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Differential
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acoustic neurinoma
acoustic neurinoma, bilateral
acquired immunodeficiency syndrome
adrenoleukodystrophy
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
Alexanders disease
algorithm
alopecia
alpha-fetoprotein
Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, early onset
Alzheimer's disease, familial
amniocentesis
amyloid angiopathy, cerebral
amyloid angiopathy, hereditary cystatin C
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, familial
anemia
anemia, hemolytic
anesthesia, general
anosmia
apolipoprotein E
APP gene
apraxia of eye movements
arteriopathy
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, truncal
attention deficit disorder with hyperactivity
autonomic dysfunction
basal ganglia, degeneration
basal ganglia, lesion of
Bassen-Kornzweig syndrome
benign familial neonatal convulsions
brachial neuritis
brachial plexus neuropathy
brachial plexus neuropathy, familial
brain biopsy
brainstem, lesion of
brainstem, neoplasms of
bulbar palsy, progressive
cafe au lait spots
carcinoembryonic antigen
carcinoma
carcinoma of pancreas
CAT scan
CAT scan, abnormal
cataracts
cavernous hemangioma
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebellar lesion
cerebellum, neoplasms of
cerebral atherosclerosis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral infarction
cerebral infarction, subcortical
cerebral ischemia
cerebro hepato renal syndrome
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, young adult
Charcot-Marie-Tooth
chorea
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 17
chromosome 2
chromosome 22
chromosome 3
chromosome 7
chromosome 9
clindamycin
clonazepam
clubfoot as related to neurologic disease
Cockayne's syndrome
coma
compression neuropathy
compression neuropathy, recurrent
cost effectiveness
creatine phosphokinase(CPK)elevated
Creutzfeldt-Jakob disease, genetic
cryptococcal meningitis
cyst, neoplastic cerebellum
cytomegalovirus infection
degenerative diseases of CNS
dementia
dementia, familial
dementia, presenile
dementia, rapidly progressive
dementia, transmissible
dentate nuclei
dentate nuclei, lesion of
developmental retardation
diabetes mellitus
DNA probes
drooling
drug induced neurologic disorders
dysarthria
dysmorphic
dystonia
dystonia musculorum deformens
dystonia, paroxysmal
dystrophin
ear, abnormal
electroencephalogram
electronystagmography
electroretinograph
encephalitis
encephalitis, focal
encephalitis, Rasmussen's
encephalitis, viral
enzyme, muscle disease
epidemiology of neurology
ethics in neurology
eye movement, disorders of
face, elongated
facial appearance, abnormal
familial
fasciculation
fatal familial insomnia
fragile-X syndrome
Friedreich's ataxia
fundus, abnormality of
gadolinium
gait disorder
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann-Straussler-Scheinker disease
GFAP gene
gonadotropin-releasing hormone
growth retardation
gynecomastia
Hallervorden Spatz disease
hallucination
hamartoma
headache
headache, positional
hearing loss
hemangioblastoma
hemiparesis
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatosplenomegaly
Hispanics
HTRA1 gene
Hunter's syndrome
huntingtin
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's chorea, presymptomatic detection of
hyperactivity
hyperekplexia
hyperhidrosis
hyperkalemic periodic paralysis
hyperreflexia
hyperthermia
hypogonadism
hypotelorism
hypotonia
hypotonia, infants
imbalance
immunodeficiency
immunohistochemistry
immunoperoxidase staining
immunosuppression
in situ hybridization
inclusion bodies, intracytopasmic
insomnia
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracerebral hemorrhage, young adult
Jakob-Creutzfeldt disease
joint hypermobility
Kallmann's syndrome
Kearns-Sayre syndrome
KRIT1 gene
Kugelberg-Welander syndrome
Laurence-Moon-Bardet-Biedl syndrome
leukemia
leukodystrophy
leukoencephalopathy
lymphoma
macrocephaly
macular degeneration
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
malignant hyperpyrexia
manic-depressive
medulla oblongata
medulla oblongata, atrophy
medulla oblongata, lesion of
meningitis
meningitis, recurrent
meningitis, relapse
mental retardation
mental retardation, familial
Mexican
Mexico
misdiagnosis
molecular genetics
mongolism
mononeuropathy
mononeuropathy, recurrent
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
mucopolysaccharidoses
mucopolysacchariduria
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle biopsy
muscle spasm
muscle stiffness
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, Duchenne, presymptomatic detection
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
myelin basic protein gene
myoclonus
myopathy
myopathy, mitochondrial
myopathy, proximal
myopia
myotonia
myotonia dystrophica
neonatal screening, genetic neurologic disorders
neoplasm, metastatic to CNS
neoplasm, posterior fossa
neoplasm, primary intracranial
neoplasm, primary of CNS
neurocutaneous disease
neuroendocrinology
neurofibroma
neurofibromatosis 1
neurofibromatosis 2
neurofibromatosis 2, presymptomatic
neurologic disease
neurologic disease, diagnoses of
neuronal ceroid-lipofuscinosis
neuronal migration disorder
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, hereditary peripheral
neuropathy, peripheral
night blindness
Notch3 gene
ocular motility, disorders of
oculopharyngeal muscular dystrophy
olfactory bulb
optic atrophy
optic glioma
optic nerve
optic neuropathy
pain
pain, flank
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paroxysmal dystonic choreoathetosis
paroxysmal neurologic deficits
pathology
patient information and support
periodic paralysis
peroxisomal disease
pheochromocytoma
pigmentary retinopathy
polycystic kidneys
polymerase chain reaction
polyneuropathy, familial
posterior fossa, lesion of
practice guidelines
prenatal diagnosis by amniocentesis
prion disease
progeria
prognosis
progressive multifocal leucoencephalopathy
progressive spinal muscular atrophy
proximal myotonic myopathy
radiation hypersensitivity
recombinant DNA
recurrent
refractive errors
Refsum's disease
renal cell carcinoma
renal cyst
retinal degeneration
retinal hemangioma
retinal lesion
retinal tumor
retinitis pigmentosa
retinopathy
review article
RFLPs
rigidity
risk factors
Rosenthal fibers
seizure
seizure, familial
seizure, focal
seizure, intractable, treatment of
seizure, neonatal
sensorineural hearing loss
simian crease
skin, lesions in neurologic disorders
skull x-ray, abnormal
sleep pathology and physiology
small vessel disease
Southern immunoblot test
spasticity
spinal cord
spinal cord, lesion of
spinal cord, neoplasm
spinal muscular atrophy
spine, metastasis to
spinocerebellar ataxia
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar degeneration
spondylosis
spongy degeneration of brain
startle reaction
stuporous
subarachnoid hemorrhage
synkinesis
tapetoretinal degeneration
telangiectases
testicular enlargement
thalamus, lesion of
tinnitus
tomaculous neuropathy
trauma
treatment of neurologic disorder
trinucleotide repeats
Usher's syndrome
ventricular garlands
vibratory sensation, abnormal
viral infection
viral infection, CNS
visual field defect
visual loss
Von Hippel Lindau
Von Hippel Lindau, carrier
Von Hippel Lindau, screening protocol for
walking, difficulty with
Werdnig-Hoffman disease
Western immunoblot test
wheelchair
white matter disease
X-linked bulbospinal neuronopathy
x-linked mental retardation
X-linked neuropathy
Showing articles 100 to 150 of 349 << 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

