Neudle.com: ataxia acute onset

Differential
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abdominal distention

abdominal protrusion

abducens nerve paralysis, bilateral

abscess, brainstem

abscess, intracerebral

abscess, lung

acute ataxia of childhood

acute cerebellar ataxia

adult polyglucosan body disease

advances in neurology

Alexanders disease

Alexanders disease, adult onset

alternating hemiplegia

alternating hemiplegia of childhood

AMPA receptor antibodies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

aneurysm, abdominal aortic

aneurysm, aortic arch

angiography, cerebral

angiography, posterior fossa

animal exposure

anti GQ1b IgG antibody

anticonvulsants

anticonvulsants, effectiveness

arterial dissection, carotid

arterial dissection, intracranial

arterial dissection, multiple

arterial dissection, ruptured

arterial dissection, vertebral

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

axonal degeneration

Babinski sign

bacterial infection

bacterial infection, CNS

basal ganglia, lesion of

basilar artery migraine

Bassen-Kornzweig syndrome

brachial plexus neuropathy

bradykinesia

brain atrophy

brainstem, infarction of

brainstem, lesion of

Brown-Vialetto-Van Laere syndrome

bulbar palsy

bulbar palsy, progressive

carotid artery disease

cauda equina, enhancement

CD4 counts

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar cognitive affective syndrome

cerebellar degeneration

cerebellar infarction

cerebral venous thrombosis

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, genetic

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, risk factors in

cerebrovascular disease, surgical treatment of

chromosomal abnormality

chromosome 2

Clinical Pathologic Conference(C.P.C.)

counterimmunoelectrophoresis

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cyanide poison

deafness

degenerative diseases of CNS

delirium

dementia

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

demyelinating disease

dermatitis

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty climbing stairs

dilantin

disability, neurological

distal muscle atrophy

doll's head maneuver

Dravet syndrome

drug induced neurologic disorders in children

electroencephalogram, abnormalities of

electromyogram

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, postinfectious

encephalopathy

enterovirus

enterovirus infection of CNS

epidemic

epileptic encephalopathy

Epstein-Barr virus

extraocular muscle lesion

eye movement, disorders of

face, numbness of

facial nerve palsy

facial nerve palsy, recurrent

fine motor function, impaired

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

gait disorder

gait, spastic

gait, waddling

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastroenteritis

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic neurologic disorders

genetic testing

GFAP gene

glutamic acid decarboxylase, antibody

glycogen storage disease

gram negative rod

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, variant forms of

gynecomastia

hand deformity

hand-foot-mouth disease

headache, sudden onset of

heralding manifestation

herpes simplex virus

herpes virus

herpes virus infection

herpes, genital

heterophile antibody test

hiccoughs

histochemistry of muscle

hypertension, cerebrovascular disease with

hyperthyroidism

hypoglycemia

hypokalemia

hypokalemic periodic paralysis

hyponatremia

hyporeflexia

hypotension, systemic

hypotonia

hypoxia

iatrogenic neurologic disorders

imbalance

immunization, neurologic complications with

immunotherapy

inappropriate antidiuretic(A.D.H.)hormone

inborn errors of metabolism

inclusion bodies

inclusion bodies, intranuclear

infection

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

learning disability, in children

leg numbness

leg weakness, bilateral

Leigh's disease

lethargy

leucine rich glioma inactivated 1 antibodies

listeria monocytogenes

lymphadenopathy, paraaortic

macrocephaly

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningismus

meningitis

meningitis, aseptic

meningitis, carcinomatous

meningitis, CSF cell count-normal

meningitis, recurrent

meningoencephalitis

meningoencephalitis, mumps

mental status, abnormal

microcephaly

migraine

migraine, children

migraine, visual symptoms in

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, brachial plexus

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, negative

MRI, spinal cord

MRI, susceptibility weighted

multiple sclerosis

mumps virus

muscle atrophy, progressive

muscle weakness, proximal

myasthenia gravis

mycobacterial infection

mycobacterium bovis

mycoplasma

mycoplasma pneumoniae

mycotic aneurysm

myelinolysis, extrapontine

myelomalacia

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myoclonus, stimulus sensitive

nemaline rod myopathy

nemaline rod myopathy, adult onset

nerve conduction studies

nerve conduction studies, motor

neurogenic bladder

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neuromuscular disease, electrodiagnosis of

neuronal intranuclear inclusion disease

neuropathy

neuropathy, acute

neuropathy, motor

neuropathy, motor, multifocal

old age, neurology of

osmotic demyelination syndrome

otitis, neurologic complications with

paralysis, acute areflexic

paraparesis

paraparesis, familial spastic

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

paresthesias

Parkinson disease, dystonia with

Parkinsonism syndrome

parotitis

paroxysmal hemiplegia

paroxysmal neurologic deficits

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

periodic paralysis

periodic paralysis, thyrotoxic

pleocytosis of cerebrospinal fluid

poison, mercury

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuritis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

pons, lesion of

post infectious cerebellar ataxia

postinfectious

potassium

potassium channel antibodies

practice guidelines

precipitating factors

prion disease

prognosis

progressive neurologic disorder

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, progressive

quadriplegia, transient

radiculopathy

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

real-time quaking-induced conversion

recurrent

Refsum's disease

regional enteritis

renal tubular acidosis

respiratory failure

respiratory tract infection

retina, abnormal

retinal lesion

review article

riboflavin transporter deficiency

sedimentation rate, elevated

seizure, photosensitive

seizure, tonic-clonic

seizure, treatment of

sensorineural hearing loss

sensory loss, band distribution

serologic testing

serologic testing, false negative

seronegative

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

sleep pathology and physiology

slurred speech

sodium channel dysfunction

spinal cord, cervical

splenomegaly

standing difficulty

status epilepticus

stem cell transplantation

steroid

steroid therapy, CNS treatment and complications with

stooped posture

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

subarachnoid hemorrhage

subarachnoid hemorrhage, recurrent

suspended sensory loss

systemic illness

tandem gait, ataxic

temporal lobe, atrophy

tongue, fasciculations of

topiramate

toxins, nervous system

transient ischemic attack

treatment of neurologic disorder

vertebral-basilar insufficiency

vertigo

viral infection

viral infection, CNS

visual acuity, decreased

visual impairment

visual loss

visual loss, sudden-unilateral

visual loss, transient

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

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