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An update on clinical presentation and responses to therapy of patients with hereditary hypophosphatemic rickets with hypercalciuria (HHRH).
Zhu Z, Bo-Ran Ho B, Chen A, Amrhein J, Apetrei A, Carpenter TO, Lazaretti-Castro M, Colazo JM, McCrystal Dahir K, Geßner M, Gurevich E, Heier CA, Simmons JH, Hunley TE, Hoppe B, Jacobsen C, Kouri A, Ma N, Majumdar S, Molin A, Nokoff N, Ott SM, Peña HG, Santos F, Tebben P, Topor LS, Deng Y, Bergwitz C. Zhu Z, et al. Among authors: gurevich e. Kidney Int. 2024 May;105(5):1058-1076. doi: 10.1016/j.kint.2024.01.031. Epub 2024 Feb 15. Kidney Int. 2024. PMID: 38364990
Accentuated hyperparathyroidism in type II Bartter syndrome.
Landau D, Gurevich E, Sinai-Treiman L, Shalev H. Landau D, et al. Among authors: gurevich e. Pediatr Nephrol. 2016 Jul;31(7):1085-90. doi: 10.1007/s00467-016-3337-1. Epub 2016 Feb 8. Pediatr Nephrol. 2016. PMID: 26857709
[SEVERE INFANTILE HYPOPHOSPHATASIA].
Gurevich E, Landau D. Gurevich E, et al. Harefuah. 2017 Jan;156(1):27-28. Harefuah. 2017. PMID: 28530318 Hebrew.
High prevalence of hypophosphatasia in Southern Israel.
Gurevich E, Hershkovitz E, Yarza S, Landau D. Gurevich E, et al. Acta Paediatr. 2020 Apr;109(4):851-852. doi: 10.1111/apa.14760. Epub 2019 Mar 10. Acta Paediatr. 2020. PMID: 30788858 No abstract available.
223 results