Associations Between Hyperphagia, Symptoms of Sleep Breathing Disorder, Behaviour Difficulties and Caregiver Well-Being in Prader-Willi Syndrome: A Preliminary Study

- Mackay, Jessica, Nixon, Gillian M., Vora, Komal, Crock, Patricia, Verge, Charles, Musthaffa, Yassmin, Blecher, Greg, Caudri, Daan, Leonard, Helen, Jacoby, Peter, Wilson, Andrew, Choong, Catherine S., Lafferty, Antony R., Downs, Jenny, Ambler, Geoff, Kapur, Nitin, Bergman, Philip B., Schofield, Cara, Seton, Chris, Tai, Andrew, Tham, Elaine

Daytime sleepiness and emotional and behavioral disturbances in Prader-Willi syndrome

- Choong, Catherine S., Nixon, Gillian M., Schofield, Cara, Seton, Chris, Tai, Andrew, Tham, Elaine, Vora, Komal, Crock, Patricia, Verge, Charles, Musthaffa, Yassmin, Blecher, Greg, Wilson, Andrew, Blackmore, A. Marie, Downs, Jenny, Chen, Wai, Jacoby, Peter, Leonard, Helen, Lafferty, Antony R., Ambler, Geoff, Kapur, Nitin, Bergman, Philip B.

Growth Hormone Increases BDNF and mTOR Expression in Specific Brain Regions after Photothrombotic Stroke in Mice

- Sanchez-Bezanilla, Sonia, Beard, Daniel J., Hood, Rebecca J., Åberg, N. David, Crock, Patricia, Walker, Frederick R., Nilsson, Michael, Isgaard, Jörgen, Ong, Lin Kooi

Sleep-disordered breathing in Australian children with Prader-Willi syndrome following initiation of growth hormone therapy

- Caudri, Daan, Nixon, Gillian M., Bergman, Philip B., Vora, Komal A., Crock, Patricia, Verge, Charles F., Tham, Elaine, Musthaffa, Yassmin, Lafferty, Antony R., Jacoby, Peter, Wilson, Andrew C., Downs, Jenny, Nielsen, Aleisha, Choong, CS, Mai, Linda, Hafekost, Claire R., Kapur, Nitin, Seton, Chris, Tai, Andrew, Blecher, Greg, Ambler, Geoff

Long-Term Efficacy of T3 Analogue Triac in Children and Adults with MCT8 Deficiency: A Real-Life Retrospective Cohort Study

- van Geest, Ferdy S., Groeneweg, Stefan, Cappuccio, Gerarda, Chatterjee, Krishna, Chesover, Alexander D., Christian, Peter, Coutant, Régis, Craiu, Dana, Crock, Patricia, Dewey, Cheyenne, Dica, Alice, Dimitri, Paul, van den Akker, Erica L. T., Dubey, Rachana, Enderli, A, Fairchild, J, Gallichan, J, Garibaldi, LR, George, B, Hackenberg, A, Heinrich, B, Huynh, T, Klosowska, A, Bacos, Iuliu, Lawson-Yuen, A, Linder-Lucht, M, Lyons, G, Lora, FM, Moran, C, Muller, KE, Paone, L, Paul, PG, Polak, M, Porta, F, Barca, Diana, Reinauer, C, de Rijke, YB, Seckold, Rowen, Menevse, TS, Simm, P, Simon, A, Spada, M, Stoupa, A, Szeifert, L, Tonduti, D, van den Berg, Sjoerd A. A., van Toor, H, Turan, S, Vanderniet, Joel, de Waart, M, van der Wal, R, van der Walt, A, Van Wermeskerken, A-M, Wierzba, J, Zibordi, F, Zung, A, Bertini, Enrico, Peeters, RP, Visser, WE, Brunner, Doris, Brunetti-Pierri, Nicola, Cappa, Marco

Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study

- Groeneweg, Stefan, van Geest, Ferdy S., Brunetti-Pierri, Nicola, Bugiani, Marianna, Cappa, Marco, Cappuccio, Gerarda, Castellotti, Barbara, Castiglioni, Claudia, Chatterjee, Krishna, de Coo, Irenaeus F. M., Coutant, Régis, Craiu, Dana, Abaci, Ayhan, Crock, Patricia, DeGoede, C, Demir, K, Dica, A, Dimitri, P, Dolcetta-Capuzzo, A, Dremmen, MHG, Dubey, R, Enderli, A, Fairchild, J, Alcantud, Alberto, Gallichan, J, George, B, Gevers, EF, Hackenberg, A, Halász, Z, Heinrich, B, Huynh, T, Klosowska, A, van der Knaap, MS, van der Knoop, MM, Ambegaonkar, Gautem P., Konrad, D, Koolen, DA, Krude, H, Lawson-Yuen, A, Lebl, J, Linder-Lucht, M, Lorea, CF, Lourenço, CM, Lunsing, RJ, Lyons, G, Armour, Christine M., Malikova, J, Mancilla, EE, McGowan, A, Mericq, V, Lora, FM, Moran, C, Müller, KE, Oliver-Petit, I, Paone, L, Paul, PG, Bakhtiani, Priyanka, Polak, M, Porta, F, Poswar, FO, Reinauer, C, Rozenkova, K, Menevse, TS, Simm, P, Simon, A, Singh, Y, Spada, M, Barca, Diana, van der Spek, J, Stals, MAM, Stoupa, A, Subramanian, Gopinath M., Tonduti, D, Turan, S, den Uil, CA, Vanderniet, Joel, van der Walt, A, Wémeau, JL, Bertini, Enrico S., Wierzba, J, de Wit, MCY, Wolf, NI, Wurm, M, Zibordi, F, Zung, A, Zwaveling-Soonawala, N, Visser, WE, van Beynum, Ingrid M.

Requirements for improving health and well-being of children with Prader-Willi syndrome and their families

- Mackay, Jessica, McCallum, Zoe, Ambler, Geoffrey R., Vora, Komal, Nixon, Gillian, Bergman, Philip, Shields, Nora, Milner, Kate, Kapur, Nitin, Crock, Patricia, Caudri, Daan, Curran, Jaqueline, Verge, Charles, Seton, Chris, Tai, Andrew, Tham, Elaine, Musthaffa, Yassmin, Lafferty, Antony R., Blecher, Greg, Harper, Jessica, Schofield, Cara, Nielsen, Aleisha, Wilson, Andrew, Leonard, Helen, Choong, Catherine S., Downs, Jenny

Growth hormone improves cognitive function after experimental stroke

- Ong, Lin Kooi, Chow, Wei Zhen, Walker, Frederick R., Nilsson, Michael, Isgaard, Jörgen, Tebay, Clifford, Kluge, Murielle, Pietrogrande, Giovanni, Zalewska, Katarzyna, Crock, Patricia, Åberg, Daivd, Bivard, Andrew, Johnson, Sarah J.

Young children with type 1 diabetes can achieve glycemic targets without hypoglycemia: Results of a novel intensive diabetes management program

- Phelan, Helen, King, Bruce, Anderson, Donald, Crock, Patricia, Lopez, Prudence, Smart, Carmel

Molecular and clinical characterization of a series of patients with childhood-onset lysosomal acid lipase deficiency. Retrospective investigations, follow-up and detection of two novel LIPA pathogenic variants

- Pisciotta, Livia, Tozzi, Giulia, Vora, Komal, Nightingale, Scott, Michelakakis, Helen, Garoufi, Anastasia, Lykopoulou, Lilia, Bertolini, Stefano, Calandra, Sebastiano, Travaglini, Lorena, Taurisano, Roberta, Lucchi, Tiziano, Indolfi, Giuseppe, Papadia, Francesco, Di Rocco, Maja, D'Antiga, Lorenzo, Crock, Patricia

Disorders of sex development: insights from targeted gene sequencing of a large international patient cohort

