Objects
Nyunt, Ohn, Cotterill, Andrew M., Archbold, Sinead M., Wu, Joyce Y., Leong, Gary M., Verge, Charles F., Crock, Patricia A., Ambler, Geoffrey R., Hofman, Paul, Harris, Mark. The Endocrine Society; 2010. Normal cortisol response on low-dose synacthen (1 μg) test in children with Prader Willi Syndrome.
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. BioMed Central; 2016. Disorders of sex development: insights from targeted gene sequencing of a large international patient cohort.
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. Wiley-Blackwell Publishing; 2013. Response to growth hormone treatment in Prader - Willi syndrome: auxological criteria versus genetic diagnosis.
King, Bruce R., Howard, Neville J., Verge, Charles F., Jack, Michelle M., Govind, Natalie, Jameson, Karen, Middlehurst, Angela, Jackson, Lilian, Morrison, Melinda, Bandara, D. M. Wajira S. Wiley-Blackwell Publishing; 2012. A diabetes awareness campaign prevents diabetic ketoacidosis in children at their initial presentation with type 1 diabetes.
Scheermeyer, Elly, Harris, Mark, Davies, Peter S. W., , Hughes, Ian, Crock, Patricia A., Ambler, Geoffrey, Verge, Charles F., Bergman, Phil, Werther, George, Craig, Maria E., Choong, Catherine S.. Elsevier; 2017. Low dose growth hormone treatment in infants and toddlers with Prader-Willi syndrome is comparable to higher dosage regimens.
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. Wiley-Blackwell; 2022. Sleep-disordered breathing in Australian children with Prader-Willi syndrome following initiation of growth hormone therapy.