Variations in the management of children with cerebral venous sinus thrombosis in the UK and Ireland by Hart, Anthony R, Ganesan, Vijeya, Pysden, Karen S

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Cogan's Syndrome: A Rare Cause of Meningoencephalitis by Pysden, Karen S., Long, Vernon, Ferrie, Colin D., Leeds Teaching Hospitals NHS Trust

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Efficacy and Safety of Vamorolone in Duchenne Muscular Dystrophy: A 30-Month Nonrandomized Controlled Open-Label Extension Trial by Mah, Jean K, Clemens, Paula R, Guglieri, Michela, Smith, Edward C, Finkel, Richard S, Tulinius, Mar, Nevo, Yoram, Ryan, Monique M, Webster, Richard, Castro, Diana, Kuntz, Nancy L, McDonald, Craig M, Damsker, Jesse M, Schwartz, Benjamin D, Mengle-Gaw, Laurel J, Jackowski, Stefan, Stimpson, Georgia, Ridout, Deborah A, Ayyar-Gupta, Vandana, Baranello, Giovanni, Manzur, Adnan Y, Muntoni, Francesco, Gordish-Dressman, Heather, Leinonen, Mika, Ward, Leanne M, Hoffman, Eric P, Dang, Utkarsh J

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Neurological Manifestations of Influenza Infection in Children and Adults: Results of a National British Surveillance Study by Goenka, Anu, Michael, Benedict D., Ledger, Elizabeth, Hart, Ian J., Absoud, Michael, Chow, Gabriel, Lilleker, James, Lunn, Michael, McKee, David, Peake, Deirdre, Pysden, Karen, Roberts, Mark, Carrol, Enitan D., Lim, Ming, Avula, Shivaram, Solomon, Tom, Kneen, Rachel

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885 A service evaluation exploring the clinical pathway offered to individuals with dystrophin gene variants identified on array CGH by Topping, Georgia, Javeria Tariq, Pysden, Karen, Sharif, Saghira, Childs, Anne-Marie

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The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications by Brunklaus, Andreas, Brünger, Tobias, Feng, Tony, Fons, Carmen, Lehikoinen, Anni, Panagiotakaki, Eleni, Vintan, Mihaela-Adela, Symonds, Joseph, Andrew, James, Arzimanoglou, Alexis, Delima, Sarah, Gallois, Julie, Hanrahan, Donncha, Lesca, Gaetan, MacLeod, Stewart, Marjanovic, Dragan, McTague, Amy, Nuñez-Enamorado, Noemi, Perez-Palma, Eduardo, Scott Perry, M, Pysden, Karen, Russ-Hall, Sophie J, Scheffer, Ingrid E, Sully, Krystal, Syrbe, Steffen, Vaher, Ulvi, Velayutham, Murugan, Vogt, Julie, Weiss, Shelly, Wirrell, Elaine, Zuberi, Sameer M, Lal, Dennis, Møller, Rikke S, Mantegazza, Massimo, Cestèle, Sandrine

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Stroke and cerebrovascular disease in childhood (International Review of Child Neurology Series) by Pysden, Karen

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Carbamazepine Improves Apneic Episodes in Congenital Central Hypoventilation Syndrome (CCHS) With a Novel PHOX2B Exon 1 Missense Mutation by Schirwani, Schaida, Pysden, Karen, Chetcuti, Philip, Blyth, Moira

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Homozygous intronic variants in TPM2 cause recessively inherited Escobar variant of multiple pterygium syndrome and congenital myopathy by Schirwani, Schaida, Sarkozy, Anna, Phadke, Rahul, Childs, Anne-Marie, Mein, Rachael, Ismail, Azzam, Smith, Audrey, Muntoni, Francesco, Hobson, Emma, Pysden, Karen

