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acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, heralded by neurologic invol
acute intermittant porphyria
advances in neurology
algorithm
allodynia
amyloid
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis, work up
amyotrophic lateral sclerosis-like syndrome
anemia
angiostrongylus cantonensis
anterior horn cell disease
anti citrullinated antibody
anti IgLON5
antiviral agents
aphasia
aphasia, progressive, primary
aphonia
apnea
areflexia
arm atrophy
arm weakness
ascending paralysis
ataxia
ataxia, progressive
ataxic gait
autoantibodies
autonomic dysfunction
Babinski sign
basophilic stippling of red blood cells
behavioral disorder
BiPAP
bone marrow biopsy
botulism
brachial amyotrophic diplegia
bulbar palsy
bulbar palsy, acute
bulbar palsy, progressive
burning feet
burning paresthesia
cachexia
CAG repeats
cane
carcinoma
CAT scan, emission, abnormal
CD4 counts
central nervous system, infection of
cerebellar atrophy, primary
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, eosinophilia of
cerebrospinal fluid, proteincytologic dissociation
cervical osteophyte
cervical spine
cervical spondylosis
cervical spondylosis, differential diagnosis of
cervical spondylosis, misdiagnosis
Chinese paralytic syndrome
chondroitin sulfate C
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
cognition
coma, episodic
conduction block
confusion
constipation
conversion reaction
cranial neuropathy
creatine phosphokinase(CPK)elevated
crying, pathologic
cyclophosphamide
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, age at onset
dementia, frontotemporal
dementia, presenile
denervation of muscle
denervation potentials
depression
dexterity, impaired
diabetes mellitus
diagnostic criteria
differential diagnosis
diphtheria
diplegia, atonic
diplegia, brachial
disorientation
distal muscle atrophy
distal muscle weakness
drooling
dying
dysarthria
dysphagia
dysphonia
dyspnea
electromyogram
electrophoretic pattern, serum
emotional lability
encephalitis
encephalitis, autoimmune
encephalopathy
endemic area
eosinophilia
epidemiology of neurology
episodic disorders
episodic neurologic deficits
episodic unconsciousness
evoked potentials
exercise
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatigue
fever
fibrillations
fine motor function, impaired
finger weakness
fish poisoning
flaccid paralysis
fluency
foot drop
frontotemporal dementia, behavioral variant
F-wave response
gag reflex, depressed
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
GM1 ganglioside antibodies
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, variant forms of
gynecomastia
hallucination
hand weakness
headache
headache, progressive
heavy metal intoxication
helminthic infection of CNS
heralding manifestation
highly active antiretroviral therapy
hoarseness
hospice
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
hypercalcemia
hyperparathyroidism
hyperreflexia
hypersomnia
hyperthyroidism
hypoglycorrhachia
hypophonia
hyporeflexia
imbalance
immunohistochemistry
immunosuppressive agents
immunotherapy
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion body myositis
inflexibility, mental
intellectual deficit
internuclear ophthalmoplegia
intrinsic hand muscles, wasting of
laminectomy, cervical
laughing, pathologic
lead and the nervous system
lead poisoning
leg atrophy
leg weakness, bilateral
leg weakness, unilateral
lid closure, weakness of
life expectancy
lobar atrophy
locked-in syndrome
Lyme disease
lymphoma
lymphoma involving CNS
Man-In-The-Barrel syndrome
masseter muscle wasting
meningismus
meningitis, eosinophilic
mimics
misdiagnosis
monoclonal gammopathy
monomelic amyotrophy
mortality
motor neuron disease
motor neuron disease, misdiagnosis
motor neuron disease, spontaneous recovery
MRI
MRI, abnormal
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, diagnosis
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelogram
myelomalacia
myelopathy
myelopathy, ischemic
myelopathy, chronic progressive
myeloradiculopathy
myoclonus
myopathy
myopathy, autoimmune
myopathy, quadriceps
myopathy, steroid responsive
myositis
nasal speech
nausea and vomiting
neck weakness
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
neuroendocrinology
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic symptoms
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronopathy
neuropathology
neuropathology, peripheral nerves
neuropathy
neuropathy, acute
neuropathy, amyloid
neuropathy, diphtheritic
neuropathy, motor
neuropathy, motor, multifocal
neuropathy, multifocal
neuropathy, painful
neuropathy, peripheral, treatment
neuropathy, toxic
neuroprotective agents
neurotoxin
next-generation sequencing
osteomalacia
pain
pain, abdominal
pain, increased response
palliative care
paralysis, acute
paralysis, acute areflexic
paralysis, asymmetric
paranoia
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paraproteinemia
parasitic infection
parasitic infection, CNS
paraspinal muscle
parathormone
parathyroid adenoma
paresthesias
Parkinsonism syndrome
pathology
patient information and support
personality change
Pick's disease
pleocytosis of cerebrospinal fluid
poison, mercury
poliomyelitis
poliomyelitis-like illness
polyglucosan body disease
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyradiculoneuropathy
porphyria
positive sharp waves
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract dysfunction
quadriceps atrophy
quadriceps weakness
quadriparesis
quadriplegia
radial nerve, palsy of
raw fish ingestion
release phenomena
REM sleep behavior disorder
remote effect of cancer on the nervous system
renal cell carcinoma
renal stones
respirator
respiratory failure
respiratory tract infection
retrovirus
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
riluzole
risk factors
screening
seizure
sensory symptoms
shell fish poisoning
single photon emission computed tomography
sleep
sleep pathology and physiology
snail
somatosensory evoked potentials
somatosensory evoked potentials, dermatomal
spastic ataxia
spasticity
speech disorder
speech, loss of
spinal cord, cervical
spinal cord, compression of
spinal cord, lesion of
spinal muscular atrophy
spondylosis
stereotyped behavior
sternocleidomastoid muscle
steroid
steroid therapy, CNS treatment and complications with
sushi
syringomyelia
tandem gait, ataxic
tick paralysis
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
toxins, nervous system
trauma
travel history
travel, foreign
treatment of neurologic disorder
tremor
tremor, postural
trinucleotide repeats
tripping
unconsciousness
unconsciousness, episodic
unconsciousness, transient
urinary incontinence
viral infection
viral infection, CNS
viral isolation
vocalizations
Waldenstrom's macroglobulinemia
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weight loss
wheelchair
word-finding difficulty
wrist drop
X-linked bulbospinal neuronopathy
Showing articles 750 to 800 of 4087 << Previous Next >>

