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Moira S Cheung

Showing results (21-30 of 34) with videos related to

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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 20, 2010
Cranial base abnormalities in osteogenesis imperfecta: phenotypic and genotypic determinantsMoira S Cheung, Heidi Arponen, Peter Roughley, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 18, 2021
Short report: craniosynostosis, a late complication of nutritional ricketsLydia Y Forestier-Zhang, Paul Arundel, Robyn Gilbey-Cross, et al.
Clinical Dysmorphology|February 19, 2021
Automated reanalysis, a novel way to diagnose an ultra-rare condition: Fibronectin-1-related spondylometaphyseal dysplasia (SMD-FN1)Ataf H Sabir, Juhi Singhal, Jessica Man, et al.
Archives of Disease in Childhood|September 5, 2020
Achondroplasia Foramen Magnum Score: screening infants for stenosisMoira S Cheung, Melita Irving, Alessandra Cocca, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|August 2, 2025
Optic neuropathy associated with vitamin A deficiency in children: a case seriesChristine Bourke, Vasiliki Panteli, Oliver R Marmoy, et al.
Bone|October 4, 2024
Meeting report from the 3rd ISCBH-ERN BOND Achondroplasia Workshop on Long Bone Pathology in Children with Achondroplasia, Salzburg, Austria 22nd June 2024Moira S Cheung, Inês Alves, Patricia Carl-Innig, et al.
Endocrinology|May 18, 2012
Mice lacking the calcineurin inhibitor Rcan2 have an isolated defect of osteoblast functionJ H Duncan Bassett, John G Logan, Alan Boyde, et al.
BMC Medical Genomics|June 7, 2021
Diagnostic yield of rare skeletal dysplasia conditions in the radiogenomics eraAtaf H Sabir, Elizabeth Morley, Jameela Sheikh, et al.
Bone|February 5, 2021
Lifetime impact of achondroplasia: Current evidence and perspectives on the natural historyJulie Hoover-Fong, Moira S Cheung, Virginia Fano, et al.
Orphanet Journal of Rare Diseases|September 19, 2025
XLH Matters 2024: expert insights and practical tools for enhancing care of people living with X-linked hypophosphataemiaLothar Seefried, Ali S Alzahrani, Carsten A Wagner, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 20, 2010
Cranial base abnormalities in osteogenesis imperfecta: phenotypic and genotypic determinantsMoira S Cheung, Heidi Arponen, Peter Roughley, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 18, 2021
Short report: craniosynostosis, a late complication of nutritional ricketsLydia Y Forestier-Zhang, Paul Arundel, Robyn Gilbey-Cross, et al.
Clinical Dysmorphology|February 19, 2021
Automated reanalysis, a novel way to diagnose an ultra-rare condition: Fibronectin-1-related spondylometaphyseal dysplasia (SMD-FN1)Ataf H Sabir, Juhi Singhal, Jessica Man, et al.
Archives of Disease in Childhood|September 5, 2020
Achondroplasia Foramen Magnum Score: screening infants for stenosisMoira S Cheung, Melita Irving, Alessandra Cocca, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|August 2, 2025
Optic neuropathy associated with vitamin A deficiency in children: a case seriesChristine Bourke, Vasiliki Panteli, Oliver R Marmoy, et al.
Bone|October 4, 2024
Meeting report from the 3rd ISCBH-ERN BOND Achondroplasia Workshop on Long Bone Pathology in Children with Achondroplasia, Salzburg, Austria 22nd June 2024Moira S Cheung, Inês Alves, Patricia Carl-Innig, et al.
Endocrinology|May 18, 2012
Mice lacking the calcineurin inhibitor Rcan2 have an isolated defect of osteoblast functionJ H Duncan Bassett, John G Logan, Alan Boyde, et al.
BMC Medical Genomics|June 7, 2021
Diagnostic yield of rare skeletal dysplasia conditions in the radiogenomics eraAtaf H Sabir, Elizabeth Morley, Jameela Sheikh, et al.
Bone|February 5, 2021
Lifetime impact of achondroplasia: Current evidence and perspectives on the natural historyJulie Hoover-Fong, Moira S Cheung, Virginia Fano, et al.
Orphanet Journal of Rare Diseases|September 19, 2025
XLH Matters 2024: expert insights and practical tools for enhancing care of people living with X-linked hypophosphataemiaLothar Seefried, Ali S Alzahrani, Carsten A Wagner, et al.
Pageof 4