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abducens nerve paralysis
acoustic nerve
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, medical precautions with
acute ataxia of childhood
acute cerebellar ataxia
adolescent medicine
advances in neurology
akinetic mute
alcohol intolerance
algorithm
alkylating agents
alpha-fetoprotein
alpha-synuclein
altered states of consciousness
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement, impaired
AMPA receptor antibodies
amphiphysin antibodies
anemia
angiotensin-converting enzyme
ankle edema
anti GQ1b IgG antibody
anti Hu antibody
anti Ri antibody
anti Yo antibody
antiamphiphysin
antibiotics
antimetabolite
aphasia
apraxia of eye movements
areflexia
arthralgia
arthritis
ascites
asparginase
ataxia
ataxia telangiectasia
ataxia, acute onset
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
atonic bladder
ATP1A3 gene
atypical
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune cerebellar ataxia
autoimmune disease
autonomic dysfunction
autonomic neuropathy
Babinski sign
bacterial infection
behavioral disorder
blindness
blood dyscrasias, neurologic findings with
Borrelia burgdorferi infection
brachial plexus neuropathy
bradykinesia
callosal angle
cane
carcinoembryonic antigen
carcinoma
carcinoma of breast
carcinoma of cervix
carcinoma of lung
carcinoma of ovary
carcinoma of uterus
cardiomyopathy
CAT scan
CAT scan, abnormal
cataracts
cauda equina, enhancement
celiac disease, adult
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebral cortex
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, drainage of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, pressure low
cerebrovascular accident
cerebrovascular accident, recurrent
cerebrovascular disease
ceruloplasmin, serum
chairbound
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
chest pain
chest x-ray, abnormal
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 9
cisternogram, radionuclide
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
cognition, slowed
coinfection
collapsin response mediator protein 5 IgG
coma
complications
consanguinity
contactin associated protein like 2 antibodies
cough
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
deep tendon reflexes
degenerative diseases of CNS
dementia
dementia, childhood
dementia, familial
dementia, rapidly progressive
dementia, reversible
depression
dermatitis
dermatomyositis
developmental retardation
dexterity, impaired
diabetes mellitus
diagnostic criteria
diarrhea
diarrhea, bloody
diet
differential diagnosis
difficulty climbing stairs
diplopia
dizziness
dopa responsive dystonia
drooling
dysarthria
dysdiadochokinesia
dyskinesia
dysmetria
dysmorphic
dysphagia
dystonia
edema, pedal
efficacy
electroencephalogram, abnormalities of
electromyogram
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, parainfectious
Epstein-Barr virus
erythema migrans
esophageal varices
evoked potentials
executive dysfunction
external lumbar drainage
eye movement, disorders of
facial expression abnormality
facial nerve palsy
facial nerve palsy, bilateral
facial nerve palsy, recurrent
facial pain
falling
familial
fever
finger nose finger test
Fisher's syndrome
fluorouracil
flush syndrome
foot drop
frataxin
Friedreich's ataxia
frontal lobe, pathologic signs of
gait disorder
gait, magnetic
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gastrointestinal disease, neurologic complications
gaze palsy, horizontal
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann-Straussler-Scheinker disease
glutamic acid decarboxylase, antibody
gluten ataxia
gluten sensitivity
gluten-free diet
granulomatous disease
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, infantile and childhood form
Guillain Barre syndrome, variant forms of
hallucination
handwriting
headache
headache, severe
hearing loss
heel-knee-shin test
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
heralding manifestation
herpes virus
high altitude sickness
hoarseness
Hodgkin's disease
human immunodeficiency virus type 1
hydrocephalus
hydrocephalus, normal pressure
hydrocephalus, normal pressure, etiology
hydrocephalus, treatment of
hyperreflexia
hypoalbuminemia
hyponatremia
hyporeflexia
hypothalamus
hypothalamus, disturbance of
hypotonia
imbalance
immune reconstitution inflammatory syndrome
immunodeficiency
immunologic disease
immunology and the nervous system
immunosuppression
immunosuppressive agents
immunotherapy
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
infection
infectious mononucleosis
infectious mononucleosis, neurologic findings with
intellectual deficit
intellectual deterioration
intracranial hypertension, benign
irritability
isoniazid
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
jaw pain
Kayser-Fleischer ring
Korsakoff's psychosis
L-dopa
leg weakness, bilateral
lethargy
leucine rich glioma inactivated 1 antibodies
leukemia
leukemia, neurologic findings assoc.with
leukopenia
limbic encephalitis
liver function enzymes
lumbar drain
lumbar puncture, repeated
Lyme disease
lymphocytic meningoradiculitis
lymphoma
malignancy screen
