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Differential
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abdominal cramps
abdominal reflex, absent
acute disseminated encephalomyelitis
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
ageusia
akinetic mute
alcohol
Alexanders disease
Alexanders disease, adult onset
aminoacidopathies
aminoacidurias
amnestic syndrome
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, prognosis
anatomy of
angiitis
angiitis, granulomatous of CNS
angiitis, isolated of CNS
angina pectoris
anhidrosis
anosmia
anti MAG antibodies
antispasticity drugs
aphasia
arteriopathy
asterixis
asymptomatic
ataxia
ataxia, cerebellar
ataxic gait
attention deficit disorder with hyperactivity
autonomic dysfunction
Babinski sign
baclofen
basal ganglia, infarction
basal ganglia, lesion of
behavioral disorder
benign essential tremor
beta adrenergic blocker
bladder dysfunction
blink reflex
bone marrow transplantation
brain biopsy
brainstem
brainstem, infarction of
brainstem, lesion of
burning paresthesia
calcification, intracranial
Canavan's disease
CAT scan
CAT scan, abnormal
CAT scan, demyelinating disease
CAT scan, serial
catecholamine
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral infarction
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral ischemia
cerebral palsy
cerebral venous infarction
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, immunoglobulins of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, multiple
cerebrovascular accident, nonvascular territory
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease, cardiovascular disease with
Charcot-Marie-Tooth
children
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
cognition
congenital malformation
congestive heart failure
corneal dystrophy
cortical blindness
cortical blindness, transient
crying, pathologic
cyst, porencephalic
cystinuria
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, cerebrovascular disease causing
dementia, presenile
dementia, subcortical
dementia, thalamic
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
depression
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
dilantin
diplopia
disability, neurological
dopamine
drug induced neurologic disorders
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dysphagia
dystonia
dystonia musculorum deformens
echocardiogram
echolalia
electrical sensation
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electron microscopy
ELISA
emotional lability
encephalitis
encephalitis, viral
encephalomalacia
encephalopathy
encephalopathy, metabolic
enzyme, defect
evoked potentials
exercise intolerance
eye, pain in
Fabry's disease
facial nerve palsy
facial weakness
facial weakness, bilateral
Fahr disease
familial
fatigue
fever
flexor spasm
gadolinium
gait disorder
gamma amino butyric acid
gamma amino butyric acid-mimetic drug
gamma knife therapy
gangliosidosis GM2
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gilles de la Tourette syndrome
glioma
glutaric acidemia
granular osmiphilic material
haloperidol
head injury
head nodding
headache
hearing loss
hearing loss, bilateral
heavy metal intoxication
hemianopia
hemianopia, transient
hemiparesis
hemiparesis, transient
hemiplegia
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatolenticular degeneration(Wilson's disease)
hiccoughs
HLA
holoprosencephaly
homovanillic acid
hormone replacement
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
hydrocephalus
hyperreflexia
hypersomnia
hypertension
hyperthyroidism
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
incoordination
intellectual deficit
intellectual deterioration
interferon
interferon beta 1-a
interferon beta 1-b
intrathecal antispasticity drugs
iron, brain
Japan
Krabbe's disease
lactic acidemia
lacunar infarction
laughing, pathologic
L-dopa
Leber's hereditary optic neuropathy
Leigh's disease
Leigh's disease, adult variety
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
level of consciousness, decreased
Lhermitte's sign
lipid storage disorder of CNS
liver disease
Lorenzo's oil
low birth weight
magnetic susceptibility
malformation, CNS, congenital
maple syrup urine disease
MELAS syndrome
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
metronidazole
microhemorrhage, intracerebral
migraine
misdiagnosis
mitochondrial disease
monoamines
