Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Nephrocalcinosis and PHEX[original query] |
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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 |
Long-term effect of conventional phosphate and calcitriol treatment on metabolic recovery and catch-up growth in children with PHEX mutation. Journal of pediatric endocrinology & metabolism : JPEM 2021 9 34 (12): 1573-1584. Alikasifoglu Ayfer, Unsal Yagmur, Gonc Elmas Nazli, Ozon Zeynep Alev, Kandemir Nurgun, Alikasifoglu Mehm |
Disease Manifestations and Complications in Dutch X-Linked Hypophosphatemia Patients. Calcified tissue international 2024 1 . A Bosman, N M Appelman-Dijkstra, A M Boot, M H de Borst, A C van de Ven, R T de Jongh, A Bökenkamp, J P van den Bergh, B C J van der Eerden, M C Zillike |
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