Mutations in KCNT1 cause a spectrum of focal epilepsies von Møller, Rikke S., Heron, Sarah E., Larsen, Line H. G., Lim, Chiao Xin, Ricos, Michael G., Bayly, Marta A., Kempen, Marjan J. A., Klinkenberg, Sylvia, Andrews, Ian, Kelley, Kent, Ronen, Gabriel M., Callen, David, McMahon, Jacinta M., Yendle, Simone C., Carvill, Gemma L., Mefford, Heather C., Nabbout, Rima, Poduri, Annapurna, Striano, Pasquale, Baglietto, Maria G., Zara, Federico, Smith, Nicholas J., Pridmore, Clair, Gardella, Elena, Nikanorova, Marina, Dahl, Hans Atli, Gellert, Pia, Scheffer, Ingrid E., Gunning, Boudewijn, Kragh‐Olsen, Bente, Dibbens, Leanne M.

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Hypothalamic hamartoma: epilepsy and neurodevelopmental profiles in a clinical cohort von Pridmore, Clair, D’Arco, Felice, Siyani, Varsha, Bull, Leah, Richardson, Hanna

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PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome von Heron, Sarah E., Grinton, Bronwyn E., Kivity, Sara, Afawi, Zaid, Zuberi, Sameer M., Hughes, James N., Pridmore, Clair, Hodgson, Bree L., Iona, Xenia, Sadleir, Lynette G., Pelekanos, James, Herlenius, Eric, Goldberg-Stern, Hadassa, Bassan, Haim, Haan, Eric, Korczyn, Amos D., Gardner, Alison E., Corbett, Mark A., Gécz, Jozef, Thomas, Paul Q., Mulley, John C., Berkovic, Samuel F., Scheffer, Ingrid E., Dibbens, Leanne M.

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Australian Clinical Consensus Guideline: The diagnosis and acute management of childhood stroke von Medley, Tanya L, Miteff, Christina, Andrews, Ian, Ware, Tyson, Cheung, Michael, Monagle, Paul, Mandelstam, Simone, Wray, Alison, Pridmore, Clair, Troedson, Christopher, Dale, Russell C, Fahey, Michael, Sinclair, Adriane, Walsh, Peter, Stojanovski, Belinda, Mackay, Mark T

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Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practice von Scheffer, Ingrid E., Bennett, Caitlin A., Gill, Deepak, Silva, Michelle G., Boggs, Kirsten, Marum, Justine, Baker, Naomi, Palmer, Elizabeth E., Howell, Katherine B., Andrews, Ian, Antony, Jayne, Ardern‐Holmes, Simone, Bye, Ann M, Cardamone, Michael, Chelakkadan, Shabeed, Clark, Damian, Curnow, Sarah R, Dabscheck, Gabriel, Fahey, Michael C, Freeman, Jeremy L, Gupta, Sachin, Harvey, A Simon, Hildebrand, Michael S, Inder, Marie, Kanhangad, Manoj, Kornberg, Andrew J, Kothur, Kavitha, Lawson, John A, Leventer, Richard J, Malone, Stephen, Menezes, Manoj P, Mohammad, Shekeeb, Nagarajan, Lakshmi, Pillai, Sekhar, Pridmore, Clair, Procopis, Peter G, Sampaio, Hugo, Silberstein, Jonathon, Sinclair, Adriane, Smith, Nicholas, Subramanian, Gopinath, Troedson, Christopher, Ware, Tyson, White, Susan M

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The spectrum of SCN1A-related infantile epileptic encephalopathies von Harkin, Louise A., McMahon, Jacinta M., Iona, Xenia, Dibbens, Leanne, Pelekanos, James T., Zuberi, Sameer M., Sadleir, Lynette G., Andermann, Eva, Gill, Deepak, Farrell, Kevin, Connolly, Mary, Stanley, Thorsten, Harbord, Michael, Andermann, Frederick, Wang, Jing, Batish, Sat Dev, Jones, Jeffrey G., Seltzer, William K., Gardner, Alison, Sutherland, Grant, Berkovic, Samuel F., Mulley, John C., Scheffer, Ingrid E.

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Characterization of the human myelin oligodendrocyte glycoprotein antibody response in demyelination von Tea, Fiona, Lopez, Joseph A, Ramanathan, Sudarshini, Merheb, Vera, Lee, Fiona X Z, Zou, Alicia, Pilli, Deepti, Patrick, Ellis, van der Walt, Anneke, Monif, Mastura, Tantsis, Esther M, Yiu, Eppie M, Vucic, Steve, Henderson, Andrew P D, Fok, Anthony, Fraser, Clare L, Lechner-Scott, Jeanette, Reddel, Stephen W, Broadley, Simon, Barnett, Michael H, Brown, David A, Lunemann, Jan D, Dale, Russell C, Brilot, Fabienne

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Ornithine Transcarbamylase Deficiency in Females: An Often Overlooked Cause of Treatable Encephalopathy von Pridmore, Clair L., Clarke, Joe T.R., Blaser, Susan

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Mutations in KCNT 1 cause a spectrum of focal epilepsies von Møller, Rikke S., Heron, Sarah E., Larsen, Line H. G., Lim, Chiao Xin, Ricos, Michael G., Bayly, Marta A., van Kempen, Marjan J. A., Klinkenberg, Sylvia, Andrews, Ian, Kelley, Kent, Ronen, Gabriel M., Callen, David, McMahon, Jacinta M., Yendle, Simone C., Carvill, Gemma L., Mefford, Heather C., Nabbout, Rima, Poduri, Annapurna, Striano, Pasquale, Baglietto, Maria G., Zara, Federico, Smith, Nicholas J., Pridmore, Clair, Gardella, Elena, Nikanorova, Marina, Dahl, Hans Atli, Gellert, Pia, Scheffer, Ingrid E., Gunning, Boudewijn, Kragh‐Olsen, Bente, Dibbens, Leanne M.

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Cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH von Nicholl, Jillian, Waters, Wendy, Mulley, John C., Suwalski, Shanna, Brown, Sue, Hull, Yvonne, Barnett, Christopher, Haan, Eric, Thompson, Elizabeth M., Liebelt, Jan, Mcgregor, Lesley, Harbord, Michael G., Entwistle, John, Munt, Chris, White, Dierdre, Chitti, Anthony, Baulderstone, David, Ketteridge, David, Friend, Kathryn, Bain, Sharon M., Sui, Y.u.

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