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abiotrophy
adult polyglucosan body disease
advance directives
advances in neurology
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
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amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
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amyotrophic lateral sclerosis-like syndrome
anti IgLON5
apnea
areflexia
arm weakness
aspiration
autoantibodies
autonomic dysfunction
axonal degeneration
Babinski sign
basal ganglia, lesion of
behavioral disorder
BiPAP
bladder dysfunction
botulinum toxin
brain atrophy
Brugada syndrome
bulbar palsy
bulbar palsy, acute
bulbar palsy, childhood
bulbar palsy, progressive
C9orf72
CAG repeats
camptocormia
CAT scan, abnormal
CAT scan, emission, abnormal
cerebral cortex
cerebral cortical atrophy
chewing, impaired
Clinical Pathologic Conference(C.P.C.)
clonus
cognition
coma, episodic
complications
creatine phosphokinase(CPK)elevated
crying, pathologic
deafness
degenerative diseases of CNS
delay in diagnosis
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dentatorubral-pallidoluysian atrophy
diabetes mellitus
differential diagnosis
disability, neurological
distal muscle weakness
DNA probes
drooling
dying
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electromyogram
electromyogram, decremental response
emotional lability
encephalitis
encephalitis, autoimmune
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epidemiology of neurology
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facial weakness
facial weakness, bilateral
falling
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fatigable chewing
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fibrillations
fine motor function, impaired
flaccid paralysis
flail arm syndrome
foot drop
fragile-X syndrome
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gag reflex, depressed
gait disorder
gait, spastic
gastrostomy
gastrostomy, percutaneous endoscopic
gene
gene mutation
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genetic neurologic disorders
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glycogen storage disease
gynecomastia
hand weakness
hearing loss
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hoarseness
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hypophonia
hyporeflexia
hypotension, systemic
imbalance
immunotherapy
inclusion bodies
intellectual deficit
intellectual deterioration
internal capsule
intrinsic hand muscles, wasting of
jaw clonus
jaw closure weakness
jaw jerk, abnormal
Jewish
Kugelberg-Welander syndrome
laughing
laughing, pathologic
leg weakness, bilateral
leg weakness, unilateral
leukoencephalopathy
life expectancy
liver disease
lobar atrophy
locked-in syndrome
masseter muscle weakness
memory, defect of recent
memory, impairment of
Mills syndrome
mimics
misdiagnosis
molecular genetics
mortality
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motor neuron disease, misdiagnosis
MRI
MRI, abnormal
multiple sclerosis, differential diagnosis of
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muscle weakness
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muscular dystrophy
mutism
myelomalacia
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myocardial injury
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myopathy
myotonia dystrophica
nasal speech
neck weakness
neoplasm, primary intracranial
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neuroendocrinology
neurogenic bladder
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neurologic disease, diagnoses of
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neuronal migration disorder
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optic atrophy
pain
pain, management of chronic
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polyglucosan body
polyglucosan body disease
polymerase chain reaction
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practice guidelines
primary lateral sclerosis
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progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
psychiatric problems in neurologic disorders
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pyramidal tract dysfunction
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quadriplegia
quality of life
radiculopathy
REM sleep behavior disorder
repetitive nerve stimulation
respirator
respiratory failure
retinitis pigmentosa
review article
riluzole
risk factors
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salivation, excessive
sensorineural hearing loss
sleep
sleep pathology and physiology
spasticity
speech disorder
speech, loss of
spinal cord, lesion of
spinal cord, pathologic exam of
spinal muscular atrophy
spinocerebellar ataxia type 1
spinocerebellar degeneration
standing difficulty
sudden death
tandem gait, ataxic
temporal lobe, atrophy
temporalis muscle wasting
testicular atrophy
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, weakness
trauma
treatment of neurologic disorder
tremor
tremor, postural
trinucleotide repeats
tripping
unconsciousness
unconsciousness, episodic
unconsciousness, transient
urinary incontinence
vestibular function, tests of
vocalizations
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weight loss
West Nile fever
wheelchair
white matter disease
X-linked bulbospinal neuronopathy
Showing articles 350 to 400 of 2707 << Previous Next >>

Primary Amyloidosis with Peripheral Neuropathy & Signs of Motor Neuron Disease
Neurol 36:1125-1127, Abarbanel,J.M.,et al, 1986

Slow Resolution of Multifocal Weakness & Fasciculation:A Reversible Motor Neuron Syndrome
Neurol 36:1260-1263, Chad,D.A.,et al, 1986

Motor Neuron Disease & Plasma Cell Dyscrasia
Neurol 36:1429-1436, Shy,M.E.,et al, 1986

