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Differential
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abdominal contractions

acrocyanosis

acute disseminated encephalomyelitis

Addison's disease

advances in neurology

adverse drug reaction

affect, flat

agitation

agnosia, visual

Aicardi-Goutieres syndrome

algorithm

alien hand syndrome

altered states of consciousness

alternating hemiplegia

alternating rapid movement

aluminum

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

ammonia

AMPA receptor antibodies

amyloid angiopathy, cerebral

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral, beaded vessels

angiography, cerebral

antibiotics, neurologic complications with

antibodies to measles

apraxia of eye movements

apraxia, constructional

apraxia, speech

aqueduct of Sylvius, stenosis

auditory evoked brainstem potentials

autoantibodies

autoimmune basal ganglia encephalitis

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavior, combative

behavioral disorder

behavioral disorder, acute

Borrelia miyamotoi infection

brain biopsy, false negative

brain purpura

brain scan

brainstem, atrophy

brainstem, infarction of

brainstem, lesion of

Brueghel's syndrome

burning feet

burning feet, differential diagnosis of

cachexia

CAG repeats

calcification, intracranial

carbon monoxide poisoning

carcinoma

cardiac arrest

cardiac arrest and resuscitation

CAT scan, emission, abnormal

CAT scan, false negative

cataracts

catatonia

caudate nucleus, lesion of, bilateral

celiac disease, adult

central nervous system, infection of

central pontine myelinolysis

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar plaques, amyloid

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral infarction

cerebral ischemia

cerebral vasculature

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure increased

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, complications with

cerebrovascular accident, multiple

cerebrovascular accident, young adult

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest pain

chest x-ray, abnormal

chilbran skin lesions

children

chorea

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cingulate gyrus

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

cortical-basal ganglionic degeneration

cough

cranial nerve enhancement

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

Creutzfeldt-Jakob disease, genetic

crying, pathologic

cytomegalic inclusion disease

cytomegalovirus infection

deep gray nuclei

degenerative diseases of CNS

dementia, rapidly progressive

dementia, transmissible

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental milestones, loss of

developmental retardation

differential diagnosis

diplopia

disorientation

downward deviation of eyes

downward gaze, paralysis of

DPPX, antibodies, encephalitis

dysequilibrium syndrome

dyskinesia

dyskinesia, buccal lingual facial

dystonia, delayed onset

dystonia, focal

echolalia

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

electromyogram

embolism, paradoxical

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, diagnosis of

encephalitis, etiology

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalitis, unknown etiology

encephalitis, viral

encephalitis, viral-causes of

encephalomyelitis

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, acute

encephalopathy, anoxic

encephalopathy, delayed

encephalopathy, metabolic

encephalopathy, parainfectious

encephalopathy, post anoxic

encephalopathy, progressive

enolase

enteritis

epidemiology of neurology

epilepsia partialis continua

extralimbic encephalitis

extrapyramidal

eye movement, disorders of

eye movement, painful

eye, pain in

facial nerve palsy

facial pain

faciobrachial dystonic seizure

fine motor function, impaired

frontal lobe, anatomy and physiology

frontal lobe, pathologic signs of

fungal infection, CNS

F-wave response

gait disorder

gait, apraxic

gamma amino butyric acid receptor antibody

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

granular osmiphilic material

hallucination, olfactory

hallucination, visual

headache, sudden onset of

headache, throbbing

headache, vascular

hearing loss

hearing loss, bilateral

hearing loss, sudden, bilateral

heart block

hemianopia, homonymous

hemiballismus

hemichorea

hemiparesis

hemiparesis, transient

hemiplegia

hemolytic-uremic syndrome

hepatomegaly

heralding manifestation

herpes simplex encephalitis

herpes simplex virus

herpes virus

HHH syndrome

human immunodeficiency virus type 1

Huntington's chorea

hydrocephalus

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hyperactivity

hyperammonemic encephalopathy

hyperekplexia

hyperkalemia

hypernatremia

hyperpyrexia, CNS disorder causing

hyperreflexia

hypersomnia

hypertension

hypertensive encephalopathy

hypotension, systemic

hypothermia

hypotonia

hypoxia, newborn

hypoxic encephalopathy

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incontinence, fecal

infection

infectious mononucleosis

infectious mononucleosis, neurologic findings with

inferior olivary nucleus

influenza

insomnia

insular cortex

insular cortex, lesion

intellectual deficit

intellectual deterioration

interferon alpha

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial pressure, increased

intrauterine

introverted

irritability

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, young adult

jaw pain

Kearns-Sayre syndrome

lactic acidemia

laminar necrosis, cortical

language disorder in adults

lateropulsion

laughing, pathologic

L-dopa

