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

Import to contacts

Publications

List by: Type | Date

Jump to: 2023 | 2022 | 2021 | 2020 | 2019 | 2018
Number of items: 13.

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)

This list was generated on Sat Apr 13 21:04:01 2024 BST.
Jump to: Articles
Number of items: 13.

Articles

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)

This list was generated on Sat Apr 13 21:04:01 2024 BST.

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

Jump to: 2020
Number of items: 1.

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]

This list was generated on Sat Apr 13 21:04:03 2024 BST.