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

Showing articles 1400 to 1450 of 2489 << Previous Next >>

TORCH Infections in the Newborn
Semin Neurol 13:106-115, Donley,D.K., 1993

Embolic Cerebral Infarction:MR Findings in the First 3 Hours AFter Onset
AJR 160:1077-1082, Shimosegawa,E.,et al, 1993

Single-Photon Emission Computed Tomographic Investigation of Patients with Motor Neuron Disease
Neurol 43:1569-1573, Abe,K.,et al, 1993

Spinal Fluid Cells and Protein in Amyotrophic Lateral Sclerosis
Arch Neurol 50:489-491, Norris,F.H.,et al, 1993

The Natural History of Amyotrophic Lateral Sclerosis
Neurol 43:1316-1322, Ringel,S.P.,et al, 1993

MRI in Acute Transverse Myelopathy
Neuroradiology 35:221-226, Holtas,S.,et al, 1993

Facial Asymmetry, Hippocampal Pathology, & Remote Symptomatic Seizures:A Temporal Lobe Epileptic Syndrome
Neurol 43:725-727, Cascino,G.D.,et al, 1993

Update on Surgical Treatment of the Epilepsies, Second Intern Palm Desert Conf on Surgical Trtm of Epilepsies (1992)
Neurol 43:1612-1617, Engel,J.Jr., 1993

Early Childhood Prolonged Febrile Convulsions, Atrophy & Sclerosis of Mesial Struc & Temporal Lobe Epilepsy:An MRI Study
Neurol 43:1083-1087, Cendes,F.,et al, 1993

Magnetic Resonance Imaging in Childhood Intractable Partial Epilepsies:Pathologic Correlations
Neurol 43:681-687, Kuzniecky,R.,et al, 1993

Detection of Hippocampal Pathology in Intractable Partial Epilepsy
Neurol 43:1793-1799, Jackson,G.D.,et al, 1993

Measurement of Whole Temporal Lobe and Hippocampus for MR Volumetry:Normative Data
Neurol 43:2006-2010, Bhatia,S.,et al, 1993

Funct'l Import of Ventric Enlarge & Cortical Atrophy in Healthy Subj & Alcoholics:PET, MR, & Neuropsych Testing
Radiology 186:59-65, Wang,G.,et al, 1993

Pick's Disease Versus Alzheimer's Disease:A Comparison of Clinical Characteristics
Neurol 43:289-292, Mendez,M.F.,et al, 1993

Clinicopath Conf
Cysticercosis Involving Basal Cisterns of Brain, Case 8-1993, NEJM 328:566-573993., , 1993

Callosal Atrophy with Reduced Cortical Oxygen Metabolism in Carotid Artery Disease
Stroke 24:88-93, Yamauchi,H.,et al, 1993

Cerebellar Infarction, Clinical and Anatomic Observations in 66 Cases
Stroke 24:76-83, Kase,C.S.,et al, 1993

Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
Neurol 43:318-325, Wullner,U.,et al, 1993

Hydrocephalus & Prominence of the Choroid Plexus:An Unusual CT Present, of Cerebral Toxoplasmosis in AIDS
Can Assoc Radiol J 43:55-59, Bourgouin,P.M.,et al, 1992

Analysis of the Prion Protein Gene in Thalamic Dementia
Neurol 42:1859-1863, Petersen,R.B.,et al, 1992

Acute Toxic Reaction to Carbamazepine:Clinical Effects and Serum Concentrations
J Pediatr 121:295-299, Tibballs,J., 1992

Magnetic Resonance Imaging in Epilepsy
Lancet 340:343-344, 1992,, , 1992

What Can the History and Physical Examination Tell Us About Low Back Pain
JAMA 268:760-765, Deyo,R.A.,et al, 1992

Diagnosis of Lumbar Spinal Stenosis in Adults:A Metaanalysis of the Accuracy of CT, MR, and Myelography
AJR 158:1135-1144, Kent,D.L.,et al, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Leksell's Posteroventral Pallidotomy in the Treatment of Parkinson's Disease
J Neurosurg 76:53-61, Laitinen,L.V.,et al, 1992

Cerebellar and Cerebral Abnormalities in Rett Syndrome:A Quantitative MR Analysis
AJR 159:177-183, Murakami,J.W.,et al, 1992

Delayed Encephalopathy after Acute Carbon Monoxide Intoxication:MR Imaging Features & Cerebral White Matter Lesions
Radiology 184:117-122, Chang,K.H.,et al, 1992

Acute Quadriplegia in Acromegaly
Ann Int Med 117:94-95, Tanigawa,K.,et al, 1992

Anti-Hu-Associated Pareneoplastic Encephalomyelitis/Sensory Neuronopathy
Medicine 71:59-72, Dalmau,J.,et al, 1992

Clinicopath Conf
Acute & Chronic BActerial Osteomyelitis & Diskitis with Epidural Abscess, Case 16-1992, NEJM 326:107, -1076,, 1992

Characteristics of Intractable Seizures Following Meningitis and Encephalitis
Neurol 42:1513-1518, Marks,D.A.,et al, 1992

Repeated Coronary Artery Spasm in a Young Woman with the Eosinophilia-Myalgia Syndrome
JAMA 267:2932-2934, Hertzman,P.A.,et al, 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

Decreased Glutamate Transport by the Brain and Spinal Cord in Amyotrophic Lateral Sclerosis
NEJM 326:1464-1468, 14931992., Rothstein,J.D.,et al, 1992

Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
Neurol 42:1488-1492, Applebaum,J.S.,et al, 1992

Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992

De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
Lancet 339:1081-1082, Hoogendijk,J.E.,et al, 1992

Amyotrophic Lateral Sclerosis and Lymphoma:Bone Marroe Examination and Other Diagnostic Tests
Neurol 42:1101-1102, Rowland,L.P.,et al, 1992

Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
Ann Neurol 32:404-407, Boylan,K.B.&Cornblath,D.R., 1992

Transsection of the Spinal Cord Associated with Breech Delivery
Am J Dis Child 146:351-352, DiMario,F.J.&Wood,B.P., 1992

Subacute Necrotizing Myelopathy:MR Imaging in Four Pathologically Proved Cases
AJR 158:163-169, 1701992., Mirich,D.R.,et al, 1992

MR Imaging Features of Medulloblastoma
AJR 158:859-865, Meyers,S.P.,et al, 1992

Complications of Acute Stroke
Lancet 339:721-724, Oppenheimer,S.&Hachinski,V., 1992

Diagnosis of Sturge-Weber Syndrome:Comparison of the Efficacy of CT & MR Imaging in 14 Cases
AJR 158:867-871, Marti-Bonmati,L.,et al, 1992

Intracranial Tuberculosis in AIDS:CT and MRI Findings
et al Neuroradiology 34:11-14, Villoria,M.F., 1992

Pure Motor Stroke:A Reappraisal
Neurol 42:789-798, Melo,T.P.,et al, 1992

Crossed Cerebellar Diaschisis and Crossed Cerebellar Atrophy:MR Findings & Clin Symptoms in 26 Pts
AJR 158:1155-1159, Tien,R.D.&Ashdown,B.C., 1992

Dementia Associated with lacunar Infarction
Stroke 23:1225-1229, Loeb,C.,et al, 1992

CNS Complications of Cocaine Abuse:Prevalence, Pathophysiology, and Neuroradiology
AJR 159:137-147, Brown,E.,et al, 1992

Showing articles 1400 to 1450 of 2489 << Previous Next >>