M. T. Collins

Clinical and molecular characterization of Chilean patients with X-linked hypophosphatemia

P. Schneider, G. Cavada, C. Carvajal, 2021, Osteoporosis International.

Hyperphosphatemic familial tumoral calcinosis secondary to fibroblast growth factor 23 (FGF23) mutation: a report of two affected families and review of the literature

G. Fuleihan, G. Nemer, A. Abchee, 2018, Osteoporosis International.

Autosomal Dominant Hypocalcemia Type 1: A Systematic Review

R. Gafni, E. Nemeth, M. Collins, 2022, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Stability and degradation of fibroblast growth factor 23 (FGF23): the effect of time and temperature and assay type

P. Andreopoulou, B. Brillante, N. Fedarko, 2016, Osteoporosis International.

A case of familial tumoral calcinosis/hyperostosis–hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic features

E. Farrow, K. White, M. Kelly, 2009, Osteoporosis International.

Vitamin D Represses Dentin Matrix Protein 1 in Cementoblasts and Osteocytes

N. Bhattacharyya, M. Somerman, M. Collins, 2014, Journal of dental research.

Fibrous Dysplasia of Bone and McCune–Albright Syndrome: A Bench to Bedside Review

M. Zhadina, A. Boyce, M. Collins, 2019, Calcified Tissue International.

Fibrous Dysplasia of Bone and McCune–Albright Syndrome: A Bench to Bedside Review

M. Zhadina, A. Boyce, M. Collins, 2019, Calcified Tissue International.