MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement von Donkervoort, S., Sabouny, R., Yun, P., Gauquelin, L., Chao, K. R., Hu, Y., Al Khatib, I., Töpf, A., Mohassel, P., Cummings, B. B., Kaur, R., Saade, D., Moore, S. A., Waddell, L. B., Farrar, M. A., Goodrich, J. K., Uapinyoying, P., Chan, S.H. S., Javed, A., Leach, M. E., Karachunski, P., Dalton, J., Medne, L., Harper, A., Thompson, C., Thiffault, I., Specht, S., Lamont, R. E., Saunders, C., Racher, H., Bernier, F. P., Mowat, D., Witting, N., Vissing, J., Hanson, R., Coffman, K. A., Hainlen, M., Parboosingh, J. S., Carnevale, A., Yoon, G., Schnur, R. E., Boycott, K. M., Mah, J. K., Straub, V., Foley, A. Reghan, Innes, A. M., Bönnemann, C. G., Shutt, T. E.

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A new automated tool to quantify nucleoid distribution within mitochondrial networks von Ilamathi, Hema Saranya, Ouellet, Mathieu, Sabouny, Rasha, Desrochers-Goyette, Justine, Lines, Matthew A., Pfeffer, Gerald, Shutt, Timothy E., Germain, Marc

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The R941L mutation in MYH14 disrupts mitochondrial fission and associates with peripheral neuropathy von Almutawa, Walaa, Smith, Christopher, Sabouny, Rasha, Smit, Ryan B., Zhao, Tian, Wong, Rachel, Lee-Glover, Laurie, Desrochers-Goyette, Justine, Ilamathi, Hema Saranya, Suchowersky, Oksana, Germain, Marc, Mains, Paul E., Parboosingh, Jillian S., Pfeffer, Gerald, Innes, A. Micheil, Shutt, Timothy E.

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Aberrant Mitochondrial Morphology and Function in the BTBR Mouse Model of Autism Is Improved by Two Weeks of Ketogenic Diet von Ahn, Younghee, Sabouny, Rasha, Villa, Bianca R., Yee, Nellie C., Mychasiuk, Richelle, Uddin, Golam M., Rho, Jong M., Shutt, Timothy E.

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Adenosine versus intravenous calcium channel antagonists for supraventricular tachycardia von Alabed, S, Sabouni, A, Providencia, R, Atallah, E, Qintar, M, Chico, TJ

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