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Differential
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abdominal distention
abducens nerve paralysis
acetazolamide
acute cerebellar ataxia
Addison's disease
adverse drug reaction
alcohol
Alexanders disease
Alexanders disease, adult onset
algorithm
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
amaurosis fugax
aminoacidopathies
aminoacidurias
amyloid angiopathy, cerebral
anemia
aneurysm
aneurysm, vertebral basilar system
angiitis
angiitis, granulomatous of CNS
angiography, cerebral, beaded vessels
angiography, cerebral
angiography, cerebral, negative
angiography, posterior fossa
angiography, vertebral artery
anomic aphasia
anorexia
anti IgLON5
anti MAG antibodies
antibodies to measles
antibodies to voltage-gated calcium channels
anxiety
aphasia
apnea
apraxia
areflexia
arteritides
arteritis, temporal
arthralgia
arthritis
astrogliopathy
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, truncal
ataxic gait
ATP1A3 gene
autoantibodies
autoimmune disease
autoimmune GFAP astrocytopathy
autonomic dysfunction
axonal injury
Babinski sign
bacterial infection
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior modification
behavior, combative
behavioral disorder
Behcet's syndrome
benign positional vertigo
bitemporal visual field defect
blindness
brain biopsy
brain biopsy, stereotaxic
brainstem, glioma
brainstem, infarction of
brainstem, lesion of
brucellosis
brucellosis, nervous system involvement with
bulbar palsy
calcification, intracranial
calcium antagonist
calcium channel dysfunction
carbamazepine
carcinoma
carpo-pedal spasm
CAT scan
CAT scan, abnormal
CAT scan, angiography
CAT scan, metrizamide
cataracts
celiac disease, adult
central core disease
central nervous system, infection of
central retinal artery occlusion
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar peduncle
cerebellar vermis
cerebral cortex
cerebral cortical atrophy
cerebral infarction
cerebrospinal fluid, abnormal
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, proteincytologic dissociation
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, young adult
channelopathy
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
chills
chloride channel dysfunction
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 19
Chvostek sign
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
collagen vascular disease
coma
coma, episodic
complications
concentration, impaired
confusion
conjunctivitis
conversion reaction
cornea, abnormal
cough
cranial nerve palsies
craniopharyngioma
cryopyrin-associated periodic syndrome
Cushing's syndrome
deafness
deafness, sudden
deafness, unilateral
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delirium
dementia
dementia, rapidly progressive
demyelinating disease
dentate nuclei, lesion of
depression
developmental retardation
diabetes insipidus
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diagnostic criteria
diarrhea
diet
differential diagnosis
digital subtraction angiography
diplopia
disability, neurological
diurnal variation
diving
dizziness
down-beat nystagmus
down-beat nystagmus, primary position of gaze
downward gaze, paralysis of
drowsiness
drug induced neurologic disorders
dysarthria
dysphagia
dystonia
dystonia, psychogenic
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electroencephalogram, triphasic delta waves
electromyogram
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, viral
encephalopathy
encephalopathy, acute
epidemiology of neurology
episodic disorders
episodic neurologic deficits
episodic unconsciousness
epistaxis
Epstein-Barr virus
exercise
exercise intolerance
exome sequencing
exophthalmus
eye movement, disorders of
face, numbness of
facial movement disorder
facial nerve palsy
facial weakness
faciobrachial dystonic seizure
failure to thrive
falling
familial
familial hemiplegic migraine
familial periodic ataxia
fasciculation
fatigue
fever
fever, recurrent
fine motor function, impaired
fingerprint bodies
Fisher's syndrome
fistula, perilymphatic
Friedreich's ataxia
frontal bossing
frontal lobe, pathologic signs of
fundus, abnormality of
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic neurologic disorders
genetic testing
GFAP gene
GFAP-IgG
glaucoma
