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You searched for: Author/Creator Mihaylova, Violeta

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1. Altered skeletal muscle (mitochondrial) properties in patients with mitochondrial DNA single deletion myopathy. Issue 1 (December 2016)

2. Clinical and genetic characteristics of late-onset Huntington's disease. (April 2019)

3. Collagen VI-Related Myopathy Caused by Compound Heterozygous Mutations of COL6A3 in a Consanguineous Kurdish Family. Issue 3 (March 2021)

5. Possible Toxicity of Tuberculostatic Agents in a Patient With a Novel TYMP Mutation Leading to Mitochondrial Neurogastrointestinal Encephalomyopathy. (June 2013)

6. Possible Toxicity of Tuberculostatic Agents in a Patient With a Novel TYMP Mutation Leading to Mitochondrial Neurogastrointestinal Encephalomyopathy. (June 2013)