Mr Martin McMillan
- Honorary Research Fellow (School of Medicine, Dentistry & Nursing)
email:
Martin.McMillan@glasgow.ac.uk
Office Block,, Ground Floor, Zone 1, Paediatrics,, The Queen Elizabeth University Hosp Campus, 1345 Govan Road, G51 4TF
Publications
2023
Tseretopoulou, X., Bryce, J. , Chen, M., McMillan, M., Lucas-Herald, A. K. , Ali, S. R. and Ahmed, S.F. (2023) The I‐CAH registry: a platform for international collaboration for improving knowledge and clinical care in congenital adrenal hyperplasia. Clinical Endocrinology, (doi: 10.1111/cen.14961) (PMID:37602832) (Early Online Publication)
2022
Broom, M. A., Bailey, E. , Kearns, R. J. , McMillan, M. and McPeake, J. (2022) Diagnostic terminology in placenta accreta spectrum: a scoping review. International Journal of Obstetric Anesthesia, 51, 103572. (doi: 10.1016/j.ijoa.2022.103572) (PMID:35868995)
2020
Steell, L. et al. (2020) Muscle deficits with normal bone microarchitecture and geometry in young adults with well controlled childhood onset Crohn’s disease. European Journal of Gastroenterology and Hepatology, 32(12), pp. 1497-1506. (doi: 10.1097/MEG.0000000000001838) (PMID:32675776)
2019
Chen, S. C., Shepherd, S., McMillan, M., Mcneilly, J., Foster, J., Wong, S. C. , Robertson, K. J. and Ahmed, S. F. (2019) Skeletal fragility and its clinical determinants in children with type 1 diabetes. Journal of Clinical Endocrinology and Metabolism, 104(8), pp. 3585-3594. (doi: 10.1210/jc.2019-00084) (PMID:30848792)
2017
Nixon, R., Cerqueira, V., Kyriakou, A., Lucas-Herald, A. , McNeilly, J., McMillan, M., Purvis, A., Tobias, E.S. , McGowan, R. and Ahmed, S.F. (2017) Prevalence of endocrine and genetic abnormalities in boys evaluated systematically for a disorder of sex development. Human Reproduction, 32(10), pp. 2130-2137. (doi: 10.1093/humrep/dex280) (PMID:28938747) (PMCID:PMC5850224)
Rodie, M.E., Mudaliar, M.A.V. , Herzyk, P. , McMillan, M., Boroujerdi, M., Chudleigh, S., Tobias, E.S. and Ahmed, S.F. (2017) Androgen-responsive non-coding small RNAs extend the potential of HCG stimulation to act as a bioassay of androgen sufficiency. European Journal of Endocrinology, 177(4), pp. 339-346. (doi: 10.1530/EJE-17-0404) (PMID:28733293)
2016
Kinning, E., McMillan, M., Shepherd, S., Helfrich, M., vant Hof, R., Adams, C., Read, H., Wall, D. M. and Ahmed, S. F. (2016) An unbalanced rearrangement of chromosomes 4:20 is associated with childhood osteoporosis and reduced caspase-3 levels. Journal of Pediatric Genetics, 5(3), pp. 167-173. (doi: 10.1055/s-0036-1584359) (PMID:27617159)
2015
Abdalrahaman, N. et al. (2015) Deficits in trabecular bone microarchitecture in young women with Type 1 diabetes mellitus. Journal of Bone and Mineral Research, 30(8), pp. 1386-1393. (doi: 10.1002/jbmr.2465) (PMID:25627460)
Mason, A., Malik, S., McMillan, M., Mcneilly, J. D., Bishop, J., McGrogan, P., Russell, R. K. and Ahmed, S. F. (2015) A prospective longitudinal study of growth and pubertal progress in adolescents with inflammatory bowel disease. Hormone Research in Paediatrics, 83(1), pp. 45-54. (doi: 10.1159/000369457) (PMID:25531796)
2011