gliadin antibodies
globus pallidus, lesion of, bilateral
glutamic acid decarboxylase, antibody
gluten sensitivity
gluten-free diet
gram positive rod
granular osmiphilic material
Guillain Barre syndrome
gynecomastia
hallucination
hallucination, auditory
hallucination, visual
Hand-Schuller-Christian disease
head circumference
head injury
head turning
head turning, neurologic complications with
headache
headache, bifrontal
headache, elderly
headache, episodic
headache, occipital
headache, recurrent
headache, severe
hearing loss
hemianopia
hemianopia, homonymous
hemimyoclonic jerks
hemiparesis
hemiplegia
hemosiderosis of CNS, superficial
hepatomegaly
hepatosplenomegaly
herpes virus
hiccoughs
hoarseness
hydrocephalus
hyperadrenalism
hypercalcemia
hyperinsulinism
hyperkalemia
hyperparathyroidism
hyperpigmentation of skin
hyperreflexia
hypersomnia
hypertension
hyperthyroidism
hypertrophic intracranial pachymeningitis
hypoglycorrhachia
hypokalemia
hypokalemic periodic paralysis
hyponatremia
hypoparathyroidism
hypophonia
hypothalamus
hypothalamus, disturbance of
hypotonia
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunomodulation
immunotherapy
impotence
inborn errors of metabolism
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
incoordination
infection
infectious mononucleosis
infectious mononucleosis, neurologic findings with
intellectual deficit
intellectual deterioration
intestinal biopsy
intracerebral hemorrhage
intracerebral hemorrhage, recurrent
intracerebral hemorrhage, young adult
intrinsic hand muscles, wasting of
iritis
irritability
islet cell tumor
Jakob-Creutzfeldt disease
jaw claudication
lactic acidemia
lateropulsion
leg numbness
leg weakness, bilateral
leptospirosis
lethargy
leucine rich glioma inactivated 1 antibodies
leukemia
leukocytosis
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
lightheaded
limbic encephalitis
lymphadenopathy
lysosomal storage disease
macrocephaly
malaise
malignant hyperpyrexia
maple syrup urine disease
mastoiditis
medulla oblongata, neoplasm of
memory, defect of recent
memory, impairment of
Meniere's disease
meningeal enhancement
meningitis
meningitis, aseptic
meningitis, bacterial
meningitis, carcinomatous
meningitis, elderly
meningitis, fungal
meningitis, Mollaret's
meningitis, recurrent
meningitis, TB
meningoencephalitis
meningoencephalomyelitis
mental status, abnormal
metabolic acidosis
metabolic disorder, primary
methotrexate
microcephaly
microhemorrhage, intracerebral
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, hemiplegic
mimics
misdiagnosis
molecular genetics
mononeuropathy
mononeuropathy multiplex
monoparesis
mortality
motor dysfunction
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
movement disorder, psychogenic
MRI
MRI pattern
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, curvilinear peppering enhancement
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, FLAIR
MRI, negative
MRI, nodular enhancement
multimodal neuroimaging
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, pain in
multiple sclerosis, paroxysmal symptoms in
muscle biopsy
muscle cramp
muscle pain
muscle weakness
muscle weakness, causes of
muscle weakness, proximal
myasthenia gravis
myasthenic syndrome
myelitis
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoedema
myokymia
myopathy
myotonia
myotonia congenita
myxedema coma
myxedema, neurologic manifestations of
nasal septum, perforation of
nausea and vomiting
negative
neoplasm, pituitary
neoplasm, primary of CNS
neoplasm, primary of CNS-metastasizing to subarachnoid space
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination, focal
neurologic signs
neurologic symptoms
neurologic symptoms, unexplained
neurologic testing
neuromyotonia
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, recurrent
neuropathy, sensory
neuropathy, vasculitic, systemic
neurotoxic
neurotoxicity, acute
night sweats
nystagmus
nystagmus, gaze-paretic
nystagmus, hereditary
nystagmus, intermittent
nystagmus, monocular
nystagmus, periodic
nystagmus, periodic alternating
nystagmus, primary position of gaze
nystagmus, vertical
ocular motility, disorders of
oculomasticatory myorhythmia
old age, neurology of
ophthalmoplegia
ophthalmoplegia, recurrent
ophthalmoplegia, total
