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Psychosocial Care for Injured Children: Worldwide Survey among Hospital Emergency Department Staff.

Alisic, E; Hoysted, C; Kassam-Adams, N; Landolt, M A; Curtis, S; Kharbanda, A B; Lyttle, M D; Parri, N; Stanley, R; Babl, F E; Pediatric Emergency Research in the UK & Ireland (PERUKI); Reuben, Adam (Elsevier, 2015-12-17)
To examine emergency department (ED) staff's knowledge of traumatic stress in children, attitudes toward providing psychosocial care, and confidence in doing so, and also to examine differences in these outcomes according ...
Measurement properties of multidimensional patient-reported outcome measures in neurodisability: a systematic review of evaluation studies.

Janssens, A.; Rogers, M.; Gumm, Rebecca; Jenkinson, C.; Tennant, A.; Logan, Stuart; Morris, Christopher (Wiley, 2015-12-11)
To identify and appraise the quality of studies that primarily assessed the measurement properties of English language versions of multidimensional patient-reported outcome measures (PROMs) when evaluated with children ...
Pulmonary oxygen uptake kinetics are slowed in young patients with cystic fibrosis during very heavy but not moderate intensity cycling exercise

Saynor, Z.; Barker, A. R.; Oades, Patrick; Williams, Craig A. (LWW, 2016)
Paediatric procedural sedation using ketamine in a UK emergency department: a 7 year review of practice.

Kidd, Lawrence R; Lyons, S C; Lloyd, Gavin (Oxford Journals, 2016-02-17)
Ketamine is growing in popularity for procedural sedation in the paediatric population, yet safety concerns remain. We performed a retrospective review of practice and outcomes of paediatric ketamine sedation using the ...
Management of children with type 1 diabetes during illness: a national survey.

Soni, A.; Agwu, J. C.; Wright, N. P.; Moudiotis, Christopher; Kershaw, M.; Edge, J.; Drew, J. H.; Ng, S. M. (BMJ, 2016-02-22)
Adequate sick-day management at home can reduce the risk of progression to diabetic ketoacidosis and admission to hospital. The aim of this project was to review the management of diabetes during illness.
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.

Crow, Y. J.; Chase, D. S.; Lowenstein Schmidt, J.; Szynkiewicz, M.; Forte, G. M. A.; Gornall, H. L.; Oojageer, A.; Anderson, B.; Pizzino, A.; Helman, G.; Abdel-Hamid, M. S.; Devriendt, K.; Di Rocco, M.; Fahey, M. C.; Fazzi, E.; Lim, M. J.; Ferrie, C. D.; Khan, N.; Gowrinathan, N. R.; McKee, S. A.; Gowrishankar, K.; Oades, Patrick; Hanrahan, D.; King, M. D.; Kirk, E. P.; Kumar, R.; Ramesh, V.; Lin, J.-P. S-M; Lagae, L.; Landrieu, P.; Lauffer, H.; Laugel, V.; Olivieri, I.; Roubertie, A.; Moroni, I.; Linnankivi, T.; Rasmussen, M.; Mackay, M. T.; Marom, D. R.; Morton, J. E. V.; Salvatici, E.; Moutard, M.-L.; Tacke, U.; Ostergaard, J. R.; Murray, K.; Nabbout, R.; Nampoothiri, S.; Nunez-Enamorado, N.; Tonduti, D.; Régal, L.; Pérez-Dueñas, B.; Tan, T. Y.; Prendiville, J. S.; Segers, K. A.; Ricci, F.; Valente, E. M.; Rio, M.; Webb, H. J.; Rodriguez, D.; Sinha, G. P.; Soler, D.; Spiegel, R.; Livingston, J. H.; te Water Naude, J.; Stödberg, T. I.; Straussberg, R.; Swoboda, K. J.; Suri, M.; Whitehouse, W. P.; Abdel-Salam, G. M.; Van Coster, R. N.; Wee Teik, K.; Rozenberg, F.; Thomas, M. M.; Till, M.; van der Knaap, M. S.; Ackroyd, S.; Vassallo, G.; Bahi-Buisson, N.; Whitney, R. N.; Vijzelaar, R.; Vogt, J.; Wallace, G. B.; Wassmer, E.; Bernard, G.; Lebon, P.; Zaki, M. S.; Bailey, K. M.; Zuberi, S. M.; Aeby, A.; Vanderver, A.; Bianchi, M.; Orcesi, S.; Cereda, C.; Rice, G. I.; Agosta, G.; Albin, C.; Allon-Shalev, S.; Crichiutti, G.; Barnerias, C.; Arellano, M.; Ariaudo, G.; Aswani, V.; Babul-Hirji, R.; Chandler, K. E.; Baildam, E. M.; Billette de Villemeur, T.; Barth, M.; Dabydeen, L.; Battini, R.; Beresford, M. W.; Blair, E. M.; Bloom, M.; Burlina, A. B.; Figueiredo, A.; Chitayat, D. A.; Carpanelli, M. L.; Carvalho, D. R.; Castro-Gago, M.; Cavallini, A.; Isidor, B.; Dale, R. C.; Collins, A. E.; Gener, B.; Sierra Corcoles, C.; Cordeiro, N.J. V.; D'Arrigo, S.; Kara, B.; De Goede, C. G E L; La Piana, R.; De Laet, C.; De Waele, L.M. H.; Denzler, I.; Desguerre, I.; Marques Lourenço, C.; Goizet, C. (Wiley, 2015-02)
Aicardi-Goutières syndrome is an inflammatory disease occurring due to mutations in any of TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR or IFIH1. We report on 374 patients from 299 families with mutations in these ...
Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study