- Eggers, Stefanie, Sadedin, Simon, Cameron, Fergus, Werther, George, Hutson, John, O'Connell, Michele, Grover, Sonia R., Heloury, Yves, Zacharin, Margaret, Bergman, Philip, Kimber, Chris, Brown, Justin, van den Bergen, Jocelyn A., Webb, Nathalie, Hunter, Matthew F., Srinivasan, Shubha, Titmuss, Angela, Verge, Charles F., Mowat, David, Smith, Grahame, Smith, Janine, Ewans, Lisa, Shalhoub, Carolyn, Robevska, Gorjana, Crock, Patricia, Cowell, Chris, Leong, Gary M., Ono, Makato, Lafferty, Antony R., Huynh, Tony, Visser, Uma, Choong, Catherine S., McKenzie, Fiona, Pachter, Nicholas, Ohnesorg, Thomas, Thompson, Elizabeth M., Couper, Jennifer, Baxendale, Anne, Gecz, Jozef, Wheeler, Benjamin J., Jefferies, Craig, MacKenzie, Karen, Hofman, Paul, Carter, Philippa, King, Richard I., Hewitt, Jacqueline, Krausz, Csilla, van Ravenswaaij-Arts, Conny M. A., Looijenga, Leendert, Drop, Sten, Riedl, Stefan, Cools, Martine, Dawson, Angelika, Juniarto, Achmad Zulfa, Khadilkar, Vaman, Khadilkar, Anuradha, Lambeth, Luke, Bhatia, Vijayalakshmi, Dũng, Vũ Chí, Atta, Irum, Raza, Jamal, thi Diem Chi, Nguyen, Hao, Tran Kiem, Harley, Vincent, Koopman, Peter, Warne, Garry, Faradz, Sultana, Bouty, Aurore, Oshlack, Alicia, Ayers, Katie L., Sinclair, Andrew H., Knarston, Ingred M., Tan, Tiong Yang

Evaluation of a novel continuous glucose monitoring guided system for adjustment of insulin dosing: PumpTune: a randomized controlled trial

- Anderson, Donald, Phelan, Helen, Jones, Katie, Smart, Carmel, Oldmeadow, Christopher, King, Bruce, Crock, Patricia

Sotos syndrome: an unusual presentation with intrauterine growth restriction, generalized lymphedema, and intention tremor

- McClelland, Jessie, Burgess, Bronwyn, Crock, Patricia, Goel, Himanshu

Spontaneous and tetracosactide-induced anti-ACTH antibodies in man

- Gan, Earn H., MacArthur, Katie, Mitchell, Anna L., Joshi, Abhijit, Crock, Patricia, Pearce, Simon H. S.

Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum

- Thorwarth, Anne, Schnittert-Hüebener, Sarah, Ebert, Grit, Steininger, Anne, Böennemann, Carsten, Brockmann, Knut, Christen, Hans-Jürgen, Crock, Patricia, deZegher, Francis, Griese, Matthias, Hewitt, Jacqueline, Ivarsson, Sten, Schrumpf, Pamela, Hüebner, Christoph, Kapelari, Klaus, Plecko, Barbara, Rating, Dietz, Stoeva, Iva, Ropers, Hans-Hilger, Grüeters, Annette, Ullmann, Reinhard, Krude, Heiko, Müeller, Ines, Jyrch, Sabine, Dame, Christof, Biebermann, Heike, Kleinau, Gunnar, Katchanov, Juri, Schuelke, Markus

Response to growth hormone treatment in Prader - Willi syndrome: auxological criteria versus genetic diagnosis

- Scheermeyer, Elly, Hughes, Ian, Davies, Peter S. W., Choong, Catherine S. Y., Harris, Mark, Ambler, Geoff, Crock, Patricia, Verge, Charles F., Craig, Maria E., Bergman, Phil, Werther, George, van Driel, Mieke

Clinical, genetic, and enzymatic characterization of P450 oxidoreductase deficiency in four patients

- Sahakitrungruang, Taninee, Huang, Ningwu, Tee, Meng Kian, Agrawal, Vishal, Russell, William E., Crock, Patricia, Murphy, Nuala, Migeon, Claude J., Miller, Walter L.

Autoimmune gastritis and parietal cell reactivity in two children with abnormal intestinal permeability

- Greenwood, Deanne L. V., Crock, Patricia, Braye, Stephen, Davidson, Patricia, Sentry, John W.