Neudle.com: myoclonic epilepsy

Differential
(Click to cross reference)

abdominal distention

abdominal x-ray

absence

acceleration-induced loss of consciousness

acetazolamide

acquired immunodeficiency syndrome

Addison's disease

advances in neurology

adverse drug reaction

affect, flat

agenesis of corpus callosum

altered states of consciousness

alternating hemiplegia

alternating rapid movement

aluminum

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

amobarbitol interview

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

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, cognitive function with

anticonvulsants, discontinuation in seizure-free epileptics

anticonvulsants, effectiveness

anticonvulsants, mechanism of action of

anticonvulsants, selection of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antioxidant

antiphospholipid antibodies

antithyroid antibodies

apraxia of eye movements

aqueduct of Sylvius, stenosis

ataxia, truncal, associated with ocular oscillations

ataxic gait

atypical

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

autonomic nervous system

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavior, combative

behavioral disorder

behavioral disorder, acute

bone marrow transplantation

bone pain

boomerang sign

Borrelia miyamotoi infection

bradykinesia

brain atrophy

brain biopsy

brain biopsy, false negative

brain scan

brainstem, atrophy

brainstem, infarction of

brainstem, lesion of

bulbar palsy

burning feet

burning feet, differential diagnosis of

burst suppression pattern, electroencephalogram

busulfan

cachexia

CAG repeats

calcification, intracranial

calcium antagonist

calcium antagonist, side effects of

carcinoma of pancreas

cardiac arrest

cardiac arrest and resuscitation

CAT scan, emission, abnormal

CAT scan, false negative

celiac disease, adult

central nervous system, infection of

central pontine myelinolysis

cephaloridine

cephalosporins

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar plaques, amyloid

cerebellum, disease of

cerebral blood flow

cerebral cortex

cerebral cortical atrophy

cerebral death

cerebral death, EEG in

cerebral edema

cerebral glucose metabolism

cerebral ischemia

cerebral vasculature

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, oligoclonal IgG in

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, young adult

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chromosomal abnormality

chronic progressive external ophthalmoplegia

cigarette smoking

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

cognition

cogwheel rigidty

collapsin response mediator protein 5 IgG

color vision, impaired

coma

coma, classification of

coma, electroencephalography in

congenital infection, CNS

cortical-basal ganglionic degeneration

corticofugal inhibition

cranial nerve palsies

Creutzfeldt-Jakob disease, genetic

crying

crying, pathologic

Cuba

cytomegalic inclusion disease

cytomegalovirus infection

deafness

deep gray nuclei

degenerative diseases of CNS

dementia, differential diagnosis of

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, transmissible

dementia, treatment of

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

downward deviation of eyes

downward gaze, paralysis of

DPPX

DPPX, antibodies

DPPX, antibodies, encephalitis

drug induced neurologic disorders

dysequilibrium syndrome

dyskinesia

dyskinesia, buccal lingual facial

dyssynergia cerebellaris myoclonica

electrical injury of nervous system

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electroencephalogram, pediatric patients

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

electroencephalogram, video monitoring with

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, diagnosis of

encephalitis, etiology

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, unknown etiology

encephalitis, viral

encephalitis, viral-causes of

encephalomyelitis

encephalomyelitis, autoimmune

encephalopathy

encephalopathy, anoxic

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, post anoxic

encephalopathy, progressive

encephalopathy, septic

enteritis

enterovirus

enterovirus infection of CNS

enzyme, defect

epidemic

epidemiology of neurology

epilepsia partialis continua

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

episodic unconsciousness

extralimbic encephalitis

extrapyramidal

eye movement, disorders of

eye movement, painful

eye, pain in

face, contractions

facial movement disorder

facial pain

faciobrachial dystonic seizure

familial adult myoclonic epilepsy

fasciculation

fatal familial insomnia

fatigue

fenfluramine

fever

fine motor function, impaired

finger nose finger test

frontal lobe, pathologic signs of

fungal infection, CNS

F-wave response

gait disorder

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gamma hydroxybutyric acid

gastrointestinal disease, neurologic complications

Gaucher's disease

Gaucher's disease, adult onset

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

glabellar sign

gliadin antibodies

globus pallidus, lesion of

glutamic acid decarboxylase, antibody

glycine

glycine receptor antibodies

granular osmiphilic material

Hallervorden Spatz disease

hallucination

hallucination, olfactory

hallucination, visual

hand-foot-mouth disease

headache, sudden onset of

heavy metal intoxication

hemianopia, homonymous

hemiballismus

hemimyoclonic jerks

hemiparesis

hemiparesis, transient

hemiplegia

hemolytic-uremic syndrome

hepatitis

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes simplex encephalitis

human immunodeficiency virus type 1

hydrocephalus

hydrocephalus, normal pressure

hydroxyindole acetic acid 5(5HIAA)

