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Differential
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aceruloplasminemia
adrenoleukodystrophy
adverse drug reaction
akathisia
algorithm
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, guamian type of
anemia
anemia, iron deficiency
anticonvulsants
aspartate aminotransferase
ataxia
ataxia, cerebellar
axonal spheroid
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
behavioral disorder
biologic markers
blood transfusion
bone marrow biopsy
bone marrow infarction
bone marrow necrosis
bradykinesia
Brueghel's syndrome
calcification, intracranial
Canavan's disease
carbamazepine
carbon monoxide poisoning
carotid angiogram
carotid artery disease
carotid artery occlusion, neck
carotid artery thrombus
carotid artery, intraluminal clot
CAT scan
CAT scan, abdomen
CAT scan, abnormal
CAT scan, false negative
cataracts
caudate nucleus
caudate nucleus, atrophy
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
centrum semiovale
cerebellar degeneration
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral infarction, hemorrhagic
cerebral ischemia
cerebral venous thrombosis, deep
cerebro hepato renal syndrome
cerebrovascular accident
ceruloplasmin, serum
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 20
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clonazepam
Cockayne's syndrome
cognition
coma
compression fracture
confusion
consanguinity
copper deficiency
copper metabolism, abnormal
cornea, opacification in infancy-causes of
corpus callosum, lesion of
cortical blindness
cyanide poison
deafness
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, childhood
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
developmental milestones, loss of
developmental retardation
diabetes mellitus
dialysis
differential diagnosis
disability rating scale, neurological
disability, neurological
disorientation
disseminated intravascular coagulation(DIC)
diurnal variation
DNA probes
dopamine agonist
dopaminergic neurons
drug abuse
drug abuse, inhalation
drug induced neurologic disorders
dysarthria
dysphagia
dyspnea
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, symptomatic
dystonia, treatment of
electrical fields, alternating
electronystagmography
electroretinograph
embolism, fat
encephalitis
encephalopathy
encephalopathy, delayed
encephalopathy, post anoxic
enzyme, defect
equinovarus
Fahr disease
familial
ferritin, elevated
ferritinemia
fever
fundus, abnormality of
gabapentin
gadolinium
gait disorder
gene
gene mutation
general paresis of the insane
genetic linkage
genetic neurologic disorders
genetic testing
gliosis
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
globus pallidus, stimulation
globus pallidus, swelling
GLUT1 deficiency syndrome
glutaric acidemia
gray matter
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
handwriting
headache
hemochromatosis
hemoglobin abnormality, neurologic complications of
hemophagocytic lymphohistiocytosis
hemophagocytosis
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
heralding manifestation
herpes virus infection
human immunodeficiency virus type 1
hydrocephalus
hyperactivity
hyperreflexia
hypoxia
hypoxic encephalopathy
imbalance
infection
insomnia
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
iron, brain
iron, serum
iron, serum, elevated
iron, serum, low
Jakob-Creutzfeldt disease
Kearns-Sayre syndrome
lactic dehydrogenase(LDH)
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
lead poisoning
Leigh's disease
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
liver biopsy
liver disease
liver function enzymes
macular degeneration
magnetic susceptibility
maple syrup urine disease
McDonald criteria for MS
MELAS syndrome
memory, impairment of
mental retardation
mental status, abnormal
metachromatic leukodystrophy
methanol intoxication
methyl benzene
metronidazole
microhemorrhage, intracerebral
midbrain
midbrain, lesion of
mineralization
mongolism
mortality
Motor Band Sign
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, complications with
MRI, contrast enhanced
MRI, demyelinating disease
MRI, diffusion weighted
MRI, eye of tiger sign
MRI, field strength
MRI, field strength, high
MRI, gradient-echo
MRI, high signal intensity of basal ganglia
MRI, hypointense signal foci on
MRI, paramagnetic effect
MRI, starfield pattern
MRI, susceptibility weighted
MRI, T1 weighted high signal foci
MRI, volumetry
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, diagnosis of
multiple sclerosis, early onset
multiple sclerosis, monosymptomatic
multiple sclerosis, plaque
multiple sclerosis, presenting manifestations
myoclonus
myoclonus, epilepsy
myopathy, mitochondrial
myopia
neoplastic angioendotheliosis
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal dystrophy, juvenile
neurodegeneration with brain iron accumulation
neurofibrillary degeneration
neurofibromatosis 1
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuronal cell death
neuronal ceroid-lipofuscinosis
neuronal degeneration
neurons
neuropathology
neuropathology, brain
neuropathy
neuropathy, hereditary peripheral
neurosyphilis
neurotoxic
neurotoxin
night blindness
normal
opiate
optic atrophy
optic nerve
optic neuropathy
osteoporosis
pain
pain, leg
palilalia
PANK2 mutation
paramagnetic rim lesion, MR
paranoia
parenteral alimentation
paresthesias
Parkinson disease
Parkinson disease, differential diagnosis of
Parkinson disease, familial
Parkinson disease, pathogenesis of
Parkinson disease, postencephalitic
Parkinsonism syndrome
pergolide
peroxisomal disease
pigmentary retinopathy
postural abnormality
practice guidelines
pramipexole
pregnancy, neurologic complications in
prognosis
progressive neurologic disorder
psychiatric disorder
psychiatric problems in neurologic disorders
pulvinar
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
refractive errors
Refsum's disease
respiratory failure
restless leg syndrome
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
rigidity
rituximab
ropinirole
Schilder's disease
sea-blue histiocytes
seizure
sensorineural hearing loss
sickle cell crisis
sickle cell disease
skin, biopsy
skin, lesions in neurologic disorders
sleep
soluble interlukin 2 receptor
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
spinocerebellar degeneration
splenomegaly
static encephalopaty of childhood with neurodegeneration in adulthood
Still's disease
stimulation, deep brain
striatal encephalitis
striatonigral degeneration
striatum, lesion of
striatum, lesion of, bilateral
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subcortical U fibers
subependymal nodules
substantia nigra
symmetric brain lesions
syphilis, neurologic complications with
systemic illness
tapetoretinal degeneration
thalamus
thalamus, atrophy of
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
thrombocytosis
treatment of neurologic disorder
tremor
tuberous sclerosis
unconsciousness
undiagnosed
uremic encephalopathy
urinary incontinence
Usher's syndrome
viral infection
viral infection, CNS
visual acuity, decreased
visual evoked response
visual field defect
visual impairment
visual loss
walking, difficulty with
weakness
white matter disease
white matter disease, periventricular
workup
Showing articles 50 to 100 of 16256 << Previous Next >>

Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
Ann Neurol 24:692-694, Sethi,K.D.,et al, 1988

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
Neurol 38:154-155, Tennison,M.B.,et al, 1988

MR Imaging in a Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 11:1057-1058, Tanfani,G.,et al, 1987

Magnetic Resonance Imaging in Multiple Sclerosis:Decreased Signal in Thalamus & Putamen
Ann Neurol 22:546-550, Drayer,B.P.,et al, 1987

Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism
Neurol 35:227-234, Jankovic,J.,et al, 1985

MR Imaging of Hallervorden-Spatz Disease
J Comput Assist Tomogr 9:491-493, Littrup,P.J.,et al, 1985

Hallervorden-Spatz Disease:Cysteine Accumulation & Cysteine Dioxygenase Deficiency in the Globus Palladus
Ann Neurol 18:482-489, Perry,T.L.,et al, 1985

Computed tomography in Hallervorden-Spatz disease
Neurol 30:1128-1130, Dooling,E.C.,et al, 1980

Alzheimer Neurofibrillary Tangles in Diseases Other Than Senile & Presenile Dementia
Ann Neurol 5:288-294, Wisniewski,K.,et al, 1979

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

Neuro CPC of MGH
Metachromatic Leukodystrophy, NEJM 267:1198-12041962., , 1962

Congenital Zika Syndrome
NEJM 394:e2, Bacin,F. & Montenegro,M.A., 2026

Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
Stroke 57:148-156, Mania-Paris,L.,et al, 2026

CT Perfusion Abnormality in Hypoglycemic Focal Neurological Deficits
Stroke 57:e6-e7, Mikito,S.,et al, 2026

A 41-Year-Old Man with Steroid-Responsive Hemiparesis
Neurol 106:e214088, Obaidi,Z.A.,et al, 2026

Reversible Leukoencephalopathy and Parkinsonism Due to CNS Involvement in Cryoglobulinemia
Neurol 106:e214622, German,A.,et al, 2026

Progressive Quadriparesis and Falls in a 66-Year-Old Man With Longstanding Human Immunodeficiency Virus
Neurol 106:e214621, Ong,B.A. & Carlson,A.K., 2026

Stroke Mechanism and Severity after Left Atrial Appendage Occlusion, Insights from the LAAOS III Randomized Clinical Trial
JAMA Neurol 83:76-82, Katsanos,A.H.,et al, 2026

Intravenous Thrombolysis Use in the Late Time Window Before Interhospital Transfer for Thrombectomy
JAMA Neurol 83:60-67, Seners,P.,et al, 2026

Clinicopathologic Conference, Disseminated Infection with Hypervirulent Klebsiella Pneumoniae
NEJM 394:282-294, Case 202026, 2026

Uncommon Faces of Disk Herniation: Atypical Imaging Presentations and Mimics
AJNR 47:244-251, Galante,M-J.,et al, 2026

