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Willis, Carol M., Cotterill, Andrew M., Conwell, Louise S., McMahon, Sarah K., Harris, Mark, Leong, Gary M., Kearney, Helen, Shann, Karen, Noud, Marina, Cardinal Sherell and Batch, Jennifer A. (2012). 10 year trend for diabetic ketoacidosis in children at diagnosis of type 1 diabetes from Brisbane. In: Australasian Paediatric Endocrine Group Annual Scientific Meeting, Queenstown, New Zealand, (). 29 July - 2 August 2012. 88  
Willis, Carol M., Cotterill, Andrew M., Conwell, Louise S., McMahon, Sarah K., Harris, Mark, Leong, Gary M., Yates, Jason M., Kearney, Helen, Shann, Karen, Noud, Marina, Cardinal, Sherell and Batch, Jennifer A. (2012). 10 year trend for diabetic ketoacidosis in children at diagnosis of type 1 diabetes from Brisbane. In: ISPAD 2012: 38th Annual Meeting of the International Society of Pediatric and Adolescent Diabetes, Istanbul, Turkey, (). 10-13 October, 2012. 20  
Conwell, L. S., Greer, R. M., Walker, R. M., Fiumara, F., Campbell, L., Harris, M. and Cotterill, A. M. (2012). [18F]-DOPA PET/CT Imaging in Congenital Hyperinsulinism - First 12 months of the Australian experience.. In: Abstracts of Monogenic Disorders of Insulin Secretion: Congenital Hyperinsulinism and Neonatal Diabetes. Monogenic Disorders of Insulin Secretion: Congenital Hyperinsulinism and Neonatal Disorders, Philadelphia Pennsylvania, (364-364). 15-16 March 2012. doi:10.1111/j.1399-5448.2012.00887.x 50   0
Conwell, Louise S., Greer, R. M., Walker, Ristan M., Fiumara, Frank, Campbell, Louise, Cowley, David, McGowan, Ivan M, Harris, Mark, Leong, Gary M., Batch, Jennifer A., McMahon, Sarah K., Dahiya, Rachana and Cotterill, Andrew M. (2012). [18F]-DOPA PET/CT imaging in congenital hyperinsulinism - first 2 years of the Queensland experience. In: Australasian Paediatric Endocrine Group Annual Scientific Meeting. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Queenstown, New Zealand, (). 28 July - 2 August 2012. 81  
Jeske, Y. W. A., McGown, I. N., Harris, M., Bowling, F. G., Choong, C. S. Y., Cowley, D. M. and Cotterill, A. M. (2009) 21-Hydroxylase Genotyping in Australasian Patients with Congenital Adrenal Hyperplasia. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 22 2: 127-141. 43   5 Cited 4 times in Scopus4
Lang, E. G., Conwell, L. S., Kamp, M. and Cotterill, A. (2009). A 10 year review of clinical outcomes and complication screening practices in young people with diabetes. In: Hormone Research. LWPES/ESPE 8th Joint Meeting Global Care in Pediatric Endocrinology in collaboration with APEG, APPES, JSPE and SLEP, New York, N.Y., USA, (322-322). 9-12 September 2009. doi:10.1159/000239668 44   0 0
Al-Agha, A., Thomsett, M., Ratcliffe, J., Cotterill, A. M. and Batch, J. A. (2001) Acquired central diabetes insipidus in children: A 12 year Brisbane experience. Journal of Paediatrics and Child Health, 37 2: 172-175. doi:10.1046/j.1440-1754.2001.00640.x 152   14 Cited 15 times in Scopus15 0
Tiong, Keith, Cotterill, Andrew and Falhammar, Henrik (2010) Adult case of partial trisomy 9q. BMC Medical Genetics, 11 26: . doi:10.1186/1471-2350-11-26 55   3 Cited 3 times in Scopus3 0
Cheung, Catherine, Vesey, David, Cotterill, Andrew, Douglas, Meaghan, Gobe, Glenda, Nicol, David and Johnson, David (2005) Altered messenger RNA and protein expressions for insulin-like growth factor family members in clear cell and papillary renal cell carcinomas. International Journal of Urology, 12 1: 17-28. doi:10.1111/j.1442-2042.2004.00993.x 104   8 Cited 8 times in Scopus8 0
