Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abducens nerve paralysis
agitation
agnosia, color
akathisia
alexia without agraphia
alien hand syndrome
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
alveolar hypoventilation
amaurosis fugax
amnesia
amnesic stroke
anatomy of
anemia
aneurysm
anorexia
anti basal ganglia antibodies
antibiotics
anticonvulsants, untoward effects of
aphasia
apraxia
apraxia of eye movements
apraxia of eyelid opening
areflexia
arrhythmia, cardiac
arteritides
arteritis, temporal
arthralgia
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic gait
athetosis
ATP1A3 gene
autoantibodies
autoimmune disease
autoimmune encephalopathy
autonomic dysfunction
Babinski sign
bacterial infection
Balint's syndrome
basal ganglia, degeneration
basal ganglia, lesion of
basilar artery
basilar artery occlusion
behavioral disorder
bilirubin encephalopathy
biologic markers
bradykinesia
bradyphrenia
brain damage
brainstem
brainstem, hemorrhage, primary
brainstem, infarction of
brainstem, lesion of
bruxism
calcium antagonist
carcinoembryonic antigen
carcinoma
carcinoma of breast
carcinoma of lung
cardiomyopathy
CAT scan, abnormal
CAT scan, pelvis
ceftriaxone
central nervous system, infection of
central retinal artery occlusion
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebellar disease, eye movement disorder in
cerebellar lesion
cerebellitis, autoimmune
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral infarction
cerebral peduncle
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, agitated delirium following
cerebrovascular accident, prognosis in
children
chills
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 20
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clonazepam
cognition
collagen vascular disease
Collier's sign
confusion
conjugate gaze, forced
convergence, impaired
cortical blindness
cortical-basal ganglionic degeneration
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
cyst, ovary
deafness
deafness, unilateral
degenerative diseases of CNS
delirium
dementia
dementia, presenile
dementia, rapidly progressive
developmental retardation
diabetes mellitus
diagnostic criteria
differential diagnosis
diplopia
dizziness
DPPX
DPPX, antibodies, encephalitis
drooling
dysarthria
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dysphagia
dyspnea
dyspraxia
dystonia
electroencephalogram, abnormalities of
embolism
embolism, vertebral-basilar artery
encephalitis
encephalitis lethargica
encephalitis, autoimmune
encephalitis, paraneoplastic
encephalomyelitis
encephalopathy
encephalopathy, neonatal
encephalopathy, parainfectious
epidemiology of neurology
epistaxis
exercise intolerance
eye movement, disorders of
face, numbness of
facial movement disorder
facial weakness
falling
familial
fever
flunarizine
fluorescent treponema antibody absorption/false positive
fundus, abnormality of
gait disorder
gammaglobulin therapy, intravenous
gastrointestinal bleeding
gaze deviation
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gender
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
geniculate body, lateral
glabellar sign
globus pallidus, lesion of
gram positive rod
grimacing
growth retardation
Guillain Barre syndrome
hallucination
hallucination, visual
headache
headache, positional
hearing loss
hemiakathisia
hemianopia
hemianopia, homonymous
hemichorea
hemiparesis
hemiplegia
hemisensory loss
hepatic failure
hepatomegaly
hepatosplenomegaly
heralding manifestation
Horner's syndrome
human immunodeficiency virus type 1
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
hyperesthesia
hyperpigmentation of skin
hyperreflexia
hypertension
hyperthermia
hypertonia
hypotonia
idiopathic
imbalance
imbalance, postural
immune reconstitution inflammatory syndrome
immunodeficiency
immunosuppression
immunosuppressive agents
inborn errors of metabolism
incoordination
infantile bilateral striatal necrosis
infection
intellectual deficit
intestinal biopsy
intracerebral hemorrhage
intracranial hypertension, benign
intracranial pressure, increased
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, young adult
jaundice
kernicterus
lacunar infarction
leukemia
level of consciousness
level of consciousness, decreased
levitation
limbic encephalitis
lipid storage disorder of CNS
lymphadenopathy
lymphoma
masked facies
mastoiditis
memory, defect of recent
memory, impairment of
meningismus
meningitis
meningitis, aseptic
