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2019 Journal Article Skeletal and extraskeletal actions of vitamin D: Current evidence and outstanding questionsBouillon, Roger, Marcocci, Claudio, Carmeliet, Geert, Bikle, Daniel, White, John H., Dawson-Hughes, Bess, Lips, Paul, Munns, Craig F., Lazaretti-Castro, Marise, Giustina, Andrea and Bilezikian, John (2019). Skeletal and extraskeletal actions of vitamin D: Current evidence and outstanding questions. Endocrine Reviews, 40 (4), 1109-1151. doi: 10.1210/er.2018-00126 |
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2019 Journal Article Bone marrow transplantation for treatment of the Col1a2+/G610C osteogenesis imperfecta mouse modelLee, Lucinda R., Peacock, Lauren, Ginn, Samantha L., Cantrill, Laurence C., Cheng, Tegan L., Little, David G., Munns, Craig F. and Schindeler, Aaron (2019). Bone marrow transplantation for treatment of the Col1a2+/G610C osteogenesis imperfecta mouse model. Calcified Tissue International, 104 (4), 426-436. doi: 10.1007/s00223-018-0504-3 |
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2019 Journal Article Long-term outcomes of adolescent anorexia nervosa on boneMumford, Jessica, Kohn, Michael, Briody, Julie, Miskovic-Wheatley, Jane, Madden, Sloane, Clarke, Simon, Biggin, Andrew, Schindeler, Aaron and Munns, Craig (2019). Long-term outcomes of adolescent anorexia nervosa on bone. Journal of Adolescent Health, 64 (3), 305-310. doi: 10.1016/j.jadohealth.2018.07.025 |
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2019 Journal Article A comparison of subtraction MRI with the standard contrast-enhanced imaging in Perthes’ diseaseJamil, K., Walker, T., Onikul, E., Munns, C. F. and Little, D. G. (2019). A comparison of subtraction MRI with the standard contrast-enhanced imaging in Perthes’ disease. Journal of Children's Orthopaedics, 13 (1), 82-88. doi: 10.1302/1863-2548.13.180136 |
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2019 Journal Article Differential diagnosis of perinatal hypophosphatasia: radiologic perspectivesOffiah, Amaka C., Vockley, Jerry, Munns, Craig F. and Murotsuki, Jun (2019). Differential diagnosis of perinatal hypophosphatasia: radiologic perspectives. Pediatric Radiology, 49 (1), 3-22. doi: 10.1007/s00247-018-4239-0 |
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2018 Journal Article Management of endocrine disease: Therapeutics of Vitamin DEbeling, P. R., Adler, R. A., Jones, G., Liberman, U. A., Mazziotti, G., Minisola, S., Munns, C. F., Napoli, N., Pittas, A. G., Giustina, A., Bilezikian, J. P. and Rizzoli, R. (2018). Management of endocrine disease: Therapeutics of Vitamin D. European Journal of Endocrinology, 179 (5), R239-R259. doi: 10.1530/EJE-18-0151 |
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2018 Journal Article Diagnosis of recurrent fracture in a pediatric cohortFiscaletti, M., Coorey, C. P., Biggin, A., Briody, J., Little, D. G., Schindeler, A. and Munns, C. F. (2018). Diagnosis of recurrent fracture in a pediatric cohort. Calcified Tissue International, 103 (5), 529-539. doi: 10.1007/s00223-018-0449-6 |
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2018 Journal Article Variations in the management of acute illness in children with congenital adrenal hyperplasia: An audit of three paediatric hospitalsChrisp, Georgina L., Maguire, Ann M., Quartararo, Maria, Falhammar, Henrik, King, Bruce R., Munns, Craig F., Torpy, David J., Hameed, Shihab and Rushworth, R. Louise (2018). Variations in the management of acute illness in children with congenital adrenal hyperplasia: An audit of three paediatric hospitals. Clinical Endocrinology, 89 (5), 577-585. doi: 10.1111/cen.13826 |
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2018 Journal Article Vitamin D assays and the definition of hypovitaminosis D: results from the First International Conference on Controversies in Vitamin DSempos, Christopher T., Heijboer, Annemieke C., Bikle, Daniel D., Bollerslev, Jens, Bouillon, Roger, Brannon, Patsy M., DeLuca, Hector F., Jones, Glenville, Munns, Craig F., Bilezikian, John P., Giustina, Andrea and Binkley, Neil (2018). Vitamin D assays and the definition of hypovitaminosis D: results from the First International Conference on Controversies in Vitamin D. British Journal of Clinical Pharmacology, 84 (10), 2194-2207. doi: 10.1111/bcp.13652 |
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2018 Journal Article Novel variant in Sp7/Osx associated with recessive osteogenesis imperfecta with bone fragility and hearing impairmentFiscaletti, Melissa, Biggin, Andrew, Bennetts, Bruce, Wong, Karen, Briody, Julie, Pacey, Verity, Birman, Catherine and Munns, Craig F. (2018). Novel variant in Sp7/Osx associated with recessive osteogenesis imperfecta with bone fragility and hearing impairment. Bone, 110, 66-75. doi: 10.1016/j.bone.2018.01.031 |