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, complications with
MRI, contrast enhanced
MRI, demyelinating disease
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, negative
MRI, paramagnetic effect
MRI, serial
MRI, spinal cord
MRI, T1 weighted high signal foci
MRI, volumetry
multiple sclerosis
multiple sclerosis, asymptomatic
multiple sclerosis, chronic progressive
multiple sclerosis, clinical patterns
multiple sclerosis, conjugal
multiple sclerosis, diagnosis of
multiple sclerosis, differential diagnosis of
multiple sclerosis, etiology of
multiple sclerosis, familial
multiple sclerosis, linoleic acid in
multiple sclerosis, misdiagnosis
multiple sclerosis, parental transmission
multiple sclerosis, pathogenesis
multiple sclerosis, prognosis
multiple sclerosis, risk factors for
multiple sclerosis, spinal form
multiple sclerosis, treatment of
muscle biopsy
myelin basic protein gene
myelinolysis, extrapontine
myelitis
myelitis, longitudinal
myelitis, transverse
myelomalacia
myelopathy
myelopathy, chronic progressive
myocardial infarction
myoclonus
mysoline
nausea and vomiting
neurochemistry
neurogenic bladder
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neuromyelitis optica (Devic's disease)
neuromyelitis optica spectrum disorder
neuromyelitis optica, IgG
neuropathology
neuropathy
neuropathy, peripheral
neurotransmitter
norepinephrine
Notch3 gene
nystagmus
obsessive-compulsive disorder
occipital lobe, infarction
occipital lobe, lesion of
old age, neurology of
optic atrophy
optic atrophy, bilateral
optic atrophy, hereditary
optic nerve, hypoplasia of
optic neuritis
optic neuritis, bilateral
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, hereditary
palatal myoclonus
palilalia
paraparesis
paraparesis, spastic
paraparesis, spastic, tropical
paraplegia
paratrigeminal syndrome
paresthesias
Parkinson disease
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
PAS positive
PAS positive material in the brain
Pelizaeus Merzbacher
periventricular leukomalacia
phenylketonuria
phenylketonuria, adult onset
pimozide
pleocytosis of cerebrospinal fluid
poison, neurologic problems with
polymerase chain reaction
pons, lesion of
posterior cerebral artery territory infarction
posterior leukoencephalopathy syndrome
premature infant
prevention of neurologic disorders
primary lateral sclerosis
prognosis
propranolol
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
pyramidal tract dysfunction
quadriparesis
quadriplegia
quality of life
radiation therapy, stereotactic
ragged-red fibers
Red flags
regional enteritis
renal stones
retrovirus
reversible neurologic disorder
review article
rigidity
Riley-Day syndrome
risk factors
Rosenthal fibers
Sandhoff's disease
Schilder's disease
scotoma
scotoma, central
seizure
seizure, children
seizure, neonatal
sensorineural hearing loss
sick sinus syndrome
skin, biopsy
skin, lesions in neurologic disorders
smell
spasticity
spasticity, treatment of
speech disorder
speech, loss of
spinal cord
spinal cord, injury of
spinal cord, injury, management of
spinal cord, lesion of
spontaneous remission
steroid therapy, CNS treatment and complications with
stimulation, deep brain
symmetric brain lesions
systemic lupus erythematosus
tardive dyskinesia
taste
Tay-Sachs disease
temporal lobe, lesion, bilateral
thalamic tumors
thalamic tumors, bilateral
thalamotomy
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine deficiency
thyrotoxicosis
tic
tinnitus
tongue, impaired movements of
top of the basilar syndrome
torticollis
transient ischemic attack
transient ischemic attack, recurrent
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, classification
tremor, differential diagnosis of
tremor, intention
tremor, jaw
tremor, leg
tremor, rubral
tremor, surgical treatment of
tremor, thalamic stimulation for suppression of
tremor, treatment of
twins
ulcerative colitis
uremia
urinary frequency
urinary incontinence
urinary urgency
vasculitides
vasculopathy
vasospasm, cerebral
vertigo
vertigo, episodic
very long chain fatty acids
viral infection
viral infection, CNS
vision loss, sequential
visual acuity, decreased
visual evoked response
visual loss
visual loss, progressive
visual loss, sudden
visual loss, transient
walking, difficulty with
water channel antibodies
weakness
Wernicke's encephalopathy
white matter disease
workup
Showing articles 450 to 500 of 5423 << Previous Next >>

