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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 8, 2009
A randomized, controlled dose-ranging study of risedronate in children with moderate and severe osteogenesis imperfectaNick Bishop, Rachel Harrison, Faisal Ahmed, et al.Nutrients|April 30, 2021
Growth and Body Composition in PKU Children-A Three-Year Prospective Study Comparing the Effects of L-Amino Acid to Glycomacropeptide Protein SubstitutesAnne Daly, Wolfgang Högler, Nicola Crabtree, et al.Archives of Disease in Childhood|November 9, 2021
Non-collagen pathogenic variants resulting in the osteogenesis imperfecta phenotype in children: a single-country observational cohort studyPatrick Thornley, Nicholas Bishop, Duncan Baker, et al.BMC Public Health|May 20, 2026
Identifying online only delivery food outlets in the North of England using data from food delivery appsHannah Groves, Daniel Clarkson, Emma Boyland, et al.Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry|April 30, 2008
Dual-energy X-ray aborptiometry assessment in children and adolescents with diseases that may affect the skeleton: the 2007 ISCD Pediatric Official PositionsNick Bishop, Pierre Braillon, Jon Burnham, et al.BMJ (Clinical Research Ed.)|February 26, 2008
Supplementation with antioxidants and folinic acid for children with Down's syndrome: randomised controlled trialJill M Ellis, Hooi Kuan Tan, Ruth E Gilbert, et al.The Journal of Clinical Endocrinology and Metabolism|June 17, 2021
Genetic Characterization of Short Stature Patients With Overlapping Features of Growth Hormone Insensitivity SyndromesAfiya Andrews, Avinaash Maharaj, Emily Cottrell, et al.Nutrients|July 2, 2021
A Three-Year Longitudinal Study Comparing Bone Mass, Density, and Geometry Measured by DXA, pQCT, and Bone Turnover Markers in Children with PKU Taking L-Amino Acid or Glycomacropeptide Protein SubstitutesAnne Daly, Wolfgang Högler, Nicola Crabtree, et al.Human Molecular Genetics|March 2, 2010
Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidismMichael R Bowl, Samantha M Mirczuk, Irina V Grigorieva, et al.EMBO Molecular Medicine|March 14, 2023
Bi-allelic mutation in SEC16B alters collagen trafficking and increases ER stressAhmed El-Gazzar, Barbara Voraberger, Frank Rauch, et al.Pageof 6