Evelina London Children's Hospital

Prenatal diagnosis of hypoplastic left heart syndrome on ultrasound using artificial intelligence: How does performance compare to a current screening programme? (2023) Day TG, Budd S, Tan J, Matthew J, Skelton E, Jowett V, Lloyd D, et al. Journal article Cardiac and placental imaging (CARP) in pregnancy to assess aetiology of preeclampsia (2022) Colford K, Price AN, Sigurdardottir J, Fotaki A, Steinweg J, Story L, Ho A, et al. Journal article Long-term methylphenidate exposure and 24-hours blood pressure and left ventricular mass in adolescents and young adults with attention deficit hyperactivity disorder. (2022) Buitelaar JK, van de Loo-Neus GH, Hennissen L, Greven CU, Hoekstra PJ, Nagy P, Ramos-Quiroga A, et al. Journal article Identifying Isolated Systolic Hypertension From Upper-Arm Cuff Blood Pressure Compared With Invasive Measurements (2021) Picone DS, Schultz MG, Armstrong MK, Black JA, Bos WJW, Chen CH, Cheng HM, et al. Journal article Unsupervised Human Pose Estimation through Transforming Shape Templates (2021) Schmidtke L, Vlontzos A, Ellershaw S, Lukens A, Arichi T, Kainz B Conference contribution ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder (2021) Oates S, Absoud M, Goyal S, Bayley S, Baulcomb J, Sims A, Riddett A, et al. Journal article Reduced structural connectivity in cortico-striatal-thalamic network in neonates with congenital heart disease (2020) Ni Bhroin M, Seada SA, Bonthrone AF, Kelly CJ, Christiaens D, Schuh A, Pietsch M, et al. Journal article Disruptive recessive TTN missense mutations cause a wide range of clinico-pathological features (2019) Rees M, Fukuzawa A, Nikoopour R, Kho A, Qi J, Fernandez-Garcia M, Wraige E, et al. Conference contribution Three-dimensional visualisation of the fetal heart using prenatal MRI with motion-corrected slice-volume registration: a prospective, single-centre cohort study (2019) Lloyd DF, Pushparajah K, Simpson JM, van Amerom JF, van Poppel MP, Schulz A, Kainz B, et al. Journal article Mutations in KEOPS-complex genes cause nephritic syndrome with primary microcephaly (2017) Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, et al. Journal article