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Differential
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abducens nerve paralysis
abscess, intracerebral
abscess, intracerebral, treatment of
acquired immunodeficiency syndrome
adverse drug reaction
alternating hemiplegia
alternating hemiplegia of childhood
amaurosis fugax
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
ANA
anemia
aneurysm
aneurysm, cavernous sinus
angiitis, isolated of CNS
angiography, cerebral
angiography, cerebral, negative
anorexia
anterior cerebral artery, occlusion of
antibiotics
aphasia
aphasia, progressive
apraxia
area postrema
areflexia
arm weakness
arteritides
arthralgia
arthritis
astrocytoma
ataxia
ataxia, cerebellar
ataxic gait
ATP1A3 gene
auditory and vestibular pathways
autoantibodies
autoimmune disease
automobile accidents
autonomic dysfunction
B cell lymphoma
Babinski sign
bacteremia
bacterial infection
bacterial infection, CNS
basal ganglia, calcification of
behavioral disorder
Behcet's syndrome
blindness, sudden
border zone infarct
Borrelia miyamotoi infection
bradykinesia
bradyphrenia
brain biopsy
brain biopsy, stereotaxic
brainstem, dysfunction
brainstem, infarction of
brainstem, lesion of
bulbar palsy
cachexia
calcification, intracranial
camptocormia
cardiomyopathy
carotid angiogram
carotid artery disease
carotid artery occlusion, neck
carotid artery stenosis
carotid artery stenosis, intracranial
carotid siphon
carotid-siphon stenosis
carphology
case studies
CAT scan
CAT scan, abnormal
CAT scan, disappearing lesion on
CAT scan, emission, abnormal
CAT scan, ring sign
CD4 counts
central nervous system, infection of
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellum
cerebral cortex
cerebral cortical atrophy
cerebral edema, vasogenic
cerebral embolism
cerebral infarction
cerebral peduncle
cerebral venous thrombosis
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, misdiagnosis
cerebrovascular accident, nonarterial territory
cerebrovascular accident, nonvascular territory
cerebrovascular accident, recurrent
cerebrovascular disease
chemotherapy, CNS treatment and complications with
children
chills
chorea
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
coinfection
collagen vascular disease
comorbidities
complications
confusion
conversion reaction
corpus callosum
corpus callosum, lesion of
cortical blindness
cortical infarction
cortical muscular atrophy
cortical ribbon sign
cough
cranial nerve palsies
cranial neuropathy, multiple
C-reactive protein
C-reactive protein, elevated
deafness
deafness, bilateral progressive vs.unilateral acute
deafness, unilateral
delay in diagnosis
delirium
dementia
dementia, rapidly progressive
demyelinating disease
dental abscess
dental procedure, neurologic complications with
depression
developmental retardation
diabetes mellitus
diagnostic criteria
diencephalon
differential diagnosis
diplopia
disorientation
distal muscle weakness
dysarthria
dysphagia
dyspnea
dystonia
ecchymoses
echocardiogram
electrocorticogram
electroencephalogram, abnormalities of
emergencies, ocular
encephalitis
encephalitis, focal
encephalitis, paraneoplastic
encephalitis, Rasmussen's
encephalitis, viral
encephalopathy
epilepsia partialis continua
epistaxis
erythema nodosum
extrapyramidal movement disorder, progressive
eye movement, disorders of
eye movement, painful
eye, pain in
face, numbness of
facial nerve
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
failure to thrive
falling
false negative
fasciculation
fatigue
fever
floaters
