Dr Salma Ali
- Honorary Clinical Lecturer (School of Medicine, Dentistry & Nursing)
email:
Salma.Ali@glasgow.ac.uk
Department of Child Health, Zone 1, Office Block, RHC & QEUH Campus, 1345 Govan Road, Glasgow, G51 4TF
Publications
2024
Ali, S. R., Gardner, M., Xin, Y. , O'Toole, S., Flett, M., Lee, B., Steven, M., Sandberg, D. E. and Ahmed, S. F. (2024) Development and validation of a short version of the quality of life-DSD questionnaire for parents of young children with conditions affecting sex development. Endocrine Connections, (doi: 10.1530/EC-24-0300) (PMID:39255500) (Accepted for Publication)
Tseretopoulou, X. et al. (2024) Temporal trends in acute adrenal insufficiency events in children with congenital adrenal hyperplasia during 2019-2022. Journal of the Endocrine Society, (doi: 10.1210/jendso/bvae145) (In Press)
2023
Ali, S.R. et al. (2023) Electronic reporting of rare endocrine conditions within a clinical network: Results from the EuRRECa project. Endocrine Connections, 12(12), e230434. (doi: 10.1530/EC-23-0434) (PMID:37902973) (PMCID:PMC10692689)
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)
Righi, B. et al. (2023) Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia. Endocrine, 80(3), pp. 630-638. (doi: 10.1007/s12020-023-03330-w) (PMID:36857009) (PMCID:PMC10199864)
2022
Lawrence, N. et al. (2022) Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry. Clinical Endocrinology, 97(5), pp. 551-561. (doi: 10.1111/cen.14796) (PMID:35781728)
2021
Ali, S. R., Bryce, J. , Kodra, Y., Taruscio, D., Persani, L. and Ahmed, S. F. (2021) The quality evaluation of rare disease registries—an assessment of the essential features of a disease registry. International Journal of Environmental Research and Public Health, 18(22), 11968. (doi: 10.3390/ijerph182211968) (PMID:34831724) (PMCID:PMC8620980)
Ali, S.R., Bryce, J. , Smythe, C., Hytiris, M., Priego, A.L., Appelman-Dijkstra, N.M. and Ahmed, S.F. (2021) Supporting international networks through platforms for standardised data collection—the European Registries for Rare Endocrine Conditions (EuRRECa) model. Endocrine, 71(3), pp. 555-560. (doi: 10.1007/s12020-021-02617-0) (PMID:33512655) (PMCID:PMC7844549)
Ali, S. R. et al. (2021) Real world estimates of adrenal insufficiency related adverse events in children with congenital adrenal hyperplasia. Journal of Clinical Endocrinology and Metabolism, 106(1), e192-e203. (doi: 10.1210/clinem/dgaa694) (PMID:32995889) (PMCID:PMC7990061)
2020
Ali, S. R. et al. (2020) The EuRRECa project as a model for data access and governance policies for rare disease registries that collect clinical outcomes. International Journal of Environmental Research and Public Health, 17(23), 8743. (doi: 10.3390/ijerph17238743) (PMID:33255540) (PMCID:PMC7727867)
Ali, S. R., Macqueen, Z., Gardner, M., Xin, Y. , Kyriakou, A., Mason, A., Shaikh, M. G., Wong, S. C. , Sandberg, D. E. and Ahmed, S. F. (2020) Parent-reported outcomes in young children with disorders/differences of sex development. International Journal of Pediatric Endocrinology, 2020, 3. (doi: 10.1186/s13633-020-0073-x) (PMID:32082389) (PMCID:PMC7020572)
2019
Flück, C. et al. (2019) Standardised data collection for clinical follow-up and assessment of outcomes in differences of sex development (DSD): recommendations from the COST action DSDnet. European Journal of Endocrinology, 181(5), pp. 545-564. (doi: 10.1530/eje-19-0363)
Ali, S. R., Lucas-Herald, A. , Bryce, J. and Ahmed, S. F. (2019) The role of international databases in understanding the aetiology and consequences of differences/disorders of sex development. International Journal of Molecular Sciences, 20, 4405. (doi: 10.3390/ijms20184405)
Ali, S. R. et al. (2019) The current landscape of European registries for rare endocrine conditions. European Journal of Endocrinology, 180(1), pp. 89-98. (doi: 10.1530/EJE-18-0861) (PMID:30407922) (PMCID:PMC6347278)
2018
Ali, S.R., Shaheen, I., Young, D., Ramage, I., Maxwell, H., Hughes, D.A., Athavale, D. and Shaikh, M.G. (2018) Fludrocortisone-a treatment for tubulopathy post-paediatric renal transplantation: A national paediatric nephrology unit experience. Pediatric Transplantation, 22(2), e13134. (doi: 10.1111/petr.13134) (PMID:29345400)
Articles
Ali, S. R., Gardner, M., Xin, Y. , O'Toole, S., Flett, M., Lee, B., Steven, M., Sandberg, D. E. and Ahmed, S. F. (2024) Development and validation of a short version of the quality of life-DSD questionnaire for parents of young children with conditions affecting sex development. Endocrine Connections, (doi: 10.1530/EC-24-0300) (PMID:39255500) (Accepted for Publication)