Effect of Glatiramer Acetate on Conversion to Clinically Definite Multiple Sclerosis in Patients with Clinically Isolated Syndrome (PreCISe study): A Randomised, Double-Blind, Placebo-Controlled Trial
Lancet 374:1503-1511, 1475, Martinelli,G.,et al, 2009

Acute Limbic Encephalitis and Glutamic Acid Decarboxylase Antibodies:A Reality?
J Neurosci 287:69-71, Blanc,F.,et al, 2009

Voltage-gated Potassium Channel-associated Limbic Encepahlitis in the West of Scotland:Case Reports and Literature Review
Scott Med J 54:27-31, Reid,J.M.,et al, 2009

Reversible Cerebral Vasoconstriction Syndrome
Pract Neurol 9:256-267, Ducros,A. &Bousser,M.-G., 2009

Fully-Automated Quantification of Regional Brain Volumes for Improved Detection of Focal Atrophy in Alzheimers Disease
AJNR 30:578-580, Brewer, J.B.,et al, 2009

Oral Fingolimod (FTY720) in Multiple Sclerosis: Two-Year Results of a Phase II Extension Study
Neurol 72:73-79, OConnor,P.,et al, 2009

Relapse Management in Multiple Sclerosis
The Neurologist 15:1-5, Thrower,B.W., 2009

Human Natural Autoantibodies in the Treatment of Neurologic Disease
Neurol 72:1269-1276, Rodriguez,M.,et al, 2009

Cortical Lesions in Primary Progressive Multiple Sclerosis: A 2-Year Longitudinal MR Study
Neurol 72:1330-1336, Calabrese,M.,et al, 2009

Association Between Clinical Conversion to Multiple Sclerosis in Radiologically Isolated Syndrome and Magnetic Resonance Imaging, Cerebrospinal Fluid, and Visual Evoked Potential: Follow-Up of 70 Patients
Arch Neurol 66:841-846, Lebrun,C.,et al, 2009

Cyclophosphamide Therapy in Pediatric Multiple Sclerosis
Neurol 72:2076-2082,2064, Makhani,N.,et al, 2009

Efficacy of Treatment of MS with IFN B-1b or Glatiramer Acetate by Monthly Brain MRI in the BECOME Study
Neurol 72:1976-1983,1972, Cadavid,D.,et al, 2009

Exclusive Breastfeeding and the Risk of Postpartum Relapses in Women with Multiple Sclerosis
Arch Neurol 66:958-963, Langer-Gould,A.,et al, 2009

Smoking Is Associated with Increased Lesion Volumes and Brain Atrophy in Multiple Sclerosis
Neurol 73:504-510, Zivadinov,R.,et al, 2009

Primary Central Nervous System Lymphoma in a Patient Treated with Natalizumab
Ann Neurol 66:403-406, 261, 262, Schweikert,A.,et al, 2009

Natalizumab: A Double-Edged Sword?
Ann Neurol 66:262-263, DeAngelis,L., 2009

Real-Life Impact of Early Interferon� Therapy in Relapsing Multiple Sclerosis
Ann Neurol 66:513-520, Trojano,M.,et al, 2009

A 52-Year-Old Woman With Disabling Peripheral Neuropathy: Review of Diabetic Polyneuropathy
JAMA 302:1451-1458, Rutkove,S., 2009

Moderate Hypothermia to Treat Perinatal Asphyxial Encephalopathy
NEJM 361:1349-1358, Azzopardi,D.,et al, 2009

The Present Efficacy of Multiple Sclerosis Therapeutics
Neurol 73:984-990, Klawiter,E.,et al, 2009

Severe Cardiac Failure in a Patient with Multiple Sclerosis Following Low-Dose Mitoxantrone Treatment
Neurol 73:991-993, D�rr,J.,et al, 2009

Nineteen Episodes of Recurrent Myelitis in a Woman with Neuromyelitis Optica and Systemic Lupus Erythematosus
Arch Neurol 66:1160-1163, Nasir, S.,et al, 2009

Treatment of Neuromyelitis Optica with Mycophenolate Mofetil
Arch Neurol 66:1128-1133, Jacob,A.,et al, 2009

Multiple Sclerosis with Predominant, Severe Cognitive Impairment
Arch Neurol 66:1139-1143, Staff,N.,et al, 2009

Progressive Multifocal Leukoencephalopathy After Natalizumab Monotherapy
NEJM 361:1081-1087, Linda,H.,et al, 2009

