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Differential
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acetylcholine receptor antibody
adverse drug reaction
amyotrophic lateral sclerosis, differential diagnosis
anterior tibial muscle weakness
antistriational muscle antibody
areflexia
arrhythmia, cardiac
Bell's phenomenon
botulism
brainstem, lesion of
bulbar palsy
calf atrophy
canned food
cardiac arrest
cardiac arrest and resuscitation
cataracts
central core disease
chewing, impaired
children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
Coats syndrome
Collier's sign
congenital myopathy
creatine phosphokinase(CPK)elevated
descending paralysis
diplopia
distal muscle weakness
dysarthria
dysphagia
dyspnea
electromyogram
electromyogram, decremental response
eye closure
face, elongated
facial appearance, abnormal
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
false negative
familial
fatigable chewing
fatigue
fibrillations
food poisoning
foot drop
gag reflex, depressed
gait disorder
gammaglobulin therapy, intravenous
gaze palsy
gaze palsy, horizontal
gaze palsy, vertical
gene mutation
genetic neurologic disorders
genetic testing
hand weakness
histochemistry of muscle
hypophonia
hypotonia
immunohistochemistry
immunosuppressive agents
inclusion body myositis
internuclear ophthalmoplegia
intrinsic hand muscles, wasting of
Kearns-Sayre syndrome
leg weakness, bilateral
lid abnormalities
lid closure, weakness of
lid twitch
lordosis
mediastinum, mass of
Melkersson's syndrome
mestinon
misdiagnosis
mitochondrial disease
motor neuron disease
multicore myopathy
muscle atrophy, progressive
muscle biopsy
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, diagnosis
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, drug induced
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, ocular
myasthenia gravis, presenting manifestations
myasthenia gravis, prognosis of
myasthenia gravis, remission of
myasthenia gravis, seronegative
myasthenia gravis, treatment of
myasthenic sneer
myopathy
myopathy, centronuclear
myopathy, inflammatory
myopathy, mitochondrial
myotonia
myotonia dystrophica
nasal regurgitation
nasal speech
nausea and vomiting
neck weakness
nemaline rod myopathy
nerve conduction studies
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuroophthalmology
neurotoxin
nystagmus
ocular motility, disorders of
ocular myopathy
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
orbicularis oculi muscle
oropharyngeal weakness
overlap syndrome
penicillamine
percussion induced muscle contraction
plasmapheresis
polymyositis
positive sharp waves
prognosis
progressive neurologic disorder
pseudointernuclear ophthalmoplegia
ptosis
ptosis, alternating
ptosis, bilateral
quadriparesis, acute
quinine
ragged-red fibers
rapidly progressing neurologic illness
repetitive nerve stimulation
respiratory failure
review article
saccadic eye movements
saccadic eye movements, abnormal
scoliosis
seronegative
shoulder-girdle wasting
single-fiber electromyography
sleep
sloped shoulders
spinal muscular atrophy
standing difficulty
steroid
steroid therapy, CNS treatment and complications with
temporalis muscle wasting
tensilon
tensilon test, false negative
tensilon test, false positive
tensilon test, paradoxical
thymectomy
thymoma
tongue, weakness
toxins, nervous system
transverse smile
treatment of neurologic disorder
trinucleotide repeats
upgaze, paralysis of
voice, abnormality of
walking, difficulty with
weakness
weakness, acute
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weaning from respirator, failure to
weight loss
wheelchair
whistle, inability to
winging of scapula
Showing articles 1400 to 1450 of 3180 << Previous Next >>

Another Kind of Knapsack Palsy
Neurol 46:585-586, Pringle,C.E.,et al, 1996

A 64-Year-Old Man with Diabetes and Ascending Paraplegia
Lancet 347:516, Gliemroth,J.,et al, 1996

Autonomic Ganglionitis with Severe Hypertension, Migraine, and Episodic but Fatal Hypotension
Neurol 47:817-821, Lee,H.C.,et al, 1996

Infarction of Superior Cerebellar Artery Presenting as Cerebellar Symptoms
Stroke 27:1679-1681, Terao,S.,et al, 1996

Risk of Stroke During Long-Term Anticoagulant Therapy in Patients After Myocardial Infarction
Ann Neurol 39:301-307, 2811996., Azar,A.J.,et al, 1996

Palliative Care in Neurology
Neurol 46:870-872, 5981996., Bernat,J.L.,et al, 1996

Restless Legs Syndrome and Leg Cramps in Fibromyalgia Syndrome:A Controlled Study
BMJ 312:1339, Yunus,M.B.&Aldag,J.C., 1996

Campylobacter Jejuni Infection and Anti-GM1 Antibodies in Guillain-Barre Syndrome
Ann Neurol 40:181-187, Jacobs,B.C.,et al, 1996

Antiamphiphysin Antibodies with Small-Cell Lung Carcinoma and Paraneoplastic Encephalomyel; itis
Ann Neurol 39:659-667, Dropcho,E.J., 1996