meningitis, carcinomatous
mental retardation
mesencephalic artery syndrome
metamorphopsia
microcephaly
midbrain, atrophy
midbrain, infarction of
migraine
migraine, children
migraine, visual symptoms in
mimics
miosis
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
molecular genetics
mononeuropathy
mononeuropathy multiplex
mortality
movement disorder
movement disorder, delayed onset
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, negative
multiple system atrophy
muscle biopsy
muscle pain
myasthenia gravis
myelitis
myoclonic jerks
myoclonus
myopathy
myositis
nasal septum, perforation of
nausea and vomiting
neurocutaneous disease
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neuropathy, vasculitic, systemic
neurotoxic
neurotoxin
Niemann-Pick disease
night sweats
NMDA antagonists
NMDA receptors
noncommunicative
nystagmus
nystagmus, cerebellar
nystagmus, monocular
nystagmus, pendular
occipital lobe, infarction
occipital lobe, infarction, bilateral
ocular bobbing
ocular dipping
ocular dyskinesia
ocular dysmetria
ocular flutter
ocular motility, disorders of
oculogyric crisis
oculomasticatory myorhythmia
ophthalmoplegia
ophthalmoplegia, progressive external
opsoclonus
opsoclonus, differential diagnosis of
opsoclonus-myoclonus syndrome
optic atrophy
optic neuritis
optic neuropathy
optic neuropathy, ischemic
optokinetic nystagmus, abnormal
oscillopsia
otitis, neurologic complications with
pain
pain, abdominal
pain, testicular
palinopsia
papilledema
Parkinson disease
Parkinson disease, atypical
Parkinson disease, dystonia with
Parkinson disease, postencephalitic
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
pathology
peduncular hallucinosis
periarteritis nodosa
pericarditis
personality change
phenothiazine
phenothiazine, dyskinesia associated with
pleocytosis of cerebrospinal fluid
POLG1 gene
polymerase chain reaction
polyneuropathy
pontine hemorrhage
posterior cerebral artery
posterior cerebral artery embolism
posterior cerebral artery territory infarction
posterior choroidal artery
posterior inferior cerebellar artery syndrome
postural abnormality
precipitating factors
preclinical
premature infant
prevention of neurologic disorders
prion disease
progeria
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
pseudoabducens palsy
psychiatric problems in neurologic disorders
psychosis
psychotic behavior
ptosis
pulmonary infiltrates
pupil
pupil, abnormality in neurologic disorders
pupil, ectopic-acquired
pure sensory stroke
quadrantanopsia, homonymous
quadriparesis
quadriplegia
radiation hypersensitivity
radiculopathy
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
reading disorder, acquired
reading problem, causes of
recurrent
release phenomena
remote effect of cancer on the nervous system
respirations in CNS disease
retinal artery occlusion
retinal infarction
retinopathy
Rett's syndrome
review article
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rhinorrhea
rigidity
rigidity, axial
saccadic eye movements
saccadic eye movements, abnormal
salivation, excessive
schizophrenia
scotoma
sedimentation rate, elevated
seizure
sensorineural hearing loss
sensory loss
sensory loss, cortical
seroconversion
simultanagnosia
sinusitis
skew deviation
skin, lesions in neurologic disorders
somnolence
speech disorder
spinal muscular atrophy
splenomegaly
status epilepticus
steroid therapy, CNS treatment and complications with
striatum, lesion of
strokelike episodes
subarachnoid hemorrhage
subthalamic nucleus
suck reflex
sweating
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
tachycardia
tardive dyskinesia
tardive dyskinesia, treatment of
tardive dystonia
tau protein
tauopathy
telangiectases
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
term infant
testicular biopsy
tetrabenazine
thalamoperforating arteries
thalamus, infarction of
thalamus, lesion of
thalamus, lesion of-bilateral
third nerve palsy
tinnitus
titubation
tonic spasms
top of the basilar syndrome
toxic encephalopathy
transient ischemic attack
treatment of neurologic disorder
tremor
trigeminal neuropathy
trigeminal neuropathy, sensory
upgaze, paralysis of
uremia
urinary incontinence
vertigo
viral infection
vision, blurred
visual field defect
visual impairment
visual loss
visual obscurations, transient
walking, difficulty with
weakness, generalized
web sites
weight loss
wheelchair
Whipple's disease
wide based gait
workup
Showing articles 50 to 100 of 1797 << Previous Next >>