malignancy, occult
masked facies
Melkersson's syndrome
memory, impairment of
meningismus
meningitis
meningitis, aseptic
meningitis, carcinomatous
meningitis, neurologic aspects and complications of
meningitis, recurrent
meningoencephalitis
meningoencephalopathy
mental retardation
mental status, abnormal
methotrexate
methylhydrazine derivatives
microcephaly
mimics
misdiagnosis
molecular genetics
monoamine oxidase inhibitors
monoclonal antibodies
monoclonal gammopathy
mononeuritis multiplex
mood change
mortality
motor neuron disease
mountain climbing
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, brachial plexus
MRI, diffusion weighted
MRI, flow void, CSF
MRI, high signal foci on
MRI, negative
MRI, periventricular hyperintensity
MRI, punctate pattern
multiple sclerosis
multiple system atrophy
muscle biopsy
muscle pain
muscle weakness
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, paraneoplastic
myasthenic syndrome
mycoplasma
mycoplasma pneumoniae
myelitis
myelopathy
myelopathy, chronic progressive
myopathy
myopathy, vacuolar
myositis
myositis, ocular
nausea and vomiting
nemaline rod myopathy
nerve conduction studies
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neurocutaneous disease
neuroendocrinology
neurologic complications of, surgery
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic disease, tempo
neurologic signs
neurologic symptoms
neuromuscular junction
neuronal cell surface antigen
neuronal intranuclear inclusion disease
neuronopathy
neuronopathy, sensory
neuropathology
neuropathy
neuropathy, acute
neuropathy, ataxic
neuropathy, painful
neuropathy, paraneoplastic
neuropathy, peripheral
neuropathy, recurrent
neuropathy, sensory
neurotoxin
next-generation sequencing
nitrogen mustard
NMDA antagonists
nystagmus
nystagmus, monocular
ocular motility, disorders of
oculomasticatory myorhythmia
onconeural antibodies
ophelia syndrome
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, recurrent
opsoclonus
opsoclonus-myoclonus syndrome
optic atrophy
optic disc edema
optic nerve
optic neuritis
optic neuropathy
orthostatic hypotension
ovarian tumor
pain
pain, abdominal
pain, back
pain, leg
papilledema
paraneoplastic cerebellar degeneration
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paresthesias
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
pathology
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
penicillamine
peripheral nerve, lesion of
personality change
pes cavus
photophobia
picking at skin
pleocytosis of cerebrospinal fluid
pneumonia
POLG1 gene
poliomyelitis-like illness
polyclonal gammopathy
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic idiopathic
polyneuropathy, chronic idiopathic, ataxic
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic relapsing
postural abnormality
potassium channel antibodies
practice guidelines
precipitating factors
pregnancy, neurologic complications in
prion disease
prion protein gene
PRKN gene
procarbazine
progeria
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
proprioception, abnormal
protein 14-3-3, cerebrospinal fluid
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
pulmonary infiltrates
quadriplegia
radiation hypersensitivity
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
real-time quaking-induced conversion
recurrent
Red flags
regional enteritis
remote effect of cancer on the nervous system
renal stones
respiratory failure
retinopathy
reversible neurologic disorder
review article
rhinorrhea
rigidity
risk factors
rituximab
safety
sarcoidosis
sarcoidosis, CNS
scoliosis
screening
sedimentation rate, elevated
seizure
sensorineural hearing loss
sensory polyneuropathy
serologic testing
serologic testing, false negative
seronegative
short steps
shunt procedure, lumboperitoneal
shunt procedure, ventricular
shunt procedure, ventricular-complications of
sinemet
skin, biopsy
skin, lesions in neurologic disorders
sleep pathology and physiology
slit lamp examination
spastic ataxia
spasticity
spinal cord
spinal cord, lesion of
spinal muscular atrophy
spirochete infection
splenomegaly
startle myoclonus
status epilepticus
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
striatal encephalitis
striatum, lesion of
striatum, lesion of, bilateral
subarachnoid hemorrhage
synucleinopathy
systemic illness
tandem gait, ataxic
telangiectases
temporal lobe, lesion
thrombocytopenia
tick bite
tinnitus
tonic foot response
transglutaminase antibodies
transient ischemic attack
treatment of neurologic disorder
tremor
tremor, postural
trientine dihydrochloride
trinucleotide repeats
ulcerative colitis
upgaze, paralysis of
urinary incontinence
urinary retention
vasculitides
ventricular enlargement
ventriculostomy
vinblastine
vincristine neurotoxicity
viral infection
viral infection, CNS
vision, blurred
vision, failure of in childhood
visual acuity, decreased
visual evoked response
visual impairment
visual loss
vocal cord paralysis
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
wheelchair
Whipple's disease
wide based gait
workup
wrist drop
zinc
Showing articles 800 to 850 of 6548 << Previous Next >>