Rice, G. I.; Forte, G. M. A.; Szynkiewicz, M.; Chase, D. S.; Aeby, A.; Abdel-Hamid, M. S.; Ackroyd, S.; Allcock, R.; Bailey, K. M.; Balottin, U.; Barnerias, C.; Bernard, G.; Bodemer, C.; Botella, M. P.; Cereda, C.; Chandler, K. E.; Dabydeen, L.; Dale, R. C.; De Laet, C.; De Goede, C. G E L; del Toro, M.; Effat, L.; Enamorado, N. N.; Fazzi, E.; Gener, B.; Haldre, M.; Lin, J.-P. S-M; Livingston, J. H.; Lourenco, C. M.; Marques, W.; Oades, Patrick; Peterson, P.; Rasmussen, M.; Roubertie, A.; Schmidt, J. L.; Shalev, S. A.; Simon, R.; Spiegel, R.; Swoboda, K. J.; Temtamy, S.A.; Vassallo, G.; Vilain, C.N.; Vogt, J.; Wermenbol, V.; Whitehouse, W. P.; Soler, D.; Olivieri, I.; Orcesi, S.; Aglan, M. S.; Zaki, M. S.; Abdel-Salam, G. M. H.; Vanderver, A.; Kisand, K.; Rozenberg, F.; Lebon, P.; Crow, Y. J. (Elsevier, 2013-12)
Airflow limitation following cardiopulmonary exercise testing and heavy-intensity intermittent exercise in children with cystic fibrosis.

Stevens, D.; Oades, Patrick; Williams, Craig A. (Springer, 2015-02)
The clinical importance of exercise testing and training in the healthcare management of young patients with cystic fibrosis (CF) is growing. The aim of the present study was to determine the incidence of airflow limitation ...
Impaired aerobic function in patients with cystic fibrosis during ramp exercise.

Saynor, Z.; Barker, A. R.; Oades, Patrick; Williams, Craig A. (Wolters Kluwer, 2014-12)
This study aimed to document the matching of muscle O2 delivery to O2 use in young patients with cystic fibrosis (CF) from muscle deoxygenation (HHb) dynamics during ramp exercise.
Exercise metabolism during moderate-intensity exercise in children with cystic fibrosis following heavy-intensity exercise.

Stevens, D.; Oades, Patrick; Armstrong, N.; Williams, Craig A. (NRC Research Press, 2011-12)
Muscle metabolism is increased following exercise in healthy individuals, affecting exercise metabolism during subsequent physical work. We hypothesized that following heavy-intensity exercise (HIE), disease factors in ...

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