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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 600 to 650 of 5474 << Previous Next >>

Atypical Presentation of Primary Angiitis of Central Nervous System Responsive to Rituximab
Stroke 53:e490-e494, Kesav, P.,et al, 2022

External Validation of e-ASPECTS Software for Interpreting Brain CT in Stroke
Ann Neurol 92:943-957, Mair,G.,et al, 2022

Patient with Prior Spinal Cord Injury Who Developed Altered Mental Status After a Fall
Neurol 99:1122-1127, Dessy,A.,et al, 2022

Extracranial Etiology of Acute Onset Ataxia and Weakness
Neurol 99:898-899, Nordli,D.,et al, 2022

New Onset Focal Tremor in Patient with Human Immunodeficienccy Virus
Clin Infect Dis 75:1861-1863, Finelli,P.F., 2022

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

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

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

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022

A 51-Year-Old Woman with Diplopia and Headache
Neurol 99:524-530, Kathuria, G.,et al, 2022

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

Torticollis in a Child with Otalgia
BMJ 378:e070608, Sarathi, C.I.P.,et al, 2022

A 31-year-Old Man with Bilateral Limited Mobility of Joints
JAMA Neurol 79:1083-1084, Wang, Z.,et al, 2022

Clinical Manifestations and Diagnosis of Listeria Monocytogenes Infection
UptoDate Aug, Gelfand, M.S.,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

Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease
Ann Neurol 91:158-159, Jokela, M.,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 57-Year-Old Man with Stepwise Progressive Paraparesis, Sensory Loss, Urinary Retention, and Constipation
Neurol 98:e555-e560, Alkabie, S.,et al, 2022

Stroke Mimics in the Acute Setting: Role of Multimodal CT Protocol
AJNR 43:216-222, Prodi, E.,et al, 2022

Clinicopathologic Conference, Neurosyphilis
NEJM 386:583-590, Case 4-2022, 2022

Leptomeningeal Enhancement Associated with Cerebral Venous Thrombosis
JAMA Neurol 79:195-196, Lozano-Chinga, M.,et al, 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

A 55-Year-Old Woman with Recurrent Episodes of Aphasia and Vision Changes
Neurol 98:330-335, Jeanneret, V.,et al, 2022

Efficacy and Safety of Selumetinib in Pediatric Patients with Neurofibromatosis Type 1
Neurol 98:e938-e946, Hwang, J.,et al, 2022

Contemporary Trends in the Nationwide Incidence of Primary Intracerebral Hemorrhage
Stroke 53:e70-e74, Bako, A.T.,et al, 2022

Brain Tumors in Children
NEJM 386:1922-1931, Cohen, A.R., 2022

Rituximab Therapy in the Treatment of Juvenile Myasthenia Gravis
Neurol 98:e2368-e2376, Molimard, A.,et al, 2022

Thalamus L-Sign: A Potential Biomarker of Neonatal Partial, Prolonged Hypoxic-Ischemic Brain Injury or Hypoglycemic Encephalopathy
AJNR 43:919-925, Misser, S.K.,et al, 2022

Vision Loss in Giant Cell Arteritis
Pract Neurol 22:138-140, Donaldson, L. & Margolin, E., 2022

Neurological Events Reported after COVID-19 Vaccines: An Analysis of Vaccine Adverse Event Reporting System
Ann Neurol 91:756-771, Frontera, J.A.,et al, 2022

Case Report of Lambl Excrescences in a Pediatric Patient with Multifocal Strokes
Neurol 99:73-76, Robertson, D.M.,et al, 2022

Inconsistency and Incongruence: The Two Diagnostic Pillars of Functional Movement Disorder
Lancet 400:328, Hess, C.H.,et al, 2022

A 48-Year-Old Woman with 6 Months of Vivid Visual Hallucinations
Neurol 99:166-171, Kizza, J.,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

Rare Cause of Hemiparesis and Ataxia in a 36-Year-Old Man
Neurol 98:251-255, Decker, J. & Singh, M., 2022

Multisystem Involvement in Post-Acute Sequelae of Coronavirus Disease 19
Ann Neurol 91:367-379, Novak, P.,et al, 2022

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

Recent Advances in the Diagnosis and Management of Cluster Headache
BMJ 376:e059577, Schindler, E. & Burish, M.J., 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

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

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

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

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



Showing articles 600 to 650 of 5474 << Previous Next >>