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Differential
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advances in neurology
algorithm
Alzheimer's disease
aminoacidopathies
amyloid
amyloid angiopathy, cerebral
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
anterior horn cell disease
aphasia
aphasia, progressive, primary
areflexia
arm atrophy
arm weakness
ascending paralysis
aspiration
asthma
asthma, poliomyelitis-like syndrome with
ataxia
ataxia, progressive
Babinski sign
behavioral disorder
biologic markers
BiPAP
brain atrophy
bulbar palsy
bulbar palsy, acute
bulbar palsy, progressive
C9orf72
CAG repeats
calf hypertrophy
camptocormia
cane
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
central nervous system, infection of
cerebellar atrophy, primary
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cervical osteophyte
cervical spine
cervical spondylosis
cervical spondylosis, differential diagnosis of
cervical spondylosis, misdiagnosis
children
chorea
chromosomal abnormality
chromosome 5
cognition
concussion
congenital heart disease
constipation
controversies in neurology
cost
cost effectiveness
creatine phosphokinase(CPK)elevated
crying, pathologic
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, age at onset
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
developmental retardation
dexterity, impaired
diagnostic criteria
differential diagnosis
diplegia, atonic
diplegia, brachial
disability, neurological
distal muscle weakness
drooling
dying
dysarthria
dysphagia
dysphonia
dystonia
electromyogram
emotional lability
epidemiology of neurology
episodic neurologic deficits
evidence-based research
evoked potentials
exercise intolerance
facial weakness, bilateral
falling
familial
fasciculation
fatigue
fever
fibrillations
finger weakness
flaccid paralysis
flail arm syndrome
fluency
foot drop
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
F-wave response
gag reflex, depressed
gait disorder
gait, waddling
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, variant forms of
hallucination
hand weakness
head injury
headache
health insurance
hemiparesis
hemiplegia
hemiplegia, progressive
heralding manifestation
hospice
Huntington's chorea
hyperreflexia
hyporeflexia
hypotonia
hypotonia, infants
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, ubiquitin
inclusion body myositis
inflexibility, mental
intellectual deficit
internal capsule
intrinsic hand muscles, wasting of
iron, brain
Jakob-Creutzfeldt disease
jaw jerk, abnormal
lactic acidemia
laminectomy, cervical
laughing, pathologic
leg weakness, bilateral
leg weakness, unilateral
leukodystrophy
Lewy body disease, diffuse
life expectancy
lobar atrophy
locked-in syndrome
lysosomal storage disease
metabolic disorder, primary
Mills syndrome
mimics
misdiagnosis
mobility
mobility aids
molecular genetics
monomelic amyotrophy
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, functional
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, susceptibility weighted
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
mutism
myasthenia gravis
myelopathy
myelopathy, ischemic
myopathy
myopathy, autoimmune
myopathy, quadriceps
myositis
nasal speech
neck weakness
nerve biopsy
neurologic complications of, surgery
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic symptoms
neurologic testing
neuronal degeneration
neuropathology
neuropathy
neuropathy, motor, multifocal
neuroprotective agents
next-generation sequencing
nusinersen
owl's eye sign of spinal cord
pain
pain, increased response
palliative care
paralysis, acute
paralysis, acute areflexic
paralysis, asymmetric
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
Parkinson disease
Parkinsonism syndrome
paroxysmal neurologic deficits
patient information and support
peroxisomal disease
personality change
pes cavus
physical therapy
Pick's disease
pleocytosis of cerebrospinal fluid
poliomyelitis
poliomyelitis-like illness
polyglucosan body disease
polymyositis
practice guidelines
pregnancy, neurologic complications in
primary lateral sclerosis
prognosis
progranulin
progressive neurologic disorder
proximal muscle atrophy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract
pyramidal tract dysfunction
quadriceps atrophy
quadriceps weakness
quadriparesis
quadriplegia
release phenomena
respirator
respiratory failure
review article
riluzole
risk factors
saccadic eye movements, abnormal
scoliosis
scoliosis, neurologic association with
scooters
screening
seizure
shoulder, subluxation
single photon emission computed tomography
skin, lesions in neurologic disorders
sleep
sleep pathology and physiology
SMN1 gene
somatosensory evoked potentials
somatosensory evoked potentials, dermatomal
spastic ataxia
spasticity
speech disorder
speech, loss of
spinal cord
spinal cord degeneration
spinal cord, compression of
spinal cord, lesion of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spondylosis
stereotyped behavior
sternocleidomastoid muscle
stiff legs
superoxide dismutase
survival motor neuron gene
syringomyelia
tau protein
teleconsulting
telemedicine
teleneurology
telestroke
temporal lobe, atrophy
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
trauma
treatment of neurologic disorder
trinucleotide repeats
tripping
ubiquitin
urea-cycle enzymopathies
urinary incontinence
viral infection
viral infection, CNS
viral isolation
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
wheelchair
word-finding difficulty
X-linked bulbospinal neuronopathy
Showing articles 750 to 800 of 4644 << Previous Next >>

