Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abducens nerve paralysis
acoustic nerve
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, medical precautions with
adolescent medicine
akinetic mute
alcohol intolerance
algorithm
alkylating agents
alpha-fetoprotein
altered states of consciousness
alternating rapid movement, impaired
amphiphysin antibodies
anemia
ankle edema
anti Yo antibody
antimetabolite
apraxia of eye movements
areflexia
arthralgia
arthritis
ascites
asparginase
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
atonic bladder
atypical
autoantibodies
autoimmune cerebellar ataxia
autoimmune disease
autonomic dysfunction
autonomic neuropathy
Babinski sign
blindness
blood dyscrasias, neurologic findings with
brachial plexus neuropathy
bradykinesia
callosal angle
cane
carcinoembryonic antigen
carcinoma
carcinoma of breast
carcinoma of lung
carcinoma of ovary
cardiomyopathy
cataracts
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebral cortex
cerebral venous thrombosis
cerebrospinal fluid, abnormal
cerebrospinal fluid, drainage of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, pressure low
cerebrovascular accident
cerebrovascular accident, recurrent
cerebrovascular disease
ceruloplasmin, serum
chairbound
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 9
cisternogram, radionuclide
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
cognition, slowed
collapsin response mediator protein 5 IgG
complications
consanguinity
contactin associated protein like 2 antibodies
cranial neuropathy
cranial neuropathy, multiple
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
deep tendon reflexes
degenerative diseases of CNS
dementia
dementia, childhood
dementia, familial
dementia, rapidly progressive
dementia, reversible
depression
dermatitis
dermatomyositis
dexterity, impaired
diabetes mellitus
diagnostic criteria
diarrhea
diarrhea, bloody
diet
differential diagnosis
difficulty climbing stairs
diplopia
dizziness
dopa responsive dystonia
drooling
dysarthria
dysdiadochokinesia
dyskinesia
dysmetria
dysmorphic
dysphagia
dystonia
edema, pedal
efficacy
electromyogram
emotional lability
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalomyelitis
encephalopathy
esophageal varices
executive dysfunction
external lumbar drainage
eye movement, disorders of
facial expression abnormality
facial nerve palsy
facial nerve palsy, bilateral
facial nerve palsy, recurrent
facial pain
falling
familial
fever
finger nose finger test
fluorouracil
flush syndrome
foot drop
frataxin
Friedreich's ataxia
frontal lobe, pathologic signs of
gait disorder
gait, magnetic
gaze palsy, horizontal
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann-Straussler-Scheinker disease
glutamic acid decarboxylase, antibody
growth retardation
Guillain Barre syndrome
hallucination
handwriting
headache
hearing loss
heel-knee-shin test
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
heralding manifestation
high altitude sickness
human immunodeficiency virus type 1
hydrocephalus
hydrocephalus, normal pressure
hydrocephalus, normal pressure, etiology
hydrocephalus, treatment of
hyperreflexia
hypoalbuminemia
hyponatremia
hypotonia
imbalance
immunodeficiency
immunologic disease
immunology and the nervous system
immunosuppression
immunotherapy
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inclusion bodies, intranuclear
intellectual deficit
intellectual deterioration
isoniazid
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
jaw pain
Kayser-Fleischer ring
Korsakoff's psychosis
L-dopa
leg weakness, bilateral
leucine rich glioma inactivated 1 antibodies
leukemia
leukemia, neurologic findings assoc.with
leukopenia
limbic encephalitis
liver function enzymes
lumbar drain
lumbar puncture, repeated
lymphoma
malignancy screen
malignancy, occult
masked facies
Melkersson's syndrome
memory, impairment of
meningismus
meningitis
meningitis, neurologic aspects and complications of
meningoencephalopathy
mental retardation
mental status, abnormal
methotrexate
methylhydrazine derivatives
mimics
misdiagnosis
molecular genetics
monoamine oxidase inhibitors
monoclonal antibodies
monoclonal gammopathy
mononeuritis multiplex
mood change
mortality
motor neuron disease
mountain climbing
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, brachial plexus
MRI, diffusion weighted
MRI, flow void, CSF
MRI, high signal foci on
MRI, negative
MRI, periventricular hyperintensity
MRI, punctate pattern
multiple sclerosis
multiple system atrophy
muscle biopsy
muscle pain
muscle weakness
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, paraneoplastic
myasthenic syndrome
myelopathy
myelopathy, chronic progressive
myopathy
myopathy, vacuolar
myositis
myositis, ocular
nausea and vomiting
nemaline rod myopathy
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neurocutaneous disease
neuroendocrinology
neurologic complications of, surgery
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic signs
neuromuscular junction
neuronal cell surface antigen
neuronal intranuclear inclusion disease
neuronopathy, sensory
neuropathology
neuropathy
neuropathy, ataxic
neuropathy, painful
neuropathy, paraneoplastic
neuropathy, peripheral
neuropathy, sensory
neurotoxin
next-generation sequencing
nitrogen mustard
NMDA antagonists
nystagmus
ocular motility, disorders of
onconeural antibodies
ophthalmoplegia, progressive external
opsoclonus-myoclonus syndrome
optic atrophy
optic neuritis
orthostatic hypotension
pain
pain, abdominal
paraneoplastic cerebellar degeneration
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paresthesias
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinsonism syndrome
pathology
penicillamine
peripheral nerve, lesion of
personality change
pes cavus
picking at skin
pleocytosis of cerebrospinal fluid
POLG1 gene
polyclonal gammopathy
polymyositis
polyneuropathy
polyneuropathy, chronic idiopathic
polyneuropathy, chronic idiopathic, ataxic
polyneuropathy, chronic inflammatory demyelinating
postural abnormality
practice guidelines
pregnancy, neurologic complications in
prion disease
prion protein gene
PRKN gene
procarbazine
progeria
prognosis
progressive neurologic disorder
proprioception, abnormal
protein 14-3-3, cerebrospinal fluid
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
quadriplegia
radiation hypersensitivity
real-time quaking-induced conversion
Red flags
regional enteritis
remote effect of cancer on the nervous system
renal stones
retinopathy
reversible neurologic disorder
review article
rigidity
scoliosis
screening
sedimentation rate, elevated
seizure
sensorineural hearing loss
sensory polyneuropathy
serologic testing
short steps
shunt procedure, lumboperitoneal
shunt procedure, ventricular
shunt procedure, ventricular-complications of
sinemet
skin, biopsy
skin, lesions in neurologic disorders
slit lamp examination
spastic ataxia
spasticity
spinal muscular atrophy
splenomegaly
startle myoclonus
subarachnoid hemorrhage
tandem gait, ataxic
telangiectases
thrombocytopenia
tinnitus
tonic foot response
transient ischemic attack
treatment of neurologic disorder
tremor
tremor, postural
trientine dihydrochloride
trinucleotide repeats
ulcerative colitis
upgaze, paralysis of
urinary incontinence
ventricular enlargement
ventriculostomy
vinblastine
vincristine neurotoxicity
vision, failure of in childhood
visual evoked response
visual impairment
visual loss
vocal cord paralysis
walking frame
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
weight loss
wheelchair
wide based gait
workup
wrist drop
zinc
Showing articles 400 to 450 of 6232 << Previous Next >>

