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Addison's disease
adrenomyeloneuropathy
advances in neurology
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agitation
algorithm
alternative medicine
Alzheimer's disease
Alzheimer's disease, behavioral symptoms
Alzheimer's disease, treatment of
amyotrophic lateral sclerosis
Angelman syndrome
anticholinesterase
antidepressant
anxiety
aphasia
apolipoprotein E
Asperger's syndrome
aspiration
ataxia
ataxia, cerebellar
ataxia, sensory
attention span
auditory evoked brainstem potentials
autism
autism, screening for
behavior
behavior, combative
behavioral disorder
bladder dysfunction
body odor
bone marrow transplantation
brain atrophy
C0ORF72
CAG repeats
calcification, intracranial
caregiver
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataplexy
caudate nucleus, atrophy
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral glucose metabolism
cerebral infarction, subcortical
cerebrospinal fluid
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, prognosis in
cerebrovascular accident, recurrent
cerebrovascular accident, rehabilitation of
children
chorea
chromosomal abnormality
chromosome 19
chromosome 7
Clinical Pathologic Conference(C.P.C.)
clonus
cobalamin C deficiency
cognition
compulsivity
corpus callosum, lesion of
cultured skin fibroblasts
cystinosis
degenerative diseases of CNS
delirium
delusion
dementia
dementia, familial
dementia, frontal lobe type
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dementia, rapidly progressive
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developmental evaluation
developmental milestones, loss of
diet
differential diagnosis
dying
dysarthria
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dysphagia
dysphasia
dyspraxia
dystonia
ear, abnormal
eczema
electroconvulsive therapy
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
emotional lability
employment
enzyme, defect
epidemiology of neurology
epsilon sarcoglycan gene
ethics in neurology
evoked potentials
Fabry's disease
falling
familial
family function
fasciculation
fetal alcohol syndrome
flow study, carotid artery
foam cells
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
frontal lobe, atrophy
frontal lobe, pathologic signs of
frontotemporal dementia, behavioral variant
gait disorder
gait, spastic
galactocerebrosidase
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
giant axonal neuropathy
Gilles de la Tourette syndrome
gout
grasp reflex
grief reaction
hallucination
health insurance
hemiplegia
hepatic failure
hepatosplenomegaly
hoarding
homocystinuria
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's disease, children
hyperactivity
hyperhomocysteinemia
hyperreflexia
hypomyelination
hypotonia
imbalance
impulsivity
inappropriate behavior
inattention
inborn errors of metabolism
inborn errors of metabolism, screening
incoordination
intellectual deficit
intellectual deterioration
intelligence quotient
internet
intracerebral hemorrhage
intrauterine
irritability
jaundice
karyotyping
Krabbe's disease
lacunar infarction
language delay
laughing, pathologic
learning disability
learning disability, in children
leg weakness, bilateral
leukodystrophy
leukoencephalopathy
lipid storage disorder of CNS
lobar atrophy
lysosomal storage disease
lysosomes, abnoral
magnetoencephalography
mania
memantine
memory
memory, evaluation of
memory, impairment of
mental retardation
mental retardation, family psychological problems in
methylmalonic acidemia
microangiopathy, brain
microhemorrhage, intracerebral
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine with aura
misdiagnosis
mongolism
mortality
motor neuron disease
mousy odor
movement disorder
MRI
MRI, abnormal
MRI, diffusion tensor
MRI, disappearing lesion on
MRI, functional
MRI, spinal cord
multiple system atrophy
myelomalacia
myelopathy
myoclonic dystonia
myoclonus
myoclonus, action
nerve conduction studies
neurofibrillary degeneration
neuroleptic
neuroleptic, atypical
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neuropathology
neuropathology, brain
neuropathy
neuropathy, demyelinating
next-generation sequencing
Niemann-Pick disease
Notch3 gene
nystagmus
olanzapine
old age, neurology of
optic ataxia
optic atrophy
paraparesis, spastic
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, nonmotor problems of
Parkinsonism syndrome
Pelizaeus Merzbacher
personality change
pes cavus
phenylketonuria
Pick's disease
Prader-Labhart-Willi syndrome
prognosis
progressive neurologic disorder
pseudobulbar palsy
pseudoxanthoma elasticum
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosocial aspects
pulmonary embolism
pyramidal
pyramidal tract dysfunction
quality of life
quetiapine
release phenomena
renal failure
repetitive questioning
review article
rigidity
risk factors
risperidone
rummaging
sarpropterin
screening
seizure
selective serotonin reuptake inhibitors
senile plaques
sensory loss
shadowing
single photon emission computed tomography
skin, biopsy
skin, lesions in neurologic disorders
sleep pathology and physiology
small vessel disease
small vessel disease, cerebral
snout reflex
socialisation
somatosensory evoked potentials
spastic dysphonia
spasticity
speech disorder
splenomegaly
stem cell transplantation
stereotyped behavior
stereotyped behavior, drug induced
stimulant drugs
subarachnoid hemorrhage
subcortical U fibers
suck reflex
suicide
temporal lobe, atrophy
thrombophlebitis
tic
tongue, fasciculations of
treatment of neurologic disorder
treatment, non-pharmacologic
tremor
trinucleotide repeats
twins
umbilical-cord blood transplantation
vasculopathy
venous thrombosis, non-cerebral
vibratory sensation, abnormal
violent behavior
visual loss
wandering
weight loss
white matter disease
white matter disease, subcortical
workup
x-linked mental retardation
Showing articles 900 to 950 of 6255 << Previous Next >>