Jeske, Y. W. A., McGown, I. N., Cowley, D. M., Oley, C., Thomsett, M. J., Choong, C. S. Y. and Cotterill, A. M. (2007) Androgen receptor genotyping in a large Australasian cohort with androgen insensitivity syndrome; identification of four novel mutations. Journal of Pediatric Endocrinology & Metabolism, 20 8: 893-908. 14   6
Rowland, J. E., Marshall, N. J., Leung, K. C., Ho, K.K.Y, Cotterill, A. M., Rowlinson, S.W. and Waters, M. J. (2002) A novel bioassay for human somatogenic activity in serum samples supports the clinical reliability of immunoassays. Clinical Endocrinology, 56 4: 475-485. doi:10.1046/j.1365-2265.2002.01507.x 75   12 Cited 14 times in Scopus14 0
Wu, Joyce Y., McGown, Ivan N., Lint, Lin, Achermann, John C., Harris, Mark, Cowley, David M., Aftimos, Salim, Neville, Kristen A., Choong, Catherine S. and Cotterill, Andrew M. (2013) A novel NR5A1 variant in an infant with elevated testosterone from an Australasian cohort of 46,XY patients with disorders of sex development. Clinical Endocrinology, 78 4: 545-550. doi:10.1111/cen.12012 67   3 Cited 3 times in Scopus3 1
Cotterill, A. M., Cowley, D., Harris, M., Huynh, T., Leong, G. M., McGown, I. and Nyunt, O. (2009) A novel V185DfsX4 mutation of the AAAS gene in a 2-year-old boy with Triple A Syndrome. Clinical Pediatric Endocrinology, 18 2: 73-75. doi:10.1297/cpe.18.73 62   Cited 0 times in Scopus0 0
Huynh, Tony, Trebbin, Andrea, Cowley, David, Bowling, Francis, Leong, Gary M., Cotterill, Andrew M., Harris, Mark, De Bosscher, Karolien, Haegeman, Guy and Hoey, Andrew J. (2009). A selective glucocorticoid receptor modulator improves muscle function in a mouse model for Duchenne muscular dystrophy. In: Hormone Research. , , (163-163). . 6   0
Nyunt, O, Cotterill, AM, Archbold, SM, Wu, JY, Leong, GM, Verge, CF, Crock, PA and Harris, M (2009). Assessment of adrenocorticotropin deficiency in children with Prader Willi syndrome using a low dose (1 mcg) synacthen test. In: LWPES/ESPE 8th Joint Meeting Global Care in Pediatric Endocrinology, New York, United States, (196-196). 9-12 September 2009. doi:10.1159/000239668 47   0 0
Greer, R. M., Rogers, M. A., Bowling, F. G., Buntain, H. M., Harris, M., Leong, G. M. and Cotterill, A. M. (2007) Australian children and adolescents with type 1 diabetes have low vitamin D levels. MJA, 187 1: 59-60. 133   34 Cited 41 times in Scopus41
Nyunt, O., Harris, M., Hughes, I., Huynh, T., Davies, P. S. W. and Cotterill, A. M. (2009) Benefit of early commencement of growth hormone therapy in children with Prader-Willi syndrome. Journal of Pediatric Endocrinology and Metabolism, 22 12: 1151-1158. 105   4 Cited 5 times in Scopus5
Nyunt, O, Archbold, SM, Donnelly, JM, Cotterill, AM, Harris, M and Leong, GM (2009). BMI changes and metabolic factors in children with Prader Willi syndrome (PWS). In: LWPES/ESPE 8th Joint Meeting Global Care in Pediatric Endocrinology, New York, United States, (296-296). 9-12 September 2009. doi:10.1159/000239668 39   0 0
Nyunt, O., Galligo, P. H., Archbold, S. M., Donnelly, J. M., Cotterill, A. M. and Harris, M. (2009) Bone age advancement in children with Prader Willi syndrome (PWS). Hormone Research in Paediatrics, 72 Suppl. 3: 83-83. 50   0
Nyunt, O, Archbold, SM, Donnelly, JM, Cotterill, AM and Harris, M (2009). Case reports of premature adrenarche in children with Prader Willi syndrome. In: LWPES/ESPE 8th Joint Meeting Global Care in Pediatric Endocrinology, New York, United States, (96-96). September 9–12 2009. doi:10.1159/000239668 45   0 0
Rogers, M. A., Greer, R. M., Harris, M. and Cotterill, A. M. (2008). Changes in presentation of new cases of type 1 diabetes in south Brisbane. In: Australasian Paediatric Endocrine Group Annual Scientific Meeting 2008, Canberra, Australia, (). 17-19 November 2008. 48  
