Items where authors include "Daniel, E."
Up a levelArticle
Righi, B. orcid.org/0000-0003-4084-1077, Ali, S.R., Bryce, J. et al. (19 more authors) (2023) Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia. Endocrine, 80 (3). pp. 630-638. ISSN 1355-008X
Newell-Price, J., Huatan, H., Quirke, J. et al. (7 more authors) (2021) An oral lipidic native testosterone formulation that is absorbed independent of food. European Journal of Endocrinology, 185 (5). pp. 607-615. ISSN 0804-4643
Bacila, I., Freeman, N., Daniel, E. et al. (42 more authors) (2021) International practice of corticosteroid replacement therapy in congenital adrenal hyperplasia - data from the I-CAH registry. European Journal of Endocrinology, 184 (4). pp. 553-563. ISSN 0804-4643
Daniel, E. orcid.org/0000-0003-4699-420X, Digweed, D., Quirke, J. et al. (3 more authors) (2019) Hydrocortisone granules are bioequivalent when sprinkled onto food or given directly on the tongue. Journal of the Endocrine Society, 3 (5). pp. 847-856. ISSN 2472-1972
Daniel, E. orcid.org/0000-0003-4699-420X, Whitaker, M.J. orcid.org/0000-0003-2388-4753, Keevil, B. orcid.org/0000-0002-0684-9318 et al. (2 more authors) (2018) Accuracy of hydrocortisone dose administration via nasogastric tube. Clinical Endocrinology, 90 (1). pp. 66-73. ISSN 0300-0664
Daniel, E. orcid.org/0000-0003-4699-420X, Debono, M., Caunt, S. et al. (6 more authors) (2018) A prospective longitudinal study of Pasireotide in Nelson's syndrome. Pituitary, 21. pp. 247-255. ISSN 1386-341X
Daniel, E. orcid.org/0000-0003-4699-420X and Newell-Price, J. (2017) Recent advances in understanding Cushing disease: resistance to glucocorticoid negative feedback and somatic USP8 mutations. F1000Research, 6. p. 613. ISSN 2046-1402
Karunasena, N., Han, T.S., Mallappa, A. et al. (4 more authors) (2017) Androgens correlate with increased erythropoiesis in women with congenital adrenal hyperplasia. Clinical Endocrinology, 86 (1). pp. 19-25. ISSN 0300-0664
Daniel, E. orcid.org/0000-0003-4699-420X, Jones, R., Bull, M. et al. (1 more author) (2016) Rapid-sequence MRI for long-term surveillance for paraganglioma and phaeochromocytoma in patients with succinate dehydrogenase (SDHx) mutations. European Journal of Endocrinology , 175. pp. 561-570. ISSN 0804-4643
Jones, R., McDonald, K.E., Willson, J.A. et al. (15 more authors) (2016) Mutations in succinate dehydrogenase B (SDHB) enhance neutrophil survival independent of HIF-1α expression. Blood, 127 (21). pp. 2641-2644. ISSN 0006-4971
Daniel, E. orcid.org/0000-0003-4699-420X, Aylwin, S., Mustafa, O. et al. (25 more authors) (2015) Effectiveness of Metyrapone in Treating Cushing's Syndrome: A Retrospective Multicenter Study in 195 Patients. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 100 (11). pp. 4146-4154. ISSN 0021-972X
Proceedings Paper
Daniel, E. orcid.org/0000-0003-4699-420X, Sandrk, M., Blankenstein, O. et al. (25 more authors) (2017) Defining the dose, type and timing of glucocorticoid and mineralocorticoid replacement in 256 children and adults with congenital adrenal hyperplasia (CAH) in the I-CAH registry. In: Hormone Research in Paediatrics. 10th International Meeting of Pediatric Endocrinology, 14-17 Sep 2017, Washington D.C.. 10th Individual Abstracts for International Meeting of Pediatric Endocrinology: Free Communication and Poster Sessions, Abstracts, 88, S1 . Karger Publishers , p. 358.
Karunasena, N., Daniel, E. orcid.org/0000-0003-4699-420X, Bryce, J. et al. (14 more authors) (2016) Adrenal crisis and sick day episodes among CAH patients: preliminary report based on international CAH (I-CAH) registry. In: Endocrine Abstracts. 18th European Congress of Endocrinology, 28-31 May 2016, Munich, Germany. Bioscientifica .