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Publication Year	Title	Author(s)
2022	Young peoples’ lived experiences of multidisciplinary mental health assessment in an intensive day program	McFerran, K. S.; Aitchison, K. A.
2022	You can’t have one without the other: The case for integrated perinatal and infant mental health services	Powrie, R.; Matacz, R.; Paul, C.; Priddis, L.; Sundram, S.; Newman, L.; Wright, T.; Raykar, V.; Lim, I.; Newman-Morris, V.; Hill, R.; Hoehn, E.; Kowalenko, N.
2017	Year in review 2016: Interstitial lung disease, pulmonary vascular disease, pulmonary function, paediatric lung disease, cystic fibrosis and sleep	Jee, A. S.; Eves, N. D.; Wort, S. J.; Corte, T. J.; Piper, A.; Wainwright, C. E.
2016	Year in review 2015: Interstitial lung disease, pulmonary vascular disease, pulmonary function, sleep and ventilation, cystic fibrosis and paediatric lung disease	Piper, A.; Corte, T. J.; Wainwright, C.; Wort, S. J.; Eves, N. D.; Jo, H. E.
2017	Xq26.3 duplication suspected as X-lag in a boy with motor delay and low muscle tone and no gigantism: The impact of high-resolution molecular cytogenetics	Hijazi, H.; Lupski, J. R.; Cotterill, A. M.; Lodish, M. B.; Stratakis, C. A.; Brown, K. T.; Trivellin, G.; Sharwood, E.; Coman, D.; Yuan, B.; Carvalho, C. M. B.
2018	Xq26.3 duplication in a boy with motor delay and low muscle tone refines the X-linked acrogigantism genetic locus	Stratakis, C. A.; Hijazi, H.; Carvalho, C. M. B.; Yuan, B.; Tatton-Brown, K.; Coman, D.; Lupski, J. R.; Cotterill, A. M.; Lodish, M. B.; Trivellin, G.; Sharwood, E.
2022	WT1 complete gonadal dysgenesis with membranoproliferative glomerulonephritis: case series and literature review	Burke, J.; Trnka, P.; Coman, D.; Anderson, E.; Aldridge, M.; Turner, R.; Harraway, J.; McManus, S.; Stewart, A.; Borzi, P.
2020	World Sepsis Day: a global agenda to target a leading cause of morbidity and mortality	Malik, I.; Aljuaid, M. H.; Daniels, R.; Gorordo-Delsol, L. A.; Machado, F.; Nsutebu, E. F.; Reinhart, K.; Finfer, S.; Schlapbach, L. J.; Kissoon, N.; Alhawsawi, A.
2013	Wrapping and swaddling infants: child health nurses' knowledge, attitudes and practice	Young, Jeanine; Watson, Karen; Gorman, Barbara; Gore, Rosemary
2016	Working perinatally to change intergenerational pathways: Approaches to early intervention and prevention are vital to clinicians and government policy	Kinley, S.; Williams, A. S.; Hoehn, E.; Chandra, P.; Luty, S.
2022	Women with type 1 diabetes exhibit a progressive increase in gut Saccharomyces cerevisiae in pregnancy associated with evidence of gut inflammation	Harris, Mark ; Penno, Megan A. S.; Bediaga, Naiara G.; Naselli, Gaetano; Ngui, Katrina M.; Smith, Alannah D.; Huang, Dexing; Zozaya-Valdes, Enrique; Thomson, Rebecca L.; Brown, James D.; Vuillermin, Peter J.; Barry, Simon C.; Craig, Maria E.; Rawlinson, William D.; Davis, Elizabeth A.; Soldatos, Georgia; Colman, Peter G.; Bandala-Sanchez, Esther; Roth-Schulze, Alexandra J.; Oakey, Helena
2021	Women and children first? Gender equity in paediatric medicine	Goldstein, H.; Lawton, B.; Davis, T.; Hall, D.; Tagg, A.; Yoshida, R.; Leo, G. S. Y.
2021	Work-related musculoskeletal injuries among obstetricians and gynaecologists: A cross-sectional survey of Fellows of Royal Australian and New Zealand College of Obstetricians and Gynaecologists (RANZCOG)	Mahomed, K.; Kapoor, V.; Kapoor, S.
2021	Widespread acneiform eruption in a young child secondary to histone deactylase inhibitor	Blake, T.; Wheller, L.; Mazzoni, D.
2019	Widening Evidence-Base of Risk with Hyperoxia	Raman, S.; Peters, M. J.; Ray, S.
2018	Why not colonoscopy? An audit of lower gastrointestinal endoscopy in children	Mealing, S. L.; Ee, L. C.
2018	Whole-exome sequencing reanalysis at 12 months boosts diagnosis and is cost-effective when applied early in Mendelian disorders	Dinger, Marcel E.; Turner, Anne; Mowat, David; Worgan, Lisa; Freckmann, Mary-Louise; Lipke, Michelle; Sachdev, Rani; Miller, David; Field, Michael; Buckley, Michael F.; Roscioli, Tony; Cowley, Mark J.; Ewans, Lisa J.; Schofield, Deborah; Shrestha, Rupendra; Zhu, Ying; Gayevskiy, Velimir; Ying, Kevin; Walsh, Corrina; Lee, Eric; Kirk, Edwin P.; Colley, Alison; Ellaway, Carolyn
2018	Whole-exome sequencing for the identification of primary immunodeficiency in children with sepsis-a prospective population-based cohort study (swiss pediatric sepsis study)	Aebi, C.; Fellay, J.; Berger, C.; Schlapbach, L. J.; Borghesi, J.; Trueck, J.; Asgari, S.; Sancho-Shimizu, V.; Agyeman, P.; Levin, M.
2020	Whole-exome sequencing for the identification of rare variants in primary immunodeficiency genes in children with sepsis: A prospective, population-based cohort study	Kuijpers, T. W.; Niederer-Loher, A.; Kahlert, C. R.; Natalucci, G.; Relly, C.; Riedel, T.; Kuehni, C. E.; Thorball, C. W.; Chaturvedi, N.; Martinon-Torres, F.; Bernhard-Stirnemann, S.; Coin, L.; Wright, V.; Herberg, J.; Levin, M.; Aebi, C.; Berger, C.; Fellay, J.; Schlapbach, L. J.; Borghesi, A.; Trück, J.; Asgari, S.; Sancho-Shimizu, V.; Agyeman, P. K. A.; Bellos, E.; Giannoni, E.; Stocker, M.; Posfay-Barbe, K. M.; Heininger, U.
2018	Whole-exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinism	Duncan, E. L.; Johnson, S. R.; Leo, P. J.; McInerney-Leo, A. M.; Anderson, L. K.; Marshall, M.; McGown, I.; Newell, F.; Brown, M. A.; Conwell, L. S.; Harris, M.