Phenotypic, Electrophysiologic, and Imaging Spectrum of Hirayama Disease from Northern India by Gomathy, Saranya B, Priyanka, Yamini, Garg, Ajay, Macken, William L, Agarwal, Ayush, Ahmed, Tanveer, Bhatia, Rohit, Goel, Vinay, Garg, Kanwaljeet, Pitceathly, Robert Ds, Reilly, Mary M, Hanna, Michael G, Srivastava, Mv Padma, Vishnu, Venugopalan Y

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Effects of ketosis in mitochondrial myopathy: potential benefits of a mitotoxic diet by Pitceathly, Robert DS, Viscomi, Carlo

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Novel Biallelic NSUN3 Variants Cause Early-Onset Mitochondrial Encephalomyopathy and Seizures by Paramasivam, Arumugam, Meena, Angamuthu K., Venkatapathi, Challa, Pitceathly, Robert D.S., Thangaraj, Kumarasamy

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Interventions for dysphagia in long-term, progressive muscle disease by Jones, Katherine, Pitceathly, Robert D S, Rose, Michael R, McGowan, Susan, Hill, Marguerite, Badrising, Umesh A, Hughes, Tom

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Rhabdomyolysis: a genetic perspective by Scalco, Renata Siciliani, Gardiner, Alice R, Pitceathly, Robert Ds, Zanoteli, Edmar, Becker, Jefferson, Holton, Janice L, Houlden, Henry, Jungbluth, Heinz, Quinlivan, Ros

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Adults with RRM2B-related mitochondrial disease have distinct clinical and molecular characteristics by PITCEATHLY, Robert D. S, SMITH, Conrad, DESCHAUER, Marcus, POHL, Ute, ROBERTS, Mark E, JACKSON, Matthew C, HALFPENNY, Christopher A, TURNPENNY, Peter D, LUNT, Peter W, HANNA, Michael G, SCHAEFER, Andrew M, MCFARLAND, Robert, FRATTER, Carl, HORVATH, Rita, CHINNERY, Patrick F, TURNBULL, Douglass M, POULTON, Joanna, TAYLOR, Robert W, GORMAN, Grainne S, ALSTON, Charlotte L, LANGPING HE, CRAIG, Kate, BLAKELY, Emma L, EVANS, Julie C, TAYLOR, John, SHABBIR, Zarfishan

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Moving towards clinical trials for mitochondrial diseases by Pitceathly, Robert D.S., Keshavan, Nandaki, Rahman, Joyeeta, Rahman, Shamima

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Extra-ocular muscle MRI in genetically-defined mitochondrial disease by Pitceathly, Robert D. S., Morrow, Jasper M., Sinclair, Christopher D. J., Woodward, Cathy, Sweeney, Mary G., Rahman, Shamima, Plant, Gordon T., Ali, Nadeem, Bremner, Fion, Davagnanam, Indran, Yousry, Tarek A., Hanna, Michael G., Thornton, John S.

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Mitochondrial DNA Analysis from Exome Sequencing Data Improves Diagnostic Yield in Neurological Diseases by Poole, Olivia V., Pizzamiglio, Chiara, Murphy, David, Falabella, Micol, Macken, William L., Bugiardini, Enrico, Woodward, Cathy E., Labrum, Robyn, Efthymiou, Stephanie, Salpietro, Vincenzo, Chelban, Viorica, Kaiyrzhanov, Rauan, Maroofian, Reza, Amato, Anthony A., Gregory, Allison, Hayflick, Susan J., Jonvik, Hallgeir, Wood, Nicholas, Houlden, Henry, Vandrovcova, Jana, Hanna, Michael G., Pittman, Alan, Pitceathly, Robert D.S., Alkhawaja, Issam, Banu, Selina, Bonsignore, Maria, Breza, Marianthi, Di Rosa, Gabriella, Heidari, Morteza, Koutsis, Georgios, Maagdenberg, Arn M.J.M., Macaya, Alfons, Münchau, Alexander, Scuderi, Carmela, Zharkinbekova, Nazira

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A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial Disease: e0145500 by Rajakulendran, Sanjeev, Pitceathly, Robert DS, Taanman, Jan-Willem, Costello, Harry, Sweeney, Mary G, Woodward, Cathy E, Jaunmuktane, Zane, Holton, Janice L, Jacques, Thomas S, Harding, Brian N

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