Neudle.com: "cortical myoclonus"

Differential
(Click to cross reference)

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

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

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, anoxic

encephalopathy, delayed

encephalopathy, metabolic

encephalopathy, parainfectious

encephalopathy, post anoxic

encephalopathy, progressive

enolase

enteritis

epidemiology of neurology

epilepsia partialis continua

escherichia coli

euphoria

evoked potentials

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

genetic testing

glabellar sign

gliomatosis cerebri

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

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

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

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 0 to 50 of 7899 Next >>

A 66-Year-Old Woman With Progressive Encephalopathy and Bilateral Hearing Loss
Neurol 100:254-258, Rivers,D.,et al, 2023

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

Clinicopathologic Conference, Borrelia Miyamotoi Infection
NEJM 383:1578-1586, Case 32-2020, 2020

Progressive Ataxia and Palatal Tremor
Neurol 94:e1445-e1447, Pradeep, S.,et al, 2020

A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
Neurol 92:e274-e281, Chen, Z. & Neo, S., 2019

A 22-year-old Man Presenting with Headache and Right Leg Jerks
Neurol 91:891-895, Schupper, A.J.,et al, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

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

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
Neurol 89:e182-e187, Tabuas-Pereira, M.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Clinicopathologic Conference, Primitive Neuroectodermal Tumor of CNS, with Involvement of Thalamus, Medial Cerebral Cortex, Brainstem, Cerebellum and Subarachnoid Space
NEJM 372:1550-1562, Case 12-2015, 2015

A Variegated Squirrel Bornavirus Associated with Fatal Human Encephalitis
NEJM 373:154-162, Hoffmann, B.,et al, 2015

A 27-Year Old Man with Rapidly Progressive Coma
Neurol 85:e74-e78, Wong,J.M.,et al, 2015

A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
Neurol 85:e116-e122, Baker, J.M.,et al, 2015

The Acquired Metabolic Disorders of the Nervous System, Dialysis Encephalopathy (Dialysis Dementia)
Adams & Victors Principles of Neurology Chp 40, pg 1146, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Acute Encephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 748, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Creutzfeldt-Jakob Disease (Subacute Spongiform Encephalopathy)
Adams & Victors Principles of Neurology, Chp 33, pg 769, Ropper, A.H.,et al, 2014

Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Cocaine
Adams & Victors Principles of Neurology Chp 43, pg 1213, Ropper, A.H.,et al, 2014

Mycoplasma Pneumoniae Infection: Neurologic Complications
www.MedLink.com, Oct, Greenlee, J.E., 2013

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Opsoclonus and Multiple Cranial Neuropathy as a Manifestation of Neuroborreliosis
Neurol 77:1013-1014, Sabien Van Erp, W.,et al, 2011

Treatment of Severe Neurological Deficits with IgG Depletion through Immunoadsorption in Patients with Escherichia coli O104:H4-Associated Haemolytic Uraemic Syndrome: A Prospective Trial
Lancet 378:1166-1173,1120, Greinacher, A.,et al, 2011

Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
Acta Radiologica 52:336-339, Talbott,S.D.,et al, 2011

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Clinicopath conf., Human Prion Disease, Sporadic CJD
Neurol 69:1881-1887, Geschwind,M.D., et al, 2007

The Acoustic Startle Reflex in Ischemic Stroke
Neurol 62:114-116, Jankelowitz,S.K. & Colebatch,J.G., 2004

Post-Stroke Movement Disorders; Report of 56 Patients
JNNP 75:1568-1574, Alarcon,F.,et al, 2004

Cortical Myoclonus During Lithium Exposure
Arch Neurol 60:401-404, Caviness,J.N.,&Evidente,V.G.H., 2003

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Subacute Sclerosing Panencephalitis Clinical and Magnetic Resonance Imaging Evaluation of 36 Patients
J Child Neurol 17:25-29, Ozturk, A.,et al, 2002

Subacute Sclerosing Panencephalitis
Postgrad Med J 78:63-70, Garg, R.K.,et al, 2002

Clinical Features of Nipah Virus Encephalitis Among Pig Farmers in Malaysia
NEJM 342:1229-1235, Goh,K.J.,et al, 2000

Rapidly Progressive Dementia
Lancet 353:1150, Bornke,C.,et al, 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Clinicopath Conf
Dementia with Lewy Bodies, Anaplastic Astrocytoma of Right Insular Region, Case 7-1998, NEJM 338:603, 61098., 1998

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Cortical Myoclonus
Neurol 50:933-942, Mima,T.T.,et al, 1998

Acute Leukoencephalopathies:Differential Diagnosis and Investigation
The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996

Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
Neurol 46:68-74, Scott,B.L.,et al, 1996

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Clinicopath Conf
Arteritis, Unclassified, with Giant-Cell Reaction & Multiple Infarcts of the Brain & Neuropathy, Cas, 5-199532:452-459,1995., 1995

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

Showing articles 0 to 50 of 7899 Next >>