fluorescein angiography
foot drop
fourth ventricle, floor
fundus, abnormality of
gait disorder
gammaglobulin therapy, intravenous
gastrointestinal perforation
gene
gene mutation
genetic neurologic disorders
genetic screening
genetic testing
genital ulcerations
glaucoma
glioblastoma multiforme(astrocytoma Gr.III)
glioma
gliomatosis cerebri
GNAQ gene
granulomatosis with polyangiitis
granulomatous disease
Guillain Barre syndrome
hallucination
hallucination, visual
hand weakness
headache
headache, focal
hearing loss
hemangioma
hemangioma, leptomeningeal
hemianopia
hemianopia, homonymous
hemianopia, transient
hemiatrophy, cerebral
hemifacial atrophy
hemiparesis
hemiparesis, recurrent
hemiplegia
hemiplegia, progressive
hemispherectomy
hepatomegaly
heralding manifestation
heterochromia iridis
highly active antiretroviral therapy
Hodgkin's disease
human immunodeficiency virus type 1
hydrocephalus
hypercalcemia
hypernatremia
hypernatremia with cerebral disorders
hyperreflexia
hypertension
hypoglycorrhachia
hyponatremia
hyponatremia with cerebral disorders
hypophonia
hypopyon
hypotonia
iatrogenic neurologic disorders
IgG4-related disease
imbalance
imbalance, postural
immune checkpoint inhibitors
immune-related adverse events
immunodeficiency
immunohistochemistry
immunomodulation
immunosuppression
immunosuppressive agents
immunotherapy
in situ hybridization
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incoordination
infection
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
intrinsic hand muscles, wasting of
jaw jerk, abnormal
JC virus
ketogenic diet
lactic acidemia
lactic dehydrogenase(LDH)
leg weakness, bilateral
leg weakness, unilateral
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
leukopenia
level of consciousness, decreased
lymph node biopsy
lymphadenopathy
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
lymphomatoid granulomatosis
malformation, vascular
malformation, vascular, cerebral
marche a petits pas
Marcus Gunn pupil
mastoiditis
MELAS syndrome
memory, defect of recent
memory, impairment of
meningeal enhancement
meningitis
meningitis, aseptic
meningitis, carcinomatous
meningitis, neutrophilic
meningitis, noninfectious
meningitis, treatment of
meningoencephalitis
mental status, abnormal
microaneurysm, retinal
microcephaly
midbrain, lesion of
middle cerebral artery, emboli to
middle cerebral artery, occlusion of
migratory lesion pattern
Mills syndrome
mimics
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
monoclonal antibodies
monomelic amyotrophy
mononeuropathy
mononeuropathy multiplex
monoparesis
monoparesis, focal
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, ADC maps
MRI, angiography, false negative
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, ring sign
MRI, ring sign, open
MRI, serial
MRI, spinal cord
MRI, sulcal hyperintensity
MRI, susceptibility weighted
MRS
multiple myeloma
multiple sclerosis
multiple sclerosis, tumefactive
multiple system atrophy
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle pain
mutism
myelitis
myelopathy
myelopathy, chronic progressive
myoclonus
myopathy
myopathy, mitochondrial
nasal septum, perforation of
nausea and vomiting
neck stiffness
neck weakness
neoplasm, intracranial
neoplasm, metastatic
neoplasm, primary intracranial
neoplasm, primary of CNS
neoplastic angioendotheliosis
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic disease, multiple
neurologic examination, focal
neurologic signs
neuromyelitis optica (Devic's disease)
neuromyelitis optica spectrum disorder
neuroophthalmology