HIV Encephalitis Presenting with Severe Generalized Chorea
Neurol 46:1163-1165, Gallo,B.V.,et al, 1996

Intravenous Immunoglobulin Treatment of Neurological Disease
JNNP 60:359-361, Otten,A.,et al, 1996

A Woman with a Relapsing Psychosis Who Got Better with Prednisone
Lancet 347:1288, Cohen,L.,et al, 1996

Cost-Effectiveness Analysis:What Is It and How Will It Influence Neurology
Ann Neurol 39:818-823, Holloway,R.G., 1996

The"Gulf War Syndrome"-Is There Evidence of Dysfunction in the Nervous System
JNNP 60:449-451, Jamal,G.A.,et al, 1996

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

A New Variant of Creutzfeldt-Jakob Disease in the UK
Lancet 347:921-925, 915, 916, 91796., Will,R.G.,et al, 1996

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

Cytomegalovirus Infection and Guillain-Barre Syndrome:The Clinical, Electrophysiologic, and Prognostic Features
Neurol 47:668-673, Visser,L.H.,et al, 1996

Prospective Evaluation of MRI Lumbosacral Nerve Root Enhancement in Acute Guillain-Barre Syndrome
Neurol 47:813-817, Gorson,K.C.,et al, 1996

Intravenous IgG in Guillain-Barre Syndrome
BMJ 313:376-377, Hughes,R.A.C., 1996

Lyme Radiculoneuritis Treated with Intravenous Immunoglobin
Neurol 46:1174-1175, Crisp,D.&Ashby,P., 1996

Sustained Myoglobinuria:The Presenting Manifestation of Dermatomyositis
Neurol 47:119-123, Rose,M.R.,et al, 1996

Multiple Mitochondrial DNA Deletions in Sporadic Inclusion Body Myositis:A Study of 56 Patients
Ann Neurol 39:789-795, Santorelli,F.M.,et al, 1996

Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
JNNP 61:1-3, Shneerson,J.M., 1996

Inclusion Body Myositis
JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996

Acute Type II Myofiber Atrophy in Critical Illness
Neurol 46:819-821, 6001996., Gutman,L.,et al, 1996

Muscle is Electrically Inexcitable in Acute Quadriplegic Myopathy
Neurol 46:731-736, 6001996., Rich,M.M.,et al, 1996

Neurogenic Muscle Hypertrophy
Muscle & Nerve 19:811-818996., Gutmann,L., 1996

Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
Neurol 47:579-580, El-Schahawi,M.,et al, 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Mushroom Myopathy
Muscle & Nerve 19:790-792996., Gonzalez,J.,et al, 1996

Isolated Neck Extensor Myopathy:A Common Cause of Dropped Head Syndrome
Neurol 46:917-921, Katz,J.S.,et al, 1996

Kobberling-Dunnigan Syndrome:A Rare Cause of Generalized Muscular Hypertrophy
Muscle & Nerve 19:843-847996., Wildermuth,S.,et al, 1996

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

Brain and Spinal Cord MRI in Motor Neuron Disease
JNNP 61:314-317, Thorpe,J.W.,et al, 1996

Amyotrophic Lateral Sclerosis and Occupational History
Arch Neurol 53:730-733, Strickland,D.,et al, 1996

Avoiding False Positive Diagnoses of Motor Neuron Disease:Lessons from the Scottish Motor Neuron Disease Register
JNNP 60:147-151, Davenport,R.J.,et al, 1996

Diagnosing Motor Neurone Disease
BMJ 312:650-651, Chancellor,A.M., 1996

Motor Neuron Disease
BMJ 313:244, Shneerson,J.M., 1996

Motor Neuron Disease Presenting as Acute Respiratory Failure:A Clinical and Pathological Study
JNNP 60:455-458, Chen,R.,et al, 1996

Dose-Ranging Study of Riluzole in Amyotrophic Lateral Sclerosis
Lancet 347:1425-1431, Lacomblez,L.,et al, 1996

Skin Involvement in Amyotrophic Lateral Sclerosis
lancet 347:1226-1227, Kolde,G.,et al, 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

AAEM Case Report#13:Diabetic Amyotrophy
Muscle & Nerve 19:939-945996., Chokroverty,S.&Sander,H.W., 1996

Ethylene Oxide Neurotoxicity:A Cluster of 12 Nurses with Peripheral and Central Nervous System Toxicity
Neurol 46:992-998, Brashear,A.,et al, 1996

Blepharospasm:Report of a Workshop
Neurol 46:1213-1218, Hallett,M.&Daroff,R.B., 1996

Clinicopath Conf
Hypertension, MI, and Cerebral Infarctions with Pheochromocytoma, Am J Med 100:357-36496., , 1996

Motor Neuron Disease:A Paraneoplastic Process Associated with Anti-Hu Antibody and Small-Cell Lung Carcinoma
Ann Neurol 40:112-116, Verma,A.,et al, 1996

Opsoclonus
Semin Neurol 16:21-26, Averbuch-Heller,L.&Remler,B., 1996



Showing articles 1400 to 1450 of 3180 << Previous Next >>