Myasthenia gravis: Association of British Neurologists’ management guidelines von Sussman, Jon, Farrugia, Maria E, Maddison, Paul, Hill, Marguerite, Leite, M Isabel, Hilton-Jones, David

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A retrospective study of acetylcholine receptor antibody positive ocular myasthenia in the West of Scotland von Farrugia, Maria E., Cleary, Marie, Carmichael, Caroline

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COVID-19-associated risks and effects in myasthenia gravis (CARE-MG) von Muppidi, Srikanth, Guptill, Jeffrey T, Jacob, Saiju, Li, Yingkai, Farrugia, Maria E, Guidon, Amanda C, Tavee, Jinny O, Kaminski, Henry, Howard, James F, Cutter, Gary, Wiendl, Heinz, Maas, Matthew B, Illa, Isabel, Mantegazza, Renato, Murai, Hiroyuki, Utsugisawa, Kimiaki, Nowak, Richard J, Guidon, Amanda C, Tyagi, Alok, Sousa, Ana Paula, Amato, Anthony A, Pinto, Ashwin, Roy, Bhaskar, Carmichael, Caroline, Dodig, Dubravka, Burke, Georgina, Cutter, Gary R, Kaminski, Henry J, Wiendl, Heinz, Murai, Hiroyuki, Lee, Ikjae, Illa, Isabel, Guptill, Jeffrey, Howard, James F., Caress, James, Pritchard, Jane, Tavee, Jinny O, Vissing, John, Best, Kamla, Utsugisawa, Kimiaki, Ramezani, Mahtab, Maas, Mathew, Farrugia, Maria E, Hehir, Michael K, Kaku, Michelle, Esquivel, Natalia Jiménez, Gallagher, Paul, Maddison, Paul, Ambrose, Philip A, Mantegazza, Renato E, Nowak, Richard J, Do Campo, Rocio Vazquez, Jacob, Saiju, Saba, Sami, Nafissi, Shahriar, Itoyama, Shannon, Muppidi, Srikanth, Viegas, Stuart Viegas, Marshall, Victoria, Li, Yingkai Li

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Mutations in GMPPB cause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathies von Belaya, Katsiaryna, Rodríguez Cruz, Pedro M, Liu, Wei Wei, Maxwell, Susan, McGowan, Simon, Farrugia, Maria E, Petty, Richard, Walls, Timothy J, Sedghi, Maryam, Basiri, Keivan, Yue, Wyatt W, Sarkozy, Anna, Bertoli, Marta, Pitt, Matthew, Kennett, Robin, Schaefer, Andrew, Bushby, Kate, Parton, Matt, Lochmüller, Hanns, Palace, Jacqueline, Muntoni, Francesco, Beeson, David

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A Practical Approach to Managing Patients With Myasthenia Gravis—Opinions and a Review of the Literature von Farrugia, Maria Elena, Goodfellow, John A.

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The Association of British Neurologists' myasthenia gravis guidelines von Sussman, Jon, Farrugia, Maria E., Maddison, Paul, Hill, Marguerite, Leite, M. Isabel, Hilton‐Jones, David

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Clinical Features, Molecular Heterogeneity, and Prognostic Implications in YARS2-Related Mitochondrial Myopathy von Sommerville, Ewen W, Ng, Yi Shiau, Alston, Charlotte L, Dallabona, Cristina, Gilberti, Micol, He, Langping, Knowles, Charlotte, Chin, Sophie L, Schaefer, Andrew M, Falkous, Gavin, Murdoch, David, Longman, Cheryl, de Visser, Marianne, Bindoff, Laurence A, Rawles, John M, Dean, John C. S, Petty, Richard K, Farrugia, Maria E, Haack, Tobias B, Prokisch, Holger, McFarland, Robert, Turnbull, Douglass M, Donnini, Claudia, Taylor, Robert W, Gorman, Gráinne S

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Elevated plasma levels of cardiac troponin-I predict left ventricular systolic dysfunction in patients with myotonic dystrophy type 1: A multicentre cohort follow-up study von Hamilton, Mark J, Robb, Yvonne, Cumming, Sarah, Gregory, Helen, Duncan, Alexis, Rahman, Monika, McKeown, Anne, McWilliam, Catherine, Dean, John, Wilcox, Alison, Farrugia, Maria E, Cooper, Anneli, McGhie, Josephine, Adam, Berit, Petty, Richard, Longman, Cheryl, Findlay, Iain, Japp, Alan, Monckton, Darren G, Denvir, Martin A

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Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure von Pfeffer, Gerald, Barresi, Rita, Wilson, Ian J, Hardy, Steven A, Griffin, Helen, Hudson, Judith, Elliott, Hannah R, Ramesh, Aravind V, Radunovic, Aleksandar, Winer, John B, Vaidya, Sujit, Raman, Ashok, Busby, Mark, Farrugia, Maria E, Ming, Alec, Everett, Chris, Emsley, Hedley C A, Horvath, Rita, Straub, Volker, Bushby, Kate, Lochmüller, Hanns, Chinnery, Patrick F, Sarkozy, Anna