Asymptomatic Reactivation of JC Virus in Patients Treated with Natalizumab
NEJM 361:1067-1074, Chen,Y.,et al, 2009

Treatment of Progressive Multifocal Leukoencephalopathy Associated with Natalizumab
NEJM 361:1075-1080, Wenning,W.,et al, 2009

Reemergence of PML in Natalizumab-Treated Patients--New Cases, Same Concerns
NEJM 361:1041-1043, Major,E., 2009

Immunologic, Clinical, and Radiologic Status 14 Months After Cessation of Natalizumab Therapy
Neurol 72:396-401,392, Stuve,O.,et al, 2009

Early MRI in Optic Neuritis: The Risk for Disability
Neurol 72:542-550, Swanton,.K.,et al, 2009

Neuromyelitis Optica and Concentric Rings of Bal� in the Brainstem
Arch Neurol 66:274-275, Graber,J.J.,et al, 2009

Incidental MRI Anomalies Suggestive of Multiple Sclerosis: The Radiologically Isolated Syndrome
Neurol 72:800-805,780, Okuda,D.T.,et al, 2009

Posterior Reversible Encephalopathy Syndrome in Neuromyelitis Optica Spectrum Disorders
Neurol 72:712-717, Maga�a,S.M.,et al, 2009

Pediatric Optic Neuritis: Brain MRI Abnormalities and Risk of Multiple Sclerosis
Neurol 72:881-885, Bonhomme,G.R.,et al, 2009

Hepatitis B Vaccine and the Risk of CNS Inflammatory Demyelination in Childhood
Neurol 72:873-880,870, Mikaeloff,Y.,et al, 2009

Neurosarcoidosis: A Study of 30 New Cases
JNNP 80:297-304, Joseph,F.G. &Scolding,N.J., 2009

Sustained-Release Oral Fampridine in Multiple Sclerosis: A Randomised, Double-Blind, Controlled Trial
Lancet 373:732-738, Goodman,A.D.,et al, 2009

NMO-IgG Detected in CSF in Seronegative Neuromyelitis Optica
Neurol 72:1101-1003, Klawiter,E.C.,et al, 2009

MRI in the Diagnosis of Pediatric Multiple Sclerosis
Neurol 72:961-967, Callen,D.J.A.,et al, 2009

Multiple Sclerosis Therapeutics: Unexpected Outcomes Clouding Undisputed Successes
Neurol 72:1008-1015, Wiendl,H. &Hohlfeld,R., 2009

Opportunistic Infections and Other Risks with Newer Multiple Sclerosis Therapies
Ann Neurol 65:367-377, Berger,J.R. &Houff,S., 2009

Memantine Induces Reversible Neurologic Impairment in Patients with MS
Neurol 72:1630-1633, Villoslada,P.,et al, 2009

MRI Features of Benign Multiple Sclerosis: Toward a New Definition of This Disease Phenotype
Neurol 72:1693-1701, Rovaris,M.,et al, 2009

A Single, Early Magnetic Resonance Imaging Study in the Diagnosis of Multiple Sclerosis
Arch Neurol 66:587-592, Rovira,A.,et al, 2009

Diffusely Abnormal White Matter in Chronic Multiple Sclerosis: Imaging and Histopathologic Analysis
Arch Neurol 66:601-609, Seewann,A.,et al, 2009

Progressive Multifocal Leukoencephalopathy and Relapsing-Remitting Multiple Sclerosis: A Comparative Study
Arch Neurol 66:593-599, Boster,A.,et al, 2009

"Cloud-like Enhancement" Is a Magnetic Resonance Imaging Abnormality Specific to Neuromyelitis Optica
Ann Neuro l 66:425-428, Ito, S.,et al, 2009

Tumefactive Demyelination: An Approach to Diagnosis and Management
JNNP 84:1047-1053, Hardy, T.A. & Chataway, J., 2009

The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
Eur J Neurol 16:513-516, Lee, Y.-C.,et al, 2009

Sporadic Adult-Onset Leukoencephalopathy with Neuroaxonal Spheroids Mimicking Cerebral MS
Neurol 70:1128-1133, Keegan,B.M.,et al, 2008



Showing articles 450 to 500 of 5423 << Previous Next >>