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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
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, treatment of
demyelinating disease
depression
developmental disability
developmental evaluation
developmental milestones, loss of
diet
differential diagnosis
dying
dysarthria
dysmorphic
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 1450 to 1500 of 6255 << Previous Next >>

Course and Outcome of Patients in Vegetative State of Nontraumatic Aetiology
JNNP 56:407-409, Sazbon,L.,et al, 1993

Psychogenic Myoclonus
Neurol 43:349-352, Monday,K.&Jankovic,J., 1993

A Population-Based Study of Dementia in 85-Year-Olds
NEJM 328:153-158, 203-2051993., Skoog,I.,et al, 1993

Use of Twin Cohorts for Research in Alzheimer's Disease
Neurol 43:261-267, Breitner,J.C.S.,et al, 1993

The Visual Variant of Alzheimer's Disease, A Clinicopathologic Case Study
Neurol 43:305-313, Levine,D.N.,et al, 1993

Wilson's Disease:Evidence of Subgroups Derived from Clinical Findings and Brain Lesions
Neurol 43:120-124, Oder,W.,et al, 1993

Predicting the Occurrence of Adverse Events after Coronary Artery Bypass Surgery
Ann Int Med 118:18-24, Geraci,J.M.,et al, 1993

Real and Imagined Clinicopathological Limits of"Prior Dementia"
Lancet 341:127-129, Brown,P.,et al, 1993

Infectious Prions or Cytotoxic Metabolites?
Lancet 341:159-161, Pablos-Mendez,A.,et al, 1993

Acute Bacterial Meningitis in Adults, A Review of 493 Episodes
NEJM 328:21-28, Durand,M.L.,et al, 1993

Nonepileptic Seizures and Childhood Sexual and Physical Abuse
Neurol 43:1950-1953, Alper,K.,et al, 1993

Weeping as a Common Element of Pseudoseizures
Arch Neurol 50:1059-1060, Bergen,D.&Ristanovic,R., 1993

Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
JAMA 270:1569-1575, Brown,W.,et al, 1993

Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
JAMA 270:2838-2842, Dobyns,W.B.,et al, 1993

Twinning and Cerebral Palsy:Experience in Four Northern California Counties, Births 1983 Through 1985
Pediatrics 92:854-858, Grether,J.K.,et al, 1993

Choroido-Cerebral Calcification Syndrome with Retardation
Neurol 43:2387-2389, Singh,B.,et al, 1993

Schizophrenia as a Brain Disease, The Dopamine Receptor Story
Arch Neurol 50:1093-1095, 10971993., Seeman,P., 1993

Schizophrenia as a Brain Disease
Arch Neurol 50:1096-1097, Williamson,P.C., 1993

Intranasal Midazolam for Claustrophobia in MRI
J Comput Assist Tomogr 17:991-992, Moss,M.L.,et al, 1993

Pre-and Postcontrast MR Studies in Tuberous Sclerosis, Wippold
J Comput Assist Tomogr 16:69-72, II,F.J.,et al, 1992

Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
NEJM 326:444-449, Medori,R.,et al, 1992

Physicians, Elderly Drivers, and Dementia
Lancet 339:41-43, O'Neill,D., 1992

Cerebromeningeal Haemophagocytic Lymphohistiocytosis
Lancet 239:104-107, Henter,J.&Elinder,G., 1992

Transient Unresponsiveness in the Elderly, Report of Five Cases
Arch Neurol 49:35-37, Haimovic,I.C.&Beresford,H.R., 1992

Detection of Full Fragile X Mutation
Lancet 339:271-272, Pergolizzi,R.G.,et al, 1992

The Management of"Psychogenic"Orofacial Pain, A Collaborative Attitude and Antidepressants May Help
BMJ 304:329-330, Hunter,S., 1992

Encephalitis in Cat Scratch Disease with Persistent Dementia
JNNP 55:133-135, Revol,A.,et al, 1992

Electroconvulsive Therapy Treatment of Depression in a Patient with Adult GM2 Gangliosidosis
Ann Neurol 31:342-344, Renshaw,P.F.,et al, 1992

Nervous System Lyme Borreliosis-Revisited
Arch Neurol 49:102-107, Finkel,M.J.&Halperin,J.J., 1992

A Familial Disorder with Subcortical Ischemic Strokes, Dementia, and Leukoencephalopathy
Neurol 42:1015-1019, Mas,J.L.,et al, 1992

The Older Driver, Clinical Assessment and Injury Prevention
Arch Int Med 152:735-740, Underwood,M., 1992

Murder, Insanity, and Medical Expert Witnesses
ARch Neurol 49:608-611, Ciccone,J.R., 1992

Wilson's Disease:The Problem of Delayed Diagnosis
JNNP 55:692-696, Walshe,J.M.&Yealland,M., 1992

Small Infarctions of Cochlear, Retinal, and Encephalic Tissue in Young Women
Stroke 23:903-907, Schwitter,J.,et al, 1992

Paramedian Thalamopeduncular Infarction:Clinical Syndromes and Magnetic REsonance Imaging
Ann Neurol 32:162-171, Tatemichi,T.K.,et al, 1992

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992

Aluminium Intoxication in Undialysed Adults with Chronic Renal Failure
JNNP 55:697-700, Russo,L.S.,et al, 1992

Delayed Encephalopathy after Acute Carbon Monoxide Intoxication:MR Imaging Features & Cerebral White Matter Lesions
Radiology 184:117-122, Chang,K.H.,et al, 1992

Clinicopath Conf
Metastatic Malignant Melanoma, "Encephalitic"Form, in Leptomeninges and Cerebral Cortex, Case 28-199, , NE27:107-116,1992., 1992

Nerve Agents:A Review
Neurol 42:946-950, Gunderson,C.H.,et al, 1992

Clinicopath Conf
Cat-Scratch Disease, with Encephalopathy, Case 22-1992, NEJM 326:1480-148992., , 1992

The Biology of Developmental Dyslexia
JAMA 268:912-915, Rumsey,J.M., 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

National General Practice Study of Epilepsy:The Social & Psychological Effects of A Recent Diagnosis of Epilepsy
BMJ 304:1416-1418, Chaplin,J.E.,et al, 1992

Epilepsy and Stress, Time for Proper Studies of the Association
BMJ 305:378-379, Betts,T., 1992

Behavior Changes Following Temporal Lobectomy, With Special Reference to Psychosis
JNNP 55:89-91, Trimble,M.R., 1992

HIV Encephalopathy and Dementia
Psychiatr Clin North Am 15:455-466, Pajeau,A.K.&Roman,G.C., 1992

Withdrawal Syndrome after the Double-Blind Cessation of Caffeine Cunsumption
NEJM 327:1109-1114, 11601992., Silverman,R.,et al, 1992

Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992

Causes of Persistent Dizziness, A Prospective Study of 100 Patients in Ambulatory Care
Ann Int Med 117:898-904, Kroenke,K.,et al, 1992



Showing articles 1450 to 1500 of 6255 << Previous Next >>