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

A 25-Year-Old Woman With Eye Swelling and HEadache
Neurol 100:879-883, Hehir,A.,et al, 2023

Neonatal Seizures
NEJM 388:1692-1700, Ropper.A.H., 2023

Extrapulmonary Manifestations of Sarcoidosis
Rheum Dis Clin North Am 39:277-297, Rao,D.A. & Dellaripa,P.F., 2023

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
UptoDate.com, March, Flanagan,E.P. & Tillema,J-M, 2023

Monkeypox-Associated Central Nervous System Disease:A Case Series and Review
Ann Neurol 93:893-905, Money,K.M.,et al, 2023

Management of Possible Multiple Sclerosis
NEJM 388:2195-2190, , 2023

Prevalence of Venous Infarction in Patients with Cerebral Venous Thrombosis:Baseline Diffusion-Weighted MRI and Follow-Up MRI
Stroke 54:1808-1814, Alajmi.E.,et al, 2023

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

Artificial Intelligence and Machine Learning in Clinical Medicine, 2023
NEjM 388:1201-1208,1220, Haug,C.H. & Drazen,J.M., 2023

Clinicopathologic Conference, Functional Seiaures
NEJM 388:1210-1218, Case 10-2023, 2023

Benefits, Limits, and Risks of GPT-4 as an AI Chatbot for Medicine
NEJM 388:1233-1239, Lee,P., et al, 2023

A 23-Year-Olf Man With Progressibe Asymmetric Weakness and Numbness
Neurol 100:674-682, Kaplan,E.H.,et al, 2023

Cutaneous a-Synuclein Signatures in Patients with MultipleSystem Atrophy and Parkinson Disease
Neurol 100:e1529-e1539, Gibbons,C.,et al, 2023

Cerebral Amyloid Angiopathy-How to Translate Updated Diagnostic Criteria for this Multifaceted Disorder to Clinical Practice?
JAMA Neurol 80:225-226, Biessels,G.J., 2023

Diagnosis, Workup, Risk Reduction of Transient Ischemic Attack in the Emergency Department Setting:A Scientific Statement From the American HEart Association
Stroke 54:e109-e121, Hardik,P.A.,et al, 2023

