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The New Zealand Medical Journal|November 27, 2012
Understanding the new HbA1c units for the diagnosis of Type 2 diabetesGeoff D Braatvedt, Tim Cundy, Michael Crooke, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 18, 2004
Susceptibility to Paget's disease of bone is influenced by a common polymorphic variant of osteoprotegerinAnna Daroszewska, Lynne J Hocking, Fiona E A McGuigan, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 5, 2015
Reversible Deterioration in Hypophosphatasia Caused by Renal Failure With Bisphosphonate TreatmentTim Cundy, Toshimi Michigami, Kanako Tachikawa, et al.The Journal of Clinical Endocrinology and Metabolism|November 6, 2008
Absence of somatic SQSTM1 mutations in Paget's disease of boneBrya G Matthews, Dorit Naot, Usha Bava, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 30, 2006
Differential gene expression in cultured osteoblasts and bone marrow stromal cells from patients with Paget's disease of boneDorit Naot, Usha Bava, Brya Matthews, et al.The Journal of Clinical Endocrinology and Metabolism|January 31, 2008
Failure to detect measles virus ribonucleic acid in bone cells from patients with Paget's diseaseBrya G Matthews, Muhammad A Afzal, Philip D Minor, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 14, 2005
Ubiquitin-associated domain mutations of SQSTM1 in Paget's disease of bone: evidence for a founder effect in patients of British descentGavin J A Lucas, Lynne J Hocking, Anna Daroszewska, et al.The Journal of Clinical Endocrinology and Metabolism|April 19, 2007
Addition of monofluorophosphate to estrogen therapy in postmenopausal osteoporosis: a randomized controlled trialIan R Reid, Tim Cundy, Andrew B Grey, et al.Gastro Hep Advances|August 12, 2024
Defining and Phenotyping Gastric Abnormalities in Long-Term Type 1 Diabetes Using a Novel Body Surface Gastric Mapping DeviceWilliam Xu, Armen A Gharibans, Stefan Calder, et al.Human Molecular Genetics|October 11, 2002
Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's diseaseLynne J Hocking, Gavin J A Lucas, Anna Daroszewska, et al.Pageof 12