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 57-Year-Old Man with Stepwise Progressive Paraparesis, Sensory Loss, Urinary Retention, and Constipation
Neurol 98:e555-e560, Alkabie, S.,et al, 2022

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

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

Leptomeningeal Enhancement Associated with Cerebral Venous Thrombosis
JAMA Neurol 79:195-196, Lozano-Chinga, M.,et al, 2022

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma
NEJM 386:977-986, Case 7-2022, 2022

MR Three-Territory Sign in Cancer-Associated Hypercoagulation Stroke (Trousseau Syndrome)
Neurologist 27:37-40, Finelli, P.F., 2022

Catastrophic Cerebral Fat Embolism Syndrome Lacks Hyperacute MRI Findings
Neurol: Clin Pract 6:e962-e964, Gusler, M.T.,et al, 2021

Differential Diagnosis Checklists Reduce Diagnostic Error Differentially: A Randomised Experiment
Med Educ 55:1172-1182, Kammer, J.E.,et al, 2021

COVID-19 Associated Myelitis Involving the Dorsal and Lateral White Matter Tracts
AJNR 42:1912-1917, Huang, H.Y.,et al, 2021

Automated Brain Perfusion Imaging in Acute Ischemic Stroke: Interpretation Pearls and Pitfalls
Stroke 52:3728-3738, Nicolas-Jilwan, M. & Wintermark, M., 2021

The First Examination of Diagnostic Performance of Automated Measurement of the Callosal Angle in 1856 Elderly Patients and Volunteers Indicates that 12.4% of Exams Met the Criteria for Possible Normal Pressure Hydrocephalus
AJNR 42:1942-1948, Morzage, M.,et al, 2021

An Unexpected Response to Therapy in a Patient with HIV and Focal Seizures
Neurol 97:1084-1089, Chishimba, L.,et al, 2021

Clinicopathologic Conference, Lead Poisoning
NEJM 385:2378-2388, Case 38-2021, 2021

Clinicopathologic Conference, Fat Embolism Syndrome
NEJM 385:2464-2474, Case 39-2021, 2021

"Disappearing Infarct" Is Late-Onset MELAS
Ann Neurol 90:1001-1002, Landis,T.M.,et al, 2021

Pembrolizumab-Induced Migrating Cortico-Subcortical Brain Lesions
Ann Neurol 89:1255-1256, Lambert, N.,et al, 2021

A 59-Year-Old Woman Presenting with Diplopia, Dysarthria, Right-sided Weakness, and Encephalopathy
Neurol 97:e859-e864, Manzano, G.S.,et al, 2021

A Teenager with Shortness of Breath and Difficulty Walking
Neurol 96:e2346-e2350, Liu, S.C.,et al, 2021

Adults with Cerebral Palsy Require Ongoing Neurologic Care
Ann Neurol 89:860-871, Smith, S.E.,et al, 2021

A 71-Year-Old Man with Horizontal Gaze Palsy, Anarthria, and Quadriparesis
Neurol 96:1146-1150, Cheema, I.,et al, 2021

