Natural History of Leigh Syndrome: A Study of Disease Burden and Progression by Lim, Albert Z., Ng, Yi Shiau, Blain, Alasdair, Jiminez‐Moreno, Cecilia, Alston, Charlotte L., Nesbitt, Victoria, Simmons, Louise, Santra, Saikat, Wassmer, Evangeline, Blakely, Emma L., Turnbull, Doug M., Taylor, Robert W., Gorman, Gráinne S., McFarland, Robert

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Consensus-based statements for the management of mitochondrial stroke-like episodes by Ng, Yi Shiau, Bindoff, Laurence A, Gorman, Gráinne S, Horvath, Rita, Klopstock, Thomas, Mancuso, Michelangelo, Martikainen, Mika H, Mcfarland, Robert, Nesbitt, Victoria, Pitceathly, Robert D S, Schaefer, Andrew M, Turnbull, Doug M

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1404 Education health care plans for children with mitochondrial diseases by Nesbitt, Victoria, Moore, Rebecca

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Mitochondrial respiratory chain disease in children undergoing cardiac transplantation: A prospective study by Bates, Matthew G.D, Nesbitt, Victoria, Kirk, Richard, He, Langping, Blakely, Emma L, Alston, Charlotte L, Brodlie, Malcolm, Hasan, Asif, Taylor, Robert W, McFarland, Robert

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Forecasting stroke-like episodes and outcomes in mitochondrial disease by Ng, Yi Shiau, Lax, Nichola Z, Blain, Alasdair P, Erskine, Daniel, Baker, Mark R, Polvikoski, Tuomo, Thomas, Rhys H, Morris, Christopher M, Lai, Ming, Whittaker, Roger G, Gebbels, Alasdair, Winder, Amy, Hall, Julie, Feeney, Catherine, Farrugia, Maria Elena, Hirst, Claire, Roberts, Mark, Lawthom, Charlotte, Chrysostomou, Alexia, Murphy, Kevin, Baird, Tracey, Maddison, Paul, Duncan, Callum, Poulton, Joanna, Nesbitt, Victoria, Hanna, Michael G, Pitceathly, Robert D S, Taylor, Robert W, Blakely, Emma L, Schaefer, Andrew M, Turnbull, Doug M, McFarland, Robert, Gorman, Gráinne S

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Disease progression in patients with single, large-scale mitochondrial DNA deletions by GRADY, John P, CAMPBELL, Georgia, TURNBULL, Doug M, McFARLAND, Robert, RATNAIKE, Thiloka, BLAKELY, Emma L, FALKOUS, Gavin, NESBITT, Victoria, SCHAEFER, Andrew M, MCNALLY, Richard J, GORMAN, Grainne S, TAYLOR, Robert W

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Digenic Leigh syndrome on the background of the m.11778G>A Leber hereditary optic neuropathy variant by Blickhäuser, Beryll, Stenton, Sarah L, Neuhofer, Christiane M, Floride, Elisa, Nesbitt, Victoria, Fratter, Carl, Koch, Johannes, Kauffmann, Birgit, Catarino, Claudia, Schlieben, Lea Dewi, Kopajtich, Robert, Carelli, Valerio, Sadun, Alfredo A, McFarland, Robert, Fang, Fang, La Morgia, Chiara, Paquay, Stéphanie, Nassogne, Marie Cécile, Ghezzi, Daniele, Lamperti, Costanza, Wortmann, Saskia, Poulton, Jo, Klopstock, Thomas, Prokisch, Holger

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Age at diagnosis, anthropometry and birthweight in two ethnically different cohorts of children with type 1 diabetes living in Northwest England or Singapore by Ng, Sze May, Chandrasekaran, Surendran, Nesbitt, Victoria, Grey, Alexandra, Lim, Pei Kwee, Hui, Yuen Ching, Lek, Ngee

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Epilepsy in adults with mitochondrial disease: A cohort study by Whittaker, Roger G., Devine, Helen E., Gorman, Grainne S., Schaefer, Andrew M., Horvath, Rita, Ng, Yi, Nesbitt, Victoria, Lax, Nichola Z., McFarland, Robert, Cunningham, Mark O., Taylor, Robert W., Turnbull, Douglass M.

