未登录 Overcoming silos in health care systems through meso-level organisations - a case study of health reforms in New South Wales, Australia Peiris, David; Feyer, Anne-Marie; Barnard, Justine; Billot, Laurent; Bouckley, Tristan; Campain, Anna; Cordery, Damien; de Souza, Alexandra; Downey, Laura; Elshaug, Adam G.; Ford, Belinda; Hanfy, Hannah; Hales, Lynelle; Khalaj, Behnoosh Hosseinloui; Schneider, Carmen Huckel; Inglis, James; Jan, Stephen; Jorm, Louisa; Landon, Bruce; Lujic, Sanja; Mulley, John; Pearson, Sallie-Anne; Schierhout, Gill; Sivaprakash, Prithivi; Stanton, Cynthia; Stephens, Anna; Willcox, Deborah 分享 收藏
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A digital health intervention for cardiovascular disease management in primary care (CONNECT) randomized controlled trial Redfern, Julie; Coorey, Genevieve; Mulley, John; Scaria, Anish; Neubeck, Lis; Hafiz, Nashid; Pitt, Chris; Weir, Kristie; Forbes, Joanna; Parker, Sharon; Bampi, Fiona; Coenen, Alison; Enright, Gemma; Wong, Annette; Nguyen, Theresa; Harris, Mark; Zwar, Nick; Chow, Clara K.; Rodgers, Anthony; Heeley, Emma; Panaretto, Katie; Lau, Annie; Hayman, Noel; Usherwood, Tim; Peiris, David 分享 收藏
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Multiplex families with epilepsy Success of clinical and molecular genetic characterization Afawi, Zaid; Oliver, Karen L.; Kivity, Sara; Mazarib, Aziz; Blatt, Ilan; Neufeld, Miriam Y.; Helbig, Katherine L.; Goldberg-Stern, Hadassa; Misk, Adel J.; Straussberg, Rachel; Walid, Simri; Mahajnah, Muhammad; Lerman-Sagie, Tally; Ben-Zeev, Bruria; Kahana, Esther; Masalha, Rafik; Kramer, Uri; Ekstein, Dana; Shorer, Zamir; Wallace, Robyn H.; Mangelsdorf, Marie; MacPherson, James N.; Carvill, Gemma L.; Mefford, Heather C.; Jackson, Graeme D.; Scheffer, Ingrid E.; Bahlo, Melanie; Gecz, Jozef; Heron, Sarah E.; Corbett, Mark; Mulley, John C.; Dibbens, Leanne M.; Korczyn, Amos D.; Berkovic, Samuel F. 分享 收藏
Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome Grinton, Bronwyn E.; Heron, Sarah E.; Pelekanos, James T.; Zuberi, Sameer M.; Kivity, Sara; Afawi, Zaid; Williams, Tristiana C.; Casalaz, Dan M.; Yendle, Simone; Linder, Ilan; Lev, Dorit; Lerman-Sagie, Tally; Malone, Stephen; Bassan, Haim; Goldberg-Stern, Hadassa; Stanley, Thorsten; Hayman, Michael; Calvert, Sophie; Korczyn, Amos D.; Shevell, Michael; Scheffer, Ingrid E.; Mulley, John C.; Berkovic, Samuel F. 分享 收藏
Genetics of epilepsy The testimony of twins in the molecular era Vadlamudi, Lata; Milne, Roger L.; Lawrence, Kate; Heron, Sarah E.; Eckhaus, Jazmin; Keay, Deborah; Connellan, Mary; Torn-Broers, Yvonne; Howell, R. Anne; Mulley, John C.; Scheffer, Ingrid E.; Dibbens, Leanne M.; Hopper, John L.; Berkovic, Samuel F. 分享 收藏
Cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH 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.; Yu, Sui 分享 收藏
Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome 钠通道SCN9A在热性惊厥和Dravet综合征的遗传性癫痫中的作用 Mulley, John C.; Hodgson, Bree; McMahon, Jacinta M.; Iona, Xenia; Bellows, Susannah; Mullen, Saul A.; Farrell, Kevin; Mackay, Mark; Sadleir, Lynette; Bleasel, Andrew; Gill, Deepak; Webster, Richard; Wirrell, Elaine C.; Harbord, Michael; Sisodiya, Sanyjay; Andermann, Eva; Kivity, Sara; Berkovic, Samuel F.; Scheffer, Ingrid E.; Dibbens, Leanne M. 分享 收藏
Mutations in DEPDC5 cause familial focal epilepsy with variable foci Dibbens, Leanne M.; de Vries, Boukje; Donatello, Simona; Heron, Sarah E.; Hodgson, Bree L.; Chintawar, Satyan; Crompton, Douglas E.; Hughes, James N.; Bellows, Susannah T.; Klein, Karl Martin; Callenbach, Petra M. C.; Corbett, Mark A.; Gardner, Alison E.; Kivity, Sara; Iona, Xenia; Regan, Brigid M.; Weller, Claudia M.; Crimmins, Denis; O'Brien, Terence J.; Guerrero-Lopez, Rosa; Mulley, John C.; Dubeau, Francois; Licchetta, Laura; Bisulli, Francesca; Cossette, Patrick; Thomas, Paul Q.; Gecz, Jozef; Serratosa, Jose; Brouwer, Oebele F.; Andermann, Frederick; Andermann, Eva; van den Maagdenberg, Arn M. J. M.; Pandolfo, Massimo; Berkovic, Samuel F.; Scheffer, Ingrid E. 分享 收藏
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KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy Weckhuysen, Sarah; Mandelstam, Simone; Suls, Arvid; Audenaert, Dominique; Deconinck, Tine; Claes, Lieve R. F.; Deprez, Liesbet; Smets, Katrien; Hristova, Dimitrina; Yordanova, Iglika; Jordanova, Albena; Ceulemans, Berten; Jansen, An; Hasaerts, Daniele; Roelens, Filip; Lagae, Lieven; Yendle, Simone; Stanley, Thorsten; Heron, Sarah E.; Mulley, John C.; Berkovic, Samuel F.; Scheffer, Ingrid E.; de Jonghe, Peter 分享 收藏
PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome 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.; Gecz, Jozef; Thomas, Paul Q.; Mulley, John C.; Berkovic, Samuel F.; Scheffer, Ingrid E.; Dibbens, Leanne M. 分享 收藏
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De novo SCN1A mutations in migrating partial seizures of infancy Rojo, D. Carranza; Hamiwka, L.; McMahon, J. M.; Dibbens, L. M.; Arsov, T.; Suls, A.; Stoedberg, T.; Kelley, K.; Wirrell, E.; Appleton, B.; Mackay, M.; Freeman, J. L.; Yendle, S. C.; Berkovic, S. F.; Bienvenu, T.; De Jonghe, P.; Thorburn, D. R.; Mulley, J. C.; Mefford, H. C.; Scheffer, I. E. 分享 收藏
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