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Child Abuse & Neglect|March 3, 2024
Bone biochemistry in children with fractures presenting with non-accidental injuryAngela K Lucas-Herald, Owen Forbes, Heather McDonald, et al.
Archives of Disease in Childhood|January 18, 2020
Nutritional rickets under 16 years: UK surveillance resultsPriscilla Julies, Richard M Lynn, Karina Pall, et al.
Bone Reports|March 20, 2023
Progressive osseous heteroplasia: A case report with an unexpected triggerAlessandra Boncompagni, Angela K Lucas-Herald, Paula Beattie, et al.
Hormone Research in Paediatrics|March 21, 2015
Early identification of pituitary dysfunction in congenital nasal pyriform aperture stenosis: recommendations based on experience in a single centreSuet Ching Chen, Helen McDevitt, W Andrew Clement, et al.
Calcified Tissue International|May 2, 2025
Developing a Standardised Dataset for Natural History Studies in Fibrous Dysplasia/McCune-Albright SyndromeAna Luisa Priego Zurita, Oana O Bulaicon, Jillian Bryce, et al.
The New England Journal of Medicine|November 18, 2024
Oral Infigratinib Therapy in Children with AchondroplasiaRavi Savarirayan, Josep Maria De Bergua, Paul Arundel, et al.
Archives of Disease in Childhood|January 21, 2026
UK consensus guidelines for multidisciplinary care of children and young people with achondroplasia: a modified Delphi processToby P Candler, Kate Ali, Emma Bewick, et al.
Therapeutic Advances in Musculoskeletal Disease|March 28, 2022
Infigratinib in children with achondroplasia: the PROPEL and PROPEL 2 studiesRavi Savarirayan, Josep Maria De Bergua, Paul Arundel, et al.
Frontiers in Endocrinology|November 29, 2023
Standardised practices in the networked management of congenital hyperinsulinism: a UK national collaborative consensusM Guftar Shaikh, Angela K Lucas-Herald, Antonia Dastamani, et al.
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