Leber's hereditary optic neuropathy

left handedness

Leigh's disease

lethargy

leucine rich glioma inactivated 1 antibodies

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

level of consciousness, differential diagnosis in

levitation

Lewy body

Lewy body disease, diffuse

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, neutrophilic

meningitis, syphilitic

meningitis, TB

meningitis, treatment of

meningoencephalitis

mental retardation

mental status, abnormal

mental status, abnormal, acute

MERRF syndrome

mesial temporal lobe

microangiopathic hemolytic anemia

microcephaly

micrographia

microinfarcts

midbrain, infarction of

migraine

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoclonal antibodies

movement disorder, delayed onset

movement disorder, extrapyramidal

movement disorder, treatment of

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, FLAIR

MRI, high signal intensity of basal ganglia

MRI, negative

MRI, sulcal hyperintensity

MRI, susceptibility weighted

multinucleated giant cell

multiple sclerosis

multiple system atrophy

muscle weakness, proximal

mutism

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

mycoplasma

mycoplasma pneumoniae

myelination of nervous system

myelitis, transverse, recurrent

myoclonus, differential diagnosis of

myoclonus, epilepsy

myoclonus, segmental

myoclonus, stimulus sensitive

myoclonus-ataxia syndrome

myopathy

myopathy, mitochondrial

nausea and vomiting

neck stiffness

negative

neoplasm, intracranial, congenital

neoplasm, intracranial, infants

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve conduction studies

neurexin-3 alpha antibodies

neuroendocrinology

neurologic complications

neurologic complications of, chronic pulmonary disease

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, multifocal

neurologic signs

neurologic symptoms

neuron specific enolase

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

occupational neurologic disorders

ocular bobbing

ocular bobbing, atypical

ocular bobbing, monocular

ocular motility, disorders of

ocular myoclonus

ocular myorhythmia

olivary degeneration, hypertrophic

ophthalmoplegia

opportunistic infection

opsoclonus

opsoclonus-myoclonus syndrome

optic atrophy

optic neuropathy

ornithine transcarbamylase deficiency

orthostatic hypotension

Parkinson disease, misdiagnosis

Parkinsonism syndrome

PAS positive

PAS positive material in the brain

persistent vegetative state

pigmentary retinopathy

piracetam

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pleurisy

pneumoencephalogram(PEG)

pneumonia

poliomyelitis-like illness

polymerase chain reaction

polyneuropathy

polyneuropathy, uremic

pons, lesion of

pontocerebellar atrophy

posterior inferior cerebellar artery syndrome

posterior leukoencephalopathy syndrome

precipitating factors

prenatal

primitive neuroectodermal tumors

prion disease

prognosis

progressive ataxia and palatal tremor

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

protein 14-3-3, cerebrospinal fluid

protein 14-3-3, cerebrospinal fluid, false negative

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary infiltrates

pyramidal tract dysfunction

quadriparesis

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

recurrent

release phenomena

remote effect of cancer on the nervous system

renal failure

renal transplantation

respiratory failure

restless leg syndrome

reticulum cell sarcoma

sedimentation rate, elevated

seizure

seizure, children

seizure, drug resistance

seizure, focal

sensorineural hearing loss

sensory loss

sensory loss, cortical

serologic testing

serologic testing, false negative

Shiga toxin

short stature

skin, lesions in neurologic disorders

slow virus infection of CNS

slurred speech

snout reflex

sodium valproate

somatosensory evoked potentials

somnolence

sonophobia

speech disorder

speech disorder, childhood

speech, unintelligible

spinal cord, injury of

spinal cord, lesion of

spinocerebellar ataxia

spirochete infection

spongy degeneration of brain

squirrels

staphylococcal protein A column therapy

status epilepticus, intractable

steroid therapy, CNS treatment and complications with

stimulant drugs

storage disease of CNS

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

stuporous

stuttering

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

subdural hematoma

suicide

symmetric brain lesions

systemic illness

tandem gait, ataxic

tauopathy

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

thrombotic microangiopathy

thymoma

tonic cerebellar fits

toxoplasmosis, acquired

toxoplasmosis, CNS

transient neurologic deficit

treatment of neurologic disorder

urea-cycle enzymopathies

uremia

uremic encephalopathy

uremic twitching

urinary incontinence

uveitis

varicella zoster virus

vasculitides

vasculopathy

ventricular enlargement

vision, blurred, monocular

visual acuity, decreased

visual field defect

visual fields, constricted

visual impairment

visual loss

visuospatial disturbance

vitreous opacities

walking, difficulty with

weakness

weakness, acute

weakness, focal

weakness, generalized

weight loss

Wernicke's encephalopathy

wheelchair

Whipple's disease

white matter disease

white matter disease, periventricular

white matter disease, subcortical

wide based gait

word-finding difficulty

workup

wrist drop

zoster sine herpete

Showing articles 50 to 100 of 8109 << Previous Next >>

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Cortical Myoclonus in Huntington's Disease
Movement Disorders 9:633-641, Thompson,P.D.,et al, 1994

