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activities of daily living
activities of daily living scale
Addison's disease
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
aggression
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 1950 to 2000 of 6255 << Previous Next >>

The Uveomeningoencephalitic Syndrome
Neurol 16, 6031966., Riehl,J.L.,et al, 1966

CNS Involvement in SLE
Arch Neurol l4:157, O'Connor,J.,et al, 1966

Infectious Mononucleosis:Neurologic & EEG Findings
Medicine 45:5l, Schnell,R.,et al, 1966

Cerebellar Disease in Infectious Monoucleosis
Arch Neurol 15:270, Dowling,M.&Slyck,E., 1966

Central Nervous System Manifestations of Periarteritis Nodosa
Neurol 15:114, Ford,R.G.,et al, 1965

The Neurological Sequelae of Electrical Injury
Can Med Assn J 91:195, Silversides,J., 1964

Non-Aphasia Disorders of Speech
International Jour Neurol 4:207-214, Geschwind,N., 1964

Unusual Brain Syndrome Seen with Diphenylhydantoin & Phenobarbitol
Am J Psych 120:282-283, Hoaken,P.C.S.,et al, 1963

The Cornelia de Lange Syndrome
J Pediatr 63:1000-1020, Ptacek,L.J., 1963

Hysterical Hemiplegia and Hemianesthesia
Postgrad Med 31:339-345, Magee,K.R., 1962

Microcephaly
Arch Dis Child 37:623-627, Davies,H.,et al, 1962

Delayed Neurological Deterioration After Anoxia
Arch Int Med 110-18-25, Plum,F.,et al, 1962

Abnormal Hemoglobin as a Cause of Neurolic Disease
Neurol 12:114, Greer,M.,et al, 1962

Spinal Fluid Pleocytosis in SLE
Journal, Lancet Nov 1962, pp 458., Pierce,R.&Logothetis,J., 1962

Neurologic Manifestations of Myxedema
NEJM 266:547, Sanders,V., 1962

Angiokeratoma Corporis Diffusum
Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962

Cerebral Manifestations of Rheumatic Fever
World Neurol 2:920, Mitkov,V., 1961

Abducens Nerve Palsy in Dilantin Intoxication
J Pediatr 55:73-77, Manlapaz,J.S., 1959

Prognostic Significance of Incidental Acute Somatic Disorders in the Course of Psychoses
Arch Neurol Psych 59:646, Gordon,A., 1948

Rheumatic Brain Disease
JAMA 134:450, Bruetsch,W.L., 1947

Polyopia & Monocular Diplopia of Cerebral Origin
Arch Neurol & Psych 54:323945., Bender,M., 1945

Neurologic Effects of Lightning & of Electricity
Lancet l:68, Critchley,M., 1934

Mirror Writing (Book)
Psyche Miniatures Med. Series1928., Critchley,M., 1928

Tubero Sclerosis
1/5/77, Neuroscience Seminar CPC., Pogacar,S., 1850

Neurology & Psychiatry Section-Year book of Pediatrics
Pediatr Abstract p. 406-449., , 1850

Position Statement on Laws and Regulations Concerning Life-Sustaining Treatment, Including Artificial Nutrition and Hydration, for Patients Lacking Decision-Making Capacity
, Bacon,D.,et al,

Clinicopathological Conference, Eosinophilic meningitis due to Angiostrongylus cantonensis infection
NEJM 392:699-709, Case 5-2025, 2025

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Wildfire Smoke Exposure and Incident Dementia
JAMA Neurol 82:40-48, Elser,H.,et al, 2025

Palliative and End-of-Life Care in Stroke:A Scientific Statement from the American Heart Association
Stroke 56;e75-e86, Creutzfeldt,C.J.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
Neurol 104:e213496, Gheihman,G.,et al, 2025

A 72-Year-Old Man With Meningoencephalitis
Neurol 104:e213658, Isaza-Pierotti,D.F.,et al, 2025

Clinicopathologic Conference, Cryptococcus Neoformans and Cushings Syndrome
NEJM 392:1847-1856, Case 13-2025, 2025

Long-Term Consumption of Ultraprocessed Foods and Prodromal Features of Parkinson Disease
Neurol 104:e213562, Wang,P.,et al, 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
Neurol 104:e213636, Chanda,G.,et al, 2025

RNF213 Polymorphisms in Intracranial Artery Dissection
Genes doi.org/10.3390/genesis 15060725, Zedde,M.,et al, 2024

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024

Vascular Malformations of the Central Nervous System
www.UptoDate.Com, March, Singer,R.J.,et al, 2024

Behcets Syndrome
NEJM 390:640-651, Saadoun,D.,et al, 2024

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

Fluorodeoxyglucose PET/CT as Possible Early Diagnostic Tool Preceding MRI Changes in Borna Disease Virus 1 Encephalitis
Lancet 403:665-666, Bayas, A., et al, 2024

Cavernous Maliformations of the Central Nervous System
NEJM 390:1022-1028, Smith,E.R., 2024

Risk Assessment and Prevention of Falls In Older Community-Dwelling Adults
JAMA doi.10.1001/JAMA.2024.1416, Colon-Emeric,C.S.,et al, 2024

Lecanemab for Alzheimer Disease, Is It Worth It?
Neurol 102:e209265, Nelson,S.E. & Lopez,O.L., 2024

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

Clinical and Imaging Features of Cobb Syndrome
Neurol 102:e208118, Yang,X.,et al, 2024

Patent Foramen Ovale Management for Secondary Stroke Prevention:State-of-the-Art Appraisal of Current Evidence
Stroke 55:236-247, Sposato,L.A.,et al, 2024

A 24-Year-Old Man with Spastic Ataxia and Hypodontia
JAMA Neurol 81:658-659, Marien,L.,et al, 2024



Showing articles 1950 to 2000 of 6255 << Previous Next >>