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Year Number of Results
2010 1
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Page 1
Coenzyme Q and mitochondrial disease.
Quinzii CM, Hirano M. Quinzii CM, et al. Dev Disabil Res Rev. 2010;16(2):183-8. doi: 10.1002/ddrr.108. Dev Disabil Res Rev. 2010. PMID: 20818733 Free PMC article. Review.
Primary and secondary CoQ(10) deficiencies in humans.
Quinzii CM, Hirano M. Quinzii CM, et al. Biofactors. 2011 Sep-Oct;37(5):361-5. doi: 10.1002/biof.155. Epub 2011 Oct 11. Biofactors. 2011. PMID: 21990098 Free PMC article. Review.
Cerebellar Ataxia and CoQ10 Deficiency.
Quinzii CM, Hirano M, Naini A. Quinzii CM, et al. J Neurol Disord Stroke. 2013;1(1):1004. J Neurol Disord Stroke. 2013. PMID: 25126613 Free PMC article. No abstract available.
Fhl1 W122S causes loss of protein function and late-onset mild myopathy.
Emmanuele V, Kubota A, Garcia-Diaz B, Garone C, Akman HO, Sánchez-Gutiérrez D, Escudero LM, Kariya S, Homma S, Tanji K, Quinzii CM, Hirano M. Emmanuele V, et al. Hum Mol Genet. 2015 Feb 1;24(3):714-26. doi: 10.1093/hmg/ddu490. Epub 2014 Sep 30. Hum Mol Genet. 2015. PMID: 25274776 Free PMC article.
ANO10 mutations cause ataxia and coenzyme Q₁₀ deficiency.
Balreira A, Boczonadi V, Barca E, Pyle A, Bansagi B, Appleton M, Graham C, Hargreaves IP, Rasic VM, Lochmüller H, Griffin H, Taylor RW, Naini A, Chinnery PF, Hirano M, Quinzii CM, Horvath R. Balreira A, et al. J Neurol. 2014 Nov;261(11):2192-8. doi: 10.1007/s00415-014-7476-7. Epub 2014 Sep 3. J Neurol. 2014. PMID: 25182700 Free PMC article.
17 results