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Differential
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acridine orange-RNA fluorescence
adult polyglucosan body disease
algorithm
aneurysm
aneurysm, intracranial
aneurysm, intracranial, treatment of
angiography, spinal
ankylosing spondylitis
aqueduct of Sylvius, stenosis
aqueductal stenosis
astrocytoma
ataxia
ataxia, cerebellar
autonomic dysfunction
axonal degeneration
Babinski sign
bladder dysfunction
brainstem, atrophy
Brugada syndrome
bulbar palsy
CAT scan
CAT scan, abnormal
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
F-wave response
gait disorder
gait, spastic
gene mutation
genetic neurologic disorders
genetic testing
glucose tolerance test, abnormal
glycogen storage disease
gynecomastia
head injury
headache
headache, severe
headache, sudden onset of
hearing loss
histochemistry
histochemistry of muscle
H-reflex testing
hydrocephalus
hydrocephalus, non-communicating(obstructive)
hyperinsulinism
hyperreflexia
hypertension
hyposmia
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
mental retardation
monoparesis
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, spine
multiple system atrophy
muscle biopsy
muscle cramp
muscle weakness
muscular dystrophy
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
muscular dystrophy, neurogenic hypothesis of
myasthenia gravis
myelogram
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myeloradiculopathy
myocardial injury
myocytolysis
myopathy
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
nystagmus
Onufrowicz nucleus
optic atrophy
pain
pain, back
pain, central
pain, foot
pain, leg
paraparesis
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
quadriparesis
quadriplegia
radiculopathy
retinopathy
review article
risk factors
seizure
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
unconsciousness
urinary incontinence
urinary urgency
vasospasm
vasospasm, cerebral
walking, difficulty with
weakness
weakness, progressive
wheelchair
white matter disease
Wolfram syndrome
X-linked bulbospinal neuronopathy
x-ray, spine
Showing articles 1450 to 1500 of 2489 << Previous Next >>

DDAVP in the Management of Nocturia in Multiple Sclerosis
Ann Neurol 31:577, Valiquette,G.,et al, 1992

Multiple Sclerosis as a Cause of Atrial Fibrillation and Electrocardiographic Changes
Arch Neurol 49:422-424, Schroth,W.S.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Motor Neurone Disease
BMJ 304:459-460, Norris,F.H., 1992

Motor Neurone Disease:A Hospice Perspective
BMJ 304:471-473, O'Brien,T.,et al, 1992

Physical Examination of Patients with Cerebrospinal Fluid Shunts:Is There Useful Information in Pumping the Shunt?
Pediatrics 89:470-473, Piatt,J.H., 1992

Acute Ventricular Dilatation in Adult Meningococcal Meningitis
Neurol 42:458-459, Walls,T.J.&Allcutt,D.A., 1992

Paraneoplastic Syndrome Manifesting as Chronic Cerebellar Ataxia in a Child with Hodgkin Disease
J Pediatr 120:275-277, Topeu,M.,et al, 1992

Intra-arterial Cisplatin-Associated Optic and Otic Toxicity
Arch Neurol 49:83-86, Maiese,K.,et al, 1992

Multifocal Demyelinating Motor Neuropathy:Cranial Nerve Involvement and Immunoglobulin Therapy
Neurol 42:506-509, Kaji,R.,et al, 1992

Multifocal Motor Neuropathy with Conduction Block:Is It a Distinct Clinical Entity?
Neurol 42:497-505, Lange,D.J.,et al, 1992

Clinicopath Conf
Spinal Dural Arteriovenous Fistula, Case 12-1992, NEJM 326:816-824992., , 1992

Surgical Treatment of Cervical Spondylotic Myelopathy:Time for a Controlled Trial
Neurol 42:5-13, Rowland,L.P., 1992

Optic Neuropathy and Central Nervous System Disease Associated with Primary Sjogren's Syndrome
Am J Med 92:686-692, Tesar,J.T.,et al, 1992

Brain Imaging in Human Immunodeficiency Virus Infection
Semin Neurol 12:57-69, Ketonen,L.&Tuite,M.J., 1992

Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
NEJM 326:1752-1755, 17751992., Bick,D.,et al, 1992

Accelerated Aging of the Brain in Werner's Syndrome
Neurol 42:922-924, Kakigi,R.,et al, 1992

Normal-Pressure Hydrocephalus
Arch Neurol 49:366-370, Vanneste,J.,et al, 1992

Acute Hydrocephalus in Nonaneurysmal Perimesencephalic Hemorrhagee:Evidence of CSF Block at the Tentorial Hiatus
Neurol 42:1805-1807, Rinkel,G.J.E.,et al, 1992

Morphometry, Histopathology, and Tomography of Cerebral Atrophy in the Acquired Immunodeficiency Syndrome
F. C. , Ann Neurol 32:31-40-1992., Gelman,B.B.&Guinto,Jr, 1992

