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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.
Hyperuricemia and gout caused by missense mutation in d-lactate dehydrogenase.
Drabkin M, Yogev Y, Zeller L, Zarivach R, Zalk R, Halperin D, Wormser O, Gurevich E, Landau D, Kadir R, Perez Y, Birk OS. Drabkin M, et al. Among authors: gurevich e. J Clin Invest. 2019 Dec 2;129(12):5163-5168. doi: 10.1172/JCI129057. J Clin Invest. 2019. PMID: 31638601 Free PMC article.
Hemolytic Uremic Syndrome: A Contemporary Pediatric Experience.
Alfandary H, Rinat C, Gurevich E, Eisenstein I, Goldberg O, Kropach N, Landau D. Alfandary H, et al. Among authors: gurevich e. Nephron. 2020;144(3):109-117. doi: 10.1159/000505401. Epub 2020 Jan 14. Nephron. 2020. PMID: 31935726
223 results