hydroxytryptophan L-5(L-5 HTP)

hyperactivity

hyperammonemic encephalopathy

hyperekplexia

hyperglycinemia

hyperglycinemia, nonketotic

hypertensive encephalopathy

hypotension, systemic

hypothalamus, disturbance of

hypoxic encephalopathy

iatrogenic neurologic disorders

immune reconstitution inflammatory syndrome

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deterioration

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral of CNS

introverted

irritability

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

jaw pain

juvenile myoclonus epilepsy

juvenile paresis

Kearns-Sayre syndrome

Korsakoff's psychosis

kuru plaques

lactic acidemia

lactic dehydrogenase(LDH)

L-dopa, drug interactions with and side effects of

Leber's hereditary optic neuropathy

Leigh's disease

Leigh's disease, adult variety

lethargy

leucine rich glioma inactivated 1 antibodies

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

levitation

Lewy body disease, diffuse

life expectancy

limbic encephalitis

linear lesion

lipid storage disorder of CNS

lithium

liver biopsy

liver function enzymes

lymphadenopathy

lymphocyte fingerprint profiles

lymphoma

lymphoma involving CNS

macular degeneration

maculopathy

malabsorption

malabsorption syndrome

malaise

malformation, CNS, congenital

marihuana

mediastinum, mass of

MELAS syndrome

memory, defect of recent

memory, impairment of

meningitis, neutrophilic

meningitis, syphilitic

meningitis, TB

meningitis, treatment of

meningoencephalitis

mental retardation

mental status, abnormal

meperidine

MERRF syndrome

mesial temporal lobe

metabolic disorder, primary

metronidazole

microangiopathic hemolytic anemia

microangiopathy, brain

microangiopathy, retina

midbrain, infarction of

migraine

migraine, seizures in

migraine, treatment of

mimics

miosis

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

monoclonal antibodies

motor neuron disease, misdiagnosis

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, paroxysmal

movement disorder, psychogenic

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, sulcal hyperintensity

MRI, susceptibility weighted

multinucleated giant cell

muscle weakness, proximal

mutism

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelination of nervous system

myelitis

myelitis, longitudinal

myelitis, transverse

myelitis, transverse, recurrent

myelopathy

myoclonic ataxia

myoclonic encephalopathy of infancy

myoclonus, differential diagnosis of

myoclonus, epilepsy

myoclonus, face

myoclonus, post anoxic

myoclonus, segmental

myoclonus, sleep

myoclonus, stimulus sensitive

myoglobinuria

myopathy

myopathy, mitochondrial

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve conduction studies

neuralgia, treatment of

neuraminidase deficiency

neurexin-3 alpha antibodies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroendocrinology

neurologic complications

neurologic complications of, burns

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, multifocal

neurologic signs

neurologic symptoms

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, ataxia, retinitis pigmentosa

next-generation sequencing

ocular motility, disorders of

oculomasticatory myorhythmia

ophthalmoplegia

ophthalmoplegia, progressive external

opportunistic infection

opsoclonus

opsoclonus-myoclonus syndrome

optic atrophy

optic atrophy, hereditary

optic neuropathy

oral ulcerations

organ transplantation

ornithine transcarbamylase deficiency

paralysis, acute areflexic

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

peripheral nerve, lesion of

persistent vegetative state

pigmentary retinopathy

PLEDs

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pleurisy

pneumoencephalogram(PEG)