McMillan, M., MacKay, W.G., Williams, C., Shepherd, A.J., Malcolm, C. and Weaver, L.T. (2011) Intrafamilial genotyping of Helicobacter pylori from faecal DNA. Gastroenterology Research and Practice, 2011, Art. 491035. (doi: 10.1155/2011/491035)
Articles
Tseretopoulou, X., Bryce, J. , Chen, M., McMillan, M., Lucas-Herald, A. K. , Ali, S. R. and Ahmed, S.F. (2023) The I‐CAH registry: a platform for international collaboration for improving knowledge and clinical care in congenital adrenal hyperplasia. Clinical Endocrinology, (doi: 10.1111/cen.14961) (PMID:37602832) (Early Online Publication)
Broom, M. A., Bailey, E. , Kearns, R. J. , McMillan, M. and McPeake, J. (2022) Diagnostic terminology in placenta accreta spectrum: a scoping review. International Journal of Obstetric Anesthesia, 51, 103572. (doi: 10.1016/j.ijoa.2022.103572) (PMID:35868995)
Steell, L. et al. (2020) Muscle deficits with normal bone microarchitecture and geometry in young adults with well controlled childhood onset Crohn’s disease. European Journal of Gastroenterology and Hepatology, 32(12), pp. 1497-1506. (doi: 10.1097/MEG.0000000000001838) (PMID:32675776)
Chen, S. C., Shepherd, S., McMillan, M., Mcneilly, J., Foster, J., Wong, S. C. , Robertson, K. J. and Ahmed, S. F. (2019) Skeletal fragility and its clinical determinants in children with type 1 diabetes. Journal of Clinical Endocrinology and Metabolism, 104(8), pp. 3585-3594. (doi: 10.1210/jc.2019-00084) (PMID:30848792)
Nixon, R., Cerqueira, V., Kyriakou, A., Lucas-Herald, A. , McNeilly, J., McMillan, M., Purvis, A., Tobias, E.S. , McGowan, R. and Ahmed, S.F. (2017) Prevalence of endocrine and genetic abnormalities in boys evaluated systematically for a disorder of sex development. Human Reproduction, 32(10), pp. 2130-2137. (doi: 10.1093/humrep/dex280) (PMID:28938747) (PMCID:PMC5850224)
Rodie, M.E., Mudaliar, M.A.V. , Herzyk, P. , McMillan, M., Boroujerdi, M., Chudleigh, S., Tobias, E.S. and Ahmed, S.F. (2017) Androgen-responsive non-coding small RNAs extend the potential of HCG stimulation to act as a bioassay of androgen sufficiency. European Journal of Endocrinology, 177(4), pp. 339-346. (doi: 10.1530/EJE-17-0404) (PMID:28733293)
Kinning, E., McMillan, M., Shepherd, S., Helfrich, M., vant Hof, R., Adams, C., Read, H., Wall, D. M. and Ahmed, S. F. (2016) An unbalanced rearrangement of chromosomes 4:20 is associated with childhood osteoporosis and reduced caspase-3 levels. Journal of Pediatric Genetics, 5(3), pp. 167-173. (doi: 10.1055/s-0036-1584359) (PMID:27617159)
Abdalrahaman, N. et al. (2015) Deficits in trabecular bone microarchitecture in young women with Type 1 diabetes mellitus. Journal of Bone and Mineral Research, 30(8), pp. 1386-1393. (doi: 10.1002/jbmr.2465) (PMID:25627460)
Mason, A., Malik, S., McMillan, M., Mcneilly, J. D., Bishop, J., McGrogan, P., Russell, R. K. and Ahmed, S. F. (2015) A prospective longitudinal study of growth and pubertal progress in adolescents with inflammatory bowel disease. Hormone Research in Paediatrics, 83(1), pp. 45-54. (doi: 10.1159/000369457) (PMID:25531796)
McMillan, M., MacKay, W.G., Williams, C., Shepherd, A.J., Malcolm, C. and Weaver, L.T. (2011) Intrafamilial genotyping of Helicobacter pylori from faecal DNA. Gastroenterology Research and Practice, 2011, Art. 491035. (doi: 10.1155/2011/491035)