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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

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

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

degenerative diseases of CNS

dementia

dementia, cerebrovascular disease causing

dementia, presenile

dementia, subcortical

dementia, thalamic

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

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

encephalopathy, metabolic

facial weakness, bilateral

gamma amino butyric acid

gamma amino butyric acid-mimetic drug

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gilles de la Tourette syndrome

glioma

glutaric acidemia

granular osmiphilic material

hearing loss, bilateral

heavy metal intoxication

hemianopia

hemianopia, transient

hemiparesis

hemiparesis, transient

hemiplegia

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatolenticular degeneration(Wilson's disease)

human immunodeficiency virus type 1

human T-lymphotropic virus type I(HTLV-I)

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance

incoordination

intellectual deficit

intellectual deterioration

interferon

interferon beta 1-a

interferon beta 1-b

intrathecal antispasticity drugs

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

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

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

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

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

psychiatric problems in neurologic disorders

pyramidal tract dysfunction

quadriparesis

quadriplegia

quality of life

radiation therapy, stereotactic

reversible neurologic disorder

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

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, surgical treatment of

tremor, thalamic stimulation for suppression of

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 200 to 250 of 5423 << Previous Next >>

Natalizumab-Associated PML
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Long-Term Outcomes after Autologous Hematopoietic Stem Cell Transplantation for Multiple Sclerosis
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High Hypothetical Interest in Physician-Assisted Death in Multiple Sclerosis
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Clinical Presentation and Prognosis in MOG-antibody Disease: A UK Study
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Ocrelizumab versus Interferon Beta-1a in Relapsing Multiple Sclerosis
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Ocrelizumab versus Placebo in Primary Progressive Multiple Sclerosis
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Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man
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Transient Smartphone Blindness: Relevance to Misdiagnosis in Neurologic Practice
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Myasthenia Gravis
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Long-Term Treatment of Epilepsy with Everolimus in Tuberous Sclerosis
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Acute Cholecystitis During Treatment with Alemtuzumab in 3 Patients with RRMS
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The Contemporary Spectrum of Multiple Sclerosis Misdiagnosis
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Superior MRI Outcomes with Alemtuzumab Compared with Subcutaneous Interferon �-1a in MS
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Rebound Syndrome in Patients with Multiple Sclerosis after Cessation of Fingolimod Treatment
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Incidence of Radiologically Isolated Syndrome: A Population-Based Study
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Neuromyelitis Optica: Evaluation of 871 Attacks and 1,153 Treatment Courses
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Discriminating Long Myelitis of Neuromyelitis Optica from Sarcoidosis
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Acute Disseminated Encephalomyelitis in 228 Patients
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Malignancies after Mitoxantrone for Multiple Sclerosis
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Fulminant Central Nervous System Nocardiosis in a Patient Treated with Alemtuzumab for Relapsing-Remitting Multiple Sclerosis
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A 34-Year-Old Man with Headache, Diploplia, and Hemiparesis
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Magnetic Resonance Imaging of Cerebral Aspergillosis: Imaging and Pathological Correlations
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Persistent Hyperthermia in a Patient with Aquaporin-4-Antibody-Positive Neuromyelitis Optica Spectrum Disorder
J Clin Neurol 12:515-516, Hsu,C-L.,et al, 2016

Very Late-Onset Neuromyelitis Optica Spectrum Disorder Beyond the Age of 75
J Neurol 262:1379-1384, Krumbholz, M.,et al, 2015

MRI Characteristics of Neuromyelitis Optica Spectrum Disorder
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Marburgs Variant of Multiple Sclerosis with Extensive Brain Lesions
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Molybdenum Cofactor Deficiency
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Cardiovascular Dysfunction in Multiple Sclerosis
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Responsibilities of Health Care PRofessionals in Counseling and Educating Patients with Incurable Neurological Diseases Regarding "Stem Cell Tourism"
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Reactivation of Herpesvirus under Fingolimod: A Case of Severe Herpes Simplex Encephalitis
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International Consensus Diagnostic Criteria for Neuromyelitis Optica Spectrum Disorders
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Neurological Manifestations of Scrub Typhus
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Outcome Following Decompressive Hemicraniectomy for Malignant Cerebral Infarction
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Oral Versus Intravenous High-Dose Methylprednisolone for Treatment of Relapses in Patients with Multiple Sclerosis (COPOUSEP):A Randomised, Controlled, Double-Blind,Non-Inferiority Trial
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Treatment Outcomes with Rituximab in 100 Patients with Neuromyelitis Optica
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Daclizumab HYP versus Interferon Beta-1a in Relapsing Multiple Sclerosis
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Isolated Lingual Dyskinesia in Multiple Sclerosis
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Cryptococcal Meningoencephalitis in a Patient with Multiple Sclerosis Treated with Fingolimod
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Outcome after Resuscitation Beyond 30 Minutes in Drowned Children with Cardiac Arrest and Hypothermia: Dutch Nationwide Retrospective Cohort Study
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Acute Idiopathic Transverse Myelitis in Children
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Varicella-Zoster Virus Infections in Patients Treated with Fingolimod
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Short Myelitis Lesions in Aquaporin-4-IgG-Positive Neuromyelitis Optica Spectrum Disorders
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Investigation of Leptomeningeal Enhancement in MS
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Characteristics of Lumbar Disc Herniation with Exacerbation of Presentation Due to Spinal Manipulative Therapy
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Relapse in Multiple Sclerosis
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Stent-Retriever Thrombectomy after Intravenous t-PA vs. t-PA Alone in Stroke
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Thrombectomy within 8 Hours after Symptom Onset in Ischemic Stroke
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Showing articles 200 to 250 of 5423 << Previous Next >>