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Differential
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allodynia
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, cluster
amyotrophic lateral sclerosis, conjugal
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis, work up
angiostrongylus cantonensis
anterior horn cell disease
anticonvulsants
areflexia
arm weakness
arthrogryposis multiplex
atlanto axial dislocation, congenital
Babinski sign
bulbar palsy
bulbar palsy, progressive
burning feet
burning paresthesia
cavernous sinus, syndrome
central core disease
central nervous system, infection of
cerebrospinal fluid, abnormal
cerebrospinal fluid, eosinophilia of
Charcot-Marie-Tooth
children
climate change
Clinical Pathologic Conference(C.P.C.)
cluster, geographic
confusion
constipation
cranial neuropathy
crying, pathologic
degenerative diseases of CNS
dementia
dementia, frontotemporal
diarrhea
diet
differential diagnosis
disorientation
drooling
dying
dysarthria
dysphagia
electromyogram
emotional lability
encephalitis
encephalitis, Powassan
encephalitis, viral
encephalocele
encephalopathy
endemic area
enterovirus
enterovirus infection of CNS
eosinophilia
epidemiology of neurology
fasciculation
Fazio-Londe's disease
fever
fibrillations
flaccid paralysis
flail arm syndrome
foot drop
gene
genetic neurologic disorders
headache
headache, progressive
heavy metal intoxication
helminthic infection of CNS
hemangioma
heralding manifestation
hyperreflexia
hypoglycorrhachia
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
infantile tremor syndrome
infection
intellectual deficit
Kugelberg-Welander syndrome
laughing, pathologic
leg weakness, bilateral
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
meningismus
meningitis, eosinophilic
mental status, abnormal
mimics
misdiagnosis
mortality
motor neuron disease
motor neuron disease, juvenile form
MRI
MRI, abnormal
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
multiple sclerosis
muscle atrophy, progressive
muscle cramp
muscle wasting, diffuse
muscle weakness
myasthenia gravis
myelitis
myelitis, longitudinal
myelitis, transverse
myotonia dystrophica
nausea and vomiting
neck pain
neurofibrillary degeneration
neurologic disease, diagnoses of
neuropathology
neurotoxic
neurotoxin
occupational neurologic disorders
ophthalmoplegia
ophthalmoplegia, painful
owl's eye sign of spinal cord
pain
pain, back
palliative care
paralysis, acute
paralysis, acute areflexic
paraparesis, flaccid
parasitic infection
parasitic infection, CNS
paresthesias
patient information and support
periodic paralysis
periodic paralysis, thyrotoxic
pleocytosis of cerebrospinal fluid
poison, mercury
poison, neurologic problems with
poliomyelitis
poliomyelitis-like illness
polymerase chain reaction
primary lateral sclerosis
prognosis
progressive neurologic disorder
pseudobulbar palsy
public health
quadriparesis
rapidly progressing neurologic illness
raw fish ingestion
respiratory failure
respiratory tract infection
review article
risk factors
rodents
seizure
snail
solvent
spasticity
speech disorder
spina bifida
spinal cord, lesion of
steroid therapy, CNS treatment and complications with
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subarachnoid hemorrhage
sushi
tick bite
Tolosa Hunt syndrome
tongue, atrophy
tongue, fasciculations of
trauma
travel history
travel, foreign
treatment of neurologic disorder
tremor
tricresylphosphate
viral infection
viral infection, CNS
walking, difficulty with
weakness
Werdnig-Hoffman disease
Showing articles 200 to 250 of 3492 << Previous Next >>

Signal Loss in the Motor Cortex on Magnetic Resonance Images in Amyotrophic Lateral Sclerosis
Ann Neurol 33:218-222, Ishikawa,K.,et al, 1993

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

Lymphocytic Infiltrates in the Spinal Cord in Amyotrophic Lateral Sclerosis
Arch Neurol 50:30-36, Engelhardt,J.I.,et al, 1993

Poliomyelitis:Hyperintensity of the Anterior Horn Cells on MRI Images of the Spinal Cord
AJR 161:863-865, Malzberg,M.S.,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

Polyglucosan Body Disease Simulating Amyotrophic Lateral Sclerosis
Neurol 43:785-790, McDonald,T.D.,et al, 1993

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

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

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

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

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

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

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

Pick's Disease:A Case Clinically Resembling Amyotrophic Lateral Sclerosis
Neurol 41:1831-1833, Sam,M.,et al, 1991

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

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

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

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

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

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

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

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

Neuromuscular Blockade
Lancet 335:382-384, , 1990

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



Showing articles 200 to 250 of 3492 << Previous Next >>