Neudle.com: neurogenic atrophy

Differential
(Click to cross reference)

acridine orange-RNA fluorescence

adult polyglucosan body disease

algorithm

aneurysm

aneurysm, intracranial

aneurysm, intracranial, treatment of

angiography, spinal

ankylosing spondylitis

aqueduct of Sylvius, stenosis

autonomic dysfunction

CAT scan, metrizamide

CAT scan, myelogram with

CAT scan, spine

cataracts

cerebellar atrophy, primary

cerebellum, neoplasms of

cerebral cortical atrophy

cervical spine

Charcot-Marie-Tooth

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

complications

corpus callosum, thinning

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

dementia

diabetes insipidus

diabetes mellitus

differential diagnosis

diffuse idiopathic skeletal hyperostosis

dysarthria

dystonia

ears of the Lynx MR sign

electrocardiogram, abnormal

enzyme, muscle disease

epidemiology of neurology

exome sequencing

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

falling

familial

fistula, arterio-venous, dural

genetic neurologic disorders

genetic testing

glucose tolerance test, abnormal

glycogen storage disease

headache, sudden onset of

hearing loss

histochemistry

histochemistry of muscle

H-reflex testing

hydrocephalus

hydrocephalus, non-communicating(obstructive)

hypotension, systemic

imbalance

inclusion bodies

intellectual deterioration

intracerebral hemorrhage

intracranial pressure, increased

intrinsic hand muscles, wasting of

Japan

Jewish

Kugelberg-Welander syndrome

laminectomy, cervical

laminectomy, lumbar

laughing

laughing, pathologic

leg weakness, bilateral

leukoencephalopathy

life expectancy

liver disease

malformation, vascular

malformation, vascular, dural

memory, defect of recent

memory, impairment of

MRI, contrast enhanced

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

multiple system atrophy

muscular dystrophy, differential diagnosis of

muscular dystrophy, facioscapulohumeral

muscular dystrophy, neurogenic hypothesis of

myelopathy, chronic progressive

myopathy, mitochondrial

myopathy, neurogenic hypothesis of

myotonia dystrophica

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve root hypertrophy

neurogenic atrophy

neurogenic bladder

neurogenic stunned myocardium

neurogenic vs.myopathic atrophy

neurologic disease, diagnoses of

neuropathy

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, peripheral

neuropathy, sensory

next-generation sequencing

paraparesis, familial spastic

paraparesis, spastic

pigmentary retinopathy

polyglucosan body

polyglucosan body disease

polymyositis

polyneuropathy, familial

posterior longitudinal ligament, ossification of

prognosis

progressive neurologic disorder

pseudobulbar palsy

psychiatric problems in neurologic disorders

pulmonary edema

pyramidal tract

pyramidal tract dysfunction

sensorineural hearing loss

sensory loss

Shy-Drager syndrome

spastic ataxia

spastic paraplegia, type 11

spastic paraplegia, type 7

spasticity

spinal cord, compression of

spinal cord, enlargement

spinal cord, infarction of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, vascular malformation of

spinal muscular atrophy

spinal stenosis

spinal stenosis, cervical canal

spinal stenosis, familial

spondylosis

stiff legs

subarachnoid hemorrhage

sudden death

syncope

treatment of neurologic disorder

trinucleotide repeats

walking, difficulty with

weakness

weakness, progressive

wheelchair

white matter disease

Wolfram syndrome

X-linked bulbospinal neuronopathy

x-ray, spine

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