The "Chameleon Eyes Sign" in Myasthenia Gravis
Neurol 103:e209756, Zara,P.,et al, 2024

A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
Neurol 103:e209708, Wannarong,T.,et al, 2024

Photophobia as the Presenting Symptom of Internal Carotid Artery Dissection
Neuroophthalmology 44:315-318, Pellegrini,F.,et al, 2024

Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
Neurol 103:e209844, Dhawan,A.,et al, 2024

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

Clinicopathologic Conference, Psychotic Disorder Due to a General Medical Condition (postictal psychosis)
NEJM 391:2036-2046, Case 37-2024, 2024

A 63-Year-Old Man With Progressive Multicranial Neuropathy and Leptomeningeal Enhancement
Neurol 103:e210100, Taga,A.,et al, 2024

Clinical Reasoning: A 39-Year-Old Returning traveler with Acute Encephalopathy and Strokes
Neurol 104:e210177, Buback,ClT.,et al, 2024

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Ischemic Retinopathy from Prolonged Orbital Compression
NEJM 390::e14, Chen,Y-K and Chen C-L, 2024

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

IgG4-Related Orbital Inflammation
https://EyeWiki.org, Oct, Chelnis,J. & Gervasio,K.A., 2023

Clinicopathologic Conference, Systemic Immunoglobulin Light-Chain (AL) Amyloidosis
NEJM 389:166-175, Case 21-2023, 2023

Woman With Acute Bilateral Ophthalmoplegia
Neurol 101:140-144, Giacobbe,Alket al, 2023

An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
Neurol 101:e570-e575, Rodrigo-Gisbert,M.,et al, 2023

Idiopathic Orbital Inflammation and Tolosa-Hunt Syndrome with Intracranial Extension
Neurol 101:371-374, Yu,S. & Chen,T., 2023

A 62-Year-Old Woman with Transient Vision Loss
Neurol 101:e1097-e1103, Silva,L.M.T.,et al, 2023

Clinicopathologic Conference,Limb-Shaking Transient Ischemia Attacks
NEJM 389:1416-1423, Case 31-2023, 2023

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

Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
Neurol 101:e1884-e1892, van der Veen,S.,et al, 2023

A Woman with Progressive Painless Sequential Monocular Vision Loss
Neurol 101:e2197-e2201, Ditrapani,J.,et al, 2023

Will Generative Artificial Intelligence Deliver on Its Promise in Health Care?
JAMA doi.10.1001, Nov, Wachter R.M. & Brynjolfsson,E., 2023

Progressive Cranial Neuropathy
JAMA Neurol 80:1375-1376, Buchberger,D.S.,et al, 2023

Clinicopathologic Conference, Antiphospholipid Syndrome due to SLE with Hypocomplimentemia
NEJM 389: 2277-2285, Case 38-2023, 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

Trial of Globus Pallidus Focused Ultrasound Ablation in Parkinsons Disease
NEJM 388:683-693, 759, Krishna,V.,et al, 2023

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

Clinicopathologic Conference, Factitious Disorder
NEJM 388:1609-1615, Case 13-2023, 2023

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

Cavernous Sinus Thrombosis
StatPearls PMID:28846357, Plewa,M.C.,et al, 2023

Paroxysmal Exercise-Induced Dyskinesias Due to Pyruvate Dehydrogenase Deficiency
Neurol 101:46-49, deGusmao,C.M.,et al, 2023

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

Reversible Symmetric Basal Ganglia Lesions in a Patient with Diabetes Undergoing Dialysis
Neurol 98:773-774, Quigley, S., 2022

Cases with IgG4-related Ophthalmic Disease with Mass Lesions Surrounding the Optic Nerve
Am J Ophthalmol 25:101324, Hamaoka, S.,t al, 2022

Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
Acta Sci Clin Case Reports 3:19-24, Chau,T.C. & Muhamad,N.A.N., 2022

A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
Neurol 99:26-30, Cao, T.Q.,et al, 2022

Bilateral Complete Ophthalmoplegia in a 50-Year-Old Man
JAMA Neurol 79:724-725, Arora, N.,et al, 2022

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

A 48-Year-Old Woman with 6 Months of Vivid Visual Hallucinations
Neurol 99:166-171, Kizza, J.,et al, 2022

Functional Neurological Disorders
Neurologist 27:276-289, Mishra, A. & Pandey, S., 2022

Diplopia and Ptosis in an Older Woman
JAMA Neurol 79:947-948, Stallworth, J.Y.,et al, 2022

A 51-Year-Old Woman with Diplopia and Headache
Neurol 99:524-530, Kathuria, G.,et al, 2022

Torticollis in a Child with Otalgia
BMJ 378:e070608, Sarathi, C.I.P.,et al, 2022

Neuroimaging Biomarkers in a Patient with Probable Psychiatric-Onset Prodromal Dementia with Lewy Bodies
Neurol 99:654-657, Urso, D.,et al, 2022

Clinical and Structural Findings in Patients with Lesion-Induced Dystonia
Neurol 99:e1957-e1967, Corp, D.T.,et al, 2022

Confused About Confusion
NEJM 386:80-87, Spanjaart, A.M.,et al, 2022

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

Clinicopathologic Conference, Neurosyphilis
NEJM 386:583-590, Case 4-2022, 2022

A Dizzy Architect
Neurol 98:543-549, Scutelnic, A.,et al, 2022

Idiopathic Intracranial Hypertension (Pseudotumor Cerebri): Prognosis and Treatment
www.UptoDate.com Mar, Wall, M. & Lee, A.G., 2022



Showing articles 50 to 100 of 1797 << Previous Next >>