Clinicopathologic Conference, Lyme Neuroborreliosis and Coinfection with Babesia Microti
NEJM 394:383-391, Case 3-2026, 2026

Disseminated Brain Infarcts Associated with Uterine Myoma
Stroke 57:e61-e62, Elbischger,J.,et al, 2026

Increased Prevalence of Nitrous Oxide-Induced Subacute Combined Degeneration of the Spinal Cord: Clinical and Imaging Findings
AJNR 47:513-520, Bruen,R.,et al, 2026

Tenecteplase for Acute Non-Large Vessel Occlusion 4.5 to 24 Hours After IschemicStroke, The OPTION Randomized Clinical Trial
JAMA doi:10.1001/JAMA.2026.0210, Ma,G.,et al, 2026

Mucormycosis
NEJM 394:684-698, Kontoyiannia,D.P. & Walsh, T.J., 2026

Treatment for Brain Metastases with Stereotactic Radiation vs Hippocampal-Avoidance Whole Brain Radiation, A Randomzid Clinical Trial
JAMA doi.10.1001/JAMA.2026.0076;2026, Aizer,A.A.,et al, 2026

Secondary Prevention after Ischemic Stroke
NEJM 394:784-792, Frie,K.L.,et al, 2026

Neurosyphilis with Abnormal in the Bilateral Pons and Multifocal Cranial Nerve Enhancement
Ann Neurol 99:283-284, Zhang,Y.,et al, 2026

Miliary Perivascular Space Enhancement in Sepsis-Associated Posterior Reversible Encephalopathy Syndrome
Neurol 106:e214654, Hutchinson,V.A.,et al, 2026

Restless Legs Syndrome, A Review
JAMA 335:703-714, Winkelmen,J.W. & Wipper, B., 2026

Unilateral Primary Angiitis of the Central Nervous System: A Rare and Under-Recognized Entity
AJNR 47:589-595, Rai,P.,et al, 2026

Brain CT for Diagnosis of Intracranial Disease in Ambulatory Patients with Cancer:Assessment of the Diagnostic Value of Scanning without Contrast Prior to With Contrast
AJNR 47:694-698, Wang,E.,et al, 2026

Zorevunersen in Children and Adolescents with Dravet Syndrome
NEJM 394:969-982, Laux,L.,et al, 2026

Niemann-Pick Type C Disease
www.UpToDate.com, Nov, Schiffmann, R., 2026

Association of Changes in Activity Patterns with Brain Atrophy and Disability Progression in People with Multiple Sclerosis
Neurol 106:e214678, e214742, Fitzgerald,K.C.,et al, 2026

Using Susceptibility-Based Imaging in Highly Active Late-Onset Multiple Sclerosis
Neurol 106:e214794, Sosa,S.M.,et al, 2026

A 49-Year-Old Man with Meningoencephalitis and Persistent Altered Mental Status
Neurol 106:e214777, Hariswar,P.T.,et al, 2026

Multiple Giant Perivascular Spaces in Hypomelanosis of Ito
Ann Neurol 99:825-826, Chammas,D.E.,etal, 2026

Iatrogenic Cerebral Amyloid Angiopathy after Cardiac Surgery, Two Case Reports
Neurol 106:e214819, Brunet de Courssou,J-B.,et al, 2026

Clinical Manifestations of Primary CNS T-Cell Lymphoma, Retrospective Study of Histopathologic, Molecular, and Neuroimaging Fetures
Neurol 106:e24744, Muller,K.J.,et al, 2026

A 52-Year Old Man with Acute-Onset Blindness
Neurol 106:e214827, Brown,A.M.,et al, 2026

Frequency of AQP4 and MOG Antibodies in Patients with Optic Neuritis Fulfilling Minimal New Multiple Sclerosis MRI Criteria
Neurol 106:e214753, Deschamps,R.,et al, 2026

Patterns and Factors Associated with Cerebral Infarction on MRi in Tuberculous Meningitis: Secondary Anlysis of the ACT-TBM Trial
Stroke 57:856-864, Chandu,M.,et al, 2026

Syphilis as an Important Modern-Day Risk Factor for Intracranial Vasculopathy and Ischemic Stroke:A Teaching Case
Stroke 57:e108-e111, Higham-Kessler,C.,et al, 2026

Ribbon-Like Sign in Convexity Subarachnoid Hemorrhage
Ann Neurol 99:881-882, Liu,S-X.,et al, 2026

Minimally Invasive Surgery Versus Open Craniotomy with Clot Evacuation after Intracerebral Hemorrhage
Ann Neurol 99:871-880, Murthy, S.B.,et al, 2026

Multiple Giant Perivascular Spaces in Hypomelanosis of Ito
Ann Neurol 99:825-826, Chammas,D.E.,et al, 2026



Showing articles 50 to 100 of 16256 << Previous Next >>