Clinical and NEuroradiol Findings of Congen Hydroceph in Infant Born to Mother with HTLV-I-Assoc Myelopathy
Neurol 42:1406-1408, Tohyama,J.,et al, 1992

MRI of Anterior Spinal Artery Syndrome of the Cervical Spinal Cord
Neuroradiology 35:25-29, Takahashi,S.,et al, 1992

CT of 338 Active Professional Boxers
Radiology 185:509-512, Jordan,B.D.,et al, 1992

Chronic Myelopathy Associated with Human T-Lymphotropic Virus Type I (HTLV-I)
Ann Int Med 117:933-946, Gessain,A.&Gout,O., 1992

Serum Antibodies to L-Type Calcium Channels in Patients with Amyotrophic Lateral Sclerosis
NEJM 327:1721-1728, 17521992., Smith,R.G.,et al, 1992

Paraneoplastic Cerebellar Degener III, Cerebellar Degener, Cancer & Lambert-Eaton Myasthenic Synd
Neurol 42:1944-1950, Clouston,P.D.,et al, 1992

Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
Ann Neurol 32:577-580, vanEngelen,B.G.M.,et al, 1992

MRI and SPECT in Amyotrophic Lateral Sclerosis, Demonstr of Upper Motor Neurone Invol by Neuroimaging
Neuroradiology 34:389-393, Udaka,F.,et al, 1992

Giant Axonal Neuropathy:Progressive Clinical and Radiologic CNS Involvement
Neurol 42:2220-2221, Richen,P.&Tandan,R., 1992

The Use of Magnetic Resonance Imaging in Diagnosing Infantile Neuroaxonal Dystrophy
Neurol 43:110-113, Tanabe,Y.,et al, 1992

Outlook for the Child with a Cephalocele
Pediatrics 90:914-919, Brown,M.S.,et al, 1992

Bilateral Thalamic Glioma-Review of Eight Cases with Personality Change and Mental Deterioration
AJNR 13:1225-1230, Partlow,G.D.,et al, 1992

Paraneoplastic Cerebellar Degener II, Clin & Immunologic Find in 21 Pts with Hodgkin's Disease
Neurol 42:1938-1943, Hammack,J.,et al, 1992

Paraneoplastic Cerebellar Degener I A Clinical Analysis of 55 Anti-Yo Antibody-Positive Pts
Neurol 42:1931-1937, Peterson,K.,et al, 1992

Clinicopath Conf
Motor Neuron Disease, Progressive-Muscular-Atrophy Type, Case 43-1992, NEJM 327:1298-130592., , 1992

Serial Changes of Cerebral Glucose Metab & Caudate Size in Persons at Risk for Huntington's Dis
Arch Neurol 49:1161-1167, Grafton,S.T.,et al, 1992

Detection in Life of Confirmed Alzheimer's Disease, Medial Temporal Lobe Atrophy by Computed Tomography
Lancet 340:1179-1183, Jobst,K.A.,et al, 1992

Clinicopath Conf
Tethered-Cord Syndrome, Occult Myelomeningocele, with Dermal Sinus, Case 47-1992, NEJM 327:1581-1588, 1992, 1992

Bacterial Spinal Epidural Abscess, Review of 43 Cases and Literature Survey
Medicine 71:369-385, Darouiche,R.O.,et al, 1992

Cerebral Venous Thrombosis
Bousser, M-G & Barnett, H. J. M. , in Stroke, Pathophysiol, Diag & Manage, 2nd Ed, Churchhill Living, tone, NY, Ch 19,, 1992

Quantitative Cerbral Anatomy of the Aging Human Brain:A Cross-Sectional Study Using Magnetic Resonance Imaging
Neurol 42:527-536, Coffey,C.E.,et al, 1992

Progressive Language Disorder Due to Lobar Atrophy
Ann Neurol 31:174-183, Snowden,J.S.,et al, 1992

Clinical Outcome in Aggressively Treated Meningeal Gliomatosis
Neurol 42:252-254, Grant,R.,et al, 1992

Clinicopath Conf
Pick's Diseae, Case 6-1992, NEJM 326:397-405992., , 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Subarachnoid Haemorrhage
Lancet 339:653-655, Van Gijn,J., 1992

GM-1 Ganglioside for Spinal-Cord Injury
NEJM 326:493, Schonhofer,P.S., 1992

Congenital Central Hypoventilation Syndrome:Diagnosis, Management, and Long-Term Outcome in Thirty-Two Children
J Pediatr 120:381-387, Weese-Mayer,D.E.,et al, 1992

Recurrent Encephalopathy and Seizures in a US Native with HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis
Neurol 42:658-661, Smith,C.R.,et al, 1992



Showing articles 1450 to 1500 of 2489 << Previous Next >>