Overlapping Anti-NMDAR Encephalitis and Multiple Sclerosis: A Case Report and Literature Review
Front Immunol doi:10.3389/Fimmun.2023.1088801, Liu,P.,et al, 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 Teenager With Right-Sides Headache and Periorbital Changes
Neurol 100:144-150, Lax,D.M.,et al, 2023

Differentiating Multiple Sclerosis from AQP4-Neuromyelitis Optica Spectrum Disorder and MOG-Antibody Disease with Imaging
Neurol 100:e308-e323, Cortesa,R.,et al, 2023

A Case of Cerebral Venous Sinus Thrombosis Presented with SAH and Isolated Headache
Sci Direct 18:4580-4584, Ahmed,N.,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

Major Neurological Deficit Following Neck Hyperextension During Dental Treatment
Neurologist 6:361-363, El-Hajj, V.G.,et al, 2022

Horizontal Diplopia Due to Extraocular Muscle Metastasis
Neurol 99:669-670, Atik, M.,et al, 2022

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,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

Progressive Vertebrobasilar Vasculopathy and Stroke Secondary to Giant Cell Arteritis
Stroke 53:e435-e438, Mahjoub, Y.,et al, 2022

Subacute Encephalopathy with Seizures in Alcoholics (SESA) - Related Abnormalities on EEG and MRI
Neurol 99:354-355, Suh, J.,et al, 2022

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

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

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 387:1022-1032, Case 28-2022, 2022

An 80-Year-Old Woman with a Homonymous Hemianopsia
Neurol 99:713-717, Tajfirouz, D.,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

Reversal of Imaging Findings of Idiopathic Intracranial Hypertension after Lumbar Puncture
JAMA Neurol 79:416-417, Kapadia, A.,et al, 2022

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

Evaluation of Revised Classification Criteria for Giant Cell Arteritis and Its Clinical Phenotypes
Rheumatology (Oxford), 61:383-387, Wiberg,F.,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 56-Year-Old Man with Unusual Presentation of Subacute Encephalopathy and Seizure
Neurol 98:e95-e102, Wang, T.,et al, 2022

Confused About Confusion
NEJM 386:80-87, Spanjaart, A.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

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

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

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

Biopsy Negative Giant Cell Arteritis - Revised Diagnostic Criteria
J Stroke Cerebrovasc Dis 31:106660, Finelli, P.F., 2022

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

The Boston Criteria Version 2.0 for Cerebral Amylois Angiopathy:A Multicentre, Retrospective, MRI-Neuropathology Diagnostic Accuracy Study
Lancet Neurol 21:714-725, Charidimou,A.,et 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 New Case of Neuromyelitis Optica Spectrum Disorders with Unknown Fever and Subacute Cognitive Decline with Normal Images
Cureus 14:e24950, Furuya,K. & Itoh,M., 2022

Evaluation of Medical Decision Support Systems (DDX Generators) Using Real Medical Cases of Varying Complexity and Origin
BMC Med Inform Dcis Mak 22:254, Fritz,P.,et al, 2022

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

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

Molecular and Neurological Features of MELAS Syndrome in Paediatric Patients: A Case Series and Review of the Literature
Mal Genet Genomic Med 10:e1955, Seed,L.M.,et al, 2022

Autoimmune Nodopathies, An Emerging Dignostic Category
Curr Opin Neurol 35:579-585, Martin-Agullar, L.,et al, 2022



Showing articles 750 to 800 of 4644 << Previous Next >>