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Differential
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abiotrophy
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, childhood
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, post-encephalitic
amyotrophic lateral sclerosis, treatment of
anterior horn cell disease
areflexia
arm weakness
asthma
asthma, poliomyelitis-like syndrome with
brain biopsy
bulbar palsy
bulbar palsy, childhood
bulbar palsy, progressive
central nervous system, infection of
cerebral embolism
cerebrovascular accident
cerebrovascular accident, young adult
cerebrovascular disease, cardiovascular disease with
children
chromosome 5
cranial neuropathy
deafness
degenerative diseases of CNS
dementia
dementia, cerebrovascular disease causing
diarrhea
differential diagnosis
dysphagia
dyspnea
efficacy
electromyogram
enterovirus
enterovirus infection of CNS
epidemiology of neurology
familial
fasciculation
fever
fibrillations
flaccid paralysis
floppy infant
gammaglobulin therapy, intravenous
gene
gene mutation
gene therapy
genetic neurologic disorders
granular atrophy, cerebral cortex
Guillain Barre syndrome
headache
hearing loss
hoarseness
hyperreflexia
hypotonia
hypotonia, infants
infant, evaluation of
infection
Jakob-Creutzfeldt disease
Kugelberg-Welander syndrome
leg weakness, bilateral
leg weakness, unilateral
meningismus
mental status, abnormal
microinfarcts
mitral valve lesion
molecular genetics
monomelic amyotrophy
mortality
motor neuron disease
motor system
MRI, abnormal
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
muscle atrophy, progressive
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, treatment of
myelitis
myelitis, longitudinal
myelitis, transverse
myocardial infarction
nasal speech
nausea and vomiting
neck pain
neck weakness
neurologic disease, diagnoses of
neuronal degeneration
neuropathology
neuropathy
neuropathy, peripheral, treatment
nusinersen
optic atrophy
owl's eye sign of spinal cord
pain
pain, back
paralysis, acute
paralysis, acute areflexic
paraparesis, flaccid
paraparesis, spastic
Parkinson disease
patient information and support
peripheral vascular disease
pes cavus
poliomyelitis-like illness
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
prognosis
progressive neurologic disorder
quadriparesis
respiratory tract infection
review article
safety
seizure
seizure, children
seizure, treatment of
SMN1 gene
spasticity
spinal cord
spinal cord degeneration
spinal cord, lesion of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
survival motor neuron gene
term infant
tongue, atrophy
tongue, fasciculations of
tongue, weakness
treatment of neurologic disorder
vestibular function, tests of
viral infection
viral infection, CNS
visual field defect
weakness
weakness, generalized
weakness, infant
weight loss
Werdnig-Hoffman disease
Showing articles 200 to 250 of 4802 << Previous Next >>

Amyotrophic Lateral Sclerosis:Hyperintensity of the Corticospinal Tracts on MR of Spinal Cord
AJR 160:604-606, Friedman,D.P.&Tartaglino,L.M., 1993

Clinicopath Conf
Acquired Demyelinating Neuropathy, ? CIDP, ? Motor Neuropathy with Multifocal Conduction Blocks, Cas, 41-1EJM 329:1182-1190,1993., 1993

Brain Imaging in Late-Onset CM2 Gangliosidosis
Neurol 43:2055-2058, Streifler,J.Y.,et al, 1993

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

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

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

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

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

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

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Olfactory Impairment in Motor Neuron Disease:A Pilot Study
JNNP 54:927-928, Elian,M., 1991

Subacute, Reversible Motor Neuron Disease
Neurol 41:1541-1544, Tucker,T.,et al, 1991

Pick's Disease:A Case Clinically Resembling Amyotrophic Lateral Sclerosis
Neurol 41:1831-1833, Sam,M.,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

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

Lymphoma, Motor Neuron Diseases, and Amyotrophic Lateral Sclerosis
Ann Neurol 29:78-86, Younger,D.S.,et al, 1991

Acute Paralytic Poliomyelitis Presenting as Guillain-Barre Syndrome
J Infection 22:129-133, Yohannan,M.D.,et al, 1991

Progressive Motor Neuron Disease Associated with Electrical Injury
Muscle & Nerve 14:977-980991., Sirdofsky,M.D.,et al, 1991

Clinicopath Conf
Case 40-1991, Inclusion-Body Myositis, NEJM 325:1026-1035991., , 1991

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

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

What Causes Motoneuron Disease?
Editorial, Lancet 336:1033-10351990., , 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

Non Alzheimer's Disease Forms of Cerebral Atrophy
Editorial, JNNP 53:929-9311990., Neary,D., 1990

Anti-GM1 IgM Antibodies in Motor Neuron Disease and Neuropathy
Neurol 40:1747-1750, Nobile-Orazio,E.,et al, 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Paraneoplastic Motor Neuron Disease and Renal Cell Carcinoma:Improvement after Nephrectomy
Neurol 40:960-962, Evans,B.K.,et al, 1990

The Spectrum of Neurologic Disease Associated with Anti-GM1 Antibodies
Neurol 40:1067-1072, Sadiq,S.A.,et al, 1990

Lower Motor Neuron Disease in a Patient with Autoantibodies Against Gangliosides GM1 and GD1b:Improvement with Immunotherapy
Neurol 40:842-844, Shy,M.E.,et al, 1990

Polyclonal IgM Anti-GM1 Ganglioside Antibody in Patients with Motor Neuron Disease and Variants
Ann Neurol 27:558-563, Salazar-Grueso,E.F.,et al, 1990

Immunologic Reactivity Against Borrelia Burgdorfi in Patients with Motor Neuron Disease
Arch Neurol 47:586-594, Halperin,J.J.,et al, 1990

2-Amino-3- (methylamino) -Propanoic Acid (BMAA) in Cycad Flour:An Unlikely Cause of ALS & Parkinsonism-Dementia of Guam
Neurol 40:767-772, Duncan,M.W.,et al, 1990

HIV-Related Neuromuscular Syndrome Simulating Motor Neuron Disease
Neurol 40:544-546, Verma,R.K.,et al, 1990

How Frequently Does Classic Amyotrophic Lateral Sclerosis Develop in Survivors of Poliomyelitis
Neurol 40:172-174, Armon,C.,et al, 1990

Amyotrophic Lateral Sclerosis:A Case-Control Study Following Detection of a Cluster in a Small Wisconsin Community
Arch Neurol 47:38-41, Sienko,D.G.,et al, 1990

Neuromuscular Blockade
Lancet 335:382-384, , 1990

HTLV-1 Associated Myelopathy and Polymyositis in a US Native
Neurol 39:1572-1575, Evans,B.K.,et al, 1989

Rising Mortality From Motoneuron Disease in the USA, 1962-84
Lancet 1:710-712, Lilienfeld,D.E.,et al, 1989

Amyotrophic Lateral Sclerosis:Abnormalities of the Tongue on Magnetic Resonance Imaging
Ann Neurol 25:468-472, Cha,C.H.&Patten,B.M., 1989



Showing articles 200 to 250 of 4802 << Previous Next >>