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Differential
(Click to cross reference)
bulbar palsy
chromosome 11
compartment syndrome
creatine phosphokinase(CPK)elevated
electrocardiogram, abnormal
electromyogram
enzyme, defect
enzyme, muscle disease
exercise
exercise intolerance
exercise-related muscle strength increase
familial
fatigue
floppy infant
gene
genetic neurologic disorders
glycogen storage disease
hypotonia, infants
iatrogenic neurologic disorders
ischemic exercise test
leukocytes
McArdle's disease
McArdle's disease, adult onset
misdiagnosis
molecular genetics
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle stiffness
muscle weakness
muscle weakness, proximal
myoglobinuria
myopathy
myopathy, metabolic
neurologic disease, diagnoses of
pain
pain, arm
PAS positive
phosphorylase b kinase deficiency
polymerase chain reaction
proximal muscle atrophy
renal failure
respiratory failure
review article
RFLPs
second wind phenomena
seizure
treatment of neurologic disorder
urine, dark
weakness
weakness, generalized
Showing articles 1450 to 1454 of 1454 << Previous

The Diagnosis & Treatment of Seizures
Pediatr Clin North Am 9:353, Scholl,M.L., 1962

Hysterical Hemiplegia and Hemianesthesia
Postgrad Med 31:339-345, Magee,K.R., 1962

A Case of Cerebellar Ataxia, with a Discussion of Classification
Arch Neurol 3:71, Locke,S.,et al, 1960

Neuro CPC of MGH
Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958

Cerebellar Ataxia in Children
Handout & References., Gilbert,J.J., 1850



Showing articles 1450 to 1454 of 1454 << Previous