Neudle.com: progressive myoclonic epilepsy

Differential
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abdominal x-ray

adverse drug reaction

Alzheimer's disease, early onset

Alzheimer's disease, familial

ammonia

amyloid angiopathy, cerebral

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

anorexia

anti IgLON5

antibiotics

antibodies to measles

anticonvulsants

anticonvulsants, selection of

antithyroid antibodies

autonomic dysfunction

Babinski sign

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion, bilateral

behavioral disorder

biologic markers

bismuth

Borrelia miyamotoi infection

bradykinesia

brain atrophy

brain biopsy

brain biopsy, false negative

calcification, intracranial

CAT scan, emission, abnormal

CAT scan, false negative

cataracts

celiac disease, adult

central nervous system, infection of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar plaques, amyloid

cerebral cortex

cerebral cortical atrophy

cerebral glucose metabolism

cerebral vasculature

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

cherry red spot-myoclonus syndrome

chromosomal abnormality

chronic progressive external ophthalmoplegia

cigarette smoking

cingulate gyrus

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

cognition

color vision, impaired

congenital infection, CNS

congenital paresis

cortical blindness

cranial nerve palsies

Creutzfeldt-Jakob disease, genetic

crying, pathologic

deep gray nuclei

degenerative diseases of CNS

dementia, differential diagnosis of

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

dementia, treatment of

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental milestones, loss of

differential diagnosis

diplopia

doll's head maneuver

downward deviation of eyes

dyssynergia cerebellaris myoclonica

dystonia

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

electroencephalogram, video monitoring with

electromyogram

electron microscopy

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, autoimmune

encephalopathy

encephalopathy, acute

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, progressive

enterovirus

enterovirus infection of CNS

epidemic

episodic disorders

episodic neurologic deficits

episodic unconsciousness

exome sequencing

extralimbic encephalitis

eye movement, disorders of

eye movement, painful

eye, pain in

faciobrachial dystonic seizure

fatal familial insomnia

fatigue

fever

fine motor function, impaired

finger nose finger test

flaccid paralysis

floaters

gait disorder

gamma amino butyric acid receptor antibody

genetic neurologic disorders

genetic testing

globus pallidus, lesion of

glutamic acid decarboxylase, antibody

gluten ataxia

gluten sensitivity

gluten-free diet

glycine receptor antibodies

granular osmiphilic material

gray matter

growth retardation

hallucination

hallucination, visual

hand-foot-mouth disease

hemianopia, homonymous

hemimyoclonic jerks

hemiparesis

hepatosplenomegaly

heralding manifestation

HHH syndrome

hoarseness

hyperammonemic encephalopathy

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

insular cortex, lesion

intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral of CNS

introverted

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

juvenile paresis

Kearns-Sayre syndrome

Leber's hereditary optic neuropathy

Leigh's disease

Leigh's disease, adult variety

lethargy

leucine rich glioma inactivated 1 antibodies

leukocyte enzyme abnormality

memory, defect of recent

memory, impairment of

meningitis

meningitis, aseptic

meningitis, neutrophilic

meningitis, treatment of

meningoencephalitis

mental retardation

mental status, abnormal

MERRF syndrome

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

motor neuron disease, misdiagnosis

movement disorder

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, sulcal hyperintensity

MRI, susceptibility weighted

multinucleated giant cell

muscle biopsy

muscle weakness

muscle weakness, proximal

mutism

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelination of nervous system

myelitis

myelitis, longitudinal

myoclonus, multifocal

myoclonus, segmental

myoclonus, stimulus sensitive

myoclonus, treatment of

myoclonus-ataxia syndrome

myopathy

myopathy, mitochondrial

neurologic complications

neurologic complications of, systemic cancer

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, ataxia, retinitis pigmentosa

next-generation sequencing

ophthalmoplegia, progressive external

opsoclonus

opsoclonus-myoclonus syndrome

optic atrophy

optic atrophy, hereditary

optic neuropathy

oral ulcerations

ornithine transcarbamylase deficiency

paralysis, acute areflexic

paraparesis, spastic

parasomnia

paratonia

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

persistent vegetative state

personality change

phonophobia

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polyneuropathy

pontocerebellar atrophy

potassium channel antibodies

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 problems in neurologic disorders

psychomotor retardation

psychosis

psychosis, acute

ptosis

pursuit eye movements, abnormal

pyruvate metabolism, abnormality of

quadriparesis

ragged-red fibers

Ramsay Hunt syndrome

rapidly progressing neurologic illness

real-time quaking-induced conversion

REM sleep behavior disorder

remote effect of cancer on the nervous system

reversible neurologic disorder

rubella encephalitis, progressive

rubella syndrome

rubella virus

rubeola virus

saccadic eye movements, abnormal

seizure

seizure, children

seizure, drug resistance

seizure, treatment of

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

short stature

skin, biopsy

sleep pathology and physiology

slow virus infection of CNS

spinal cord, lesion of

spinocerebellar ataxia

spirochete infection

spongy degeneration of brain

status epilepticus, intractable

steroid

steroid therapy, CNS treatment and complications with

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

sudden death

symmetric brain lesions

systemic illness

tandem gait, ataxic

tau protein

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

teratoma, ovarian

thalamus, lesion of-bilateral

thymoma

thyroiditis

toxins, nervous system

transient neurologic deficit

transplacental virus infections

treatment of neurologic disorder

unconsciousness, episodic

unconsciousness, transient

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

vision, blurred, monocular

visual loss

visuospatial disturbance

vocalizations

walking, difficulty with

weakness

weakness, acute

weakness, focal

weakness, generalized

weight loss

wheelchair

white matter disease

white matter disease, subcortical

wide based gait

word-finding difficulty

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