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Differential
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abducens nerve paralysis
abortion, spontaneous
advances in neurology
adverse drug reaction
ageusia
algorithm
alpha-fetoprotein
Alzheimer's disease
amaurosis fugax
amaurosis fugax, unilateral vs.bilateral
amyloid angiopathy, cerebral
amyotrophic lateral sclerosis
anemia
aneurysm
aneurysm, multiple intracranial
anosmia
anticardiolipin antibodies
anticoagulant, treatment
antiphospholipid antibodies
antiphospholipid antibody syndrome
apraxia of eye movements
Argyll Robertson pupil
arteritides
arthralgia
arthritis
aspirin
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
atrial myxoma
autoantibodies
autoimmune disease
bacterial infection
biologic markers
blindness, transient
calcification, gyral
calcification, intracranial
calf hypertrophy
carcinoembryonic antigen
carcinoma
cardiomyopathy
cardiopulmonary bypass
carpal tunnel syndrome
CAT scan, abnormal
CAT scan, venography
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebral edema
cerebral embolism
cerebral infarction
cerebral venous infarction
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebral venous thrombosis, etiology
cerebral venous thrombosis, recurrent
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, gold sol.curve of
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, atrial myxoma
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, nonvascular territory
cerebrovascular accident, prevention of
cerebrovascular accident, thrombolytic agents in treatment
cerebrovascular accident, young adult
cerebrovascular disease
children
chorea
chorea, causes of
choreoathetosis
chromosomal abnormality
chromosome 11
Clinical Pathologic Conference(C.P.C.)
collagen vascular disease
complications
confusion
conversion reaction
coronary artery disease
coronavirus
cortical blindness
coumarin
COVID-19
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
craniectomy, decompressive
crawl regression
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
D-dimer
deafness
decision analysis
delay in diagnosis
dementia
dementia, frontotemporal
developmental milestones, loss of
developmental retardation
diabetes mellitus
diagnostic criteria
difficulty climbing stairs
drooling
dural sinus thrombosis
dysarthria
dyskinesia
dyskinesia, drug induced
dyspnea
dystonia
dystonia, drug induced
dystrophin
echoencephalogram
embolism
encephalitis
encephalitis, focal
encephalopathy
encephalopathy, metabolic
endocarditis, marantic
endovascular therapy
epidemiology of neurology
erythema migrans
evidence-based research
eye movement, disorders of
Factor V Leiden
falling
false positive
false positive VDRL
familial
fever
fibrinolytic agents
fibrinolytic agents, intra-venous local infusion
fine motor function, impaired
fungal infection, CNS
gadolinium
gait disorder
gammaglobulin therapy, intravenous
gender
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glaucoma
Gowers maneuver
growth retardation
Guillain Barre syndrome
headache
heart murmur
heparin
heparin, low-molecular-weight
hepatomegaly
heralding manifestation
Horner's syndrome
Horner's syndrome, childhood
Huntington's chorea
hydrocephalus
hypergammaglobulinemia
hypotonia
hypoxia
immunodeficiency
immunosuppression
incidence
inclusion body myositis
infection
intellectual deficit
intracranial pressure, increased
iritis
Jakob-Creutzfeldt disease
juvenile idiopathic inflammatory myopathy
lactic acidemia
learning disability
learning disability, in children
leukemia
leukocytosis
level of consciousness, decreased
Lewy body disease, diffuse
livedo reticularis
liver disease
liver function enzymes
lupus anticoagulant
Lyme disease
lymphadenopathy
lymphadenopathy, axillary
lymphadenopathy, paraaortic
lymphoma
malformation, vascular
MELAS syndrome
meningeal enhancement
meningitis
meningitis, aseptic
mental retardation
microangiopathy, brain
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve lesion
mortality
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, functional
MRI, venography
multiple organ failure
multiple system atrophy
multisystem inflammatory syndrome in children
muscle biopsy
muscle pain
muscle weakness
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
myelopathy
myocardial infarction
myocardial injury
myoglobinuria
myopathy
myopathy inflammatory, classification
myopathy, inflammatory
myopathy, inflammatory, classification
myositis
myositis specific autoantibody
myositis, juvenile
neurocutaneous disease
neuroendocrinology
neurologic complications
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neurologic symptoms
neuroophthalmology
neuropathology
neuropathy
neuropathy, vasculitic, systemic
neurotoxin
next-generation sequencing
obstetric complications
ocular motility, disorders of
ophthalmoplegia
ophthalmoplegia, painful
optic atrophy
optic neuropathy
oral contraceptives
pain
pandemic
papilledema
Parkinson disease
pars planitis
partial thromboplastin time, prolonged
pathology
peripheral blood smear
petechiae
photosensitivity, skin
pitfalls
plasmapheresis
platelet inhibiting drugs
polycythemia, primary
polymerase chain reaction
port wine nevus
postinfectious
postpartum
practice guidelines
pregnancy, neurologic complications in
prethrombotic state
prevention of neurologic disorders
progeria
prognosis
progressive neurologic disorder
protein C deficiency
protein S deficiency
pulmonary embolism
pupil
pupil, abnormality in neurologic disorders
quadriparesis
radiation hypersensitivity
ragged-red fibers
rash
Raynaud's phenomenon
Red flags
renal failure
renal infarct
renal vein thrombosis
review article
risk factors
schistocytes
scleroderma
scleroderma, neurologic involvement with
screening
sedimentation rate, elevated
seizure
seizure, children
sensorineural hearing loss
serologic testing
seronegative
serositis
severe acute respiratory syndrome
skin, lesions in neurologic disorders
speech disorder, childhood
speech, delayed development of
spinal cord, lesion of
spinal muscular atrophy
spirochete infection
splenomegaly
spontaneous remission
steroid therapy, CNS treatment and complications with
stiff joints
strokelike episodes
Sturge-Weber syndrome
syncope
systemic illness
systemic juvenile idiopathic arthritis
systemic lupus erythematosus
telangiectases
temporal lobe, lesion
temporal lobe, lesion, bilateral
third nerve palsy
thrombocytopenia
thrombocytosis
thrombophlebitis
thrombotic microangiopathy
tissue plasminogen activator, intravenous
Tolosa Hunt syndrome
toxins, nervous system
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
trigeminal neuropathy
tripping
trochlear nerve palsy
uveitis
valvulopathy
vasculopathy
venous thrombosis, non-cerebral
viral infection
viral infection, CNS
visual field defect
walking, difficulty with
weakness
weakness, progressive
weight loss
wheelchair
white matter disease
whole genome sequencing
workup
Showing articles 400 to 450 of 5474 << Previous Next >>

