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Neutrophil function in duchenne muscular dystrophy
Journal article   Peer reviewed

Neutrophil function in duchenne muscular dystrophy

U. Karagol, D. Gardner-Medwin and F.L. Mastaglia
Journal of the Neurological Sciences, Vol.73(1), pp.73-77
1986
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Abstract

Spontaneous migration, chemotactic and bactericidal activity and nitrobluetetrazolium (NBT) reduction by neutrophils from patients with Duchenne muscular dystrophy were evaluated using quantitative techniques. Significant reductions in spontaneous migration and chemotaxis were found in the DMD group when compared with a control group of subjects. No significant differences were found in bactericidal activity or NBT reduction. The findings suggest that there is a defect in the contractile system or cell membrane function of neutrophils in DMD and that the genetic defect is expressed in leucocytes as well as other tissues.

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Citation topics
1 Clinical & Life Sciences
1.127 Molecular & Cell Biology - Pharmacology
1.127.938 NADPH Oxidase
Web Of Science research areas
Clinical Neurology
Neurosciences
ESI research areas
Neuroscience & Behavior
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