d'Emden, Helen, McDermott, Brett, Gibbons, Kristen, Harris, Mark and Cotterill, Andrew (2015) Choosing a screening tool to assess disordered eating in adolescents with type 1 diabetes mellitus. Journal of Diabetes and its Complications, 29 1: 2-4. doi:10.1016/j.jdiacomp.2014.09.008 23   0 Cited 0 times in Scopus0 0
McLennan, K., Jeske, Y., Cowley, D. M., Thomsett, M., Cotterill, A. M. and Choong, C. (1999). Combined pituitary hormone deficiency: Clinical and genetic correlates. In: Australasian Paediatric Endocrine Group Annual Scientific Meeting. APEG 1999, Hyatt Coolum, Maroochydore, Qld., (A2). 8 - 10 Oct, 1999. 53  
McLennan, Kim, Jeske, Yvette, Cotterill, Andrew, Cowley, David, Penfold, James, Jones, Tim, Howard, Neville, Thomsett, Michael and Choong, Catherine (2003) Combined pituitary hormone deficiency in Australian children: clinical and genetic correlates. Clinical Endocrinology, 58 6: 785-794. doi:10.1046/j.1365-2265.2003.01781.x 57   29 Cited 31 times in Scopus31 0
Hughes, Ian, Harris, Mark, Cotterill, Andrew, Garnett, Sarah, Bannink, Ellen, Pennell, Craig, Sly, Peter, Leong, Gary M., Cowell, Chris, Ambler, Geoff, Werther, George, Hofman, Paul, Cutfield, Wayne and Choong, Catherine S. (2014) Comparison of Centers for Disease Control and Prevention and World Health Organization references/standards for height in contemporary Australian children: analyses of the Raine Study and Australian National Children's Nutrition and Physical Activity cohorts. Journal of Paediatrics and Child Health, 1-7. doi:10.1111/jpc.12672 37   0 Cited 0 times in Scopus0 0
Hughes, Ian P., Harris, Mark, Cotterill, Andrew, Ambler, Geoffrey, Cowell, Christopher T., Cutfield, Wayne S., Werther, George and Choong, Catherine S. (2013) Comparison of weight- vs body surface area-based growth hormone dosing for children: implications for response. Clinical Endocrinology, 80 3: 384-394. doi:10.1111/cen.12315 26 2 1 Cited 1 times in Scopus1 0
d’Emden, Helen, Holden, Libby, McDermott, Brett, Harris, Mark, Gibbons, Kristen, Gledhill, Anne and Cotterill, Andrew (2012) Concurrent validity of self-report measures of eating disorders in adolescents with type 1 diabetes. Acta Paediatrica, 101 9: 973-978. doi:10.1111/j.1651-2227.2012.02738.x 93 4 4 Cited 5 times in Scopus5 1
Huynh, Tony, McGown, Ivan, Cowley, David, Harris, Mark, Leong, Gary M. and Cotterill, Andrew M. (2009). Congenital adrenal hyperplasia genotyping strategy using MLPA and DNA sequencing: an Australian cohort. In: Hormone Research. , , (235-235). . 3   0
Smith, C., Thomsett, M., Choong, C., Rodda, C., McIntyre, H. D. and Cotterill, A. M. (2001) Congenital thyrotoxicosis in premature infants. Clinical Endocrinology, 54 3: 371-376. doi:10.1046/j.1365-2265.2001.01173.x 125   27 Cited 34 times in Scopus34 0
Vuckovic, Slavica, Withers, Geoff, Harris, Mark, Khalil, Dalia, Gardiner, Damien, Flesch, Inge, Tepes, Sonia, Greer, Ristan, Cowley, David, Cotterill, Andrew and Hart, Derek N.J. (2007) Decreased blood dendritic cell counts in type 1 diabetic children. Clinical Immunology, 123 3: 281-288. doi:10.1016/j.clim.2007.03.002 129   36 Cited 38 times in Scopus38 0
Valery, Patricia C., Ibiebele, Torukiri, Harris, Mark, Green, Adele C., Cotterill, Andrew, Moloney, Aletia, Sinha, Ashim K. and Garvey, Gail (2012) Diet, physical activity, and obesity in school-aged indigenous youths in northern Australia. Journal of Obesity, 2012 893508.1-893508.12. doi:10.1155/2012/893508 56 1 Cited 2 times in Scopus2 0