Polyneuritis in Children
Pediatrics 22:972-990, Low,N.L.,et al, 1958

Occlusive Rheum Arteritis Brain & Other Organs in Pat with Rheum Valvular Heart Dis
IV Inter Cong Neuropath, III:309, D. H. Jacob, G. T. Verlag, eds. , Stuttgart., Bruetsch,W.L., 1850

Unilateral Primary Angiitis of the Central Nervous System: A Rare and Under-Recognized Entity
AJNR 47:589-595, Rai,P.,et al, 2026

Zorevunersen in Children and Adolescents with Dravet Syndrome
NEJM 394:969-982, Laux,L.,et al, 2026

Increased Prevalence of Nitrous Oxide-Induced Subacute Combined Degeneration of the Spinal Cord: Clinical and Imaging Findings
AJNR 47:513-520, Bruen,R.,et al, 2026

Mucormycosis
NEJM 394:684-698, Kontoyiannia,D.P. & Walsh, T.J., 2026

Turning Slowly Predicts Future Diagnosis of Parkinsons Disease:A Decade-Long Longitudinal Analysis
Ann Neurol 99:114-123, Elshehabi,M.,, 2026

Restless Legs Syndrome, A Review
JAMA 335:703-714, Winkelmen,J.W. & Wipper, B., 2026

Paramagnetic Rim Lesions and Development of Clinical MS in Radiologically Isolated Syndrome
JAMA Neurol 83:250-258, Lim,T.R.et al, 2026

Polymyalgia Rheumatica
NEJM 394:1097-1109, Dejaco,C.,et al, 2026

Clinical Manifestations of Primary CNS T-Cell Lymphoma, Retrospective Study of Histopathologic, Molecular, and Neuroimaging Fetures
Neurol 106:e24744, Muller,K.J.,et al, 2026

Frequency of AQP4 and MOG Antibodies in Patients with Optic Neuritis Fulfilling Minimal New Multiple Sclerosis MRI Criteria
Neurol 106:e214753, Deschamps,R.,et al, 2026

The 2024 McDonld Criteria for Dignosis of Multiple Sclerosis, The Rubber meets the Road
Neurol 106:e214688, Miller, A.E., 2026

Syphilis as an Important Modern-Day Risk Factor for Intracranial Vasculopathy and Ischemic Stroke:A Teaching Case
Stroke 57:e108-e111, Higham-Kessler,C.,et al, 2026

A 41-Year-Old Man Presenting with Right Foot Tingling
Neurol 106:214781, Lu,V.,et al, 2026

Using Susceptibility-Based Imaging in Highly Active Late-Onset Multiple Sclerosis
Neurol 106:e214794, Sosa,S.M.,et al, 2026

Can AI Say "I Dont Know"?
NEJM 394:1873-1875, Sikora,A.,et al, 2026

A 28-Year-Old Man with Seizures and Thalamic Lesions
Neurol 106:e218065, Santos-Rojo,A.B.,et al, 2026

A 55-Year-Old Man with Rapidly Progressive Weakness and Numbness
Neurol 106:e218063, Li,X.,et al, 2026