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Correction: Elevated plasma levels of cardiac troponin-I predict left ventricular systolic dysfunction in patients with myotonic dystrophy type 1: A multicentre cohort follow-up st... von Hamilton, Mark J, Robb, Yvonne, Cumming, Sarah, Gregory, Helen, Duncan, Alexis, Rahman, Monika, McKeown, Anne, McWilliam, Catherine, Dean, John, Wilcox, Alison, Farrugia, Maria E, Cooper, Anneli, McGhie, Josephine, Adam, Berit, Petty, Richard, Longman, Cheryl, Findlay, Iain, Japp, Alan, Monckton, Darren G, Denvir, Martin A

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A novel MT-CO2 variant causing cerebellar ataxia and neuropathy: The role of muscle biopsy in diagnosis and defining pathogenicity von Baty, Karen, Farrugia, Maria E., Hopton, Sila, Falkous, Gavin, Schaefer, Andrew M., Stewart, William, Willison, Hugh J., Reilly, Mary M., Blakely, Emma L., Taylor, Robert W., Ng, Yi Shiau

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Real-World Data on Access to Standards of Care for People With Spinal Muscular Atrophy in the UK von Muni-Lofra, Robert, Murphy, Lindsay B, Adcock, Kate, Farrugia, Maria E, Irwin, Joseph, Lilleker, James B, McConville, John, Merrison, Andria, Parton, Matt, Ryburn, Liz, Scoto, Mariacristina, Marini-Bettolo, Chiara, Mayhew, Anna

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The modified rankin scale to assess disability in myasthenia gravis: Comparing with other tools von Farrugia, Maria E., Carmichael, Caroline, Cupka, Bryan J., Warder, Judy, Brennan, Kathryn M., Burns, Ted M.

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Two recurrent mutations are associated with GNE myopathy in the North of Britain von Chaouch, Amina, Brennan, Kathryn M, Hudson, Judith, Longman, Cheryl, McConville, John, Morrison, Patrick J, Farrugia, Maria E, Petty, Richard, Stewart, Willie, Norwood, Fiona, Horvath, Rita, Chinnery, Patrick F, Costigan, Donald, Winer, John, Polvikoski, Tuomo, Healy, Estelle, Sarkozy, Anna, Evangelista, Teresinha, Pogoryelova, Oksana, Eagle, Michelle, Bushby, Kate, Straub, Volker, Lochmüller, Hanns

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International clinimetric evaluation of the MG-QOL15, resulting in slight revision and subsequent validation of the MG-QOL15r von Burns, Ted M., Sadjadi, Reza, Utsugisawa, Kimiaki, Gwathmey, Kelly G., Joshi, Amruta, Jones, Sarah, Bril, Vera, Barnett, Carolina, Guptill, Jeffrey T., Sanders, Donald B., Hobson-Webb, Lisa, Juel, Vern C., Massey, Janice, Gable, Karissa L, Silvestri, Nicholas J., Wolfe, Gil, Cutter, Gary, Nagane, Yuriko, Murai, Hiroyuki, Masuda, Masayuki, Farrugia, Maria Elena, Carmichael, Caroline, Birnbaum, Simone, Hogrel, Jean-Yves, Nafissi, Shahriar, Fatehi, Farzad, Ou, Changyi, Liu, Weibin, Conaway, Mark

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Extract from the Marine Seaweed Padina pavonica Protects Mitochondrial Biomembranes from Damage by Amyloidogenic Peptides von Caruana, Mario, Camilleri, Angelique, Farrugia, Maria Ylenia, Ghio, Stephanie, Jakubíčková, Michaela, Cauchi, Ruben J, Vassallo, Neville

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Clinical features of the myasthenic syndrome arising from mutations in GMPPB von Rodríguez Cruz, Pedro M, Belaya, Katsiaryna, Basiri, Keivan, Sedghi, Maryam, Farrugia, Maria Elena, Holton, Janice L, Liu, Wei Wei, Maxwell, Susan, Petty, Richard, Walls, Timothy J, Kennett, Robin, Pitt, Matthew, Sarkozy, Anna, Parton, Matt, Lochmüller, Hanns, Muntoni, Francesco, Palace, Jacqueline, Beeson, David

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Risk of cardiac manifestations in adult mitochondrial disease caused by nuclear genetic defects von Lim, Albert Zishen, Jones, Daniel M, Bates, Matthew G D, Schaefer, Andrew M, O'Sullivan, John, Feeney, Catherine, Farrugia, Maria E, Bourke, John P, Turnbull, Doug M, Gorman, Gráinne S, McFarland, Robert, Ng, Yi Shiau

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Detection and characterization of MuSK antibodies in seronegative myasthenia gravis von McConville, John, Farrugia, Maria Elena, Beeson, David, Kishore, Uday, Metcalfe, Richard, Newsom-Davis, John, Vincent, Angela

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Concentric and single fiber needle electrodes yield comparable jitter results in myasthenia gravis von Farrugia, Maria E., Weir, Andrew I., Cleary, Marie, Cooper, Sarah, Metcalfe, Richard, Mallik, Arup

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