optic ataxia
optic atrophy
optic atrophy, bilateral
optic neuritis
optic neuropathy, ischemic
oscillopsia
otitis, neurologic complications with
pain
pain, abdominal
pain, leg
pain, testicular
palatal myoclonus
palinopsia
papilledema
papillitis
paralysis
paralysis, acute areflexic
paramyotonia congenita
paranoia
paraparesis
paraplegia
parathyroid adenoma
paresthesias
Parkinson disease
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
paroxysmal tonic upgaze
PAS positive
PAS positive material in the brain
pathologic reflex
pathology
patient information and support
periarteritis nodosa
pericarditis
periodic paralysis
periodic paralysis, thyrotoxic
perivascular enhancement
perivascular inflammation
peroxisomal disease
Persistent postural-perceptual dizziness
personality change
personality disorder
pheochromocytoma
pleocytosis of cerebrospinal fluid
pleurisy
pneumonia
polymerase chain reaction
polyneuropathy
polyneuropathy, chronic relapsing
polyuria
pons, lesion of
posterior leukoencephalopathy syndrome
potassium
potassium channel antibodies
potassium channel dysfunction
precipitating factors
pregnancy, neurologic complications in
primary aldosteronism
primary episodic ataxia
prognosis
progressive neurologic disorder
psychiatric disorder
psychiatric problems in neurologic disorders
psychosis
psychosis, acute
ptosis
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, tonic
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriplegia, transient
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
recurrent
red eye
REM sleep behavior disorder
remote effect of cancer on the nervous system
respiratory tract infection
retinal artery occlusion
retinal detachment
retinopathy
reversible cerebral vasoconstrictive syndromes
review article
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rhinorrhea
Romberg's sign
rubeola virus
saccadic eye movements, abnormal
sarcoidosis
scleritis
scotoma
scuba diving
sedimentation rate, elevated
seizure
seizure, differential diagnosis of
seizure, focal
selective serotonin reuptake inhibitors
sensorineural hearing loss
serologic testing
serotonin norepinephrine reuptake inhibitors
short stature
sinusitis
skin, lesions in neurologic disorders
skull bone, thickening
sleep pathology and physiology
slow virus infection of CNS
slurred speech
sneeze
sodium channel dysfunction
sore throat
spinocerebellar ataxia
spinocerebellar ataxia type 6
spinocerebellar degeneration
spongy degeneration of brain
startle myoclonus
startle reaction
status epilepticus
steatorrhea
steroid responsive encephalopathy
steroid therapy, CNS treatment and complications with
storage disease of CNS
stress, emotional
strokelike episodes
stuttering
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage, cerebral convexity
superior cerebellar peduncle
supratentorial lymphocytic inflam parenchy perivasc enhanc responsive to steroids
swimming
symmetric brain lesions
syncope
systemic illness
tachycardia
tandem gait, ataxic
temporal lobe, lesion
temporal lobe, lesion, bilateral
testicular biopsy
tetany
thalamus, lesion of
third nerve palsy
thirst
thyrotoxicosis
tinnitus
tonic spasms
toxic encephalopathy
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
tremor, psychogenic
trigeminal neuralgia
trigeminal neuropathy
trigeminal neuropathy, sensory
trinucleotide repeats
Trousseau's sign
unconsciousness
unconsciousness, episodic
unconsciousness, transient
upgaze
upgaze, paralysis of
upgaze, sustained
urea-cycle enzymopathies
uremia
urinary incontinence
uveitis
vaccination, neurologic complications with
valsalva maneuver
vasculopathy
vasospasm, cerebral
vertebral artery
vertebral artery disease
vertebral artery occlusion
vertebral artery stenosis
vertebral-basilar insufficiency
vertigo
vertigo, episodic
vertigo, treatment of
violent behavior
viral infection
viral infection, CNS
Virchow-Robin spaces, dilated
vision, blurred
visual field defect
visual loss
visuospatial disturbance
vitamin E deficiency
vitreous opacities
vocalizations
Vogt-Koyanagi-Harada syndrome
walking, difficulty with
weakness
weakness, acute
weakness, episodic
weakness, generalized
weight loss
wheelchair
Whipple's disease
white matter disease
wide based gait
Showing articles 350 to 400 of 1892 << Previous Next >>