Digital Health in Primordial and Primary Stroke Prevention: A Systematic Review
Stroke 53:1008-1019, Feigin, V.L.,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

Spontaneous Subarachnoid Haemorrhage
Lancet 400:846-862, Claassen, J. & Park, S., 2022

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

Which Imaging Approach Should be Used for Stroke of Unknown Time of Onset?
Stroke 52:373-380, Simonsen, C.Z.,et al, 2021

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

Direct to Angiography Suite Without Stopping for Computed Tomography Imaging for Patients with Acute Stroke
JAMA Neurol 78:1099-1107, Requena, M.,et al, 2021

Clinicopathologic Conference, Systemic Juvenile Idiopathic Arthritis
NEJM 385:1220-1229, Case 29-2021, 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

Determination of Brain Death
NEJM 385:2554-2561, Greer, D.M., 2021

Next-Generation Artificial Intelligence for Diagnosis
JAMA doi:10.1001/JAMA/2021.22396, Dec, Adler-Milstein, J.,et al, 2021

Assessing the Utility of a Differential Diagnostic Generator in UK General Practice: A Feasibility Study
Diagnosis 8:91-99, Cheraghi-Sohi, S.,et al, 2021

Machine Learning Approach to Identify Stroke Within 4.5 Hours
Stroke 51:860-866, Lee, H.,et al, 2020

Diagnosis and Treatment of Parkinson Disease
JAMA 323:548-560, Armstrong, M.J. & Okun, M.S., 2020

