidone in Alzheimers Disease
NEJM 367:1497-1507, Devanand, D.P.,et al, 2012

Range of Genetic Mutations Associated with Severe Non-Syndromic Sporadic Intellectual Disability: An Exome Sequencing Study
Lancet 380:1674-1682, Rauch, A.,et al, 2012

Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

Brain Amyloid Imaging - FDA Approval of Florbetapir F18 Injection
NEJM 367:885-887, Yang, L.,et al, 2012

The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
Stroke 43:2871-2876, Pescini, F.,et al, 2012

Neurodegenerative causes of death among retired National Football League Players
Neurol 79:1970-1974, Lehman, E.,et al, 2012

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

MRI and EEG as long-term seizure outcome predictors in familial mesial temporal lobe epilepsy
Neurol 79:2349-2354, Morita, M.,et al, 2012

Memantine for Dementia in Adults Older than 40 years with Downs Syndrome (MEADOWS): a Randomised,double-blind,placebo-controlled Trial
Lancet 379:528-536, Hanney,M.,et al, 2012

Memory Enhancement and Deep-Brain Stimulation of the Entorhinal Area
NEJM 366:502-510, Suthana,N.,et al, 2012

Subjective Cognition and Amyloid Deposition Imaging
Arch Neurol 69:223-229, Perrotin,A.,et al, 2012

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

Donepezil and Memantine for Moderate-to Severe Alzheimers Disease
NEJM 366:893-903,957, Howard,R.,et al, 2012

Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012

CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
Neurol 78:1150-1156, Deiva,K.,et al, 2012

Inverse Association between Cancer and Alzheimers Disease: Results from the Framingham Heart Study
BMJ 344:e1442, Driver,J.A.,et al, 2012

Restricted Diffusion in Vanishing White Matter
Arch Neurol 69:723-727, Van de Lei, H.D.W.,et al, 2012



Showing articles 350 to 400 of 2374 << Previous Next >>