MELAS
MedLink.com, August, Klopstock, T., 2012

Cogan Syndrome An Analysis of Reported Neurological Manifestations
The Neurologist 18:55-63, Antonios,N. and Silliman,S., 2012

Early Surgical Therapy for Drug-Resistant Temporal Lobe Epilepsy
JAMA 307:922-930,966,985, Engel,J.,et al, 2012

Hospitalization of Psychiatric Disorders Before and After Onset of Unprovoked Seizures/Epilepsy
Neurol 78:396-401, Adelow,C.,et al, 2012

Hashimoto Encephalopathy
Neurol 78:e134, Afshari, M.,et al, 2012

Cortical Pathology in Multiple Sclerosis Patients with Epilepsy: A 3 Year Longitudinal Study
JNNP 83:49-54, Calabrese, M.,et al, 2012

Expanding the Clinical, Radiological and Neuropathological Phenotype of Chronic Lymphocytic Inflammation with Pontine Perivascular Enhancement Responsive to Steroids (CLIPPERS)
JNNP 83:15-22, Simon, N.G.,et al, 2012

Left Atrial Catheter Ablation and Ischemic Stroke
Stroke 43:265-270, Haeusler, K.G.,et al, 2012

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

Sporadic Cerebral Amyloid Angiopathy Revisited: Recent Insights Into Pathophysiology and Clinical Spectrum
JNNP 83:124-137, Charidimou,A.,et al, 2012

Stiff-Man Syndrome and Variants
Arch Neurol 69:230-238, McKeon,A.,et al, 2012

Clinicopathologic Conference,Disseminated Infection with Mycobacterium Tuberculosis of Liver,Peripancreatic Lymphnodes,Sputum,Blood & Urine with Acute Psychosis and HIV.
NEJM 366:648-657, Case 5-2012, 2012

Neurosyphilis Versus Herpes Encephalitis in a Patient with Confusion, Memory Loss, and T2-Weighted Mesiotemporal Hyperintensity
Case Rep Infect Dis 2012:154863, Vedes,E.,et al, 2012

Neuro-Sweets Disease
Pract Neurol 12:126-130, Maxwel,G.,et al, 2012

Functional Weakness: Clues to Mechanism from the Nature of Onset
JNNP 83:67-69, Stone, J.,et al, 2011