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Clinical and Molecular Spectrum of Autosomal Recessive CA8‐Related Cerebellar Ataxia by Kaiyrzhanov, Rauan, Ortigoza‐Escobar, Juan Darío, Stringer, Brett W., Ganieva, Manizha, Gowda, Vykuntaraju K., Srinivasan, Varunvenkat M., Macaya, Alfons, Laner, Andreas, Onbool, Enas, Al‐Shammari, Randa, Al‐Owain, Mohammed, Deconinck, Nicolas, Vilain, Catheline, Dontaine, Pauline, Self, Eleanor, Akram, Rabia, Hussain, Ghulam, Baig, Shahid Mahmood, Iqbal, Javed, Salpietro, Vincenzo, Neshatdoust, Maedeh, Kasiri, Mahboubeh, Yesil, Gozde, Uygur, Turkan, Pysden, Karen, Berry, Ian R., Alves, Cesar Augusto, Giacomotto, Jean, Houlden, Henry, Maroofian, Reza

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Safety and efficacy of tamoxifen in boys with Duchenne muscular dystrophy (TAMDMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial by Henzi, Bettina C, Schmidt, Simone, Nagy, Sara, Schaedelin, Sabine, Putananickal, Niveditha, Stimpson, Georgia, Ridout, Deborah, Muntoni, Francesco, Main, Marion, Abbott, Lianne, Burnett, Nicola, Rohwer, Anne-Marie, .O'Reilly, Emer, Guglieri, Michela, Bettolo, Chiara, James, Meredith, Sodhi, Jassi, Willis, Tracey, Rylance, Claire, Birchall, Nicola, Childs, Anne-Marie, Pysden, Karen, Martos-Lozano, Cristina, Pallant, Lindsey, Wadsworth, Steph, Gregson, Sarah, Clark, Stuart, Wraige, Elizabeth, Jungbluth, Heinz, Gowda, Vasantha, Sheehan, Ennie, Wolfe, Amy, Schofield, Alex, Hughes, Imelda, McCullagh, Gary, Whitehouse, Emily, Varma, Uma, Warner, Sinead, Reading, Emily, Benson, Lucy, Moustoukas, Jenny, Strachan, Kate, Emery, Nicholas, Ong, Min, Durso, Sarah, White, Kay, Hinde, Neil, Sanchez Marco, Silvia, Saxena, Anurag, Gibbon, Frances, Davis, Hayley, Murugan, Archana, Lynch, Mollie, Milton, Emily, Wills, Lucy, Robertson, Gemma, Cobb, Gavin, Burslem, Julie, Wong, Jarod, Brunklaus, Andreas, DiMarco, Marina, Brown, Sarah, Mckenzie, Susanne, Torne, Krupa, Mohamed, Rana, Velmurugan, Vel, Prasad, Manish, Williamson, Sarah, Degoede, Christian, Geary, Michelle, Palmer, Jenni, Shill, Catherine, White, Cathy, Gates, Sarah, Shah, Ayaz, .McFetridge, Jaci, Nic Fhirleinn, Grainne, Hussain, Nahin, Baskaran, Dhinesh, Lambat, Zubeida, Ambegaonkar, Gautam, Krishnakumar, Deepa, Taylor, Jacqui, Moores, Jo, Servais, Laurent, English, Hayley, Parasuraman, Deepak, Rabb, Rosanna, McMurchie, Heather, Deconinck, Nicolas, de Groot, Imelda, Horrocks, Iain, Houwen-van Opstal, Saskia, Laugel, Vincent, Lopez Lobato, Mercedes, Schara-Schmidt, Ulrike, von Moers, Arpad, Lawrence, Fiona, Hafner, Patricia, Dorchies, Olivier M

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Spontaneous Dissecting Lenticulostriate Artery Aneurysm in Children: Radiologic Findings and Clinical Management by Yap, Leesien, Patankar, Tufail, Pysden, Karen, Tyagi, Atul, Goddard, Tony

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The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications by Brunklaus, Andreas, Brünger, Tobias, Feng, Tony, Fons, Carmen, Lehikoinen, Anni, Panagiotakaki, Eleni, Vintan, Mihaela-Adela, Symonds, Joseph, Andrew, James, Arzimanoglou, Alexis, Delima, Sarah, Gallois, Julie, Hanrahan, Donncha, Lesca, Gaetan, Macleod, Stewart, Marjanovic, Dragan, Mctague, Amy, Nuñez-Enamorado, Noemi, Perez-Palma, Eduardo, Scott Perry, M, Pysden, Karen, Russ-Hall, Sophie, Scheffer, Ingrid, Sully, Krystal, Syrbe, Steffen, Vaher, Ulvi, Velayutham, Murugan, Vogt, Julie, Weiss, Shelly, Wirrell, Elaine, Zuberi, Sameer, Lal, Dennis, Møller, Rikke, Mantegazza, Massimo, Cestèle, Sandrine