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

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017

Pure Sensory Ganglionopathy as the First Sign of Relapse in Non-Hodgkin Lymphoma
Neurol 88:1976-1977, Hossack, M. & McClean, J., 2017

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

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

CNS Posttransplant Lymphoproliferative Disorder
Neurol 89:e32-e37, Kesari, N.K.,et al, 2017

TIPIC Syndrome: Beyond the Myth of Carotidynia, a New Distinct Unclassified Entity
AJNR 38:1391-1398, Lecler, A.,et al, 2017

A Demure Teenager and Her Dystonic Foot
Neurol 89:e71-e75, Cullinane, P.W.,et al, 2017

Effect of Gluten-Free Diet on Cerebellar MR Spectroscopy in Gluten Ataxia
Neurol 89:705-709, Hadjivassiliou, M.,et al, 2017

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

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 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

Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
Front Neurol soi.10.3389/fneur.2017.00376,Aug, Zhou,C.,et al, 2017

Paraneoplastic Cerebellar Degeneration with Anti-Yo Antibodies - A Review
Ann Clin Trans Neurol 3:655-663, Venkatraman,A. & Opal,P., 2016

SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
Eur J Hum Genet 24:1016-1021, Choquet,K.,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

Clinicopathologic Conference, Aqueductal Stenosis with Hydrocephalus
NEJM 375:2583-2593, Case 40-2016, 2016

Clinicopathologic Conference, Oligdendroglioma II/IV with IDH1 R132H mutation and codelation of 1p and 19q
NEJM 375:2381-2389, Case 38-206, 2016

A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
JAMA Neurol 73:1494-1495, Hughes, A.J.C.,et al, 2016

Treatment of Neurosarcoidosis
Neurol 87:2517-2521, Bitoun, S.,et al, 2016

Cystic Lesions as a Rare Complication of Deep Brain Stimulation
Mov Disord Clin Pract 3:87-90, Sharma, V.D.,et al, 2016

Extensive Vasogenic Edema in Bickerstaff Brainstem Encephalitis
Neurol 86:e38-e39, Nerrant, E.,et al, 2016

A 57-year-old Man with Subacute Gait Difficulty and Hand Tremor
Neurol 87:e110-e113, Paliwal, V.K.,et al, 2016

Neurological Management of Von Hippel-Lindau Disease
Neurologist 21:73-78, Hodgson, T.S.,et al, 2016

Transient Deficits after Inadvertent Intrathecal Trigger-point Injection with Lidocaine
Neurol 87:848-849, Bereczki, D., et al, 2016

A 57-year-old Woman with Ataxia and Oscillopsia
Neurol 87:e61-e64, Bradshaw, M.J.,et al, 2016

An 87-year-old Man with Chronic Obstructive Pulmonary Disease and Acute Encephalopathy
Neurol 87:e135-e139, Spera, K.,et al, 2016

A 52-year-old Man with Diplopia and Ataxia
Neurol 87:e140-e143, Bradshaw, M.J.,et al, 2016

Recurrent Hemorrhage Risk and Mortality in Hereditary and Sporadic Cerebral Amyloid Angiopathy
Neurol 87:1482-1487, Van Etten, E.S.,et al, 2016

Anti-LGI1 Encephalitis
Neurol 87:1449-1456,1428, Van Sonderen, A.,et al, 2016

Long-Term Preclinical Magnetic Resonance Imaging Alterations in Sporadic Creutzfeldt-Jakob Disease
Ann Neurol 80:629-632, Zanusso, G.,et al, 2016

Emerging Risk Factors for Recurrent Vascular Events in Patients with Embolic Stroke of Unertermined Source
Stroke 47:2714-2721, Ueno, Y.,et al, 2016

A Young Man with Recurrent Coma and Refractory Status Epilepticus
JAMA Neurol 73:1243-1244, Sheikh, Z.,et al, 2016

Early Start of DOAC after Ischemic Stroke
Neurol 87:1856-1862,1652, Seiffge, D.J.,et al, 2016

Cortical Superficial Siderosis Predicts Early Recurrent Lobar Hemorrhage
Neurol 87:1863-1870,1854, Roongpiboonsopit, D.,et al, 2016

Rapidly Progressive Quadriplegia and Encephalopathy
JAMA Neurol 73:1363-1366, Wynn, D.,et al, 2016

A 64-year-old Man with Visual Distortions
Neurol 87:e252-e256, McGrath, E.R.,et al, 2016

A 34-Year-Old Man with Headache, Diploplia, and Hemiparesis
Neurol 86:e28, Lincoln, M.R.,et al, 2016

A 64-year-old Man with Progressive Paraspinal Muscle Weakness
Neurol 86:e4-e9, Schneider, R.,et al, 2016

A Red Eye from Carotid Stenosis
BMJ 352:e364, Perera, S.,et al, 2016

Orthostatic Tremor
Neurol 86:458-464, Hassan, A.,et al, 2016

Leukodystrophy and Progressive Myoclonic Epilepsy Disclosing DRPLA
Neurol 86:e58-e59, Sgobbi de Souza, P.V.,et al, 2016

A 62-Year-Old Woman with Bizarre Behavior and Recurrent Episodes of Behavioral Arrest
Neurol 86:e62-e65, Briglia, H.,et al, 2016

Safety of Pregnancy After Cerebral Venous Thrombosis
Stroke 47:713-718, Aguiar de Sousa, D.,et al, 2016

Acute Bulbar Palsy as a Variant of Guillain-Barre Syndrome
Neurol 86:742-747, Kim, J.K.,et al, 2016



Showing articles 350 to 400 of 1892 << Previous Next >>