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abducens nerve paralysis
acoustic nerve
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
adenylate kinase 5 autoantibodies
agitation
alternating rapid movement
alveolar hypoventilation
Alzheimer's disease
amnesia
amyotrophic lateral sclerosis
aneurysm
aneurysm, cavernous sinus
aneurysm, internal carotid artery
anti Yo antibody
antibodies to measles
apraxia
arrhythmia, cardiac
arterial dissection, aorta
arthralgia
arthritis
ataxia
ataxia, cerebellar
ataxic gait
atypical
autoantibodies
autonomic dysfunction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
blindness
brain biopsy
brainstem, atrophy
carcinoma
carcinoma of breast
carcinoma of lung
CAT scan, abnormal
CAT scan, pelvis
cavernous sinus, syndrome
central nervous system, infection of
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortex
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, gold sol.curve of
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular disease
cervical rib
chest x-ray, abnormal
children
chorea
choreoathetosis
chorioretinitis
Clinical Pathologic Conference(C.P.C.)
confusion
cranial nerve palsies
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cryptococcal meningitis
cyst, ovary
cytomegalovirus infection
deep gray nuclei
delirium
dementia
dementia, rapidly progressive
demyelinating disease
differential diagnosis
dizziness
dysarthria
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dysmetria
ejection fraction, abnormal
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
encephalitis
encephalitis, autoimmune
encephalitis, human immunodeficiency virus type 1
encephalitis, paraneoplastic
encephalopathy
encephalopathy, metabolic
epidemiology of neurology
erythema migrans
eye movement, disorders of
facial nerve palsy
facial nerve palsy, bilateral
facial pain
facial weakness
facial weakness, bilateral
fasciculation
fever
gait disorder
gastrointestinal perforation
gender
glioma
grimacing
Guillain Barre syndrome
hallucination, visual
head nodding
headache
heel-knee-shin test
hemifacial atrophy
hepatitis
herpes simplex encephalitis
herpes simplex encephalitis, diagnosis of
herpes simplex virus
herpes virus infection
herpes zoster
heterochromia iridis
hippocampal atrophy
hippocampus
hippocampus, hyperintense
Horner's syndrome
Horner's syndrome, etiologies of
human immunodeficiency virus type 1
incidence
inclusion bodies
inclusion bodies, eosinophilic intranuclear
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
iron, brain
Klumpke palsy
lactic dehydrogenase(LDH)
level of consciousness
level of consciousness, decreased
limbic encephalitis
low back pain
Lyme disease
lymphadenopathy
lymphadenopathy, hilar
lymphoma
lymphoma involving CNS
memory, defect of recent
memory, impairment of
meningismus
meningitis
meningitis, aseptic
meningitis, carcinomatous
meningitis, chronic
mental status, abnormal
mesial temporal lobe
miosis
mononeuritis multiplex
mononeuropathy
mononeuropathy multiplex
mortality
Motor Band Sign
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, FLAIR
MRI, gradient-echo
MRI, negative
MRI, paramagnetic effect
MRI, susceptibility weighted
multiple sclerosis
multiple sclerosis, diagnosis of
muscle biopsy
muscle cramp
myelitis
myelopathy
myelopathy, vacuolar
myoclonus
nausea and vomiting
neoplasm, primary intracerebral
neoplasm, primary of CNS
nerve conduction studies
neuritis
neurologic complications of, systemic disease
neurologic disease
neuropathology
neuropathy
neuropathy, peripheral
neuropathy, sensory
NMDA antagonists
NMDA receptors
noncommunicative
ocular dipping
ophthalmoplegia
opportunistic infection
opportunistic infection, CNS
opsoclonus
optic neuropathy
optic neuropathy, bilateral
otitis, neurologic complications with
pain, back
pancoast tumor
paraneoplastic cerebellar degeneration
paratrigeminal syndrome
pericarditis
personality change
pleocytosis of cerebrospinal fluid
poliomyelitis
polymyositis
polyneuropathy
polyradiculoneuropathy
posterior inferior cerebellar artery syndrome
pregnancy, neurologic complications in
prognosis
progressive multifocal leucoencephalopathy
prosopagnosia
psychiatric problems in neurologic disorders
psychomotor retardation
psychotic behavior
pupil
pupil, abnormality in neurologic disorders
pursuit eye movements, abnormal
radiculitis
release phenomena
remote effect of cancer on the nervous system
retrovirus
review article
rubeola virus
Sabin-Feldman dye test
saccadic eye movements, abnormal
salivation, excessive
sciatica
scleroderma
screening
sedimentation rate, elevated
seizure
serum glutamic oxaloacetic transaminase
skin, lesions in neurologic disorders
somnolence
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
sweating
symmetric brain lesions
syphilis, diagnosis and treatment
syphilis, neurologic complications with
syringomyelia
tau protein
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
thalamus, lesion of
Thies's sign
third nerve palsy
tick bite
tonsillectomy
toxoplasma complement fixation test
toxoplasmosis, acquired
toxoplasmosis, CNS
treatment of neurologic disorder
tremor
tremor, intention
trigeminal neuropathy
trigeminal neuropathy, sensory
tuberculosis
uveitis
vertigo
viral infection
viral infection, CNS
vision, blurred
visual loss
visuospatial disturbance
walking, difficulty with
weight loss
white matter disease
Showing articles 50 to 100 of 4949 << Previous Next >>