pneumonia

poison, organophosphate

polymerase chain reaction

polyneuropathy

polyneuropathy, uremic

pontocerebellar atrophy

potassium channel antibodies

precipitating factors

pregnancy, neurologic complications in

prion disease

prognosis

progressive encephalomyelitis with rigidity syndrome

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

protein 14-3-3, cerebrospinal fluid

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

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, dilated, bilateral

pursuit eye movements, abnormal

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

rabies, nervous system involvement with

ragged-red fibers

Ramsay Hunt syndrome

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

recurrent

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal failure

renal stones

renal transplantation

respiratory depression

respiratory failure

restless leg syndrome

reticulum cell sarcoma

retinal artery occlusion

retinal branch artery occlusion

reversible neurologic disorder

rubella encephalitis, progressive

rubella syndrome

rubella virus

rubeola virus

saccadic eye movements, abnormal

salivation, excessive

Schilder's disease

SCN1A gene

sedimentation rate, elevated

seizure

seizure, adult onset

seizure, age of onset

seizure, children

seizure, classification of

seizure, diagnosis of

seizure, differential diagnosis of

seizure, drug resistance

seizure, drug-induced

seizure, dystonic

seizure, EEG normal during

seizure, EEG pattern in

seizure, photosensitive

seizure, prognosis in adults

seizure, stimulus sensitive

seizure, teenager

seizure, tonic-clonic

seizure, treatment of

seizure, withdrawal

selective serotonin reuptake inhibitors

sensorineural hearing loss

sensory loss

sensory loss, cortical

septicemia

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

slurred speech

snout reflex

sodium channel dysfunction

sodium valproate

sodium valproate, intravenous

sodium valproate, toxicity

spinal cord, lesion of

spinal cord, pathologic exam of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spirochete infection

splenium of corpus callosum

spongy degeneration of brain

square wave jerks

staphylococcal protein A column therapy

status epilepticus, intractable

status epilepticus, myoclonic

status epilepticus, nonconvulsive

steatorrhea

stem cell transplantation

stereotypy

steroid

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulant drugs

stiripentol

storage disease of CNS

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

stuporous

stuttering

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

subacute sclerosing panencephalitis, adult onset

subarachnoid hemorrhage

symmetric brain lesions

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

thalamus, lesion of-bilateral

theta coma

thrombocytopenia

thrombotic microangiopathy

thymoma

thyroid stimulating immunoglobulins

tonic cerebellar fits

tonic spasms

topiramate

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

transient neurologic deficit

transplacental virus infections

travel history

travel, foreign

treatment of neurologic disorder

tricyclic antidepressant

trigeminal neuralgia

trigeminal neuralgia, treatment of

trinucleotide repeats

unconsciousness, episodic

unconsciousness, transient

Unverricht-Lundborg disease

upgaze

upgaze, paralysis of

urea-cycle enzymopathies

uremia

uremic encephalopathy

varicella zoster virus

vision, blurred, monocular

visual acuity, decreased

visual field defect

visual impairment

visual loss

visuospatial disturbance

vitreous opacities

vocalizations

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

wrist drop

zoster sine herpete

Showing articles 100 to 150 of 3545 << Previous Next >>

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

The Role of Hypotension in Septic Encephalopathy Following Surgical Procedures
& Stevens, M. , Arch Neurol 49:653-656., Wijdicks,E.F.M., 1992

Aluminium Intoxication in Undialysed Adults with Chronic Renal Failure
JNNP 55:697-700, Russo,L.S.,et al, 1992

Juvenile Myoclonic Epilepsy, Underdiagnosed and Treatment May Have to be Life Long
BMJ 305:4-5, Timmings,P.L.&Richens,A., 1992

Localization of Idiopathic Generalized Epilepsy on Chromosome 6p in Families of Juvenile Myoclonic epilepsy patients
Neurol 41:1651-1655, Durner,M.,et al, 1991

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

Multistate Outbreak of Poisonings Associated with Illicit Use of Gamma Hydroxy Butyrate
JAMA 265:447-448, , 1991

Hashimoto's Encephalopathy:A Steroid-Responsive Disorder Associated with High Anti-Thyroid Antibody Titers-Report of 5 Cases
Neurol 41:228-233, Shaw,P.J.,et al, 1991

Clinicopath Conf
Cerebral Amyloid Angiopathy, Case 27-1991, NEJM 325:42-54991., , 1991

Mitochondril Encephalopathies:Molecular Genetic Diagnosis from Blood Samples
Lancet 337:1311-1313, Hammans,S.R.,et al, 1991

Progressive Myoclonic Ataxia (The Ramsay Hunt Syndrome)
Arch Neurol 47:1121-1125, Marsden,C.D.,et al, 1990

Chronic Acetazolamide Monotherapy in the Treatment of Juvenile Myoclonic Epilepsy
Neurol 40:1677-1681, Resor,S.R.&Resor,L.D., 1990