Comparison of AI, Diagnostic Generator, and Expert Opinion in Difficult Neurologic Diagnosis; Real-World Case Study
Diagnosis doi.org/10.1515/dx-2026-002, Finelli,P.F., 2026

Diagnostic Value of the Kappa Free light Chain Index to Distinguish MOGAD, NMOSD, and MS
Neurol 106:e214946, Tournier,A.,et al, 2026

Using Susceptibility-Based Imaging in highly ctive Late-Onset Multiple Sclerosis
Neurol 106:e214794, Sosa,S.M.,et al, 2026

Large Language Model Performance and Clinical Reasoning Tasks
JAMA Netw Open 9:e264003, Rao,A.S.,et al, 2026

Cerebral Amyloid Angiopathy
NEJM 394:1836-1845, Greenberg,S.M., 2026

CT Perfusion Abnormality in Hypoglycemic Focal Neurological Deficits
Stroke 57:e6-e7, Mikito,S.,et al, 2026

Atypical Diabetic Neuropathies
BMJ 390:e081109, McCray,B.A.,et al, 2025

Myelin Oligodendrocyte Glycoprotein Antibody - Associated Cerebral Cortical Encephalitis: A Case Report Highlighting Diagnostic Challenges and Therapeutic Implications
Front Immunol 16:1619807, Liu,M. & Li, D., 2025

AI: Need for Comparative Studies in Complex Neurologic Diagnosis
Ann Neurol doi:10.1002/ana.78068, Finelli,P.F., 2025

Spontaneous Calcified Cerebral Emboli from Bicuspid Aortic Valve in Young Patients: Case Series and Review
Stroke:Vasc Inter Neurol doi.org/10.1161/svi 270000.138, Sardana,S.,et al, 2025

High-Grade Gliomas with Autoimmune Encephalitis-Like Presentation: Case Report and Systematic Review of the Literature
Neurological Sci 46:3559-3572, Creda,G.S.et al, 2025

Tiger Man Sign in Sarcoid Myopathy
Neurol 105:e214323, Sun,Q.,et al, 2025

Multivessel Cerebral Occlusion in Noonan Syndrome
Stroke 56:e359-362, deLima, M.M.,et al, 2025

Neurosyphilis
Ann Neurol 98:1070-1076, Minter,D.J. & Chow,F.C., 2025

Nontrauma-Associated Cerebral Fat Embolism Syndrome in Sickle Cell-Related Hemoglobinopathies: A Case Series and Systematic Review
AJNR 46:2000-2008, Shadmani,G.,etal, 2025

Neuroimaging Findings in Children and Young Adults with Neurotoxicity after CAR T-Cell Therapy for B-Cell Malignancies
Neurol 105:e214086, McGuire,J.L.,et al, 2025

General AI May Revolutionize Neurology-Or It Might Be Bad
JAMA Neurol 82:977-978, Westover,M.B., & Westover A.M., 2025

Diagnosis of Multiple Sclerosis: 2024 Revisions of the McDonald Criteria
Lancet Neurol 24:850-865, Montalban,X.,et al, 2025

A 30-Year-Old Female Patient with Multiple Sclerosis Presenting with Rapidly Progressive Cranial Neuropathies, Weakness, and Ataxia
Neurol 105:e214429, Trentadue,T.,et al, 2025

Idiopathic Normal-Pressure Hydrocephalus
NEJM 393:2243-2253, 2264, Johnson,M.D.,& Williams, M.A., 2025

A 5-Year-Old Boy with Subacute and Refractory Myoclonus
Neurol 106:e214457, Park,P.S.,et al, 2025

Recurrent Ischemic Strokes Due to Os Odontoideum
Ann Neurol 98:1315-1317, Wang,J.,et al, 2025

A 62-Year-Old Man with Progressive Limb Weakness, Involuntary Movements, and HyperCKemia
JAMA Neurol 82L:1286-1287, Liu,Y.,et al, 2025

Complex Regional Pain Syndrome
NEJM 393:2338-2348, Goebel,A., 2025

Large Language Models in Neurological Practice: Real-World Study
J Med Internet Res 27:e73212, Maiorana,N.V.,et al, 2025

Validation of the Boston Criteria Version 2.0 for Cerebral Amyloid Angiopathy in Patients Presenting with Intracerebral Hemorrhage
Neurol 104:e213460, Downes,M.H.,et al, 2025

Granulomatosis with Polyangiitis Presenting as Isolated Ear Involvement A Case Series and Literature Review
ACTA Otorhinolaryngol Italica 45:217-230, Zorzi,S.,et al, 2025

Neurological History Both Twinned and Queried by Generative Artificial Intelligence
Front Med doi.10.3389/frmed.2024.1496866, Lee,J-H.,et al, 2025

Niemann-Pick Disease Type C
Gene Reviews www.genereview.org, Bremova-Ertl,T. & Patterson, M., 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
Neurol 104:e213636, Chanda,G.,et al, 2025



Showing articles 400 to 450 of 5474 << Previous Next >>