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acid maltase deficiency
acoustic neurinoma
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, heralded by neurologic invol
advance directives
advances in neurology
adverse drug reaction
alcoholic polyneuropathy
algorithm
alpha-fetoprotein
alveolar hypoventilation
Alzheimer's disease
aminoacidurias
amyloid angiopathy, cerebral
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, childhood
amyotrophic lateral sclerosis, cluster
amyotrophic lateral sclerosis, complications with
amyotrophic lateral sclerosis, conjugal
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, guamian type of
amyotrophic lateral sclerosis, hospitalization
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, myasthenic syndrome with
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, post-encephalitic
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, sensory symptoms in
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis, work up
amyotrophic lateral sclerosis-like syndrome
analgesic
anatomy of
aneurysm, cavernous sinus
aneurysm, internal carotid artery
animal exposure
ankylosing spondylitis
anterior horn cell disease
anterior interosseous neuropathy
anterior tibial muscle weakness
anti Hu antibody
antibodies to voltage-gated calcium channels
antiviral agents
anxiety
aphonia
apnea
apraxia of eye movements
areflexia
arm atrophy
arm weakness
arrhythmia, cardiac
arthrogryposis multiplex
aspiration
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic gait
atlanto axial dislocation, congenital
atrioventricular block
autoantibodies
autoimmune disease
autonomic dysfunction
Babinski sign
basal ganglia, lesion of
behavioral disorder
Bence Jones protein
benign congenital hypotonia
benzodiazepine
biologic markers
BiPAP
bone marrow biopsy
botulinum toxin
botulinum toxin, complications of
brachial neuritis
brain atrophy
brainstem, infarction of
brainstem, lesion of
bright tongue sign
Brown Sequard syndrome
Brugada syndrome
bulbar palsy
bulbar palsy, acute
bulbar palsy, progressive
C0ORF72
cachexia
CAG repeats
calcium channel dysfunction
calf hypertrophy
camptocormia
carbon monoxide poisoning
carcinoembryonic antigen
carcinoma
carcinoma of breast
cardiomyopathy
cardiovascular disease
caregiver
case studies
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cavernous sinus, syndrome
CD4 counts
central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebellum, neoplasms of
cerebral cortex
cerebral cortical atrophy
cerebral death
cerebral embolism
cerebral peduncle
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident
cervical osteoarthritis
cervical osteophyte
cervical spine
cervical spine injury
cervical spine injury, treatment of
cervical spondylosis
cervical spondylosis, differential diagnosis of
cervical spondylosis, misdiagnosis
Charcot-Marie-Tooth
chest x-ray, abnormal
chewing, impaired
children
chorea
chorea, Sydenham's
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 5
chronic polyneuritis, children
Clinical Pathologic Conference(C.P.C.)
clonus
cluster, geographic
cognition
coma
complications
compression neuropathy
concussion
conduction block
congenital heart disease
congenital myopathy
congestive heart failure
constipation
contractures, joint
controversies in neurology
cost
cost effectiveness
cough
coxsackievirus
coxsackievirus, myopathy with
CPAP
creatine phosphokinase(CPK)elevated
crying, pathologic
cycad seed flour
cyclosporine
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
denervation of muscle
denervation potentials
dentatorubral-pallidoluysian atrophy
depression
dermatomyositis
developmental milestones
developmental retardation
dexterity, impaired
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diabetic mononeuropathy
diagnostic criteria
diaphragmatic paralysis
diaphragmatic paralysis, causes of
diet
differential diagnosis
difficulty climbing stairs
diplegia, atonic
disability rating scale, neurological
disability, neurological
distal muscle atrophy
distal muscle weakness
DNA probes
dopamine
drooling
dropped head syndrome
drowning
drug interactions
dying
dysarthria
dysphagia
dysphonia
dyspnea
dystonia
dystrophic calcification
dystrophin
efficacy
electrical injury of nervous system
electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
electron microscopy
electrophoretic pattern, serum
emotional lability
encephalocele
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
encephalopathy, post anoxic
endocarditis, subacute bacterial
enterovirus
enterovirus infection of CNS
entrapment neuropathy
enzyme, muscle disease
epidemiology of neurology
ethics in neurology
euthanasia
evidence-based research
evoked potentials
excitotoxin
eye movement, disorders of
facial weakness, bilateral
facioscapulohumeral syndrome
falling
familial
fasciculation
fatigable chewing
