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Differential
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acrocyanosis
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
Africa
Aicardi-Goutieres syndrome
algorithm
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
ataxia
ataxia, progressive
atypical
Babinski sign
basal ganglia, calcification of
bladder dysfunction
bone marrow transplantation
brain atrophy
bulbar palsy
calcification, intracranial
camptocormia
cane
CAT scan, abnormal
cerebellar atrophy, primary
cerebrospinal fluid, abnormal
chilbran skin lesions
children
constipation
corpus callosum
corpus callosum, atrophy of
corpus callosum, thinning
cultured skin fibroblasts
degenerative diseases of CNS
dementia, childhood
demyelinating disease
dentate nuclei, lesion of
diagnostic criteria
diet
differential diagnosis
distal muscle weakness
dysarthria
dysphagia
dystonia
dystonia, children
ears of the Lynx MR sign
ELISA
emergency room
encephalopathy
endemic area
epidemiology of neurology
familial
fasciculation
fatty acid, elevated plasma content
feeding disorder
fever
foot drop
gait disorder
gait, spastic
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
geographic location
hand weakness
head lag
hemiparesis
high arched feet
human T-lymphotropic virus type I(HTLV-I)
hyperpyrexia, CNS disorder causing
hyperreflexia
hypogonadism
hypotonia
intellectual deficit
interferon alpha
intrauterine
intrinsic hand muscles, wasting of
irritability
jaw jerk, abnormal
leg weakness, bilateral
leukodystrophy
leukoencephalopathy
Lorenzo's oil
Maghreb
microcephaly
Mills syndrome
misdiagnosis
motor neuron disease
movement disorder
MRI, abnormal
MRI, emergent
multiple sclerosis, misdiagnosis
muscle cramp
myelopathy
myelopathy, chronic progressive
neck weakness
neurologic disease, diagnoses of
neurologic signs
neuropathology
next-generation sequencing
pain, leg
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, familial spastic, variants
paraparesis, spastic
paraparesis, spastic, tropical
paraplegia
peroxisomal disease
pleocytosis of cerebrospinal fluid
polymerase chain reaction
prenatal
prenatal diagnosis by amniocentesis
primary lateral sclerosis
prognosis
progressive neurologic disorder
psychomotor retardation
pyramidal tract dysfunction
review article
screening
seizure
skin, darkening of
skin, lesions in neurologic disorders
spastic ataxia
spastic paraplegia, type 11
spastic paraplegia, type 15
spasticity
spastin
speech disorder, childhood
startle reaction
stiff legs
testicular atrophy
toe walking
treatment of neurologic disorder
urinary urgency
walking frame
walking, difficulty with
weakness
weakness, progressive
wheelchair
white matter disease
Showing articles 750 to 800 of 3817 << Previous Next >>

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

HIV-Associated CD8 Encephalitis: A UK Case Series and Review of Histopathologically Confirmed Cases
Front Neurol 12:628296, Lucas,S.B.,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

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

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

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

Autoimmune Encephalitis Related to Cancer Treatment with Immune Checkpoint Inhibitors
Neurol 97:e191-e202, Nersesjan, V.,et al, 2021

Comparison of 1 vs 2 Brain Death Examinations on Time to Death Pronouncement and Organ Donation
Neurol 96:e1453-e1461, Varelas, P.N.,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

Teleneurology-Enabled Determination of Death by Neurologic Criteria After Cardiac Arrest or Severe Neurologic Injury
Neurol 96:e1999-e2005, Matiello, M.,et al, 2021

Caplan-Fisher Rules
Stroke 52:doi:10.1161/Strokeaha.121.035017, Caplan, L., 2021

National Institute of Neurological Disorders and Stroke Consensus Diagnostic Criteria for Traumatic Encephalopathy Syndrome
Neurol 96:848-863, Katz, D.I.,et al, 2021

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

HIV Infection - Screening, Diagnosis, and Treatment
NEJM 384:2131-2143, Saag, M.S., 2021

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

A 13-Year-Old Boy with Subacute-Onset Spastic Gait
JAMA Neurol 78:e1-e2, Xie, N.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,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 Juvenile Idiopathic Arthritis
NEJM 385:1220-1229, Case 29-2021, 2021

Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
NEJM 385:1317-1325, Case 30-2021, 2021

Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
Neurol 97:875-878, Dinov, D.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,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

A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
Neurol 97:958-963, Davalos, L.,et al, 2021

Single Photon Emission Computed Tomography/Positron Emission Tomography Molecular Imaging for Parkinsonism: A Fast-Developing Field
Ann Neurol 90:711-719, Verger, A.,et al, 2021

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

Headache, Cognitive Decline, and a Curious Rim-Enhancing Lesion
JAMA Neurol 78:613-614, Beaman, C.B.,et al, 2021

Clinical and Genetic Features in Patients with Reflex Bathing Epilepsy
Neurol 97:e577-e586, Accogli, A.,et al, 2021

Vitamin B12 Deficiency in a 29-Year-Old Woman
Neurol 97:e643-e646, Huddar, A.,et al, 2021

Genetics of Cluster Headache Takes a Leap
Ann Neurol 90:191-192, Palotie, A., 2021

Chronic Meningitis
NEJM 385:930-936, Aksamit, A.J., 2021

A Case-Based Review of Cerebral Venous Infarcts with Perfusion Imaging and Comparision to Arterial Ischemic Stroke
Front Radiol 1:687045, Li, A.Y.,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

Anti-cN1A Antibodies are Associated with More Severe Dysphagia in Sporadic Inclusion Body Myositis
Cells 10:1146, Lucchini,M.,et al, 2021

Leg Weakness and Paraesthesia Provide a Clue to Sudden Death due to Aortic Dissection
Lancet 397:128, Agarwal, M.,et al, 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

Molecular Diagnostic Yield of Exome Sequencing in Patients with Cerebral Palsy
JAMA 325:467-475, Moreno-De-Luca, A.,et al, 2021

Central Nervous System Involvement in Erdheim-Chester Disease
Neurol 95:e2746-e2754, Aubart,F.C.,et al, 2020

A case of COVID-19-associated pharyngeal-cervical-brachial variant of Guillain-Barre syndrome
Neurol 95:978-983, Liberatore, G.,et al, 2020

Variant Creutzfeldt-Jakob Disease Diagnosed 7.5 Years after Occupational Exposure
NEJM 383:83-85, Brandel, J.P.,et al, 2020

Imaging Review of Paraneoplastic Neurologic Syndromes
AJNR 41:2176-2187, Madhavan, A.A.,et al, 2020

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

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



Showing articles 750 to 800 of 3817 << Previous Next >>