Neudle.com: myoclonus ataxia syndrome

Differential
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abdominal distention

abdominal x-ray

adverse drug reaction

Alexanders disease, adult onset

alien hand syndrome

alopecia

altered states of consciousness

alternating rapid movement

alternating rapid movement, impaired

aluminum

AMPA receptor antibodies

amphiphysin 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

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

behavioral disorder, acute

bismuth

blindness

boomerang sign

bovine spongiform encephalopathy

brainstem, dysfunction

brainstem, dysfunction, eye movement disorders with

brainstem, infarction of

carbon monoxide poisoning

CAT scan, emission, abnormal

CAT scan, pelvis

cataracts

celiac disease, adult

central nervous system, infection of

cephalosporins

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, biochemical markers of CNS tumors

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

chest pain

chest x-ray, abnormal

chromosomal abnormality

chromosome 12

chromosome 2

chromosome 21

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

color vision, impaired

congenital infection, CNS

congenital paresis

conjugate gaze, forced

contactin associated protein like 2 antibodies

conversion reaction

cortical-basal ganglionic degeneration

cough

cranial nerve enhancement

cranial nerve palsies

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

Creutzfeldt-Jakob disease, genetic

crying

deafness

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delirium

dementia

dementia, differential diagnosis of

dementia, familial

dementia, rapidly progressive

dementia, reversible

dementia, transmissible

dementia, treatment of

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty climbing stairs

diplopia

disability, neurological

disorientation

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, Powassan

encephalitis, viral

encephalitis, viral-causes of

encephalomyelitis

encephalomyelitis, parainfectious

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

Epstein-Barr virus

exome sequencing

eye movement, disorders of

facial movement disorder

facial nerve palsy

faciobrachial dystonic seizure

fatal familial insomnia

fatigue

fever

fine motor function, impaired

finger nose finger test

fingerprint bodies

flaccid paralysis

frontal lobe, pathologic signs of

gait disorder

gait, apraxic

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gaze palsy

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

genetic neurologic disorders

globus pallidus, lesion of

GluD2

glutamic acid decarboxylase, antibody

granular osmiphilic material

grasp reflex

gray matter

gyrus, abnormal

Hallervorden Spatz disease

hallucination

hand-foot-mouth disease

heavy metal intoxication

heralding manifestation

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

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

immunologic disease

immunology and the nervous system

immunosuppressive agents

immunotherapy

impotence

inattention

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

incontinence, fecal

incoordination

infection

inferior olivary nucleus

intellectual deterioration

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

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

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

low back pain

Lyme disease

lymphadenopathy

lysosomal storage disease

malabsorption syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningoencephalomyelitis

mental retardation

mental status, abnormal

midbrain, infarction of

miglustat

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

motor neuron disease, misdiagnosis

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, FLAIR

MRI, high signal intensity of basal ganglia

MRI, negative

MRI, pelvis

MRI, punctate pattern

MRI, spinal cord

MRI, susceptibility weighted

multiple sclerosis

multiple sclerosis, misdiagnosis

muscle stiffness

mutism

myasthenia gravis, paraneoplastic

myasthenic syndrome

mycoplasma

mycoplasma pneumoniae

myelitis

myelitis, longitudinal

myoclonus, orthostatic

myoclonus, segmental

myoclonus, stimulus sensitive

myoclonus, treatment of

myoclonus-ataxia syndrome

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 disease, multifocal

neurologic signs

neurologic symptoms

neuromuscular junction

neuromuscular junction, abnormality of

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, paraneoplastic

next-generation sequencing

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

ocular dysmetria

ocular flutter

ocular motility, disorders of

oculocephalic reflex

oculomasticatory myorhythmia

old age, neurology of

olivary degeneration, hypertrophic

onconeural antibodies

ophthalmoplegia

opsoclonus

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic atrophy

optic atrophy, hereditary

optic neuropathy

oral ulcerations

organ transplantation

orthostatic hypotension

paralysis, acute areflexic

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

pathologic reflex

penicillin

pericarditis

peripheral nerve, lesion of

personality change

photophobia

pigmentary retinopathy

plasmapheresis

pleocytosis of cerebrospinal fluid

pleurisy

pneumonia

POEMS syndrome

poliomyelitis-like illness

polymerase chain reaction

polyneuropathy

pons, lesion of

pontocerebellar atrophy

potassium channel antibodies

pregnancy, neurologic complications in

prevention of neurologic disorders

prion disease

prognosis

progressive ataxia and palatal tremor

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

psychological testing

psychomotor retardation

pulmonary infiltrates

Purkinje cell

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

Red flags

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

screening

season

sedimentation rate, elevated

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

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

sleep apnea, obstructive

sleep pathology and physiology

slow virus infection of CNS

slurred speech

snout reflex

sodium channel dysfunction

speech disorder, non aphasic

speech, loss of

spinal cord

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 16

spinocerebellar ataxia type 7

spinopontine atrophy, dominant

splenium of corpus callosum

spongy degeneration of brain

square wave jerks

standing difficulty

staphylococcal protein A column therapy

stem cell transplantation

steroid

steroid therapy, CNS treatment and complications with

stiff legs

stiff man syndrome

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

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

thalamus, lesion of-bilateral

toxins, nervous system

transplacental virus infections

treatment of neurologic disorder

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

walking, difficulty with

weakness, acute

weakness, focal

weight loss

Wernekinck commissure syndrome

whole genome sequencing

Showing articles 100 to 150 of 1509 << Previous Next >>

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

Opsoclonus-Myoclonus Syndrome:Correlation of Radiographic and Pathological Observations
Neuroradiology 31:250-252, Turchman,R.F.,et al, 1989