neuropathology
neuropathy
neuropathy, peripheral
neuropathy, vasculitic, systemic
neuroretinitis
neutropenia
New England
night sweats
nivolumab
nystagmus
nystagmus, dissociated
nystagmus, monocular
nystagmus, vertical
obesity
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
opportunistic infection, CNS
optic atrophy
optic neuritis
oral ulcerations
organ transplantation
orthostatic hypotension
otitis, neurologic complications with
pain
pain, abdominal
pain, testicular
papilledema
papovavirus
paraparesis
paraparesis, spastic
parietal lobe, lesion of
parietal lobe, syndromes of
Parkinson disease, dystonia with
Parkinson disease, L-dopa nonresponsive
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
parotid gland swelling
paroxysmal hemiplegia
paroxysmal neurologic deficits
patent foramen ovale
patient information and support
pembrolizumab
periarteritis nodosa
personality change
phonophobia
plasma cell myeloma, CNS involvement associated with
pleocytosis of cerebrospinal fluid
pneumonia
polymerase chain reaction
polymerase chain reaction, false negative
polyneuropathy
pons, lesion of
port wine nevus
posterior fossa
posterior fossa, lesion of
postural abnormality
precipitating factors
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
pulmonary infiltrates
pure motor hemiplegia
pyramidal tract dysfunction
quadriparesis
quadriparesis, progressive
ragged-red fibers
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
recurrent
release phenomena
remote effect of cancer on the nervous system
renal failure
renal transplantation
retinal artery occlusion
retinal ischemia
retinal lesion
retinal vasculitis
retinal vasculopathy
retinal vasculopathy with cerebral leukodystrophy
retinopathy
retro-orbital pain
reversible neurologic disorder
review article
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rhinorrhea
rigidity
Romberg's sign
salivary gland enlargement
sarcoidosis
sarcoidosis, CNS
scleroderma
scleroderma, neurologic involvement with
scotoma
screening
sedimentation rate, elevated
seizure
seizure, focal
seizure, intractable
seizure, repetitive
seizure, surgical treatment of
seizure, treatment of
seminoma
sensorineural hearing loss
short stature
sinusitis
skin, lesions in neurologic disorders
small vessel disease
small vessel vasculitis
solitary scerlosis
somnolence
sonophobia
speech, loss of
spinal cord, cervical
spirochete infection
splenomegaly
squamous cell carcinoma of head and neck
stare
staring spells
status epilepticus
steroid therapy, CNS treatment and complications with
stroke, progression of
strokelike episodes
Sturge-Weber syndrome
sweet taste
synucleinopathy
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
tachycardia
tandem gait, ataxic
temporalis muscle wasting
tendonitis
testicular biopsy
third nerve palsy
thrombocytopenia
thrombophlebitis
tinnitus
toothache
toxic encephalopathy
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
trigeminal nerve
trigeminal nerve, lesion of
trigeminal neuropathy
trigeminal neuropathy, sensory
tumefactive lesion
uremia
uveitis
vasculitides
vertigo
viral infection
viral infection, CNS
vision, blurred
vision, blurred, monocular
visual acuity, decreased, monocular
visual field defect
visual loss
visual loss, slow
vitritis
walking frame
walking, difficulty with
water channel antibodies
weakness
weakness, generalized
weakness, progressive
weight loss
wheelchair
white matter disease
wide based gait
Wolff-Parkinson-White syndrome
word-finding difficulty
Showing articles 300 to 350 of 2570 << Previous Next >>