d'Emden, Helen, Holden, Libby, McDermott, Brett, Harris, Mark, Gibbons, Kristen, Gledhill, Anne and Cotterill, Andrew (2013) Disturbed eating behaviours and thoughts in Australian adolescents with type 1 diabetes. Journal of Paediatrics and Child Health, 49 4: E317-E323. doi:10.1111/jpc.12014 56 2 0 Cited 0 times in Scopus0 1
Greer, R. M., Loo, S. W., Walker, R. M., Bowlay, G., Venter, D. J. and Cotterill, A. M. (2009). Does pancreatic immunoreactivity of glucagon-like peptide and its receptor differ between infants with hyperinsulinism of infancy and control infants?. In: Hormone Research. LWPES/ESPE 8th Joint Meeting Global Care in Pediatric Endocrinology, New York, N.Y., USA, (339-339). 9-12 September 2009. doi:10.1159/000239668 37   0 0
Tonks, Ian D., Mould, Arne, Nurcombe, Victor, Cool, Simon M., Walker, Graeme J., Hacker, Elke, Keith, Patricia, Schroder, Wayne A., Cotterill, Andrew, Hayward, Nicholas K. and Kay, Graham F. (2009) Dual loss of Rb1 and Trp53 in melanocytes perturbs melanocyte homeostasis and genetic stability in vitro but does not cause melanoma or pigmentation defects in vivo. Pigment Cell and Melanoma Research, 22 3: 328-330. doi:10.1111/j.1755-148X.2009.00560.x 36   2 Cited 1 times in Scopus1 0
Penno, Megan A. S., Couper, Jennifer J., Craig, Maria E., Colman, Peter G., Rawlinson, William D., Cotterill, Andrew M., Jones, Timothy W., Harrison, Leonard C., ENDIA Study Group and Forbes, Josephine M. (2013) Environmental determinants of islet autoimmunity (ENDIA): a pregnancy to early life cohort study in children at-risk of type 1 diabetes. BMC Pediatrics, 13 124.1-124.15. doi:10.1186/1471-2431-13-124 31   5 Cited 6 times in Scopus6 7
Pai, S, Best, S, Roddick, J, Pahao, H, Baskerville, T, Brown, M, Harris, M, Cotterill, A and Thomas, R (2010). F.25. Activity of the REL-B and p65 subunits of NF-kappa B demonstrates innate immune activation in children at risk of type 1 diabetes. In: FOCIS 2010 Abstract Supplement :10th Annual Meeting, Federation of Clinical Immunology Societies. FOCiS 2010: Tenth Annual Meeting of the Federation of Clinical Immunology Societies, Boston, MA, U.S.A., (S82-S82). 24-27 June 2010. doi:10.1016/j.clim.2010.03.247 83   0 0
Hughes, IP, Choong, CS, Cotterill, A, Harris, M and Davies, PSW (2010) Gender bias in children receiving growth hormone treatment. Journal of Clinical Endocrinology and Metabolism, 95 3: 1191-1198. doi:10.1210/jc.2009-1563 54   8 Cited 7 times in Scopus7 0
Hughes, Ian, Choong, Catherine, Cotterill, Andrew M., Harris, Mark and Davies, Peter S. W. (2009). Gender bias in children receiving growth hormone treatment in Australia : No evidence of an ascertainment bias. In: Hormone Research in Paediatrics. LWPES/ESPE 8th Joint Meeting Paediatric Endocrinology in collaboration with APEG, APPES, JSPE and SLEP, New York, U.S., (253-253). 9-12 September 2009. doi:10.1159/000239668 51   0 0
Greer, Ristan M., Shah, Janaki, Jeske, Jeske, Yvette W., Brown, David, Walker, Rosslyn M., Cowley, David, Bowling, Francis G., Liaskou, Daphne, Harris, Mark, Thomsett, Michael J., Choong, Catherine, Bell, John R., Jack, Michelle M. and Cotterill, Andrew M. (2007) Genotype-Phenotype associations in patients with severe hyperinsulinism of infancy. Pediatric and Developmental Pathology, 10 1: 25-34. doi:10.2350/06-04-0083.1 139   7 Cited 10 times in Scopus10 0
Hughes, Ian P., Cotterill, Andrew, Harris, Mark and Davies, Peter S. W. (2009). GH treated children: difference in age at first presentation between boys and girls. In: Hormone Research. LWPES/ESPE 8th Joint Meeting Global Care in Pediatric Endocrinology in collaboration with APEG, APPES, JSPE and SLEP, New York, N.Y., USA, (253-254). 9-12 September 2009. doi:10.1159/000239668 35   0 0