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2018 Journal Article Consensus guidelines on the use of bisphosphonate therapy in children and adolescentsSimm, Peter J., Biggin, Andrew, Zacharin, Margaret R., Rodda, Christine P., Tham, Elaine, Siafarikas, Aris, Jefferies, Craig, Hofman, Paul L., Jensen, Diane E., Woodhead, Helen, Brown, Justin, Wheeler, Benjamin J., Brookes, Denise, Lafferty, Antony, Munns, Craig F. and APEG Bone Mineral Working Group (2018). Consensus guidelines on the use of bisphosphonate therapy in children and adolescents. Journal of Paediatrics and Child Health, 54 (3), 223-233. doi: 10.1111/jpc.13768 |
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2018 Journal Article A novel CASR mutation (p.Glu757lys) causing autosomal dominant hypocalcaemia type 1Kwan, Benjamin, Champion, Bernard, Boyages, Steven, Munns, Craig F., Clifton-Bligh, Roderick, Luxford, Catherine and Crawford, Bronwyn (2018). A novel CASR mutation (p.Glu757lys) causing autosomal dominant hypocalcaemia type 1. Endocrinology, Diabetes and Metabolism Case Reports, 2018 (1) 18-0107, 1-4. doi: 10.1530/EDM-18-0107 |
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2018 Book Chapter Juvenile osteoporosisGlorieux, Francis H. and Munns, Craig (2018). Juvenile osteoporosis. Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism. (pp. 419-423) wiley. doi: 10.1002/9781119266594.ch53 |
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2017 Journal Article Protocol for a randomised control trial of bisphosphonate (zoledronic acid) treatment in childhood femoral head avascular necrosis due to Perthes diseaseJamil, Kamal, Zacharin, Margaret, Foster, Bruce, Donald, Geoffrey, Hassall, Timothy, Siafarikas, Aris, Johnson, Michael, Tham, Elaine, Whitewood, Colin, Gebski, Val, Cowell, Chris T, Little, David Graham and Munns, Craig Frank (2017). Protocol for a randomised control trial of bisphosphonate (zoledronic acid) treatment in childhood femoral head avascular necrosis due to Perthes disease. BMJ Paediatrics Open, 1 (1) e000084, e000084. doi: 10.1136/bmjpo-2017-000084 |
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2017 Journal Article Long-term bisphosphonate therapy in osteogenesis imperfectaBiggin, A. and Munns, C. F. (2017). Long-term bisphosphonate therapy in osteogenesis imperfecta. Current Osteoporosis Reports, 15 (5), 412-418. doi: 10.1007/s11914-017-0401-0 |
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2017 Journal Article Monitoring guidance for patients with hypophosphatasia treated with asfotase alfaKishnani, Priya S., Rush, Eric T., Arundel, Paul, Bishop, Nick, Dahir, Kathryn, Fraser, William, Harmatz, Paul, Linglart, Agnès, Munns, Craig F., Nunes, Mark E., Saal, Howard M., Seefried, Lothar and Ozono, Keiichi (2017). Monitoring guidance for patients with hypophosphatasia treated with asfotase alfa. Molecular Genetics and Metabolism, 122 (1-2), 4-17. doi: 10.1016/j.ymgme.2017.07.010 |
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2017 Journal Article Combination sclerostin antibody and zoledronic acid treatment outperforms either treatment alone in a mouse model of osteogenesis imperfectaLittle, David G., Peacock, Lauren, Mikulec, Kathy, Kneissel, Michaela, Kramer, Ina, Cheng, Tegan L., Schindeler, Aaron and Munns, Craig (2017). Combination sclerostin antibody and zoledronic acid treatment outperforms either treatment alone in a mouse model of osteogenesis imperfecta. Bone, 101, 96-103. doi: 10.1016/j.bone.2017.04.016 |
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2017 Journal Article The importance of vitamin D in maternal and child health: A global perspectiveFiscaletti, M., Stewart, P. and Munns, C. F. (2017). The importance of vitamin D in maternal and child health: A global perspective. Public Health Reviews, 38 (1) 19. doi: 10.1186/s40985-017-0066-3 |
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2016 Journal Article Response to the letter by Sugiyama and OdaMughal, M. Z., Thacher, T. D., Specker, B. L., Shaw, N. J., Kiely, M., Munns, C. F. and Högler, W. (2016). Response to the letter by Sugiyama and Oda. Journal of Clinical Endocrinology and Metabolism, 101 (10), L97-L98. doi: 10.1210/jc.2016-3059 |
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2016 Journal Article Central adrenal insufficiency is not a common feature in CHARGE syndrome: A cross-sectional study in 2 cohortsWong, Monica T.Y., van Ravenswaaij-Arts, Conny M.A., Munns, Craig F., Hsu, Peter, Mehr, Sam and Bocca, Gianni (2016). Central adrenal insufficiency is not a common feature in CHARGE syndrome: A cross-sectional study in 2 cohorts. Journal of Pediatrics, 176, 150-155. doi: 10.1016/j.jpeds.2016.05.065 |