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

Nonalcoholic Wernicke Encephalopathy
Neurol 97:e1541-e1542, Hansen, G.,et al, 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

Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral Sclerosis
J Clin Med 9:1-12, Rizzo, G.,et al, 2020

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

Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
Neurol 94:e225-e229, Nigam, M.,et al, 2020

A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
Neurol 94:e1664-e1669, Han, F.,et al, 2020

Progressive Ataxia and Palatal Tremor
Neurol 94:e1445-e1447, Pradeep, S.,et al, 2020

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
Neurol 95:e1760-e1763, Brigham, E.,et al, 2020

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020

Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
Neurol 94:273-275, Macaron, G.,et al, 2020

A 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
Neurol 94:713-717, Silverman, A.,et al, 2020

COVID-19: A Global Threat to the Nervous System
Ann Neurol 88:1-11, Koralnik, I.J. & Tyler, K.L., 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Acute Cortical Lesions in MELAS Syndrome: Anatomic Distribution, Symmetry, and Evolution
AJNR 41:167-173, Bhatia,K.D.,et al, 2020

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Characteristic Head Jerks in Congenital Oculomotor Apraxia due to Joubert Syndrome
Neurol 93:e1125-e1126, Borngraber, F.,et al, 2019

Bilateral Claude Syndrome
Neurol 93:599-600, Witsch, J.,et al, 2019

Diagnostic Tools for Immune Causes of Encephalitis
Clin Microbiol Infect 25:431-436, Lascano, A.M.,et al, 2019

A 17-year-old Baseball Player with Right Hand Weakness
Neurol 92:e76-e80, Vachon, C. & Libdeh, A.A., 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

Relapsing-Remitting Severe Bickerstaffs Brainstem Encephalitis
BMJ 394:684, Tyrakowska, Z.,et al, 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 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

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Supplementary Motor Area Stroke Mimicking Functional Disorder
Stroke 49:e28-e30, Mathew, P.,et al, 2018

Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
Pract Neurol 18:5-13, Popkirov, S.,et al, 2018

Neurological Manifestations Among US Government Personnel Reporting Directional Audible and Sensory Phenomena in Havana, Cuba
JAMA 319:1125-1133, 1098, 1079, Swanson, R.L.,et al, 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Essential Tremor
NEJM 378:1802-1810, Haubenberger, D.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

A 54-year-old woman with Confusion and Visual Disturbances
Neurol 91:363-367, Rossi, K.C.,et al, 2018

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
Ann Neurol 81:298-309, Flanagan, E.P.,et al, 2017

Clinical Decision-Making in Functional and Hyperkinetic Movement Disorders
Neurol 88:118-123,114, van der Salm, S.M.A.,et al, 2017

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017



Showing articles 50 to 100 of 4949 << Previous Next >>