Neudle.com: ataxia myoclonic

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

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

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

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

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

Showing articles 50 to 100 of 1424 << Previous Next >>

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

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

CSF Antigliadin Antibodies and the Ramsay Hunt Syndrome
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Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Diagnostic Guidelines in Central Nervous System Whipple's Disease
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Progressive Ataxia, Focal Seizures, and Malabsorption Syndrome in a 41 Year Old Woman
JNNP 60:225-230, Mumford,C.J.,et al, 1996

A New Variant of Creutzfeldt-Jakob Disease in the UK
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Opsoclonus
Semin Neurol 16:21-26, Averbuch-Heller,L.&Remler,B., 1996

A Woman with a Relapsing Psychosis Who Got Better with Prednisone
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Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
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Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

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

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Anti-Ri Antibodies Associated with Opsoclonus and Progressive Encephalomyelitis with Rigidity
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Antineuronal (anti-Ri) Antibodies in a Pt with Steroid-Responsive Opsoclonus-Myoclonus
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Encephalopathy from Abuse of Bismuth Subsalicylate (Popto-Bismol)
Neurol 43:1265, Jungreis,A.C.&Schaumburg,H.H., 1993

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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Clinicopath Conf
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Extrapyramidal Involvement in Rett's Syndrome
Neurol 40:293-295, FitzGerald,P.M.,et al, 1990

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

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

Creutzfeldt-Jakob Disease without Periodic Sharp Wave Complexes:A Clinical, EEG, and Path Study
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Opsoclunus, Myoclonus, Ataxia & Encephalopathy in Adults with Cancer:A Distinct Paraneoplastic Syndrome
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Pontine Lesion in Opsoclonus-Myoclonus Syndrome Shown by MRI
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Rapidly Progressive Dementia Caused by Spongiform Encephalopathy
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Persisting Neurologic Sequelae of Lithium Carbonate Therapy
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Valproic Acid, Treatment of Myoclonus in Dyssynergia Cerebellaris Myoclonica
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Encephalopathy in Infants & Children With Chronic Renal Disease
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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

Creutzfeldt-Jakob Disease in a 20-year-old Woman
Neurol 30:492-496, Packer,R.J.,et al, 1980

Clin. Path. Conference
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Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979

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

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

Progressive Dialysis Encephalopathy
Ann Neurol 4:199-204, Lederman,R.J.,et al, 1978

Familial Chorea & Myoclonus Epilepsy
Neurol 28:913-919, Takahata,N.,et al, 1978

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

Progressive Rubella Encephalitis
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Chronic Progressive Panencephalitis due to Rubella Virus Simulating Subacute Sclerosing Panencephalitis
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Recurrent Rhombencephalitis Associatedwith Anti-GAD65 Antibody
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Clinicopathologic Conference, Factitious Disorder
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Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
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A 47-Year-Old Man With an Upper Respiratory Infection, Acute Confusion, Dysarthria, and Ataxia
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Showing articles 50 to 100 of 1424 << Previous Next >>