Items where authors include "Siddiqui, S"

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Number of items: 9.

Article

Evans, RA, Leavy, OC, Richardson, M et al. (1003 more authors) (2022) Clinical characteristics with inflammation profiling of long COVID and association with 1-year recovery following hospitalisation in the UK: a prospective observational study. The Lancet Respiratory Medicine, 10 (8). pp. 761-775. ISSN 2213-2600

Hardcastle, AJ, Liskova, P, Bykhovskaya, Y et al. (59 more authors) (2021) A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus. Communications Biology, 4 (1). 266. ISSN 2399-3642

Lee, MJ, Drake, TM, Sayers, AE et al. (532 more authors) (2020) Outcomes of obstructed abdominal wall hernia: results from the UK national small bowel obstruction audit. BJS Open, 4 (5). pp. 924-934. ISSN 2474-9842

Drake, TM, Lee, MJ orcid.org/0000-0001-9971-1635, Sayers, AE et al. (533 more authors) (2019) Outcomes following small bowel obstruction due to malignancy in the national audit of small bowel obstruction. European Journal of Surgical Oncology, 45 (12). pp. 2319-2324. ISSN 0748-7983

Al-Jawad, M, Addison, O, Sirovica, S et al. (4 more authors) (2018) Intracoronal stress transfer through enamel following RBC photopolymerisation: A synchrotron X-ray study. Dental Materials, 34 (10). pp. 1426-1439. ISSN 0109-5641

Bingley, R, Martin, A, Manfredi, O et al. (8 more authors) (2018) Fretting–corrosion at the modular tapers interface: Inspection of standard ASTM F1875-98. Proceedings of the Institution of Mechanical Engineers, Part H: Journal of Engineering in Medicine, 232 (5). pp. 492-501. ISSN 0954-4119

Sivakumar, S, Taccone, FS, Desai, KA et al. (2497 more authors) (2016) ESICM LIVES 2016: part two. Intensive Care Medicine Experimental, 4 (S1).

Zeng, H, Konicek, AR, Moldovan, N et al. (7 more authors) (2015) Boron-doped ultrananocrystalline diamond synthesized with an H-rich/Ar-lean gas system. Carbon, 84. pp. 103-117. ISSN 0008-6223

Siddiqui, S, Zenteno, JC, Rice, A et al. (8 more authors) (2014) Congenital hereditary endothelial dystrophy caused by SLC4A11 mutations progresses to Harboyan syndrome. Cornea, 33 (3). 247 - 251. ISSN 0277-3740

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