Pernicious Anaemia
BMJ 369:m1319, Mohamed, M.,et al, 2020

Transient Ischemic Attack
NEJM 382:1933-1941, Amarenco, P., 2020

Olfactory Dysfunction in COVID-19
JAMA doi:10.1001/JAMA.2020.8391, Whitcroft, K.L. & Hummel, T., 2020

Mechanical Thrombectomy in the Era of the COVID-19 Pandemic: Emergency Preparedness for Neuroscience Teams
Stroke 51:1896-1901, Nguyen, T.N.,et al, 2020

Protected Code Stroke
Stroke 51:1891-1895, Khosravani, H.,et al, 2020

Rapid Implementation of Virtual Neurology in Response to the COVID-19 Pandemic
Neurol 94:1077-1087, Grossman, S.N.,et al, 2020

Acute Ischemic Stroke
NEJM 383:252-260, Powers, W.J., 2020

Polymyalgia Rheumatica and Giant Cell Arteritis
JAMA 324:993-994, Buttgereit, F.,et al, 2020

Migraine
NEJM 383:1866-1876, Ashina, M., 2020

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

Contemporary Reversal of Oral Anticoagulation in Intracerebral Hemorrhage
Stroke 50:529-536, Bower, M.M.,et al, 2019

Acute Encephalitis in Immunocompetent Adults
Lancet 393:702-716, Venkatesan, A.,et al, 2019

Reimagining Specialty Consultation in the Digital Age the Potential Role of Targeted Automatic Electronic Consultations
JAMA doi:10.1001/JAMA.2019.6607, Wachter, R.M.,et al, 2019

Case 27-2019:A 16-Year-Old Girl with Head Trauma During a Sailboat Race
CPC,Concussion,Benign Paroxysmal Positional Vertigo, Case 27-2019, NEJM 381:863-871, Iaccarino,M.A.,et al, 2019

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

Automated ASPECTS in Acute Ischmeic Stroke: A Comparative Analysis with CT Perfusion
AJNR 40:2033-2038, Sundaram, V.K.,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

Management of Acute Retinal Ischemia
Ophthalmol 125:1597-1607, Viousse, V.,et al, 2018

Primary Thrombectomy in tPA (Tissue-Type Plasminogen Activator) Eligible Stroke Patients with Proximal Intracranial Occlusions
Stroke 49:265-269, Fischer, U.,et al, 2018

Diagnosing Stroke in Acute Dizziness and Vertigo
Stroke 49:788-795, Saber Tehrani, A.S.,et al, 2018

Toxidrome Recognition in Chemical - Weapons Attacks
NEJM 378:1611-1620, Ciottone, G.R., 2018

Automated DWI analysis can identify patients within the thrombolysis time window of 4.5 hours
Neurol 90:e1570-e1577, Wouters, A.,et al, 2018

A Fatal Case of Undiagnosed Candida Meningitis-Role of Computer-assisted Diagnosis
Neurologist 23:138-140, Finelli, P.F., 2018

Safety of Magnetic Resonance Imaging in Patients with Cardiac Devices
NEJM 377:2555-2564, Nazarian, S.,et al, 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Identifying Ischemic Stroke Associated with Cancer: A Multiple Model Derived from a Case-Control Analysis
J Neurol 264:781-791, Kassubek, R.,et al, 2017

Anticoagulant-Associated Intracranial Hemorrhage in the Era of Reversal Agents
Stroke 48:1432-1437, Steiner, T.,et al, 2017

Using Artificial Intelligence to Reduce the Risk of Nonadherence in Patients on Anticoagulation Therapy
Stroke 48:1416-1419, Labovitz, D.L.,et al, 2017

National Randomized Controlled Trial of Virtual House Calls for Parkinson Disease
Neurol 89:1152-1161,1103, Beck, C.A.,et al, 2017

Pacemakers in MRI for the Neuroradiologist
AJNR 38:2222-2230, Korutz, A.W.,et al, 2017

Cryptogenic Stroke
NEJM 374:2065-2074, Saver, J.L., 2016

Imaging, Intervention, and Workflow in Acute Ischemic Stroke: The Calgary Approach
AJNR 37:978-984, Zerna, C.,et al, 2016

Safety and Diagnostic Value of Brain Biopsy in HIV patients: a Case Series and Meta-Analysis of 1209 Patients
JNNP 87:722-733, Lee, A.M.,et al, 2016

Evolutionary Pressures on the Electronic Health Record
JAMA 316:923-924, Zulman, D.M.,et al, 2016



Showing articles 100 to 150 of 349 << Previous Next >>