Computer-Assisted Diagnostic Checklist in Clinical Neurology
Neurologist 21:23-27, Finelli,P.F. and McCabe, A.L., 2016

National Characteristics and Predictors of Neurology 30-day Readmissions
Neurol 86:669-675, Guterman, E.L.,et al, 2016

Guillain-Barre Syndrome Outbreak Associated with Zika Virus Infection in French Polynesia: A Case-Control Study
Lancet 387:1531-1539,1486, Cao-Larmeau, V-M., et al, 2016

Missed Ischemic Stroke Diagnosis in the Emergency Department by Emergency Medicine and Neurology Services
Stroke 47:668-673, Arch, A.E.,et al, 2016

Zika Virus as a Cause of Neurologic Disorders
NEJM 374:1506-1509, Broutet, N.,et al, 2016

Clinical Manifestations and Evaluation of Adults with Suspected Native Valve Endocarditis
UpToDate Feb, Sexton, D.J. & Fowler,Jr., V.G., 2016

Three Territory DWI Acute Infarcts: Diagnostic Value in Cancer-Associated Hypercoagulation Stroke (Trousseau Syndrome)
AJNR 37: Nov, Finelli, P.F. & Nouh, A., 2016

A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness
Neurol 86:e190-e194, McIntosh, P. & Karam, C., 2016

Definition and Diagnostic Criteria of Sleep-Related Hypermotor Epilepsy
Neurol 86:1834-1842, Tinuper, P.,et al, 2016

Clinopathologic Conference, Celiac Disease
NEJM 374:1875-1883, Case 14-2016, 2016

A Clinical Approach to Diagnosis of Autoimmune Encephalitis
Lancet Neurol 15:391-404, Graus, F.,et al, 2016

Zika Virus as a Cause of Neurologic Disorders
NEJM 374:1506-1509, Broutet, N.,et al, 2016

Outcomes Among Patients Discharged From the Emergency Department with a Diagnosis of Peripheral Vertigo
Ann Neurol 79:32-41, Atzema, C.L.,et al, 2016

The Effectiveness of Electronic Differential Diagnoses (DDX) Generators: A Systematic Review and Meta-Analysis
PLoS ONE 11:e0148991, Riches, N.,et al, 2016

Small Fiber Neuropathy in Fabry Disease:A Review of Pathophysiology and Treatment
JIEMS 4:1-5, Politeri,J.M.,et al, 2016

Emerging Cases of Powassan Virus Encephalitis in New England:Clinical Presentation, Imaging, and Review of the Literature
CID 62:707-713, Piantadosi,A.,et al, 2016

Tuberculoma of the Brain - A Diagnostic Dilemma: Magnetic Resonance Spectrosopy a New Ray of Hope
J Assoc Chest Physicians 3:3-8, Mukherjee,S.,et al, 2015

PCR Testing for the Diagnosis of Herpes Simplex Virus in Patients with Encephalitis or Meningitis
UpToDate, Dec, Caliendo, A.M., 2015

Deep Brain Stimulation of the Dentate Nucleus Improves Cerebellar Ataxia After Cerebellar Stroke
Neurol 85:2075-2076, Teixeira, M.J.,et al, 2015

A 48-year-old Man with Walking Difficulty
Neurol 85:e165-e169, Kalladka, D.,et al, 2015

A Young Woman with Blurred Vision and Distal Paresthesias
JAMA Neurol 72:1519-1523, Kung, N.H.,et al, 2015

