Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Nephrocalcinosis and FGF23[original query] |
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| Infantile hypercalcemia and hypercalciuria: new insights into a vitamin D-dependent mechanism and response to ketoconazole treatment. The Journal of pediatrics 2010 Aug 157 (2): 296-302. Nguyen Minh, Boutignon Henri, Mallet Eric, Linglart Agnes, Guillozo Huguette, Jehan Frederic, Garabedian Miche |
| Hereditary hypophosphatemia in Norway: a retrospective population-based study of genotypes, phenotypes, and treatment complications. European journal of endocrinology / European Federation of Endocrine Societies 2015 Nov . Rafaelsen Silje Hjorth, Johansson Stefan, Raeder Helge, Bjerknes Robe |
| Outcome of adult patients with X-linked hypophosphatemia caused by PHEX gene mutations. Journal of inherited metabolic disease 2018 2 41 (5): 865-876. Chesher Douglas, Oddy Michael, Darbar Ulpee, Sayal Parag, Casey Adrian, Ryan Aidan, Sechi Annalisa, Simister Charlotte, Waters Aoife, Wedatilake Yehani, Lachmann Robin H, Murphy Elai |
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