Neudle.com: neurogenic atrophy

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Differential
(Click to cross reference)

acridine orange-RNA fluorescence

adult polyglucosan body disease

aneurysm, intracranial

aneurysm, intracranial, treatment of

angiography, spinal

ankylosing spondylitis

aqueduct of Sylvius, stenosis

aqueductal stenosis

ataxia, cerebellar

autonomic dysfunction

axonal degeneration

bladder dysfunction

brainstem, atrophy

Brugada syndrome

CAT scan, abnormal

CAT scan, metrizamide

CAT scan, myelogram with

CAT scan, spine

cerebellar atrophy, primary

cerebellum, neoplasms of

cerebral cortical atrophy

Charcot-Marie-Tooth

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

corpus callosum, thinning

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

diabetes insipidus

diabetes mellitus

differential diagnosis

diffuse idiopathic skeletal hyperostosis

ears of the Lynx MR sign

electrocardiogram, abnormal

enzyme, muscle disease

epidemiology of neurology

exome sequencing

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fistula, arterio-venous, dural

F-wave response

genetic neurologic disorders

genetic testing

glucose tolerance test, abnormal

glycogen storage disease

headache, severe

headache, sudden onset of

histochemistry of muscle

H-reflex testing

hydrocephalus, non-communicating(obstructive)

hyperinsulinism

hypotension, systemic

inclusion bodies

intellectual deterioration

intracerebral hemorrhage

intracranial pressure, increased

intrinsic hand muscles, wasting of

Kugelberg-Welander syndrome

laminectomy, cervical

laminectomy, lumbar

laughing, pathologic

leg weakness, bilateral

leukoencephalopathy

life expectancy

malformation, vascular

malformation, vascular, dural

memory, defect of recent

memory, impairment of

mental retardation

motor neuron disease

MRI, contrast enhanced

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multiple system atrophy

muscle weakness

muscular dystrophy

muscular dystrophy, differential diagnosis of

muscular dystrophy, facioscapulohumeral

muscular dystrophy, neurogenic hypothesis of

myasthenia gravis

myeloneuropathy

myelopathy, chronic progressive

myeloradiculopathy

myocardial injury

myopathy, mitochondrial

myopathy, neurogenic hypothesis of

myotonia dystrophica

neoplasm, primary intracranial

neoplasm, primary of CNS

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, hereditary peripheral

neuropathy, hypertrophic

neuropathy, peripheral

neuropathy, sensory

next-generation sequencing

Onufrowicz nucleus

paraparesis, familial spastic

paraparesis, spastic

pigmentary retinopathy

polyglucosan body

polyglucosan body disease

polyneuropathy, familial

posterior longitudinal ligament, ossification of

progressive neurologic disorder

pseudobulbar palsy

psychiatric problems in neurologic disorders

pulmonary edema

pyramidal tract

pyramidal tract dysfunction

sensorineural hearing loss

Shy-Drager syndrome

spastic paraplegia, type 11

spastic paraplegia, type 7

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

subarachnoid hemorrhage

treatment of neurologic disorder

trinucleotide repeats

unconsciousness

urinary incontinence

urinary urgency

vasospasm, cerebral

walking, difficulty with

weakness, progressive

white matter disease

Wolfram syndrome

X-linked bulbospinal neuronopathy

Showing articles 1550 to 1600 of 2489 << Previous Next >>

Diagnostic Tests for Choreoacanthocytosis
Neurol 41:1000-1006, Feinberg,T.E.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Presynaptic Parkinsonism in Olivopontocerebellar Atrophy:Clinical, pathological, and Neurochemical Evidence
Ann Neurol 30:425-428, Pascual,J.,et al, 1991

Membranous Lipodystrophy:MR Imaging Appearance of the Brain
Radiology 180:793-797, Araki,T.,et al, 1991

Frontal Lobe Degeneration:Clinical, Neuropsychologicaland SPECT Characteristics
Neurol 41:1374-1382, Miller,B.L.,et al, 1991

Magnetic Resonance Imaging in Toxic Encephalopathy Due to Podophyllin Poisoning
Neuroradiology 33:372-373, Chan,Y.W., 1991

Neurologic Aspects of Cobalamin Deficiency
Medicine 70:229-245, Healton,E.B.,et al, 1991

Poliomyelitis-Like paralysis During Recovery from Acute Bronchial Asthma:Possible Etiology and Risk Fators
Pediatrics 88:276-279, Shahar,E.M.,et al, 1991

Envenomation by the Scorpion Centruroides Exilicauda (C Sculpturatus) :Severe and Unusual Manifestations
Pediatrics 87:930-933, Berg,R.A.&Tarantino,M.D., 1991

Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction
Ann Neurol 29:606-614, Mhiri,C.,et al, 1991

Serial MR Imaging in Creutzfeldt-Jakob Disease
Neuroradiology 33:364-367, Uchino,A.,et al, 1991

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

Magnetic Resonance Imaging Shows Specific Abnormalities in the MELAS Syndrome
Neurol 41:1043-1046, Matthews,P.M., 1991

Autosomal Recessive Distal Dystrophy
Neurol 41:1365-1370, Barohn,R.J.,et al, 1991