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Pathogenic variants in MT‐ATP6: A United Kingdom–based mitochondrial disease cohort study by Ng, Yi Shiau, Martikainen, Mika H., Gorman, Gráinne S., Blain, Alasdair, Bugiardini, Enrico, Bunting, Apphia, Schaefer, Andrew M., Alston, Charlotte L., Blakely, Emma L., Sharma, Sunil, Hughes, Imelda, Lim, Albert, de Goede, Christian, McEntagart, Meriel, Spinty, Stefan, Horrocks, Iain, Roberts, Mark, Woodward, Cathy E., Chinnery, Patrick F., Horvath, Rita, Nesbitt, Victoria, Fratter, Carl, Poulton, Joanna, Hanna, Michael G., Pitceathly, Robert D. S., Taylor, Robert W., Turnbull, Doug M., McFarland, Robert

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Cerebellar Ataxia in Patients With Mitochondrial DNA Disease: A Molecular Clinicopathological Study by Lax, Nichola Zoe, Hepplewhite, Philippa Denis, Reeve, Amy Katherine, Nesbitt, Victoria, McFarland, Robert, Jaros, Evelyn, Taylor, Robert William, Turnbull, Douglass Matthew

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Use of FGF-21 as a Biomarker of Mitochondrial Disease in Clinical Practice by Morovat, Alireza, Weerasinghe, Gayani, Nesbitt, Victoria, Hofer, Monika, Agnew, Thomas, Quaghebeur, Geralrine, Sergeant, Kate, Fratter, Carl, Guha, Nishan, Mirzazadeh, Mehdi, Poulton, Joanna

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Mitochondrial disease and COVID-19: An international cohort study confirms risks and long-term outcomes by Pizzamiglio, Chiara, Jonvik, Hallgeir, Brady, Stefen, Chinnery, Patrick, Galàn, Lucía, Gorman, Grainne, Horga, Alejandro, Horvath, Rita, Janssen, Mirian, Lim, Albert, Mancuso, Michelangelo, Mcfarland, Robert, Molnar, Maria, Musumeci, Olimpia, Nesbitt, Victoria, Wladimir, Primiano, Guido, Santos, Ernestina, Servidei, Serenella, Thomas, Rhys, Hanna, Michael, Machado, Pedro, Pitceathly, Robert

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A national perspective on prenatal testing for mitochondrial disease by Nesbitt, Victoria, Alston, Charlotte L, Blakely, Emma L, Fratter, Carl, Feeney, Catherine L, Poulton, Joanna, Brown, Garry K, Turnbull, Doug M, Taylor, Robert W, McFarland, Robert

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Postnatal corticosteroid use for prevention or treatment of bronchopulmonary dysplasia in England and Wales 2012–2019: a retrospective population cohort study by Yao, Sijia, Uthaya, Sabita, Gale, Chris, Babirecki, Matthew, Cane, Clare, Gupta, Aashish, Ewing, Alistair, Mittal, Anita, Halpern, Lindsay, Surana, Pinki, Nash, Matt, Wallis, Sam, Hassan, Ahmed, Schwarz, Karin, Whincup, Graham, Dangerfield, Joanne, Morris, Jocelyn, Hasib, Abdul, Allwood, Alex, Deketelaere, Abby, Klutse, Toria, Spathis, Sonia, Krishnan, Sathish, Sen, Samar, Holman, Jennifer, Lee, Geraint, Balal, Sobia, Seagrave, Cath, Bate, Tristan, Dixon, Hilary, Aladangady, Narendra, Gaili, Hassan, Lal, M, Pandey, Poornima, Filkin, Jonathan, Cusack, Jonathan, Kairamkonda, Venkatesh, Grosdenier, Michael, Birch, Jennifer, Karupaiah, Ashok, Ramadan, Ghada, Misra, I, Thiagarajan, Prakash, Muthukumar, Priya, Fragapane, Tiziana, Gupta, Subodh, Ben-Sasi, Khadija, Adams, Eleri, McDevitt, Katharine, Gupta, Ruchika, Khashu, Minesh, Al-Muzaffar, Iyad, Reddy, Chinnappa, Johnson, Mark, Bhat, Prashanth, Gandhi, Rashmi, Groves, Charlotte, Tyszcuzk, Lidia, Rewitzky, Glynis, Croft, Julia, Abdul-Malik, Bushra, Muogbo, Dominic, Das, Ambalika, Sengupta, Soma, Zipitis, Christos, Venkata, Nagendra, Winckworth, Lucinda, Vayalakkad, Anitha, Narasimhan, Raju, Obi, Ben, Jones, Stephen, Baird, Jim, Mack, Kirsten, Ramachandran, Arun, Emery, Faith, Huddy, Charlotte, Yasin, Salim, Sharp, Victoria, Heal, Carrie, Salgia, Sanjay, Ahmed, Imran, Birch, Jacqeline, Bastani, Porus, Theron, Marice, Paul, Siba, Park, Se-Yeon, Goel, Nitin, Webb, Delyth, Bird, Sue, Eyre, Elizabeth, Mohammed, Jageer, Sullivan, Caroline, Garr, Ros, Leith, Wynne, Vasu, Vimal, Gregory, Anna, Vamvakiti, Katia, Harrington, Brendan, Eaton, Megan, Cronin, Michael

