Publications by authors named "Moira Cheung"

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The Head Circumference Height Index (HCH-I) to Quantify Relative Macrocephaly and Aid Identification of Hypochondroplasia in Children.
Moira S Cheung, Ruggero Lanzafame, Karen J Low, Tim J Cole

Am J Med Genet A· February 2026

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EndoCompass Project: Research Roadmap for Calcium and Bone Endocrinology.
Katharina Jähn-Rickert, Karin Zibar Tomšić, Athanasios D Anastasilakis, Jean-Philippe Bertocchio, Maria Luisa Brandi, Moira Shang-Mei Cheung

Horm Res Paediatr· December 2025

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EndoCompass project: research roadmap for calcium and bone endocrinology.
Katharina Jähn-Rickert, Karin Zibar Tomšić, Athanasios D Anastasilakis, Jean-Philippe Bertocchio, Maria Luisa Brandi, Moira Shang-Mei Cheung

Eur J Endocrinol· October 2025

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Bone health in a U.K. cohort of youth living with perinatally acquired HIV-1: a longitudinal study.
Merle Henderson, Alexandra Blenkinsop, Oliver Ratmann, Moira Cheung, Hermione Lyall

J Int AIDS Soc· September 2025

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XLH Matters 2024: expert insights and practical tools for enhancing care of people living with X-linked hypophosphataemia.
Lothar Seefried, Ali S Alzahrani, Carsten A Wagner, Damian Eade, Danilo Fintini, Moira S Cheung

Orphanet J Rare Dis· September 2025

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Optic neuropathy associated with vitamin A deficiency in children: a case series.
Christine Bourke, Vasiliki Panteli, Oliver R Marmoy, Dorothy A Thompson, Kshitij Mankad, Moira S Cheung

J AAPOS· August 2025

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Limb lengthening in individuals with achondroplasia: Analysis of an international survey.
Christoph Beger, Inês Alves, Patricia Carl-Innig, Marco Sessa, Klaus Mohnike, Moira S Cheung

Bone· June 2025

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XLH Matters: an evolving programme to discuss new advances and share clinical experiences to improve patient outcomes.
Lothar Seefried, Ferdinando Aliberti, Cathrine Alsaker Heier, Pedro Arango-Sancho, Martin Biosse Duplan, Moira S Cheung

Orphanet J Rare Dis· February 2025

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Meeting report from the 3rd ISCBH-ERN BOND Achondroplasia Workshop on Long Bone Pathology in Children with Achondroplasia, Salzburg, Austria 22nd June 2024.
Moira S Cheung, Inês Alves, Patricia Carl-Innig, Deborah Eastwood, Mohamad Maghnie

Bone· January 2025

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Natural history of spinal cord compression stage AFMS3 in infants with achondroplasia: retrospective cohort study.
Moira Shang-Mei Cheung, Alessandra Cocca, Charlotte H Harvey, Connor Stephen S Brett, Amaka C Offiah

Arch Dis Child· November 2024

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Eiken syndrome with parathyroid hormone resistance due to a novel parathyroid hormone receptor type 1 mutation: clinical features and functional analysis.
Alistair D Calder, Jeremy Allgrove, Jakob Höppner, Moira Cheung, Saji Alexander

J Bone Miner Res· October 2024

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Association of the Achondroplasia Foramen Magnum Score and intraoperative neuromonitoring.
Claudia Craven, Ivana Jankovic, Edward Dyson, Stewart G Boyd, Felice D'Arco, Moira Shang-Mei Cheung

Arch Dis Child· August 2024

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Growth reference charts for children with hypochondroplasia.
Moira S Cheung, Tim J Cole, Paul Arundel, Nicola Bridges, Christine P Burren

Am J Med Genet A· February 2024

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Unravelling the pathogenesis of foramen magnum stenosis in patients with severe achondroplasia: a CT-based comparison with age-matched controls and FGFR3 craniosynostosis syndromes.
Catherine H Zhang, Felice D'Arco, Alessandro Borghi, Stefania Picariello, Moira Cheung

Childs Nerv Syst· December 2023

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Recommendations for neuroradiological examinations in children living with achondroplasia: a European Society of Pediatric Radiology and European Society of Neuroradiology opinion paper.
Jenny Wright, Moira Cheung, Ata Siddiqui, Jonathan Lucas, Alistair Calder

Pediatr Radiol· November 2023

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Higher rates of non-skeletal complications and greater healthcare needs in achondroplasia compared to the general UK population: a matched cohort study using the CPRD database.
Jeanne M Pimenta, Melita Irving, Moira Cheung, Louise Mazzeo, Sarah Landis

Orphanet J Rare Dis· July 2023

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Meeting Report from 2nd ICCBH-ERN BOND Spinal Complications in Children and Adults with Achondroplasia Workshop, Dublin, Ireland, 2nd July 2022.
Moira S Cheung, Klaus Mohnike

Bone· December 2022

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A challenging diagnosis of the PIK3CA-related overgrowth spectrum.
Ataf Hussain Sabir, Alessandra Cocca, Moira Cheung, Melita Irving

Clin Dysmorphol· October 2022

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Comprehensive literature review on the prevalence of comorbid conditions in patients with achondroplasia.
Monika Stender, Jeanne M Pimenta, Moira Cheung, Melita Irving, Swati Mukherjee

Bone· September 2022

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Autosomal recessive EXT2 syndrome - extending the phenotypic spectrum of an emerging condition, a further case?
Ataf H Sabir, Juhi Singhal, Jessica Man, Nicola Cooper, Moira Cheung

Clin Dysmorphol· April 2022

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Simultaneous Kidney and Parathyroid Transplantation in the Management of Genetic Hypoparathyroidism in a Child.
Natalie Vallant, Manish D Sinha, Moira Cheung, Nick Ware, Helen Jones

Transplant Direct· April 2022

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International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia.
Ravi Savarirayan, Penny Ireland, Melita Irving, Dominic Thompson, Inês Alves, Moira S Cheung

Nat Rev Endocrinol· March 2022

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Patient-Reported Complications, Symptoms, and Experiences of Living With X-Linked Hypophosphatemia Across the Life-Course.
Moira Cheung, Angela J Rylands, Angela Williams, Karen Bailey, Judith Bubbear

J Endocr Soc· August 2021

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Diagnostic yield of rare skeletal dysplasia conditions in the radiogenomics era.
Ataf H Sabir, Elizabeth Morley, Jameela Sheikh, Alistair D Calder, Ana Beleza-Meireles, Moira S Cheung

BMC Med Genomics· June 2021

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