Should We Test for IgG Antibodies Against MOG in Both Serum and CSF in Patients with Suspected MOGAD?
Neurol 100:497-498, Kim,H.J. & Palace, J., 2023

Diagnosis of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease:International MOGAD Panel Proposed Criteria
Lancet Neurol doi.org110.1016/51474-4422(22)00431-8, Banwell,B.,et al, 2023

Surgical Treatment of Atrioesophageal Fistula:A Systematic Review
Ann Thorac Surg 116:421-428, Amirkhosravi,F.,et al, 2023

Autoimmune Encephalitis Misdiagnosis in Adults
JAMA Neurol 80:30-39, Flanagan,E.P.,et al, 2023

A 67-Year-Old Woman with Progressive Tingling Sensations and Imlalance
Neurol 100:151-157, Horta,L.F.B.,et al, 2023

Infectious Mononucleosis: Rapid Evidence Review
Am Fam Physician 107:71-78, Sylventer,J.E.,et al, 2023

External Validation of e-ASPECTS Software for Interpreting Brain CT in Stroke
Ann Neurol 92:943-957, Mair,G.,et al, 2022

Updates on Sturge-Weber Syndrome
Stroke 53:3769-3779, Yeom,S.E.&Comi,A.M., 2022

Clinical Manifestation,Management,and Outcomes in Patients with COVID-19 Vaccine-Induced Acute Encephalitis:Two Case Reports and a Literature Review
Vaccines 10:1230, Shyu,S.,et al, 2022

Neuromyelitis Optica Spectrum Disorder
NEJM 387:631-639, Wingerchuk, D.M. & Lucchinetti, C.F., 2022

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022

Laboratory Diagnosis of Creutzfeldt-Jakob Disease
NEJM 386:1345-1350, Zerr, I., 2022

Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era
JAMA Neurol 79:405-413, Morton, S.U.,et al, 2022

A 48-Year-Old Woman Presenting with Vertigo, Ptosis, and Red Eyes
Neurol 98:678-683, Kim, K.T.,et al, 2022

A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

Neurological Events Reported after COVID-19 Vaccines: An Analysis of Vaccine Adverse Event Reporting System
Ann Neurol 91:756-771, Frontera, J.A.,et al, 2022

Clinicopathologic Conference, Plasm-Cell Myeloma Post-Transplant Lymphoproliferative Disorder
NEJM 386:2508-2516, Case 20-2022, 2022

Association of Amount of Weight Lost After Bariatric Surgery with Intracranial Pressure in Women with Idiopathic Intracranial Hypertension
Neurol 99:e1090-e1099, Mollan, S.P.,et al, 2022

What All Physicians Need to Know About the Polio Resurgence in New York State
JAMA online e1-e3, Larkin, H., 2022

FDG-PET/CT of Giant Cell Arteritis with Normal Inflammatory Markers
Ann Neurol 92:337-339, Koizumi, N.,et al, 2022

Magnetic Resonance Imaging or Computed Tomography for Suspected Acute Stroke: Association of Admission Image Modality with Acute Recanalization Therapies, Workflow Metrics, and Outcomes
Ann Neurol 92:184-194, Fischer, U.,et al, 2022

Inconsistency and Incongruence: The Two Diagnostic Pillars of Functional Movement Disorder
Lancet 400:328, Hess, C.H.,et al, 2022

Curtain Sign
NEJM 387:e7, Sherman, S.V., 2022

Clinicopathologic Conference, Insulinoma
NEJM 387:356-365, Case 23-2022, 2022

Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies
AJNR 43:2-10, Benjamin, P.,et al, 2022

Should Electronic Differential Diagnosis Support be Used Early or Late in the Diagnostic Process? A Multicentre Experimental Study of Isabel
BMJ Qual Saf doi:10.1136/bmjqs-2021-013493, Sibbald, M.,et al, 2022

Reaching 95%: Decision Support Tools are the Surest Way to Improve Diagnosis Now
BMJ Qual Saf doi:10.1136/bmjqs-2021-014033, Graber, M.L., 2022

A 55-Year-Old Woman with Recurrent Episodes of Aphasia and Vision Changes
Neurol 98:330-335, Jeanneret, V.,et al, 2022

Stroke Mimics in the Acute Setting: Role of Multimodal CT Protocol
AJNR 43:216-222, Prodi, E.,et al, 2022

A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
Neurol 98:e669-e674, Sakoda, M.,et al, 2022

Rare Cause of Hemiparesis and Ataxia in a 36-Year-Old Man
Neurol 98:251-255, Decker, J. & Singh, M., 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Sturge-Weber Syndrome
www.UptoDate.com,Dec, Patterson,M.C., 2022



Showing articles 400 to 450 of 6232 << Previous Next >>