A Double-Blind, Placebo-Controlled Trial of TRH in Amyotrophic Lateral Sclerosis
Neurol 36:141-145, Caroscio,J.T.,et al, 1986

Controlled Trial of Thyrotropin Releasing Hormone in Amyotrophic Lateral Sclerosis
Neurol 36:146-151, Brooke,M.H.,et al, 1986

Amyotrophic Lateral Sclerosis:Effects of Administration of Thyrotropin-Releasing Hormone
Neurol 36:152-159, Mitsumoto,H.,et al, 1986

Amyotrophic Lateral Sclerosis, Associated Clinical Disorders & Immunological Evaluations
Arch Neurol 43:234-238, Appel,S.H.,et al, 1986

Familial Adult Motor Neuron Disease:Amyotrophic Lateral Sclerosis
Neurol 36:511-517, Mulder,D.W.,et al, 1986

From Benign Fasciculations & Cramps to Motor Neuron Disease
Neurol 36:997-998, Shepherd-Fleet,W.&Watson,R.T., 1986

Classification of Peripheral Neuropathy:The Long and the Short of It
Muscle & Nerve 9:711-719986., Sabin,T.J., 1986

Post-Polio Syndrome
J Med Assoc Ga 74:510-511, Bailey,A.A., 1985

Amytrophic Lateral Sclerosis:Part 2, Etiopathogenesis
Ann Neurol 18:419-431, Tandan,R.,et al, 1985

Isolation of LAV/HTLV-III From a Patient with Amyotrophic Lateral Sclerosis
NEJM 313:324-325, Hoffman,P.M.,et al, 1985

ALS & Pet Exposure
Neurol 35:717-720, Tarras,S.,et al, 1985

Autosomal Recessive Distal Muscular Dystrophy:A Comparative Study with Distal Myopathy with Rimmed Vacuole Formation
Ann Neurol 17:51-59, Nonaka,I.,et al, 1985

Progressive Dementia, Visual Deficits, Amyotrophy, & Microinfarcts
Neurol 35:789-796, Kaplan,J.G.,et al, 1985

Congenital Hydrocephalus & Eye Abnormalities with Severe Developmental Brain Defects:Warburg's Syndrome
Ann Neurol 16:60-65, Bordarier,C.,et al, 1984

Cerebro-ocular Dysgenesis (Walker-Warberg Syndrome) :Neuropathologic & Etiologic Analysis
Neurol 34:1531-1541, Williams,R.S.,et al, 1984

Classic & Generalized Variants of Pick's Disease, A Clinicopath, Ultrastruc & Immunocyto Study
Ann Neurol 16:467-480, Munoz-Garcia,D.,et al, 1984

Amyotrophic Lateral Sclerosis:A Double-Blind Crossover Trial of Thyrotropin-Releasing Hormone
JNNP 47:1332-1334, Imoto,K.,et al, 1984

Nystagmus in Motor Neuron Disease:Clinicopathological Study of Two Cases
Ann Neurol 16:71-77, Kushner,M.J.,et al, 1984

Inhibition of Terminal Axonal Sprouting by Serum From Patients with Amyotrophic Lateral Sclerosis
NEJM 311:933-939, Gurney,M.E.,et al, 1984

Familial Occurrence of Amyotrophic Lateral Sclerosis, Parkinsonism, & Dementia
Ann Neurol 16:642-648, Schmitt,H.P.,et al, 1984

Monomelic Amyotrophy
Arch Neurol 41:388-394, Gourie-Devi,M.,et al, 1984

Benign Focal Amyotrophy
Arch Neurol 41:678-679, Riggs,J.E.,et al, 1984

Conjugal Amyotrophic Lateral Sclerosis
Ann Neurol 14:699, Paolino,E.,et al, 1983

Glutamate Dehydrogenase Deficiency in Patients with Olivopontocerebellar Atrophy
Neurol 33:1322-1326, Duvoisin,R.C.,et al, 1983

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

Quadriceps Myopathy:A Varient of the Limb-Girdle Dystrophy Syndrome
JNNP 46:355-357, Swash,M.,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

Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,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

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

Computed Tomography in Pick's Disease:Findings in a Family Affected in Three Consecutive Generations
J Comput Assist Tomogr 6:907-911, Groen,J.J.,et al, 1982

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

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

Distal Myopathy, Histochemical & Ultrastructural Studies
Arch Neurol 39:367-371, Kumamoto,T.,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

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

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

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,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

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981



Showing articles 350 to 400 of 2707 << Previous Next >>