Cerebral Fat Embolism
Stroke 46:e251-e253, Mijalski, C.,et al, 2015

Bells Palsy: Aetiology, Clinical Features and Multidisciplinary Care
JNNP 86:1356-1361, Eviston, T.J.,et al, 2015

Recognizing Autoimmune-Mediated Encephalitis in the Differential Diagnosis of Limbic Disorders
AJNR 36:2196-2205, da Rocha, A.J.,et al, 2015

Nigrosome 1 Detection at 3T MRI for the Diagnosis of Early-Stage Idiopathic Parkinson Disease: Assessment of DIagnostic Accuracy and Agreement on Imaging Asymmetry and Clinical Laterality
AJNR 36:2010-2016, Noh, Y.,et al, 2015

Reversible Cerebral Vasoconstriction Syndrome, Part 1: Epidemiology, Pathogenesis, and Clinical Course
AJNR 36:1392-1399, Miller, T.R.,et al, 2015

CIDP Diagnostic Pitfalls and Perception of Treatment Benefit
Neurol 85:498-504, Allen, J.A. & Lewis, R.A., 2015

Characyeristic features and progression of abnormalities on MRI for CARASIL
Neurol 85:459-463, Sekine, Y., etal, 2015

International Consensus Diagnostic Criteria for Neuromyelitis Optica Spectrum Disorders
Neurol 85:177-189, Wingerchuk, D.M.,et al, 2015

A 73-year-old Man with Diplopia and Ataxia
Neurol 85:e96-e100, Gupta, H.V.,et al, 2015

A Man in His 40s with Headache, Lethargy, and Altered Mental Status
JAMA Neurol 72:1061-1065, McKee, K.E.,et al, 2015

Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015

Non-Alzheimers Dementia 2 Lewy Body Dementias
Lancet 386:1683-1697, Walker, Z.,et al, 2015

Non-Alzheimers Dementia 3 Vascular Dementia
Lancet 386:1698-1706, OBrien, J.T. & Thomas, A., 2015

Autopsy Case of Severe Generalized Dystonia and Static Ataxia with Marked Cerebellar Atrophy
Neurol 85:1522-1524, Miyamoto, R.,et al, 2015

Brain Death Declaration
Neurol 84:1870-1879, Wahlster, S.,et al, 2015

Complications and Mortality in Hereditary Hemorrhagic Telangiectasia
Neurol 84:1886-1893, Donaldson, J.W.,et al, 2015

Clinicopathologic Conference, Invasive Neisseria Meningitidis Infection and Primary C8 Deficiency
NEJM 372:1454-1462, Case 11-2015, 2015

Significant Period Between Presentation and Diagnosis in Basilar Artery Occlusion
Stroke 46:e79-e81, Organek, N.,et al, 2015

Burning Hands and Feet
Neurol 84:e146-e152, Chan, A.C. & Wilder-Smith, E., 2015

Prevalence of Amyloid PET Positivity in Dementia Syndromes
JAMA 313:1939-1949,1913, Ossenkoppele, R.,et al, 2015

Identifying and Managing Common Childhood Language and Speech Impairments
BMJ 350:h2318, Reilly, S.,et al, 2015

Clinicopathologic Conference, CAT Scratch Disease (Encephalopathy Associated with Bartonella Henselae)
NEJM 372:2050-2058, Case 16-2015, 2015

Differential Diagnosis of Finger Drop
Neurologist 19:128-131, Varatharaj, A.,et al, 2015

Encephalitis of Unclear Origin Diagnosed by Brain Biopsy
JAMA Neurol 72:66-72, Gelfand, J.M.,et al, 2015

Differentiation Between Traumatic Tap and Aneurysmal Subarachnoid Hemorrhage: Prospective Cohort Study
BMJ 350:h568, Perry, J.J.,et al, 2015

Kleine-Levin Syndrome in 120 Patients: Differential Diagnosis and Long Episodes
Ann Neurol 77:529-540, Lavault, S.,et al, 2015

Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: An IOM Report on Redefining an Illness
JAMA 313:1101-1102, Clayton, E.W., 2015

Automated Differentiation between Epileptic and Nonepileptic Convulsive Seizures
Ann Neurol 77:348-351, Beniczky, S.,et al, 2015

Clinical Neurology: Why this Still Matters in the 21st Century
JNNP 86:229-233, Nicholl, D.J. & Appleton, J.P., 2015



Showing articles 800 to 850 of 6548 << Previous Next >>