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Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts.
Jaksch M, Paret C, Stucka R, Horn N, Müller-Höcker J, Horvath R, Trepesch N, Stecker G, Freisinger P, Thirion C, Müller J, Lunkwitz R, Rödel G, Shoubridge EA, Lochmüller H. Jaksch M, et al. Among authors: paret c. Hum Mol Genet. 2001 Dec 15;10(26):3025-35. doi: 10.1093/hmg/10.26.3025. Hum Mol Genet. 2001. PMID: 11751685
Acetabular labrum: MRI in asymptomatic volunteers.
Cotten A, Boutry N, Demondion X, Paret C, Dewatre F, Liesse A, Chastanet P, Fontaine C. Cotten A, et al. Among authors: paret c. J Comput Assist Tomogr. 1998 Jan-Feb;22(1):1-7. doi: 10.1097/00004728-199801000-00001. J Comput Assist Tomogr. 1998. PMID: 9448753 Clinical Trial.
90 results