fatigue
Fazio-Londe's disease
fibrillations
finger weakness
flail arm syndrome
floppy infant
foot drop
football neurologic injuries
fragile-X syndrome
free radical
Friedreich's ataxia
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gag reflex, depressed
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gangliosides
gastrostomy
gastrostomy, percutaneous endoscopic
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glioma
glutamic acid
GM1 ganglioside antibodies
growth retardation
guanidine
Guillain Barre syndrome
Gulf War syndrome
Guyon's canal
gynecomastia
hallucination
hand weakness
handlebar palsy
hanging
head injury
headache
health insurance
heart block
heavy metal intoxication
hemangioma
hemiparesis
hemiplegia
hemiplegia, progressive
heralding manifestation
herniated disc
herpes simplex encephalitis
herpes simplex encephalitis, diagnosis of
herpes zoster
highly active antiretroviral therapy
history of neurology
HLA
hoarseness
Hodgkin's disease
Hodgkin's disease, neurologic involvement with
hospice
human immunodeficiency virus type 1
hunger
huntingtin
Huntington's chorea
hypercalcemia
hypercapnia
hyperparathyroidism
hyperreflexia
hypertension
hypoglycemia
hypoglycemic coma
hypopnea
hyporeflexia
hypothyroidism
hypotonia
hypotonia, infants
hypoxia
hypoxic encephalopathy
iatrogenic neurologic disorders
immune complexes
immunodeficiency
immunoelectrophoresis, serum
immunologic disease
immunosuppression
immunosuppressive agents
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, ubiquitin
inclusion body myositis
infant, evaluation of
infantile tremor syndrome
insomnia
intellectual deficit
intermittent positive pressure breathing
internal capsule
internet
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
iron, brain
Isaacs syndrome
Jackson's syndrome
Jakob-Creutzfeldt disease
jaw clonus
jaw closure weakness
jaw jerk, abnormal
klippel feil syndrome
Kugelberg-Welander syndrome
laminectomy, cervical
laughing, pathologic
lead and the nervous system
leg weakness, bilateral
leg weakness, unilateral
leukemia
leukoencephalopathy
level of consciousness, decreased
Lewy body disease, diffuse
lid closure, weakness of
life expectancy
life support, withdrawal of
life support, withholding of
life sustaining treatment
liver disease
lobar atrophy
locked-in syndrome
lordosis
lumbar puncture
Lyme disease
lymphadenopathy
lymphoma
lymphoma involving CNS
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
masseter muscle weakness
median neuropathy
medical-legal aspects of neurology
meningitis
mental retardation
Millard Gubler syndrome
Mills syndrome
mimics
minimally conscious state
misdiagnosis
mobility
mobility aids
molecular genetics
monoclonal antibodies
monoclonal gammopathy
monomelic amyotrophy
mononeuropathy
mononeuropathy, motor
morphine
mortality
Motor Band Sign
motor neuron disease
motor neuron disease, juvenile form
motor neuron disease, spontaneous recovery
motor system
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, FLAIR
MRI, functional
MRI, gradient-echo
MRI, muscle
MRI, paramagnetic effect
MRI, spinal cord
MRI, susceptibility weighted
MRS
multiple myeloma
multiple sclerosis
multiple sclerosis, diagnosis of
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple sclerosis, treatment of
multiple system atrophy
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle relaxant
muscle stiffness
muscle strength, testing
muscle tenderness
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, drug induced
myasthenia gravis, limb-girdle
myasthenia gravis, treatment of
myasthenic crisis
myasthenic syndrome
myelogram
myelogram, cervical
myelopathy
myelopathy, ischemic
myocardial infarction
myocardial injury
myocarditis
myoclonus
myocytolysis
myokymia
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, distal
myopathy, mitochondrial
myopathy, quadriceps
myopathy, thyroid disease causing
myositis
myotonia congenita
myotonia dystrophica
N-acetyl-L-aspartic acid
narcotic analgesics
nasal speech
neck extension
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
neoplasm, primary intracerebral
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
nerve growth factor
neuritis, causes of
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurogenic vs.myopathic atrophy
neurologic complications
neurologic complications of, surgery
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic disease, incurable
neurologic evaluation
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular junction
neuromuscular junction, abnormality of
neuromyotonia
neuronal degeneration
neuronal migration disorder
neuronopathy
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, bicycle
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, motor, multifocal
neuropathy, peripheral
neuropathy, peripheral, treatment
neuroprotective agents
neurotoxic