Bedside Detection of Awareness in the Vegetative State: A Cohort Study
Lancet 378:2088-2094, Cruse, D.,et al, 2011

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

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

"Bath Salts" Intoxication
NEJM 365:967-968, Ross, E.A.,et al, 2011

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

Treatment of Severe Neurological Deficits with IgG Depletion through Immunoadsorption in Patients with Escherichia coli O104:H4-Associated Haemolytic Uraemic Syndrome: A Prospective Trial
Lancet 378:1166-1173,1120, Greinacher, A.,et al, 2011

An Acutely Confused Young Woman
Lancet 378-456, Casetta, I,.et al, 2011

Sudden, Unexpected Death in Epilepsy
NEJM 365:2902-11, Devinsky, O., 2011

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

Paraneoplastic and Autoimmune Encephalitis
UpToDate, June, Dalmau, J.,et al, 2011

Paraneoplastic Upbeat Nystagmus
Neurol 77:691-693, Wray, S.H.,et al, 2011

Clinicopathologic Conference, Susacs Syndrome (retinocochleocerebral vasculopathy)
NEJM 365:549-559, Case 24-2011, 2011

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

Patterns and Trends in Antipsychotic Prescribing for Parkinson Disease Psychosis
Arch Neurol 68:899-904, Weintraub, D.,et al, 2011

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

Late onset autism and anti-NMDA-receptor encephalitis
Lancet 378:98;378, Creten, C.,et al, 2011

A Case of Hashimoto Encephalopathy Clinical Manifestation, Imaging, Pathology, Treatment, and Prognosis
The Neurologist 17:141-143, Zhao, W.,et al, 2011

Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease
Neurol 76:1372-1376, Sone, J.,et al, 2011

Anti-Ab Autoantibodies in the CSF of a Patient With CAA-Related Inflammation: A Case Report
Neurol 76:842-844, DiFrancesco,J.C.,et al, 2011

Diagnosing variant Creutzfeldt-Jakob disease: a retrospective analysis of the first 150 cases in the UK
JNNP 82:646-651, Heath, C.A.,et al, 2011

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

Movement Disorders Emergencies Part 1
, Robottom, B.J., et al, 2011

Autoimmune Encephalopathy
Semin Neurol 31:144-157, Flanagan, E.,et al, 2011

Subacute sclerosing panencephalitis: An Update
Dev Med Child Neurol 52:901-907, Guitierrez, J.,et al, 2010

Sjogren Syndrome: Neurologic Complications
www.Medlink.com,Jan, Roman,G.C., 2010

Willful Modulation of Brain Activity in Disorders of Consciousness
NEJM 362:579-589,648, Monti,M.M.,et al, 2010

Infectious and Non-Infectious Neurologic Complications in Heart Transplant Recipients
Medicine 89:166-175, Mu�oz,P., et al, 2010

The Expanding Clinical Profile of Anti-AMPA Receptor Encephalitis
Neurol 74:857-859, Graus,F.,et al, 2010

Anti-N-Methyl-d-Aspartate Receptor Encephalitis: Characteristic Behavioral and Movement Disorder
Arch Neurol 67:250-251, Ferioli,S.,et al, 2010

Neurosacrcoidosis: Presentations and Management
Neurologist 16:2-15, Terushkin,V.,et al, 2010

Opsoclonus-Myoclonus Syndrome in Anti-N-Methyl-D-Aspartate Receptor Encephalitis
Arch Neurol 67:118-121, Kurian,M.,et al, 2010

Dopamine Agonist Withdrawal Syndrome in Parkinson Disease
Arch Neurol 67:58-63, Rabinak,C. &Nirenberg,M., 2010

Zonisamide Discontinuation Due to Psychiatric and Cognitive Adverse Events: A Case-Control Study
Neurol 75:513-518, White,J.R., 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



Showing articles 900 to 950 of 6255 << Previous Next >>