Tseretopoulou, X. et al. (2024) Temporal trends in acute adrenal insufficiency events in children with congenital adrenal hyperplasia during 2019-2022. Journal of the Endocrine Society, (doi: 10.1210/jendso/bvae145) (In Press)
Ali, S.R. et al. (2023) Electronic reporting of rare endocrine conditions within a clinical network: Results from the EuRRECa project. Endocrine Connections, 12(12), e230434. (doi: 10.1530/EC-23-0434) (PMID:37902973) (PMCID:PMC10692689)
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)
Righi, B. et al. (2023) Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia. Endocrine, 80(3), pp. 630-638. (doi: 10.1007/s12020-023-03330-w) (PMID:36857009) (PMCID:PMC10199864)
Lawrence, N. et al. (2022) Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry. Clinical Endocrinology, 97(5), pp. 551-561. (doi: 10.1111/cen.14796) (PMID:35781728)
Ali, S. R., Bryce, J. , Kodra, Y., Taruscio, D., Persani, L. and Ahmed, S. F. (2021) The quality evaluation of rare disease registries—an assessment of the essential features of a disease registry. International Journal of Environmental Research and Public Health, 18(22), 11968. (doi: 10.3390/ijerph182211968) (PMID:34831724) (PMCID:PMC8620980)
Ali, S.R., Bryce, J. , Smythe, C., Hytiris, M., Priego, A.L., Appelman-Dijkstra, N.M. and Ahmed, S.F. (2021) Supporting international networks through platforms for standardised data collection—the European Registries for Rare Endocrine Conditions (EuRRECa) model. Endocrine, 71(3), pp. 555-560. (doi: 10.1007/s12020-021-02617-0) (PMID:33512655) (PMCID:PMC7844549)
Ali, S. R. et al. (2021) Real world estimates of adrenal insufficiency related adverse events in children with congenital adrenal hyperplasia. Journal of Clinical Endocrinology and Metabolism, 106(1), e192-e203. (doi: 10.1210/clinem/dgaa694) (PMID:32995889) (PMCID:PMC7990061)
Ali, S. R. et al. (2020) The EuRRECa project as a model for data access and governance policies for rare disease registries that collect clinical outcomes. International Journal of Environmental Research and Public Health, 17(23), 8743. (doi: 10.3390/ijerph17238743) (PMID:33255540) (PMCID:PMC7727867)
Ali, S. R., Macqueen, Z., Gardner, M., Xin, Y. , Kyriakou, A., Mason, A., Shaikh, M. G., Wong, S. C. , Sandberg, D. E. and Ahmed, S. F. (2020) Parent-reported outcomes in young children with disorders/differences of sex development. International Journal of Pediatric Endocrinology, 2020, 3. (doi: 10.1186/s13633-020-0073-x) (PMID:32082389) (PMCID:PMC7020572)
Flück, C. et al. (2019) Standardised data collection for clinical follow-up and assessment of outcomes in differences of sex development (DSD): recommendations from the COST action DSDnet. European Journal of Endocrinology, 181(5), pp. 545-564. (doi: 10.1530/eje-19-0363)
Ali, S. R., Lucas-Herald, A. , Bryce, J. and Ahmed, S. F. (2019) The role of international databases in understanding the aetiology and consequences of differences/disorders of sex development. International Journal of Molecular Sciences, 20, 4405. (doi: 10.3390/ijms20184405)
Ali, S. R. et al. (2019) The current landscape of European registries for rare endocrine conditions. European Journal of Endocrinology, 180(1), pp. 89-98. (doi: 10.1530/EJE-18-0861) (PMID:30407922) (PMCID:PMC6347278)
Ali, S.R., Shaheen, I., Young, D., Ramage, I., Maxwell, H., Hughes, D.A., Athavale, D. and Shaikh, M.G. (2018) Fludrocortisone-a treatment for tubulopathy post-paediatric renal transplantation: A national paediatric nephrology unit experience. Pediatric Transplantation, 22(2), e13134. (doi: 10.1111/petr.13134) (PMID:29345400)
Grants
Grants and Awards listed are those received whilst working with the University of Glasgow.
- Validation of a Health-Related Quality of Life (HRQoL) Tool for Young Boys with Hypospadias
Glasgow Children`s Hospital Charity
2020 - 2020
Research datasets
2020
Ali, S., Bryce, J. , Haghpanahan, H., Lewsey, J. D., Tan, L. E., Atapattu, N., Birkebaek, N. H., Blankenstein, O., Neumann, U., Balsamo, A., Ortolano, R., Bonfig, W., Claahsen-van der Grinten, H. L., Cools, M., Correa Costa, E., Darendeliler, F., Poyrazoglu, S., Elsedfy, H., Finken, M. J.J., Fluck, C. E., Gevers, E., Korbonits, M., Guaragna-Filho, G., Guran, T., Guven, A., Hannema, S. E., Higham, C., Hughes, I. A., Tadokoro-Cuccaro, R., Thankamony, A., Iotova, V., Krone, N. P., Krone, R., Lichiardopol, C., Luczay, A., Mendonca, B. B., Bachega, T. A.S.S., Miranda, M. C., Milenkovic, T., Mohnike, K., Nordenstrom, A., Einaudi, S., van der Kamp, H., Vieites, A., de Vries, L., Ross, R. J. M. and Ahmed, S. F. (2020) Real World Estimates Of Adrenal Insufficiency Related Adverse Events In Children With Congenital Adrenal Hyperplasia. [Data Collection]