neurotoxin
neurotransmitter
neutropenia
newborn, evaluation of
NMDA antagonists
NMDA receptors
nusinersen
nystagmus
nystagmus, primary position of gaze
nystagmus, rotary
occupational neurologic disorders
ocular motility, disorders of
old age, neurology of
olivary degeneration, hypertrophic
Onufrowicz nucleus
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, progressive external
opiate
Oppenheim muscular dystrophy
orthopnea
osteomalacia
owl's eye sign of spinal cord
oxygen therapy
pain
pain, management of chronic
palatal myoclonus
palliative care
paranoia
paraoxonase
paraparesis
paraparesis, spastic
paraproteinemia
paraspinal muscle
parathyroid adenoma
paresthesias
Parkinson disease
Parkinson disease, motor neuron disease with
Parkinson disease, treatment of
Parkinsonism syndrome
Parkinsonism-dementia complex
pathology
patient information and support
penicillamine
periodic paralysis
periodic paralysis, thyrotoxic
persistent vegetative state
personality change
phrenic nerve pacemaker
physical activity
physical therapy
physician assisted suicide
Pick's disease
placebo
plasma cell dyscrasia
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
poison, mercury
poison, neurologic problems with
poliomyelitis
polyclonal gammopathy
polyglucosan body disease
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
porphyria
positive sharp waves
post polio syndrome
posterior fossa, differential diagnosis of lesions of
posterior inferior cerebellar artery syndrome
posterior interosseous neuropathy
practice guidelines
preclinical
pregnancy, neurologic complications in
pressure sores
prevention of neurologic disorders
primary lateral sclerosis
progeria
prognosis
progranulin
progressive muscular dystrophy
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
pseudohypertrophy
psychiatric problems in neurologic disorders
psychomotor retardation
pulmonary embolism
pulmonary function tests
pyramidal tract
pyramidal tract dysfunction
quadriceps atrophy
quadriceps weakness
quadriplegia
quality of life
radiation hypersensitivity
radiation therapy, salivary gland
radiculopathy
release phenomena
remote effect of cancer on the nervous system
renal stones
repetitive nerve stimulation
respirator
respiratory depression
respiratory failure
retrovirus
review article
RFLPs
right to die
riluzole
risk factors
risk-benefit assessment
safety
salivation, excessive
sarcoidosis
scoliosis
scoliosis, neurologic association with
scooters
screening
sedation
seizure
seizure, children
seizure, treatment of
sensory ganglia
sensory ganglia, abnormal
sensory symptoms
sensory testing
serologic testing
serum alanine aminotransferase
shoulder, subluxation
single photon emission computed tomography
skin, biopsy
skin, lesions in neurologic disorders
sleep
sleep apnea
sleep pathology and physiology
smell
Smell Identification Test
SMN1 gene
somatosensory evoked potentials
somatosensory evoked potentials, dermatomal
somnolence
spasticity
speech disorder
spina bifida
spinal cord
spinal cord degeneration
spinal cord, compression of
spinal cord, injury of
spinal cord, injury, management of
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, neoplasm, extramedullary
spinal cord, neoplasm, intramedullary
spinal cord, pathologic exam of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar degeneration
spirometry
spondylosis
standing difficulty
stem cell tourism
stem cell transplantation
sternocleidomastoid muscle
steroid
stiff legs
stiff man syndrome
strangulation
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
subdural hematoma
sudden death
suicide
superoxide dismutase
survival motor neuron gene
symptomatic
syringomyelia
tabes dorsalis
tandem gait, ataxic
tau protein
telangiectases
teleconsulting
telemedicine
teleneurology
telestroke
temporal lobe, atrophy
temporalis muscle wasting
tensilon test
tensilon test, false positive
term infant
testicular atrophy
thoracic outlet syndromes
thrombophlebitis
thyrotropin-releasing hormone
Tolosa Hunt syndrome
tongue, atrophy
tongue, enlarged
tongue, fasciculations of
tongue, weakness
torticollis
tracheostomy
trauma
treatment of neurologic disorder
tremor
tremor, postural
triangle of Guillain and Mollaret
tricresylphosphate
trinucleotide repeats
tripping
ubiquitin
ulnar nerve
ulnar nerve, deep palmar branch of
ulnar neuropathy
unconsciousness
upgaze, paralysis of
urinary incontinence
valium
vasculopathy
venous thrombosis, non-cerebral
viral infection
viral infection, CNS
Waldenstrom's macroglobulinemia
walking frame
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, infant
weakness, progressive
weaning from respirator, failure to
web sites
Weber's syndrome
weight loss
Werdnig-Hoffman disease
wheelchair
whistle, inability to
white matter disease
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 500 to 550 of 8823 << Previous Next >>

