Literature DB >> 10814901

The serum nitric oxide levels in patients with Duchenne muscular dystrophy.

K Gücüyener1, E Ergenekon, D Erbas, G Pinarli, A Serdaroğlu.   

Abstract

Nitric oxide is formed in skeletal muscle by the neuronal type nitric oxide synthase and the signalling function of dystrophin and related compounds are in part mediated by nitric oxide. Duchenne muscular dystrophy, mdx mice and patients with Becker dystrophy demonstrated neuronal type nitric oxide synthase deficiency in muscle biopsy specimens. We have intended to find out whether the plasma nitric oxide levels show any abnormality in patients with Duchenne muscular dystrophy. Serum NO levels of Duchenne patients (4.191+/-2.82 micromol/l) were significantly lower than those of the control (39.53+/-19.43 micromol/l) and cerebral palsy (77.84+/-21.70 micromol/l) groups.

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Year:  2000        PMID: 10814901     DOI: 10.1016/s0387-7604(00)00106-6

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  9 in total

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Review 6.  Therapeutic strategies to address neuronal nitric oxide synthase deficiency and the loss of nitric oxide bioavailability in Duchenne Muscular Dystrophy.

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7.  Nitric Oxide (NO) and Duchenne Muscular Dystrophy: NO Way to Go?

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Review 9.  Muscle exercise in limb girdle muscular dystrophies: pitfall and advantages.

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  9 in total

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