Coincidence of Myoclonus and Multiple Sclerosis:Dramatic Response to Clonazepam
Neurol 40:1633-1634, Smith,C.R.&Scheinberg,L., 1990

Myoclonic Status Epilepticus:A Clinical and Electroencephalographic Study
Neurol 40:1199-1202, Jumao-as,A.&Brenner,R.P., 1990

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

Bismuth Absorption and Myoclonic Encephalopathy During Bismuth Subsalicylate Therapy
Ann Int Med 112:140-141, Mendelowitz,P.C.,et al, 1990

Epileptic Seizures and Syndromes
Lancet 336:161-163, Gram,L., 1990

Acceleration-Induced Loss of Consciousness, A Review of 500 Episodes
Arch Neurol 47:764-776, Whinnery,J.E.&Whinnery,A.M., 1990

Agenesis of the Corpus Callosum and Gyral Malformations are Frequent Manifestations of Nonketotic Hyperglycinemia
Neurol 39:817-820, Dobyns,W.B., 1989

Juvenile Myoclonic Epilepsy:An Autosomal Recessive Disease
Ann Neurol 25:440-443, Panayiotopoulos,C.P.&Obeid,T., 1989

Neonatal Seizures:Current Concepts and Revised Classification
Pediatrics 84:422-428, Volpe,J.J., 1989

Busulphan and Phenytoin
Ann Int Med 111:1049-1050, Grigg,A.P.,et al, 1989

Nifedipine and Myoclonic Disorders
Nephron 51:281, Pedro-Botet,M.L.,et al, 1989

Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988

A Creutzfeldt-Jakob Like Syndrome Due to Lithium Toxicity
JNNP 51:120-123, Smith,S.J.M.&Kocen,R.S., 1988

Myoclonus During Combined Tricyclic Antidepressant and Lithium Treatment
J Clin Psychopharmacol 8:446-447, Devanand,D.P.,et al, 1988

Rapidly Progressive Dementia Caused by Spongiform Encephalopathy
West J Med 148:313-319, Enos,B.E.&Vinters,H.V., 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

Outcome from Coma After Cardiopulmonary Resuscitation:Relation to Seizures & Myoclonus
Neurol 38:401-405, Krumholz,A.,et al, 1988

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

Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986

Seizures & Myoclonus in Patients with Alzheimer's Disease
Neurol 36:1226-1230, Hauser,W.A.,et al, 1986

Mitochondrial Myopathies
Ann Neurol 17:521-538, DiMauro,S.,et al, 1985

Creutzfeldt-Jakob Disease of Long Duration:Clinicopathological Characteristics
Ann Neurol 16:295-304, Brown,P.,et al, 1984

Clinicopathological Conference
Case 49-1983, Creutzfeldt-Jakob, NEJM 309:1440-1449983., , 1983

Dialysis Encephalopathy, Clinical, Electroencephalographic & Interventional Aspects
Medicine 62:129-141, O'Hare,J.A., 1983

Meperidine-Associated Myoclonus & Seizures in Long-Term Hemodialysis Patients
Ann Neurol 14:593, Hochman,M.S., 1983

Valproate & Clonazepam in the Treatment of Severe Progressive Myoclonus Epilepsy
Arch Neurol 39:236-238, Iivanainen,M.,et al, 1982

Toxic Substances & the Nervous System:The Role of Clinical Observation
JNNP 44:1-8, LeQuesne,P.M., 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Encephalopathy in Infants & Children With Chronic Renal Disease
Arch Neurol 38:656-658, Foley,C.M.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Cephaloridine Encephalopathy
BMJ 283:409-410, Taylor,R.,et al, 1981

Myoclonic Seizures Following Chlorambucil Overdose
Jr. , Ann Neurol 9:191-194981., Byrne,T.N., 1981

Valproic Acid
NEJM 302:661-666, Brown,T.R., 1980

Neurologic Prognosis after Cardiopulmonary Arrest:III. Seizure Activity
Neurol 30:1292-1297, Snyder,B.D.,et al, 1980

Lafora Disease:Diagnosis by Liver Biopsy
Ann Neurol 8:409-415, Nishimura,R.N.,et al, 1980

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Familial Psychosis & Diverse Neurologic Abnormalities in Adult-Onset Gaucher's Disease
Arch Neurol 36:95-99, Neil,J.F.,et al, 1979

Showing articles 100 to 150 of 3545 << Previous Next >>