Clinicopath Conf
Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) , with Amyloid (KURU) Plaques, Case 17-1993, N, JM 328:66,1993., 1993

Stimulus-Sensitive Myoclonus in Akinetic-Rigid Syndromes
Brain 115:1875-1888, Chen,R.,et al, 1992

Creutzfeldt-Jakob Disease and Other Transmissible Spongiform Encephalopathies
Ed, F. O. Bastian, Mosby Year Book, St. Louis 9:153, Maertens,P.&Quindlen,E.A., 1991

Cortical-Basal Ganglionic Degeneration
Neurol 40:1203-1212, Riley,D.E.,et al, 1990

MRI Demonstration of Cortical Laminar Necrosis and Delyaed White Matter Injury in Anoxic Encephalopathy
Neuroradiology 32:319-321, Sawada,H.,et al, 1990

Diffuse Lewy Body Disease and Progressive Dementia
Neurol 38:1520-1528, Burkhardt,C.R.,et al, 1988

Photic Cortical Reflex Myoclonus
Ann Neurol 22:252-257, Shibasaki,H.&Neshige,R., 1987

Segmental Myoclonus Clinical and Pharmacologic Study
Arch Neurol 43:1025-1031, Jankovic,J.&Pardo,R., 1986

Brainstem Auditory Evoked Potentials in 20 Patients with Palatal Myoclonus
Arch Neurol 40:155-158, Westmoreland,B.F.,et al, 1983

Clinical Pathologic Conference, Creutzfeldt-Jakob Disease, (Case record 43-1977)
NEJM 297:930, Scully,R.E.,et al, 1977

Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients
Medicine 55:467, Knox,D.L.,et al, 1976

Neurologic Disorders in Renal Failure (1st of Two Parts)
NEJM 294:143, Raskin,N.H.,et al, 1976

Case Records of MGH
NEJM 29l:l4l, 1974; 29l:263, 1974 Subscute Sclerosing Panencephalitis., , 1974

Case Records of MGH-NEJM 285:621
1971., , 1971

Clinical Spectrum of Ocular Bobbing
JNNP 33:771, Susac,J.O.,et al, 1970

Encephalitis with Myoclonus in Whipple's Disease
JNNP 32:338, Stoupel,N.,et al, 1969

Neuro CPC of MGH
Jacob-Creutzfeldt Disease, NEJM 264:1359-13641961., , 1961

Clinical Picture in Creutzfeldt-Jakob Disease
Trans of Amer Neuro Assn 5:l47, Fisher,C.M., 1960

Neuro CPC of MGH
Cerebral Infarcts Due to Paradoxical Emboli, NEJM 258:338-3451958., , 1958

Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
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CT Perfusion Abnormality in Hypoglycemic Focal Neurological Deficits
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A 41-Year-Old Man with Steroid-Responsive Hemiparesis
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Stroke Mechanism and Severity after Left Atrial Appendage Occlusion, Insights from the LAAOS III Randomized Clinical Trial
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Intravenous Thrombolysis Use in the Late Time Window Before Interhospital Transfer for Thrombectomy
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Clinicopathologic Conference, Disseminated Infection with Hypervirulent Klebsiella Pneumoniae
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Spontaneous Calcified Cerebral Emboli from Bicuspid Aortic Valve in Young Patients: Case Series and Review
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Melas Syndrome
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MELAS Presenting as Bilateral Symmetric Occipital and Temporal Cortices Lesions, A Case Report and Literature Review
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Trident Sign in GFAP-Associated Meningoencephalomyelitis
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Motor Vehicle Collision Due to Left Hemineglect Associated with a Stroke
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Multivessel Cerebral Occlusion in Noonan Syndrome
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A 24-Year-Old Man With Persistent Spontaneous Dizziness
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Intravenous Thrombolysis Use Before Inter-Facility Transfer for Thrombectomy:Association with Efficacy and Safety Outcomes
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An 83-Year-Old Female Patient with a Pupil Involving Oculomotor Nerve Palsy
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Anticoagulant Usage and Risk of Thromboembolic Events After Ischemic Stroke in Adults with Cancer
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Ribbon-Like Cortical Calcifications in Hereditary Cerebral Hemorrhage With Amyloidosis-Dutch Type
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A 5-Year-Old Boy with Subacute and Refractory Myoclonus
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Necrotizing Granulomatous Encephalitis in a Patient After a Pericallosal Aneurysm Stent-Assisted Coil
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Recurrent Ischemic Strokes Due to Os Odontoideum
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Bobble-Head Doll Syndrome in a Child
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Showing articles 50 to 100 of 8109 << Previous Next >>