Oxford University Hospitals NHS Foundation Trust

Hospital


Location: Oxford, United Kingdom (GB) GB

ISNI: 0000000104401440

ROR: https://ror.org/03h2bh287

Show on Map:


close-button

Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

From
To

Abstract

Journal

Non-invasive detection of coronary inflammation using computed tomography and prediction of residual cardiovascular risk (the CRISP CT study): a post-hoc analysis of prospective outcome data (2018) Oikonomou EK, Desai MY, Mancio J, Alashi A, Centeno EH, Thomas S, Herdman L, et al. Journal article CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2018) Blok LS, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, et al. Journal article Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants (2018) Johnston JJ, Van Der Smagt JJ, Rosenfeld JA, Pagnamenta AT, Alswaid A, Baker EH, Blair E, et al. Journal article ESPEN guidelines on definitions and terminology of clinical nutrition (2017) Cederholm T, Barazzoni R, Austin P, Ballmer P, Biolo G, Bischoff SC, Compher C, et al. Journal article Criteria for the definition of Pituitary Tumor Centers of Excellence (PTCOE): A Pituitary Society Statement (2017) Casanueva FF, Barkan AL, Buchfelder M, Klibanski A, Laws ER, Loeffler JS, Melmed S, et al. Journal article Detecting human coronary inflammation by imaging perivascular fat (2017) Antonopoulos AS, Sanna F, Sabharwal N, Thomas S, Oikonomou EK, Herdman L, Margaritis M, et al. Journal article European Surveillance System on Contact Allergies (ESSCA): results with the European baseline series, 2013/14 (2017) Uter W, Amario-Hita JC, Balato A, Ballmer-Weber B, Bauer A, Fortina AB, Bircher A, et al. Journal article STAG1 mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability (2017) Lehalle D, Mosca-Boidron AL, Begtrup A, Boute-Benejean O, Charles P, Cho MT, Clarkson A, et al. Journal article Mutations in mitochondrial DNA causing tubulointerstitial kidney disease (2017) Connor TM, Hoer S, Mallett A, Gale DP, Gomez-Duran A, Posse V, Antrobus R, et al. Journal article Pieces-of-parts for supervoxel segmentation with global context: Application to DCE-MRI tumour delineation (2016) Irving B, Franklin JM, Papiez BW, Anderson EM, Sharma RA, Gleeson FV, Brady SM, Schnabel JA Journal article
1 ... 3 4 5 6 7