Severe Hippocampal Atrophy in a Patient with Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 80:642-643, Bartels,F.,et al, 2023

Dexamethasone Versus Surgery for Chronic Subdural Hematoma
NEJM 388:2230-2240, 2289, Miah,I.P.,et al, 2023

Effect of Spinal Cord Burst Stimulation vs Placebo Stimulation on Disability in Patients with Chronic Radicular Pain after Lumbar Spine Surgery
JAMA 328:1506-1514, Hara, S.,et al, 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

A 65-Year-Old Woman with Cancer History and Wrist Drop
Neurol 99:570-576, Merrill, R.,et al, 2022

An 8-Year-Old with Acute Onset Ataxia
Neurol 99:305-310, McLaren, J.R.,et al, 2022

Epidemiology, Survival, and Clinical Characteristics of Inclusion Body Myositis
Ann Neurol 92:201-212, Lindgren, U.,et al, 2022

Neurobrucellosis:The Great Mimicker
Rev Soc Bras Med Trop 55:e0567-e2012, Soares,C.N.,et al, 2022

Severe High Cervical Cord Compression Due to Large Bilateral Neurofibromas in a Patient with Neurofibromatosis Type 1: A Case Report and Review of Literature
CUREUS doi:10.7759/CUREUS.27211, Sadeh,M. & Farhat, H., 2022

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

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

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

Clinicopathologic Conference, Encephalitis due to Behcets Disease
NEJM 387:925-933, Case 27-2022, 2022

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

Longitudinally Extensive Spinal Cord Lesions in a Middle-Aged Man
Neurol 98:419-424, Xi, N. & Zhou, Y., 2022

Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
Neurol 98:468-469, Zhao, B.,et al, 2022

Durability of Clinical and Quality-of-Life Outcomes of Closed-Loop Spinal Cord Stimulation of Chronic Back and Leg Pain
JAMA Neurol 79:251-260, Mekhail, N.,et al, 2022

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

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

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

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

Fluorosis
Neurol 97:e1973-e1974, Saluja, A.,et al, 2021

A Middle-Aged Man with a History of Muscle Pain Presenting with Progressive Leukoencephalopathy and Subsequent Coma
Neurol 97:910-915, Jakobsson, A.S.,et al, 2021

Spontaneous Intracranial Hypotension
NEJM 385:2173-2178, Schievink, W.I., 2021

A 79-Year-Old Woman with Subacute Bilateral Visual Loss
Neurol 97:e1159-e1165, Rossi, S.,et al, 2021

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021

Lumbar Sediment Sign Seen in an Unusual Presentation of Meningitis
Lancet 398:1436, Hegde, A.,et al, 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 Intramedullary Mass
BMJ 374:m1948, Yang, J.S.,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

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

A 64-Year-Old Man with Multiple Cranial Neuropathies
Neurol 97:e215-e221, Lefland, A.,et al, 2021

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

Clinicopathologic Conference, Mycobacterium Tuberculosis Meningitis
NEJM 384:166-176, Case 1-2021, 2021

Paraneoplastic Myeloneuropathies
Neurol 96:e632-e639, Shah, S.,et al, 2021

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

Clinicopathologic Conference, Lympohplasmic Lymphoma of the CNS (Bing-Neel Syndrome)
NEJM 384:745-753, Case 6-2021, 2021

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

Cervical Spondylotic Myelopathy Secondary to Ochronotic Vertebral Arthropathy
Neurol 96:627-628, Pinto, W.,et al, 2021

Neurobrucellosis Brief Review
Neurologist 26:248-252, Bouferraa,Y.,et al, 2021

Caudal Epidural Steroid Injections in the Setting of Remaining on Antithrombotics: A Retrospective Study
Pain Physician 24:e821-e828, Simon,J.I.,et al, 2021

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

The Tolosa-Hunt Syndrome
NJJP 71:577-582, Kline,L.B. & Hoyt,W.F., 2021

The Durability of Minimally Invasive Lumbar Decompression Procedure in Patients with Symptomatic Lumbar Spinal Stenosis:Long-term Follow-up
Pain Practice 21:826-835, Mekhail,N.,et al, 2021

Intracranial MRI Vessel-Wall Imaging
Pract Neurol March-April:61-65, Barnes,M.,& Moftakhar,P., 2021

Vessel Wall MR Imaging for the Detection of Intracranial Inflammatory Vasculopathies
Cardiovasc Diagn Ther 10:1108-1119, Edjlali,M.,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

Antiplatelet and Anticoagulant Risk for Select Spine Interventions:A Retrospective Cohort
Pain Med 21:910-917, Ehsanian,R.,et al, 2020



Showing articles 500 to 550 of 8823 << Previous Next >>