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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 16191 << 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

Spontaneous Calcified Cerebral Emboli from Bicuspid Aortic Valve in Young Patients: Case Series and Review
Stroke:Vasc Inter Neurol doi.org/10.1161/svi 270000.138, Sardana,S.,et al, 2025

Melas Syndrome
Stat PearlsPubl Jan 25, Pia,S. & Lui,F., 2025

Opioid-Associated Amnestic Syndrome
Radiopaedia doi.org/10.53347/rid-8716, Deng,F.,et al, 2025

Stroke Associated with Patent Foramen Ovale(PFO): Evaluation
www.UptodDate.com, Dec 2025, Messe,S.R., 2025

MELAS Presenting as Bilateral Symmetric Occipital and Temporal Cortices Lesions, A Case Report and Literature Review
Neurologist 30:75-79, Liu,Q.,et al, 2025

Trident Sign in GFAP-Associated Meningoencephalomyelitis
Neurol 106:e214566, Mallett,N.S.,et al, 2025

Motor Vehicle Collision Due to Left Hemineglect Associated with a Stroke
NEJM 393:e41, Matsunaga,S. & Mikami,T., 2025

Validation of the Boston Criteria Version 2.0 for Cerebral Amyloid Angiopathy in Patients Presenting with Intracerebral Hemorrhage
Neurol 104:e213460, Downes,M.H.,et al, 2025

When the "Eye Falls", Diagnosing Orbital Varix
Neurol 106:e214568, Shor,N.,et al, 2025

Myelin Oligodendrocyte Glycoprotein Antibody - Associated Cerebral Cortical Encephalitis: A Case Report Highlighting Diagnostic Challenges and Therapeutic Implications
Front Immunol 16:1619807, Liu,M. & Li, D., 2025

From Stroke Workup to Mitochondrial Disease: A Case Report of MELAS
Radiol Case Reports 20:6248-6252, Sevencan,Y.,et al, 2025

Clinical Core Symptoms of Posterior Spinal Artery Ischemia
Eur Neurol 65:183-186, Struhal,S.,et al, 2025

Diagnosis of Multiple Sclerosis: 2024 Revisions of the McDonald Criteria
Lancet Neurol 24:850-865, Montalban,X.,et al, 2025

A 10-Year-Old Boy with Progressive Tremor, Insomnia and Autonomic Dysfunction
Neurol 105:e214297, Chen,Z., et al, 2025

A 56-Year-Old Woman with Right-Sided Weakness and Recurrent MRI Lesions
Neurol 105:e214293, Vorobyev,A.,et al, 2025

A 59-Year-Old Man with Acute-Onset Encephalopathy and Aphasia
Neurol 105:e214299, Gutierrez-Abizuri,C.,et al, 2025

Sjogren Syndrome Presenting with Craniospinal Hypertrophic Pachymeningitis
Neurol 105:e214382, Nayak,A.,et al, 2025

Tiger Man Sign in Sarcoid Myopathy
Neurol 105:e214323, Sun,Q.,et al, 2025

Multivessel Cerebral Occlusion in Noonan Syndrome
Stroke 56:e359-362, deLima, M.M.,et al, 2025

Surgical Management of ICH:Past, Present, and Future Prospects
Stroke 56:e355-358, Tarek,M.A.,et al, 2025

Endovascular Thrombectomy Versus Best Medical Therapy for Large Vessel Occlusion Stroke Beyond 24 Hours: A Systematic Review and Meta-Analysis
Stroke 56:3127-3137, Rodriguez-Caliemnes,A.,et al, 2025

Effectiveness of Endovascular Treatment for Acute Mild Basilar Artery Occlusion Stroke:A Multicenter Real-World Study
Stroke 56:3187-3198, Xiao,Y.,et al, 2025

Acute Subarachnoid MRI-FLAIR Signal in severe Tick-Borne Encephalitis: A Potential Prognostic Marker
Life 15:1655, Bohm,V.,et al, 2025

Nontrauma-Associated Cerebral Fat Embolism Syndrome in Sickle Cell-Related Hemoglobinopathies: A Case Series and Systematic Review
AJNR 46:2000-2008, Shadmani,G.,etal, 2025

Neuroimaging Findings in Children and Young Adults with Neurotoxicity after CAR T-Cell Therapy for B-Cell Malignancies
Neurol 105:e214086, McGuire,J.L.,et al, 2025

Idiopathic Intracranial Hypertension
NEJM 393:1409-1414, Horton,J.C., 2025



Showing articles 50 to 100 of 16191 << Previous Next >>