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Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy by Diggle, Christine P., Sukoff Rizzo, Stacey J., Popiolek, Michael, Hinttala, Reetta, Schülke, Jan-Philip, Kurian, Manju A., Carr, Ian M., Markham, Alexander F., Bonthron, David T., Watson, Christopher, Sharif, Saghira Malik, Reinhart, Veronica, James, Larry C., Vanase-Frawley, Michelle A., Charych, Erik, Allen, Melanie, Harms, John, Schmidt, Christopher J., Ng, Joanne, Pysden, Karen, Strick, Christine, Vieira, Päivi, Mankinen, Katariina, Kokkonen, Hannaleena, Kallioinen, Matti, Sormunen, Raija, Rinne, Juha O., Johansson, Jarkko, Alakurtti, Kati, Huilaja, Laura, Hurskainen, Tiina, Tasanen, Kaisa, Anttila, Eija, Marques, Tiago Reis, Howes, Oliver, Politis, Marius, Fahiminiya, Somayyeh, Nguyen, Khanh Q., Majewski, Jacek, Uusimaa, Johanna, Sheridan, Eamonn, Brandon, Nicholas J.

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Experience of mechanical thrombectomy for paediatric arterial ischaemic stroke by Bodey, Caroline, Goddard, Tony, Patankar, Tufail, Childs, Anne Marie, Ferrie, Colin, McCullagh, Helen, Pysden, Karen

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The prevalence of neuromuscular disease in the paediatric population in Yorkshire, UK; variation by ethnicity and deprivation status by Woodcock, Ian R, Fraser, Lorna, Norman, Paul, Pysden, Karen, Manning, Sue, Childs, Anne‐Marie

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Parental and physician beliefs regarding the provision and content of written sudden unexpected death in epilepsy (SUDEP) information by Gayatri, Neti A., Morrall, Matthew C. H. J., Jain, Vivek, Kashyape, Pawan, Pysden, Karen, Ferrie, Colin

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A Report of Novel STIM1 Deficiency and 6-Year Follow-Up of Two Previous Cases Associated with Mild Immunological Phenotype by Rice, Laura, Stockdale, Claire, Berry, Ian, O’Riordan, Sean, Pysden, Karen, Anwar, Rashida, Rushambuza, Roger, Blyth, Moira, Srikanth, Sonal, Gwack, Yousang, El-Sherbiny, Yasser M., Carter, Clive, Savic, Sinisa

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Homozygous deletion in MICU1 presenting with fatigue and lethargy in childhood by Lewis-Smith, David, Kamer, Kimberli J, Griffin, Helen, Childs, Anne-Marie, Pysden, Karen, Titov, Denis, Duff, Jennifer, Pyle, Angela, Taylor, Robert W, Yu-Wai-Man, Patrick, Ramesh, Venkateswaran, Horvath, Rita, Mootha, Vamsi K, Chinnery, Patrick F

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RMND1-Related Leukoencephalopathy With Temporal Lobe Cysts and Hearing Loss—Another Mendelian Mimicker of Congenital Cytomegalovirus Infection by Ulrick, Nicole, Goldstein, Amy, Simons, Cas, Taft, Ryan J., Helman, Guy, Pizzino, Amy, Bloom, Miriam, Vogt, Julie, Pysden, Karen, Diodato, Daria, Martinelli, Diego, Monavari, Ahmad, Buhas, Daniela, van Karnebeek, Clara D.M., Dorboz, Imen, Boespflug-Tanguy, Odile, Rodriguez, Diana, Tétreault, Martine, Majewski, Jacek, Bernard, Genevieve, Ng, Yi Shiau, McFarland, Robert, Vanderver, Adeline

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