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
Neurol 38:1056-1060, Zochodne,D.W.,et al, 1988

Opsoclunus, Myoclonus, Ataxia & Encephalopathy in Adults with Cancer:A Distinct Paraneoplastic Syndrome
Medicine 67:100-109, Anderson,N.E.,et al, 1988

Pontine Lesion in Opsoclonus-Myoclonus Syndrome Shown by MRI
JNNP 51:1572-1575, Hattori,T.,et al, 1988

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

Paraneoplastic Opsoclonus-Myoclonus, Associated with Medullary Thyroid Carcinoma & Review of the Literature
Arch Neurol 43:410-415, Dropcho,E.&Payne,R., 1986

Syndrome of Palatal Myoclonus & Progressive Ataxia:Two Cases with Magnetic Resonance Imaging
Neurol 35:1212-1214, Sperling,M.R.&Herrman,C., 1985

Persisting Neurologic Sequelae of Lithium Carbonate Therapy
Arch Neurol 40:747-751, MacDonaldson,I.,et al, 1983

Valproic Acid, Treatment of Myoclonus in Dyssynergia Cerebellaris Myoclonica
Arch Neurol 39:527-528, Sommerville,E.R.,et al, 1982

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

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

Adult Celiac Disease Presenting as Cerebellar Syndrome
Neurol 30:245-249 1980., Finelli,P.F.,et al, 1980

Creutzfeldt-Jakob Disease in a 20-year-old Woman
Neurol 30:492-496, Packer,R.J.,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 Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979

Dominant Spinopontine Atrophy
Arch Neurol 35:156, Pogacar,S.,et al, 1978

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

Clinical Pathologic Conference, Creutzfeldt-Jakob Disease, (Case record 43-1977)
NEJM 297:930, Scully,R.E.,et al, 1977

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
NEJM 292:990-993, 994-998, 1023-1024975., Townsend,J.J., 1975

Chronic Progressive Panencephalitis due to Rubella Virus Simulating Subacute Sclerosing Panencephalitis
NEJM 292:994-998,1023, Weil, M.L.,et al, 1975

Acquired Pendular Nystagmus with Oscillopsia in Multiple Sclerosis:A Sign of Cerebellar Nuclei Disease
JNNP 37:570, Aschoff,J.C.,et al, 1974

Niemann-Pick Type C Disease
www.UpToDate.com, Nov, Schiffmann, R., 2026

Clinical Insights Into CASPR1 and CASPR1/Contactin1 Com-lex Autoimmune Nodopathies
Neurol 106:e214403, Paramasivan,N.K.,et al, 2026

A 52-Year Old Man with Acute-Onset Blindness
Neurol 106:e214827, Brown,A.M.,et al, 2026

Increased Prevalence of Nitrous Oxide-Induced Subacute Combined Degeneration of the Spinal Cord: Clinical and Imaging Findings
AJNR 47:513-520, Bruen,R.,et al, 2026

A 30-Year-Old Female Patient with Multiple Sclerosis Presenting with Rapidly Progressive Cranial Neuropathies, Weakness, and Ataxia
Neurol 105:e214429, Trentadue,T.,et al, 2025

A Randomized Trial of Shunting for Idiopathic Normal-Pressure Hydrocephalus
NEJM 393:2198-2209, 2264, Luciano,M.G.,et al, 2025

A 50-Year-Old Male Patient With Acute Severe Sensory Deafferentation and Bilateral Ptosis with Rapid Recovery
Neurol 106:e214435, Pseruk,F.,et al, 2025

A 5-Year-Old Boy with Subacute and Refractory Myoclonus
Neurol 106:e214457, Park,P.S.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
Neurol 104:e213496, Gheihman,G.,et al, 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

Clinicopathological Conference, Powasan Virus Encephalitis
NEJM 393:176-184, Case 19-2025, 2025

The Spectrum of Fragile X Disorders
NEJM 393:281-288, Hagerman,R.H. & Hagerman,P.J., 2025

A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
Neurol 105:e213993, Shen,F.,et al, 2025

Gait Analysis in Neurologic Disorders, Methodology, Applications and Clinical Considerations
Neurol 105:e214154, Ali,F.,et al, 2025

Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
Neurol 105:e214099, Mizutani,H.,et al, 2025

A 58-Year-Old Man With Resting tremor, Bradykinesia, and Distal Numbness
Neurol 105:e214183, Costa,R., et al, 2025

A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
Neurol 105:e214233, Bu,S.,et al, 2025

Showing articles 100 to 150 of 1509 << Previous Next >>