An Unusual Presentation of Prolonged Delirium
BMJ 373:N1423, Bume, R.,et al, 2021

Cerebral Venous Thrombosis
NEJM 385:59-64, Ropper, A.H. & Kline, J.P., 2021

A Brewing Back Pain
NEJM 385:66-72, Pischel, L.,et al, 2021

Sequential Bilateral Vision Loss in a Woman with Scalp Tenderness and Jaw Claudication
JAMA Neurol 78:878-879, Kaufman, A.R.,et al, 2021

Clinical and Radiologic Features, Pathology, and Treatment of Balo Concentric Sclerosis
Neurol 97:e414-e422, Jolliffe, E.A.,et al, 2021

A 47-Year-Old With Headache, Vertigo, and Double Vision
Neurol 97:e535-e539, Frey, J.,et al, 2021

Clinicopathologic Conference, Systemic Primary Amyloidosis
NEJM 384:363-372, Case 3-2021, 2021

A 71-Year-Old Man Presenting with Acute Onset Dysarthria and Dysphagia
Neurol 96:180-184, Spagni, G.,et al, 2021

Acute Flaccid Myelitis: Cause, Diagnosis, and Management
Lancet 394:334-397, Murphy, O.C.,et al, 2021

Rapidly Progressive Thalamic Dementia
Neurol 96:e809-e813, Rizzo, A.C.,et al, 2021

Cranial Nerve Disorders Associated with Immune Checkpoint Inhibitors
Neurol 96:e866-e875, Vogrig, A.,et al, 2021

Diagnostic Accuracy Among Neurology Residents
Neurol 96:e1804-e1808, Schorr, E.M.,et al, 2021

Clinicopathologic Conference, Normal Pressure Hydrocephalus
NEJM 384:1350-1358, Case 10-2021, 2021

Pregnancy in Patients with AQP4-Ab, MOG-Ab, or Double-Negative Neuromyelitis Optica Disorder
Neurol 96:e2006-e2015, Collongues, N.,et al, 2021

Lateropulsion After Hemispheric Stroke
Neurol 96:e2160-e2171, Dai, S.,et al, 2021

Progressive Multifocal Leukoencephalopathy in a Patient with Progressive Multiple Sclerosis Treated With Ocrelizumab Monotherapy
JAMA Neurol 78:736-740, Patel,A.,et al, 2021

Clinical Presentation, Diagnosis, and Treatment of Atrioesophageal Fistula Resulting From Atrial Fibrillation Ablation
J Cardiovasc Electrophysiol 32:2441-2450, Della Rocca,D.G.,et al, 2021

Drug-Related Demyelinating Syndromes: Understanding Risk Factors, Pathophysiological Mechanisms and Magnetic Resonance Imaging Findings
Mult Scler Rel Dis 55:103146, Rimkus, C.M.,et al, 2021

Intracerebral Hemorrhage in Patients with Neuromyelitis Optica:Case Report with Literature Review for Possible Pathological Association
Case Rep Neurol 13:157-165, Elshony,H.S.,et al, 2021

CNS Demyelinating Attacks Requiring Ventilatory Support With Myelin Oligodendrocyte Glycoprotein or Aquaporin-4 Antibodies
Neurol 97:e1351-e1358, Zhao-Fleming,H.H.,et al, 2021

Limitations of a Commercial Assay as Diagnostic Test of Autoimmune Encephalitis
Front Immunol 12:691536, Ruiz-Garcia,R.,et al, 2021

Utility of MRI Enhancement Pattern in Myelopathies with Longitudinally Extensive T2 Lesions
Neurol Clin Pract 11:e601-e611, Mustafa,K.,et al, 2021

A Rare Complication of Cardiac Ablation:Atrial-esophageal Fistula Presenting as Odynophagia
Cureus doi:10.7759/CUREUS.6871, Khan,M.,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

Two Cases of Meningitis Associated with Ocrelizumab Therapy
Mult Scler Rel Dis 38:101866, Theriault, M. & Solomon, A.J., 2020

Bilateral Middle Cerebellar Peduncle Lesions:Neuroimaging Features and Differential Diagnoses
Brain Behav 10:e01778, Jiang,J.,et al, 2020

Paramagnetic Rim Lesions are Specific to Multiple Sclerosis:An International Multicenter 3T MRI Study
Ann Neurol 88:1034-1042, Maggi,P.,et al, 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

Hypodense Cerebral Venous Sinus Thrombosis on Unenhanced CT: A Potential Pitfall. Report of a Case and Review of the Literature
Radiol Case Reports 15:35-38, Neal,E. & Sturgeon,J., 2020



Showing articles 750 to 800 of 4087 << Previous Next >>