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Addison's disease
adrenomyeloneuropathy
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agitation
algorithm
alternative medicine
Alzheimer's disease
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amyotrophic lateral sclerosis
Angelman syndrome
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attention
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atypical
auditory evoked brainstem potentials
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behavior
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behavioral disorder
bladder dysfunction
body odor
bone marrow transplantation
brain atrophy
C9orf72
CAG repeats
calcification, intracranial
caregiver
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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
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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
delay in diagnosis
delirium
delusion
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eczema
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electroencephalogram, abnormalities of
electromyogram
emotional lability
employment
enzyme, defect
epidemiology of neurology
epsilon sarcoglycan gene
ethics in neurology
evoked potentials
executive dysfunction
exome sequencing
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
gaze palsy, vertical
gene
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genetic neurologic disorders
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giant axonal neuropathy
Gilles de la Tourette syndrome
gout
grasp reflex
grief reaction
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health insurance
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hepatic failure
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hepatosplenomegaly
hoarding
homocystinuria
Huntington's chorea
Huntington's chorea, genetic counselling
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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
miglustat
migraine
migraine with aura
Mini Mental Status Examination
misdiagnosis
mongolism
mortality
motor neuron disease
mousy odor
movement disorder
MRI
MRI, abnormal
MRI, diffusion tensor
MRI, disappearing lesion on
MRI, functional
MRI, negative
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
seizure, laughing as manifestation
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
visuospatial disturbance
wandering
weight loss
white matter disease
white matter disease, subcortical
whole genome sequencing
workup
x-linked mental retardation
Showing articles 750 to 800 of 6334 << Previous Next >>

"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019

Clinicopathologic Conference, Pernicious Anemia (Vitamin B12 Deficiency)
NEJM 380:665-674, Case 5-2019, 2019

Acute Encephalitis in Immunocompetent Adults
Lancet 393:702-716, Venkatesan, A.,et al, 2019

Acute Toxic Limbic Encephalopathy Following Glyphosate Intoxication
Neurol 92:534-536, Planche, V.,et al, 2019

Childhood Primary Angiitis of the Central Nervous System
www.UptoDate.com, Dec, Twilt, M. & Benseler, S., 2019

Medical Use of Cannabis in 2019
JAMA 322:974-975, Hill, K.P., 2019

A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
Neurol 93:557-561, Urso, D.,et al, 2019

Ehlers-Danlos Syndromes
BMJ 366:I4966, Ghali, N.,et al, 2019

Neurosyphilis
NEJM 381:1358-1363, Ropper, A.H.,et al, 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

A Case of Acute Encephalopathy and Rigidity in a 30-Year-Old Man
Neurol 93:759-763, Hurtubise, B. & MacLellan, A., 2019

Diagnosis and Management of Dementia
JAMA 322:1589-1599, Arvanitakis, Z.,et al, 2019

A 68-year-old Man with Rapid Cognitive Decline
Neurol 93:315-318, Berth, S.H.,et al, 2019

Sydenham Chorea
www.UptoDate.com, Oct, Gilbert, D.L., 2019

Bismuth Neurotoxicity from Use of Topical Bismuth Dressing for Burns
Neurol 92:680-681, Saini, V.,et al, 2019

A 23-Year-Old Man with Headaches, Confusion, and Lower Extremity Weakness
Neurol 92:863-867, Patel, N.M.,et al, 2019

Limbic-Predominant Age-Related TDP-43 Encephalopathy (LATE): Consensus Working Group Report
Brain DOI: 10.1093/brain/awz099, Nelson, P.T.,et al, 2019

Clinicopathologic Conference, Ingestion of Isopropyl Alcohol
NEJM 380:1657-1665, Case 13-2019, 2019

A 47-year-old Man with Diffuse White Matter Disease and Rapidly Progressive Dementia
Neurol 92:e2832-e2837, Di Luca, D.G.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Wilson Disease
NIDDK Oct2018, , 2018

Behcet Disease
emedicine.medscape.com Dec, Davey-Ranasinghe, N. & Diamond, H.S., 2018

Neuronal Intranuclear Inclusion Disease Showing Intranuclear Inclusions in Renal Biopsy 12 Years Earlier
Neurol 91:884-886, Motoki, M.,et al, 2018

Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
Pract Neurol 18:5-13, Popkirov, S.,et al, 2018

A 12-year-old girl with headache and change in mental status
Neurol 90:524-529, Patel, P.,et al, 2018

Clinicopathological Conference, Insulinoma
NEJM 379:376-384, Case 23-2018, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

A 60-year-old woman with ataxia
Neurol 90:e1627-e1630, Dandapat, S.,et al, 2018

Toxidrome Recognition in Chemical - Weapons Attacks
NEJM 378:1611-1620, Ciottone, G.R., 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

An unusual neuropsychiatric manifestation of systemic lupus erythematosus
Neurol 90:e1929-e1932, Dongkyung, D.,et al, 2018

Characteristics in Limbic Encephalitis with Anti-Adenylate Kinase 5 Autoantibodies
Neurol 88:514-524,508, Do, L. & Chanson, E., 2017

Outcomes after Diagnosis of Mild Cognitive Impairment in a Large Autopsy Series
Ann Neurol 81:549-559, Abner, E.L.,et al, 2017

Clinicopathologic Conference, Vascular Malformations in Liver, Stomach, Esophagus, and Lungs that are Consistent with Hereditary Hemorrhagic Telangiectasia, Complicated
NEJM 376:972-980, Case 7-2017, 2017

A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017

Autoimmune Encephalitis: Pathophysiology and Imaging Review of an Overlooked Diagnosis
AJNR 38:1070-1078, Kelley, B.P.,et al, 2017

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
Lancet 390:1758-1768, Ory, D.S.,et al, 2017

A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
Neurol 89:e193-e196, Lamb, C.J.,et al, 2017

My Weeping Patient
Neurol 89:e202, Peters, J.,et al, 2017

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

Chess Study Revives Debate Over Cognition-Enhancing Drugs
JAMA doi:10.1001/JAMA:2017.8114, Lyon, J., 2017

Clinicopathologic Conference, Advanced AIDS Complicated by HSV-1 Encephalopathy. Basal-Cell Carcinoma. Kaposis Sarcoma.
NEJM 376:2580-2589, Case 20-2017, 2017

An Older Man with Memory Impairment and Convulsions
BMJ 358:J2824, Zhao, X.,et al, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

Clinical Decision-Making in Functional and Hyperkinetic Movement Disorders
Neurol 88:118-123,114, van der Salm, S.M.A.,et al, 2017

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 2017

Autoimmune Encephalitis: Pathophysiology and Imaging Review of an Overlooked Diagnosis
AJNR 38:1070-1078, Kelley, B.P.,et al, 2017

Bilateral Hippocampal Restricted Diffusion:Same Picture Many Causes
J Neuroimaging 27:300-305, Bhattacharyya,S.,et al, 2017



Showing articles 750 to 800 of 6334 << Previous Next >>