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Differential
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advances in neurology
Alzheimer's disease
amyloid angiopathy, cerebral
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
anterior horn cell disease
arm weakness
asthma
asthma, poliomyelitis-like syndrome with
atlanto axial dislocation, congenital
biologic markers
bulbar palsy
bulbar palsy, progressive
cavernous sinus, syndrome
children
chromosomal abnormality
degenerative diseases of CNS
dementia
dementia, frontotemporal
differential diagnosis
distal muscle atrophy
distal muscle weakness
dysphagia
dyspnea
electromyogram
encephalocele
epidemiology of neurology
exercise
familial
fasciculation
fibrillations
flaccid paralysis
Friedreich's ataxia
gene
genetic linkage
genetic neurologic disorders
hemangioma
hoarseness
Huntington's chorea
hyperreflexia
infantile tremor syndrome
intrinsic hand muscles, wasting of
Jakob-Creutzfeldt disease
juvenile distal and segmental muscular atrophy
Kugelberg-Welander syndrome
leg atrophy
leg weakness, unilateral
Lewy body disease, diffuse
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
misdiagnosis
molecular genetics
monomelic amyotrophy
monoparesis
motor neuron disease
motor neuron disease, juvenile form
MRI
MRI, abnormal
MRI, disappearing lesion on
MRI, functional
MRI, spinal cord
multiple sclerosis
multiple system atrophy
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle twitching
muscle wasting, diffuse
muscle weakness
muscular dystrophy
muscular dystrophy, Duchenne
myelomalacia
myotonia dystrophica
nasal speech
neck weakness
nerve conduction studies
neurofibromatosis 1
neurofibromatosis 2
neurologic disease, diagnoses of
ophthalmoplegia
ophthalmoplegia, painful
paraparesis, spastic
Parkinson disease
periodic paralysis
periodic paralysis, thyrotoxic
pes cavus
poliomyelitis-like illness
prognosis
rash
recombinant DNA
review article
RFLPs
spasticity
spina bifida
spinal cord, cervical
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subarachnoid hemorrhage
Tolosa Hunt syndrome
tongue, atrophy
tongue, fasciculations of
tongue, weakness
trauma
treatment of neurologic disorder
tremor
trinucleotide repeats
viral infection, CNS
weight loss
West Nile fever
Showing articles 300 to 350 of 3229 << Previous Next >>

Oligoclonal IgG Bands in Cerebrospinal Fluid in Various Neurological Diseases
Ann Neurol 13:434-439, Chu,A.B.,et al, 1983

Acute Respiratory Failure in Motor Neuron Disease
Arch Neurol 40:30-32, Hill,R.,et al, 1983

Effect on Weakness & Spasticity in Amyotrophic Lateral Sclerosis of Thyrotropin-Releasing Hormone
Lancet 2:73-75, Engel,W.K.,et al, 1983

Amyotrophic Lateral Sclerosis & Pet Exposure
NEJM 309:244-245, Schenkman,M.,et al, 1983

Mercury Intoxication Simulating Amyotrophic Lateral Sclerosis
JAMA 250:642-643, Adams,C.R.,et al, 1983

Adult Polyglucosan Body Disease:Clinical & Nerve Biopsy Findings in Two Cases
Ann Neurol 13:440-444, Vos,A.L.M.,et al, 1983

Syndromes of Amytrophic Lateral Sclerosis & Dementia:Relation to Transmissible Creutzfeldt-Jakob Disease
Ann Neurol 14:17-26, Salazar,A.M.,et al, 1983

Classic Amyotrophic Lateral Sclerosis With Dementia
Arch Neurol 39:681-683, Wilkstrom,J.,et al, 1982

Neurogenic Arthrogryposis in One Identical Twin, Sul
Arch Neurol 39:717-718, Yi,C.,et al, 1982

Enigmatic Dyspnoea:An Unusual Presentation of Motor-Neuron Disease
Lancet 1:933-935, Nightingale,S.,et al, 1982

Long-Term Management of Respiratory Failure in Amyotrophic Lateral Sclerosis
Ann Neurol 12:18-23, Sivak,E.,et al, 1982

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

Clinical & Electrophysiological Studies in Primary Lateral Sclerosis
Jr. , Arch Neurol 39:662-664982., Russo,L.S., 1982

Amyotrophic Lateral Sclerosis & Paraproteinemia
Neurol 32:896-898, Krieger,C.,et al, 1982

Nonfamilial Amyotrophy with Dementia, etc
Advances in Neurology, Human Motor Neuron Diseases, Ed. Rowland, Raven Press, NY 1982 vol 36, p 173., Tyler,H.R., 1982