Long Survival Sporadic Creutzfeldt-Jakob Disease
Neurol 95:87-88, Liu, X.Y.,et al, 2020

Clinical Characteristics, Risk Factors, and Outcomes of POEMS Syndrome
Neurol 95:e268-e279, Keddie, S.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Nusinersen in Adult Patients with Spinal Muscular Atrophy
Neurol 95:e413-e416, Moshe-Lilie, O.,et al, 2020

Acetylcholine Receptor-Antibody-Positive Myasthenia Gravis Presenting with Early Atrophy and Nonfluctuating Weakness of Proximal Limb Muscles
J Clin Neurol 16:714-716, Pancheri, E.,et al, 2020

An Atypical Presentation of Creutzfeldt-Jakob Disease with a Heidenhain Variant and Balints Syndrome
Cureus DOI:10.7759/cureus,8608, Gupta,A. & Dhingra,A., 2020

Spinal Dural Arteriovernous Fistula Presented with Rapidly Progressive Myelopathy, Longitudinally Extensive Spinal Cord Lesion, Pleocytosis with Polymorphonuclear Predominance, and Decreased Cerebrospinal fluid Glucose Levels:A Case Report
Rinsho Shinkeigaku 60:699-705, Kitazaki,Y.,et al, 2020

Clinicopathologic Conference, Lymphocytic Choriomeningitis Virus Infection
NEJM 381:2553-2560, Case Record 40-2019, 2019

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

A Case of Progressive Myelopathy in a Middle-Aged Woman
JAMA Neurol 76:1253-1254, Muccilli, A.,et al, 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

A 65-year-old man with Asymmetric Weakness and Parethesias
Neurol 93:856-861, Harada, Y.,et al, 2019

Chronic Dengue Virus Panencephalitis in a Patient with Progressive Dementia with Extrapyramidal Features
Ann Neurol 86:695-703, Johnson, T.P.,et al, 2019

Progressive Neurological Impairment and an Enhancing Brainstem Lesion in a Middle-Aged Man
JAMA Neurol 76:1397-1398, Gupta, S.,et al, 2019

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

A 17-year-old Baseball Player with Right Hand Weakness
Neurol 92:e76-e80, Vachon, C. & Libdeh, A.A., 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019

A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
Neurol 92:e274-e281, Chen, Z. & Neo, S., 2019

Association of Initial Disease-Modifying Therapy with Later Conversion to Secondary Progressive Multiple Sclerosis
JAMA 32:175-187, Brown, J.W.L.,et al, 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

A 40-Year-Old Woman Presenting with Distal Leg Weakness
Neurol 92:242-247, Fam, D.,et al, 2019

Leg Weakness and Stiffness at the Emergency Room
Neurol 92:e622-e625, af Edholm, K.,et al, 2019

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

Pembrolizumab Treatment for Progressive Multifocal Leukoencephalopathy
NEJM 380:1597-1605, Cortese, I.,et al, 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

A 47-year-old Man with Diffuse White Matter Disease and Rapidly Progressive Dementia
Neurol 92:e2832-e2837, Di Luca, D.G.,et al, 2019

Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy
NEJM 381:164-172, Case 21-2019, 2019

Cervical Synovial Cyst Leading to Spinal Cord Compression
Neurol 93:e318-e319, Urits, I.,et al, 2019

Clinicopathologic Conference, Statin-Associated Autoimmune Myopathy
NEJM 381:275-283, Case 22-2019, 2019

A 68-year-old Man with Rapid Cognitive Decline
Neurol 93:315-318, Berth, S.H.,et al, 2019

A 26-Year Old Man with Right Hand and Arm Weakness
Neurol 93:e927-e933, Elliott,E.J.&Smith,J.D., 2019

Childhood Primary Angiitis of the Central Nervous System
www.UptoDate.com, Dec, Twilt, M. & Benseler, S., 2019

A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
Neurol 93:557-561, Urso, D.,et al, 2019

Rapidly Progressive Vision Loss in a Patient with Breast Cancer
JAMA 322:1098-1099, Izzo, M.C.,et al, 2019

Clinicopathologic Conference, Adenovirus Meningoencephalitis
NEJM 381:1459-1470, Case 31-2019, 2019

Diagnostic Tools for Immune Causes of Encephalitis
Clin Microbiol Infect 25:431-436, Lascano, A.M.,et al, 2019

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
www.UptoDate.com, May, Koralnik, I.J., 2018

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,et al, 2018

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Selenium Toxicity Associated with Reversible Leukoencephalopathy and Cortical Blindness
JAMA Neurol 75:1282-1283, Rae, W.,et al, 2018

Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Facial Myokymia and Myorhythmia in Anti-IgLON5 Disease
Neurol 91:e1659, Vetter, E.,et al, 2018

Clinical Presentation and Cranial MRI Findings of Listeria Monocytogenes Encephalitis
Neurologist 23:198-203, Arslan, F.,et al, 2018



Showing articles 300 to 350 of 2570 << Previous Next >>