Neudle.com: myoclonic ataxia

Differential
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abdominal distention

abdominal x-ray

adverse drug reaction

altered states of consciousness

alternating rapid movement

aluminum

AMPA receptor antibodies

antibiotics, neurologic complications with

antibodies to measles

anticonvulsants

anticonvulsants, effectiveness

anticonvulsants, selection of

antidepressant

antioxidant

antithyroid antibodies

ataxia, truncal, associated with ocular oscillations

autonomic dysfunction

axonal spheroid

Babinski sign

bacterial infection

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

bovine spongiform encephalopathy

carbon monoxide poisoning

CAT scan, emission, abnormal

cataracts

celiac disease, adult

central nervous system, infection of

cephalosporins

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellum

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral glucose metabolism

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, young adult

cherry red spot

cherry red spot-myoclonus syndrome

chromosomal abnormality

chromosome 12

chromosome 2

chromosome 21

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clonazepam

clonus

coenzyme Q10 deficiency

cognition

cogwheel rigidty

cold intolerance

color vision, impaired

congenital infection, CNS

congenital paresis

conjugate gaze, forced

contactin associated protein like 2 antibodies

cortical-basal ganglionic degeneration

cranial nerve palsies

Creutzfeldt-Jakob disease, genetic

crying

deafness

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delirium

dementia

dementia, differential diagnosis of

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

diplopia

disability, neurological

dizziness

doll's head maneuver

downward gaze, paralysis of

Dravet syndrome

drooling

drug induced neurologic disorders

dyssynergia cerebellaris myoclonica

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

electromyogram

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, diagnosis of

encephalitis, etiology

encephalitis, paraneoplastic

encephalitis, viral

encephalitis, viral-causes of

encephalomyelitis

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, parainfectious

enterovirus

enterovirus infection of CNS

enzyme, defect

epidemic

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

eye movement, disorders of

facial movement disorder

faciobrachial dystonic seizure

falling

familial

fasciculation

fatal familial insomnia

fatigue

fever

fine motor function, impaired

finger nose finger test

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

gliadin antibodies

globus pallidus, lesion of

GluD2

glutamic acid decarboxylase, antibody

gram positive rod

granular osmiphilic material

grasp reflex

gray matter

gyrus, abnormal

Hallervorden Spatz disease

hallucination

hand-foot-mouth disease

heavy metal intoxication

heralding manifestation

hoarseness

human immunodeficiency virus type 1

hydrocephalus

hyperhidrosis

hyperpigmentation of skin

hypothalamus, disturbance of

hypothyroidism

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

idiopathic

imbalance

imbalance, postural

immune reconstitution inflammatory syndrome

immunohistochemistry

immunosuppressive agents

immunotherapy

impotence

inattention

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

intellectual deterioration

intestinal biopsy

intestinal pseudoobstruction

intrauterine infection

intrauterine infection, viral of CNS

introverted

irritability

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

juvenile paresis

Kearns-Sayre syndrome

Leber's hereditary optic neuropathy

Leigh's disease

Leigh's disease, adult variety

leucine rich glioma inactivated 1 antibodies

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

limbic encephalitis

linear lesion

lipid storage disorder of CNS

lithium

liver function enzymes

malabsorption syndrome

malaise

masked facies

MELAS syndrome

memory, defect of recent

memory, impairment of

mental status, abnormal

mitochondrial disease

mitochondrial encephalomyopathy

motor neuron disease, misdiagnosis

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, diffusion weighted

MRI, false negative

MRI, FLAIR

MRI, high signal intensity of basal ganglia

MRI, negative

MRI, pelvis

MRI, spinal cord

MRI, susceptibility weighted

mutism

myelitis

myelitis, longitudinal

myoclonus, orthostatic

myoclonus, segmental

myoclonus, stimulus sensitive

myoclonus, treatment of

myopathy

myopathy, mitochondrial

neuraminidase deficiency

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroaxonal leukodystrophy

neuroblastoma

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic signs

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, ataxia, retinitis pigmentosa