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Preservation of the Phrenic Motorneurons in Werdnig-Hoffman Disease
Ann Neurol 9:506-510, Kuzuhara,S.,et al, 1981

Primary Lateral Sclerosis
Arch Neurol 38:630-633, Beal,M.F.,et al, 1981

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
Ann Neurol 8:317-324, Steiman,G.S.,et al, 1980

Gross Demonstration of Atrophic Cauda Equina Roots in Motor Neuron Disease, An Improved Method
Arch Neurol 37:394, Meneses,A., 1980

Management of Hypoventilation in Motor Neuron Disease Presenting with Respiratory Insufficiency
Ann Neurol 7:188-191, Sivak,E.D.,et al, 1980

Progressive Bulbar Paralysis Associated With Neurgl Deafness, A Nosological Entity
Arch Neurol 37:214-216, Alberica,R.,et al, 1980

Alzheimer Neurofibrillary Tangles in Diseases Other Than Senile & Presenile Dementia
Ann Neurol 5:288-294, Wisniewski,K.,et al, 1979

Spirometry in Amyotrophic Lateral Sclerosis
Arch Neurol 36:74-80, Fallat,R.J.,et al, 1979

Age & Cerebrospinal-Fluid Protein in Motor-Neuron Disease
NEJM 300:437-438, Guiloff,R.J.,et al, 1979

Double-Blind Study of Modified Neurotoxin in Motor Neuron Disease
Neurol 29:77-81, Tyler,H.R., 1979

Presenile Dementia With Motor Neuron Disease in Japan, A New Entity
Arch Neurol 36:592-593, Mitsuyama,Y.,et al, 1979

Subacute Motor Neuronopathy:A Remote Effect of Lymphoma
Ann Neurol 5:271-287, Schold,S.C.,et al, 1979

Amyotrophic Lateral Sclerosis With Ophthalmoplegia; A Cliniocopathologic Study
Arch Neurol 36:615-617, Harvey,D.G.,et al, 1979

Remission of a Syndrome Indistinguishable from Motor Neuron Disease after Resection of Bronchial Carcinoma
BMJ 2:176-177, , 1979

Clinical Pathological Conference
Amyotrophic Lateral Sclerosis, Case Record 46-1979, NEJM 301:1104-1111979., , 1979

Diaphragmatic Paralysis in Motor Neuron Disease
Neurol 28:18, Parhad,I.M.,et al, 1978

Free Amino Acid Levels in Amyotrophic Lateral Sclerosis
Ann Neurol 3:305, Patten,B.M.,et al, 1978

Amyotrophic Lateral Sclerosis
Arch Neurol 35:638-642, Rosen,A.D., 1978

Cellular Immunity In Guamanians with Amyotrophic Lateral Sclerosis & Parkinsonism-Dementia
NEJM 299:680-685, Hoffman,P.M.,et al, 1978

Sparing of the Onufrowicz Nucleus in Sacral Anterior Horn Lesions
Ann Neurol 4:245-249, Iwata,M.,et al, 1978

Lower Motor Neuron Disease with Spinocerebellar Degeneration
Ann Neurol 2:524, Page,R.W.,et al, 1977

Control of Emotional Expression in Pseudobulbar Palsy
Arch Neurol 34:717, Lieberman,A.,et al, 1977

Cervical Spondylotic Myelopathy with Reversible Fasciculations in the Lower Extremities
Arch Neurol 34:774, Kasdon,D., 1977

Viruslike Particles in Amytrophic Lateral Sclerosis:Electron Microscopical Study of a Case
Ann Neurol 1:290, Pena,C.E., 1977

Antibody Titers to Coxsackieviruses in Amyotrophic Lateral Sclerosis
NEJM 295:107, Cremer,N.E.,et al, 1976

Postradiation Motor Neuron Syndrome
Arch Neurol 33:786, Sadowsky,C.H.,et al, 1976

Frequency of Nerve Fiber Degeneration of Peripheral Motor & Sensory Neurons in Amyotrophic Lateral Sclerosis
Neurol 25:781, Dyck,P.J.,et al, 1975

Mononeuropathy of the Deep Palmar Branch of the Ulnar Nerve in a Diabetic
Arch Neurol 32:564, Finelli,P.F., 1975

Neuromuscular Disease in Primary Hyperparathyroidism
Ann Int Med 80:182, Patten,B.M.,et al, 1974

Poliomyelitis-A Persistent Problem
NEJM 288:370, Weinstein,L., 1973

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

Neuropathy in Thyrotoxicosis-Correspondence-NEJM 289:219
1973., , 1973



Showing articles 300 to 350 of 3229 << Previous Next >>