Welander's Distal Myopathy:Clinical Neurophysiol & Muscle Biopsy Obser in Young & Middle Aged Adults with Early Symptoms
JNNP 54:494-498, Borg,K., 1991

Parental Sex Effect in Familial Amyotrophic Lateral Sclerosis
Neurol 41:1292-1294, Leone,M., 1991

Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
NEJM 324:1381-1384, 1430-14321991., Siddique,T.,et al, 1991

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

Hyperintensity in the Globus Pallidus on T1-Weighted & Inversion-Recovery MRI:A Possible Marker of Advanced Liver Dise
Neurol 41:1526-1527, Pujol,A.,et al, 1991

Portal-Systemic Encephalopathy:Presence of Basal Galglia Lesions with High Signal Intensity on MR Images
Radiology 179:551-555, Inoue,E.,et al, 1991

Non-Neoplastic Pineal Cysts
Neurol 41:1034-1040, Fetell,M.R.,et al, 1991

Magnetic Resonance Imaging of Fourth Ventricular Epidermoid Tumors
Arch Neurol 48:438-440, Wagle,W.A.,et al, 1991

Central Nervous System Germinomas, A Review
Arch Neurol 48:652-657, Horowitz,M.B.&Hall,W.A., 1991

Hippocampal Sclerosis in Temporal Lobe Epilepsy Demonstrated by Magnetic Resonance Imaging
Ann Neurol 29:175-182, Berkovic,S.F.,et al, 1991

Delayed Radiation Encephalopathy after Radiotherapy for Nasopharyngeal Cancer:A CT Study of 45 Cases
J Comput Assist Tomogr 15:181-187, Hu,J.,et al, 1991

Adult Polyglucosan Body Disease:The Diagnostic Value of Axilla Skin Biopsy
Ann Neurol 29:448-451, Busard,H.L.S.M.,et al, 1991

CT Appearance of Panencephalopathic and Ataxic Type of Creutzfeldt-Jakob Disease
J Comput Assist Tomogr 15:3332-3344, Berciano,J.,et al, 1991

MRI Findings in Neuro-Behcet's Disease
Neurol 41:405-408, AlKawi,M.Z.,et al, 1991

Thyroid-Associated Eye Disease:Clinical Management
Lancet 338:29-32, Fells,P., 1991

Optic Nerve Sheath Hemorrhage
In Walsh & Hoyt's Clinical Neuro-ophthalmology, Williams & Wilkins, Baltimore, Vol4, p. 2082-2085, 2, 52-2454, 19Miller, N. R., 1991

Delayed Visual Loss Due to Trauma of the Internal Carotid Artery
Arch Neurol 48:490-497, Weinstein,J.M.,et al, 1991

MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease
Neuroradiology 33:181-182, Johnsen,D.E.,et al, 1991

Axial vs Sagittal T2-Weighted Brain MR Images in the Evaluation of Multiple Sclerosis
J Comput Assist Tomogr 15:359-364, Wilms,G.,et al, 1991

Radiation Myelopathy:Significance of Gadolinium-DTPA Enhancement in the Diagnosis
Neuroradiology 33:286-289, Michikawa,M.,et al, 1991

Corpus Callosotomy for Intractable Seizures in the Pediatric Age Group
Arch Neurol 48:364-372, Nordgren,R.E.,et al, 1991

Anterior Callosotomy in the Treatment of Medically Intractable Epilepsies:A Study of 43 Patients
Ann Neurol 30:357-364, Oguni,H.,et al, 1991

Magnetic Resonance Imaging-based Volume Studies in Temporal Lobe Epilepsy:Pathological Correlations
Ann Neurol 30:31-36, Cascino,G.D.,et al, 1991

Hyperintense Basal Ganglia on T1-Weighted MR Images in Patients Receiving Parenteral Nutrition
Radiology 181:117-120, Mirowitz,S.A.,et al, 1991

Cerebellar Atrophy Following Acute Intoxication with Phenytoin
Neurol 40:1800, Masur,H.,et al, 1990

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

Hippocampal Sclerosis Can be Reliably Detected by Magnetic Resonance Imaging
Neurol 40:1869-1875, Jackson,G.D.,et al, 1990

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

Serial Magnetic Resonance Imaging in Neonatal Hypoxic-Ischemic Encephalopathy
J Pediatr 117:694-700, Byrne,P.,et al, 1990

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

Selective Involvement of the Pyramidal Tract on Magnetic Resonance Imaging in Primary Lateral Sclerosis
Neurol 40:1799-1800, Marti-Fabregas,J.&Pujol,J., 1990

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Improved Molecular-Genetic Diagnosis of Leber's Hereditary Optic Neuropathy
NEJM 323:1488-1489, Johns,D.R., 1990

Graves Orbitopathy:Correlation of CT and Clinical Findings
Radiology 177:675-682, Nugent,R.A.,et al, 1990

Internuclear Ophthalmoplegia in the Chiari Type II Malformation
Neurol 40:1850-1854, Arnold,A.C.,et al, 1990

Physical Features of Prader-Willi Syndrome in Neonates
Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990

Showing articles 1550 to 1600 of 2489 << Previous Next >>