Hughes, Ian P., Harris, Mark, Choong, Catherine S., Ambler, Geoff, Cutfield, Wayne, Hofman, Paul, Cowell, Chris T., Werther, George, Cotterill, Andrew, Davies, Peter S.W. and on behalf of the Australasian Paediatric Endocrine Group (APEG) (2012) Growth hormone regimens in Australia: analysis of the first three years of treatment for Idiopathic Growth Hormone Deficiency and Idiopathic Short Stature. Clinical Endocrinology, 77 1: 62-71. doi:10.1111/j.1365-2265.2011.04230.x 124 6 7 Cited 6 times in Scopus6 0
Hughes, Ian P., Choong, Catherine S., Harris, Mark, Ambler, Geoffrey R., Cutfield, Wayne S., Hofman, Paul L., Cowell, Chris T., Werther, George, Cotterill, Andrew, Davies, Peter S.W. and on behalf of the Australasian Paediatric Endocrine Group (APEG) (2011) Growth hormone treatment for Turner syndrome in Australia reveals that younger age and increased dose interact to improve response. Clinical Endocrinology, 74 4: 473-480. doi:10.1111/j.1365-2265.2011.03937.x 114 2 6 Cited 9 times in Scopus9 0
Jack, Michelle M., Walker, Rosslyn M., Thomsett, Michael J., Cotterill, Andrew M. and Bell, John R. (2000) Histological findings in persistent hyperinsulinemic hypoglycemia of infancy: Australian experience. Pediatric and Developmental Pathology, 3 6: 532-547. doi:10.1007/s100240010117 37   16 Cited 18 times in Scopus18 0
Thomsett, M. J., Shield, G. J., Batch, J. A. and Cotterill, A. M. (1999) How well are we doing? Metabolic control in patients with diabetes. Journal of Paediatrics and Child Health, 35 5: 479-482. doi:10.1046/j.1440-1754.1999.355424.x 78   19 Cited 25 times in Scopus25 0
Dahiya, R., Shyng, S. L., McGown, I., Marsh, B., Leong, G., Harris, M., Lourie, R. and Cotterill, A. (2010). Hyperinsulinism linked to a novel paternally inherited alteration in KCNJ11. In: 92nd Meeting and Expo of the Endocrine Society (ENDO 2010), San Diego, CA, U.S.A., (). 19-22 June 2010. 42   0
Cotterill, A. M., Cowley, D., Dahiya, R., Greer, R. M., Harris, M., Huynh, T., Leong, G., McGown, I., Nyunt, O., Venter, D. J. and Walker, R. (2008). Hyperinsulinism of infancy associated with a novel paternally inherited alteration in the KCNJ11 gene. In: Australasian Paediatric Endocrine Group Annual Scientific Meeting, Canberra, ACT, Australia, (). 17 - 19 November 2008. 50  
Cotterill, Andrew, Cowley, David and Greer, Ristan (2010). Hypoglycemia: assessment and management. In Charles G. D. Brook, Peter E. Clayton and Rosalind S. Brown (Ed.), Brook's Clinical Pediatric Endocrinology 6th ed. (pp. 505-529) Chichester, West Sussex, UK: Blackwell Publishing. doi:10.1002/9781444316728.ch19 13   Cited 0 times in Scopus0 0
Wu, Joyce Y., Sudeep, Cowley, David M., Harris, Mark, McGown, Ivan N. and Cotterill, Andrew M. (2011) Is it time to commence newborn screening for congenital adrenal hyperplasia in Australia?. Medical Journal of Australia, 195 5: 260-262. doi:10.5694/mja11.10284 60 3 2 Cited 3 times in Scopus3 0
Shield, G. J., Stillman, J., Jeske, Y., Bowling, F., Cowley, D. M., Thomsett, M., Choong, C. and Cotterill, A. M. (1999). Islet auto-antibody status at diagnosis in children with insulin dependent diabetes relates to glycaemic control at 12 months. In: Abstracts of the Australasian Paediatric Endocrine Group Annual Scientific Meeting 1999. Australasian Paediatric Endocrine Group Annual Scientific Meeting 1999, Hyatt Coolum, Maroochydore, Qld., (a29-a29). 8 - 10 October, 1999. 40  
Lang E, Cotterill A and Conwell LS (2011). Management and health outcomes in young people with diabetes: a 10 year review.. In: Australian Diabetes Endocrine Group State Conference, Brisbane Australia, (). June 2011. 33  

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