P254 Congenitally corrected transposition of the great arteries with an ebstenoid tricuspid valve, aortic atresia, hypoplastic aortic arch and a dysplastic pulmonary valve von Rittey, L A, Parry, H, Willcoxson, F

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37 Successful insertion of an implantable cardioverter defibrillator in a 9 month old with out of hospital ventricular tachycardia who was subsequently diagnosed with brugada syndr... von Rittey, L, Hares, D, Blackburn, M

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36 Outcomes in premature or small for dates neonates with congenital heart disease von Rittey, L, Pryad, S, Bustani, P, Thomson, JDR

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Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection von Bonthron, David T, Goizet, Cyril, Déry, Catherine, Woods, C Geoffrey, Ali, Manir, Weschke, Bernhard, Jackson, Andrew P, Voit, Thomas, King, Mary D, Baumann, Clarisse, Till, Marianne, Quarrell, Oliver W, Crow, Yanick J, Cau, Daniel, Lacombe, Didier, Lyall, Hermione, Lanzi, Giovanni, Stephenson, John B P, Griffith, Elen, Garner, Anna, Parmar, Rekha, Lebon, Pierre, McKeown, Carole, Rogers, R Curtis, Hayward, Bruce E, Babul-Hirji, Riyana, Bertini, Enrico, Martínez-Frías, María Luisa, Monier, Anne, Leitch, Andrea, Rittey, Christopher D, Semple, Colin, Aicardi, Jean, Chitayat, David, Tolmie, John L, Ponting, Chris P, Baxter, Peter, Tacke, Uta, Mathieu, Michèle, Sanchis, Amparo, Tomlin, Pam, Oade, Yvette, Klepper, Joerg, Fazzi, Elisa, Chandler, Kate E

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COVID-19 in congenital heart disease (COaCHeD) study von Chivers, Sian, Cleary, Aoife, Knowles, Rachel, Babu-Narayan, Sonya V, Simpson, John M, Nashat, Heba, Dimopoulos, Konstantinos, Gatzoulis, Michael A, Wilson, Dirk, Prica, Milos, Anthony, James, Clift, Paul F, Jowett, Victoria, Jenkins, Petra, Khodaghalian, Bernadette, Jones, Caroline B, Hardiman, Antonia, Head, Catherine, Miller, Owen, Chung, Natali AY, Mahmood, Umar, Bu'Lock, Frances A, Ramcharan, Tristan KW, Chikermane, Ashish, Shortland, Jennifer, Tometzki, Andrew, Crossland, David S, Reinhardt, Zdenka, Lewis, Clive, Rittey, Leila, Hares, Dominic, Panagiotopoulou, Olga, Smith, Benjamin, Najih L, Muhammad, Bharucha, Tara, Daubeney, Piers EF

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P877Lesion Index facilitates continuous transmural radiofrequency ablation lesions in a porcine recovery model von Whitaker, J., Fish, J., Chubb, H., Harrison, J., Williams, S., Sohal, M., Van Zaen, J., Gibbs, J., Rittey, D., Thorsten, J., Donskoy, E., Mukherjee, R., O'neill, L., Wright, M., O'neill, M.

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GLRB is the third major gene of effect in hyperekplexia von Chung, S.-K., Bode, A., Cushion, T. D., Thomas, R. H., Hunt, C., Wood, S.-E., Pickrell, W. O., Drew, C. J. G., Yamashita, S., Shiang, R., Leiz, S., Longardt, A.-C., Raile, V., Weschke, B., Puri, R. D., Verma, I. C., Harvey, R. J., Ratnasinghe, D. D., Parker, M., Rittey, C., Masri, A., Lingappa, L., Howell, O. W., Vanbellinghen, J.-F., Mullins, J. G., Lynch, J. W., Rees, M. I.

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A second locus for Aicardi-Goutières syndrome at chromosome 13q14–21 von Ali, M, Highet, L J, Lacombe, D, Goizet, C, King, M D, Tacke, U, van der Knaap, M S, Lagae, L, Rittey, C, Brunner, H G, van Bokhoven, H, Hamel, B, Oade, Y A, Sanchis, A, Desguerre, I, Cau, D, Mathieu, N, Moutard, M L, Lebon, P, Kumar, D, Jackson, A P, Crow, Y J

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Aicardi-Goutières Syndrome Displays Genetic Heterogeneity with One Locus ( AGS1) on Chromosome 3p21 von Crow, Y.J., Jackson, A.P., Roberts, E., van Beusekom, E., Barth, P., Corry, P., Ferrie, C.D., Hamel, B.C.J., Jayatunga, R., Karbani, G., Kálmánchey, R., Kelemen, A., King, M., Kumar, R., Livingstone, J., Massey, R., McWilliam, R., Meager, A., Rittey, C., Stephenson, J.B.P., Tolmie, J.L., Verrips, A., Voit, T., van Bokhoven, H., Brunner, H.G., Woods, C.G.

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Congenital trigeminal anaesthesia von Hashmi, SJ, Chow, G, Bittner, SB, Rittey, CD, Williams, LHP

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First line prescribing practices and drug retention rates for focal epilepsy von Henderson, L M, Sawar, M, Rittey, C D

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COVID-19 in congenital heart disease (COaCHeD) study von Chivers, Sian, Cleary, Aoife, Knowles, Rachel, Babu-Narayan, Sonya V, Simpson, John M, Nashat, Heba, Dimopoulos, Konstantinos, Gatzoulis, Michael A, Wilson, Dirk, Prica, Milos, Anthony, James, Clift, Paul F, Jowett, Victoria, Jenkins, Petra, Khodaghalian, Bernadette, Jones, Caroline B, Hardiman, Antonia, Head, Catherine, Miller, Owen, Chung, Natali Ay, Mahmood, Umar, Bu'Lock, Frances A, Ramcharan, Tristan Kw, Chikermane, Ashish, Shortland, Jennifer, Tometzki, Andrew, Crossland, David S, Reinhardt, Zdenka, Lewis, Clive, Rittey, Leila, Hares, Dominic, Panagiotopoulou, Olga, Smith, Benjamin, Najih L, Muhammad, Bharucha, Tara, Daubeney, Piers Ef

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The allopurinol load test lacks specificity for primary urea cycle defects but may indicate unrecognized mitochondrial disease von Bonham, J. R., Guthrie, P., Downing, M., Allen, J. C., Tanner, M. S., Sharrard, M., Rittey, C., Land, J. M., Fensom, A., O'Neill, D., Duley, J. A., Fairbanks, L. D.

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