Congenital subpendymal giant cell astrocytoma in children with tuberous sclerosis complex: growth patterns and neurological outcome von Chan, Denise L., Kennedy, Sean E., Sarkozy, Vanessa E., Chung, Clara W. T., Flanagan, Danny, Mowat, David, Farrar, Michelle A., Lawson, John A.

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A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes von Bastard, Paul, Hsiao, Kuang-Chih, Zhang, Qian, Choin, Jeremy, Best, Emma, Chen, Jie, Gervais, Adrian, Bizien, Lucy, Materna, Marie, Harmant, Christine, Roux, Maguelonne, Hawley, Nicola L, Weeks, Daniel E, McGarvey, Stephen T, Sandoval, Karla, Barberena-Jonas, Carmina, Quinto-Cortés, Consuelo D, Hagelberg, Erika, Mentzer, Alexander J, Robson, Kathryn, Coulibaly, Boubacar, Seeleuthner, Yoann, Bigio, Benedetta, Li, Zhi, Uzé, Gilles, Pellegrini, Sandra, Lorenzo, Lazaro, Sbihi, Zineb, Latour, Sylvain, Besnard, Marianne, Adam de Beaumais, Tiphaine, Jacqz Aigrain, Evelyne, Béziat, Vivien, Deka, Ranjan, Esera Tulifau, Litara, Viali, Satupa'itea, Reupena, Muagututi'a Sefuiva, Naseri, Take, McNaughton, Peter, Sarkozy, Vanessa, Peake, Jane, Blincoe, Annaliesse, Primhak, Sarah, Stables, Simon, Gibson, Kate, Woon, See-Tarn, Drake, Kylie Marie, Hill, Adrian V S, Chan, Cheng-Yee, King, Richard, Ameratunga, Rohan, Teiti, Iotefa, Aubry, Maite, Cao-Lormeau, Van-Mai, Tangye, Stuart G, Zhang, Shen-Ying, Jouanguy, Emmanuelle, Gray, Paul, Abel, Laurent, Moreno-Estrada, Andrés, Minster, Ryan L, Quintana-Murci, Lluis, Wood, Andrew C, Casanova, Jean-Laurent

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Psychosocial experiences of clinicians providing care for children with severe neurological impairment von Nevin, Suzanne M., Le Marne, Fleur A., Beavis, Erin, Macintosh, Rebecca, Palmer, Elizabeth E., Sachdev, Rani, Nunn, Kenneth, Bye, Ann, Beek, Anna, Wittekind, Carola, Shalhoub, Carolyn, Lau, Christine Yuen‐Yan, Elliot, Christopher, Rogers, David, Wijetilaka, Devika, Argent, Elizabeth, Cotterell, Elizabeth, Jacobson, Erica Elizabeth, McCarthy, Hugh, Sampaio, Hugo, Dalby‐Payne, Jacqui, Ging, Joanne, Doyle, Katrina, Bhattacharya, Kaustuv, Stark, Kylie, Lorentzos, Michelle, Slade, Rob, Evans, Ruth, Pillai, Sekhar, Mohammad, Shekeeb, Piper, Susie, Sarkozy, Vanessa

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Deep Sequencing and Phenotyping in an Australian Tuberous Sclerosis Complex “No Mutations Identified” Cohort von Chung, Clara W. T., Bournazos, Adam M., Chan, Lok Chi Denise, Sarkozy, Vanessa, Lawson, John, Kennedy, Sean E., Cooper, Sandra T., Kirk, Edwin P., Mowat, David

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Understanding the ongoing learning needs of Australian paediatricians: Evaluation of a pilot paediatric video teaching programme von Le Marne, Fleur A, Briggs, Nancy, Frith, Katie, Kariyawasam, Didu, McCarthy, Hugh J, Nunn, Kenneth, Rao, Arjun, Sachdev, Rani, Sarkozy, Vanessa, Teng, Arthur, Trethewie, Susan, Williams, Gary D, Bye, Ann ME

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Early detection of Tuberous Sclerosis Complex: an opportunity for improved neurodevelopmental outcome von Ting Chung, Clara Wai, Lawson, John Anthony, Sarkozy, Vanessa, Riney, Kate, Wargon, Orli, Shand, Antonia W, Cooper, Stephen, King, Harrison, Kennedy, Sean E, Mowat, David

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