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Causes of Death in Adults with Mitochondrial Disease by Barends, Marlieke, Verschuren, Lotte, Morava, Eva, Nesbitt, Victoria, Turnbull, Doug, McFarland, Robert

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Risk and causes of death in children with a seizure disorder by NESBITT, VICTORIA, KIRKPATRICK, MARTIN, PEARSON, GALE, COLVER, ALLAN, FORSYTH, ROB

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The clinical spectrum of the m.10191T>C mutation in complex I-deficient Leigh syndrome by NESBITT, VICTORIA, MORRISON, PATRICK J, CRUSHELL, ELLEN, DONNELLY, DEIRDRE E, ALSTON, CHARLOTTE L, HE, LANGPING, MCFARLAND, ROBERT, TAYLOR, ROBERT W

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Deoxyguanosine kinase deficiency: natural history and liver transplant outcome by Manzoni, Eleonora, Carli, Sara, Gaignard, Pauline, Schlieben, Lea Dewi, Hirano, Michio, Ronchi, Dario, Gonzales, Emmanuel, Shimura, Masaru, Murayama, Kei, Okazaki, Yasushi, Barić, Ivo, Petkovic Ramadza, Danijela, Karall, Daniela, Mayr, Johannes, Martinelli, Diego, La Morgia, Chiara, Primiano, Guido, Santer, René, Servidei, Serenella, Bris, Céline, Cano, Aline, Furlan, Francesca, Gasperini, Serena, Laborde, Nolwenn, Lamperti, Costanza, Lenz, Dominic, Mancuso, Michelangelo, Montano, Vincenzo, Menni, Francesca, Musumeci, Olimpia, Nesbitt, Victoria, Procopio, Elena, Rouzier, Cécile, Staufner, Christian, Taanman, Jan-Willem, Tal, Galit, Ticci, Chiara, Cordelli, Duccio Maria, Carelli, Valerio, Procaccio, Vincent, Prokisch, Holger, Garone, Caterina

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BMJ-2021-066288.R1Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study by Schon, Katherine R, Horvath, Rita, Wei, Wei, Calabrese, Claudia, Tucci, Arianna, Ibañez, Kristina, Ratnaike, Thiloka, Pitceathly, Robert D S, Bugiardini, Enrico, Quinlivan, Rosaline, Hanna, Michael G, Clement, Emma, Ashton, Emma, Sayer, John A, Brennan, Paul, Josifova, Dragana, Izatt, Louise, Fratter, Carl, Nesbitt, Victoria, Barrett, Timothy, McMullen, Dominic J, Smith, Audrey, Deshpande, Charulata, Smithson, Sarah F, Festenstein, Richard, Canham, Natalie, Caulfield, Mark, Houlden, Henry, Rahman, Shamima, Chinnery, Patrick F, Ambrose, John C, Arumugam, Prabhu, Bevers, Roel, Bleda, Marta, Boardman-Pretty, Freya, Boustred, Christopher R, Brittain, Helen, Caulfield, Mark J, Chan, Georgia C, Elgar, Greg, Fowler, Tom, Giess, Adam, Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J P, Jackson, Rob, Jones, Louise J, Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Leigh, Sarah E A, Leong, Ivonne U S, Lopez, Javier F, Maleady-Crowe, Fiona, McEntegart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C, O’Donovan, Peter, Odhams, Chris A, Patch, Christine, Buonerimo Pereira, Mariana, Perez-Gil, Daniel, Pullinger, John, Rahim, Tahrima, Rendon, Augusto, Rogers, Tim, Savage, Kevin, Sawant, Kushmita, Scott, Richard H, Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C, Sosinsky, Alona, Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R A, Thompson, Simon R, Tucci, Arianna, Welland, Matthew J, Williams, Eleanor, Witkowska, Katarzyna, Wood, Suzanne M

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