neurosyphilis

neurotoxic

neurotoxin

next-generation sequencing

ocular motility, disorders of

oculomasticatory myorhythmia

old age, neurology of

olivary degeneration, hypertrophic

ophthalmoplegia

ophthalmoplegia, progressive external

opsoclonus

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic atrophy

optic atrophy, hereditary

optic neuropathy

oral ulcerations

organ transplantation

orthostatic hypotension

paralysis, acute areflexic

paraparesis, spastic

parasomnia

Parkinson disease

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleurisy

pneumonia

polymerase chain reaction

polyneuropathy

pons, lesion of

pontocerebellar atrophy

potassium channel antibodies

pregnancy, neurologic complications in

prevention of neurologic disorders

prion disease

prognosis

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

Purkinje cell surface antibody

pursuit eye movements, abnormal

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

ragged-red fibers

Ramsay Hunt syndrome

rapidly progressing neurologic illness

rash

rash, hand

real-time quaking-induced conversion

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal failure

respiratory failure

respiratory tract infection

rubella encephalitis, progressive

rubella syndrome

rubella virus

rubeola virus

saccadic eye movements, abnormal

salivation, excessive

SCN1A gene

sedimentation rate, elevated

seizure, photosensitive

seizure, tonic-clonic

seizure, treatment of

senile plaques

sensorineural hearing loss

sensory loss, cortical

seroconversion

serologic testing

serologic testing of cerebrospinal fluid

short stature

sleep apnea, obstructive

sleep pathology and physiology

slow virus infection of CNS

slurred speech

snout reflex

sodium channel dysfunction

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 16

spinocerebellar ataxia type 7

splenium of corpus callosum

spongy degeneration of brain

stem cell transplantation

steroid

steroid therapy, CNS treatment and complications with

stiff man syndrome

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

stuporous

stuttering

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

suck, poor

suicide

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, neurologic complications with

temporal lobe, lesion, bilateral

teratoma, ovarian

term infant

thalamus, lesion of

thalamus, lesion of-bilateral

toxins, nervous system

transplacental virus infections

treatment of neurologic disorder

tremor

tremor, intention

tremor, postural

triangle of Guillain and Mollaret

trinucleotide repeats

ultrasonography

unconsciousness

unconsciousness, episodic

unconsciousness, transient

Unverricht-Lundborg disease

visual acuity, decreased

visual impairment

visual loss

visuospatial disturbance

vitreous opacities

vocalizations

walking, difficulty with

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Paraneoplastic Syndrome Manifesting as Chronic Cerebellar Ataxia in a Child with Hodgkin Disease
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MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Clinicopath Conf
Huntington's Diseae, Case2-1992, NEJM 326:117-125992., , 1992

Angelman Syndrome: Clinical Profile
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HIV Encephalopathy and Dementia
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Stimulus-Sensitive Myoclonus in Akinetic-Rigid Syndromes
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Delayed Diagnosis of Juvenile Myoclonic Epilepsy
JNNP 55:497-499, Grunewald,R.A.,et al, 1992

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Neurological and Neuropsychiatric Spectrum of Wilson's Disease:A Prospective Study of 45 Cases
J Neurol 238:281-287, Oder,W.,et al, 1991

Neurologic Aspects of Cobalamin Deficiency
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Neurological Conversion Disorders in Childhood
Lancet 337:889-890, , 1991

Wilson Disease:Clinical Presentation, Treatment, and Survival
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Cat Scratch Disease, Acute Encephalopathy & Other Neurologic Manifestations
Am J Dis Child 145:98-101, Carithers,H.A.&Margileth,A.M., 1991

Anti-Ri:An Antibody Associated with Paraneoplastic Opsoclonus and Breast Cancer
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Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
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Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
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Clinicopath Conf
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Clinicopath Conf
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Clinicopath Conf
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Myoclonus in Adult Huntington's Disease
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Truncal Asterixis Associated with Ceftazidine, A Third-Generation Cephalosporin
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Showing articles 900 to 950 of 1450 << Previous Next >>