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Studies in Health Technology and Informatics|May 23, 2026
Comparative Post-Market Evaluation of Two Generations of Digital Devices for Growth Hormone Therapy: Adherence and Performance SupportPaul Dimitri, Lilian Arnaud, Melissande Simonin, et al.Medical Physics|June 10, 2016
Estimation of trabecular bone parameters in children from multisequence MRI using texture-based regressionKarim Lekadir, Corné Hoogendoorn, Paul Armitage, et al.Pituitary|July 18, 2018
Pituitary tumour apoplexy within prolactinomas in children: a more aggressive condition?Elizabeth Culpin, Matthew Crank, Mark Igra, et al.Pediatric Radiology|July 3, 2020
High-resolution peripheral quantitative computed tomography in children with osteogenesis imperfectaDavid J Fennimore, Maria Digby, Margaret Paggiosi, et al.Journal of Pediatric Rehabilitation Medicine|June 21, 2021
Immersive virtual reality in children with upper limb injuries: Findings from a feasibility studyIvan Phelan, Penny J Furness, Heather D Dunn, et al.Virtual Reality|March 14, 2023
Playing your pain away: designing a virtual reality physical therapy for children with upper limb motor impairmentIvan Phelan, Penny Jayne Furness, Maria Matsangidou, et al.Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry|March 18, 2014
Fracture prediction and the definition of osteoporosis in children and adolescents: the ISCD 2013 Pediatric Official PositionsNick Bishop, Paul Arundel, Emma Clark, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|July 14, 2019
Phenotypic diversity and correlation with the genotypes of pseudohypoaldosteronism type 1Jaya Sujatha Gopal-Kothandapani, Arpan B Doshi, Kath Smith, et al.Frontiers in Endocrinology|October 30, 2024
Opportunities for digitally-enabled personalization and decision support for pediatric growth hormone therapyPaul Dimitri, Paula van Dommelen, Indraneel Banerjee, et al.American Journal of Medical Genetics. Part A|May 6, 2016
An emerging, recognizable facial phenotype in association with mutations in GLI-similar 3 (GLIS3)Paul Dimitri, Elisa De Franco, Abdelhadi M Habeb, et al.Pageof 6