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Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1.
Lehnhardt A, Karnatz C, Ahlenstiel-Grunow T, Benz K, Benz MR, Budde K, Büscher AK, Fehr T, Feldkötter M, Graf N, Höcker B, Jungraithmayr T, Klaus G, Koehler B, Konrad M, Kranz B, Montoya CR, Müller D, Neuhaus TJ, Oh J, Pape L, Pohl M, Royer-Pokora B, Querfeld U, Schneppenheim R, Staude H, Spartà G, Timmermann K, Wilkening F, Wygoda S, Bergmann C, Kemper MJ. Lehnhardt A, et al. Clin J Am Soc Nephrol. 2015 May 7;10(5):825-31. doi: 10.2215/CJN.10141014. Epub 2015 Mar 27. Clin J Am Soc Nephrol. 2015. PMID: 25818337 Free PMC article.
Pathogenesis, diagnosis and management of hyperkalemia.
Lehnhardt A, Kemper MJ. Lehnhardt A, et al. Pediatr Nephrol. 2011 Mar;26(3):377-84. doi: 10.1007/s00467-010-1699-3. Epub 2010 Dec 22. Pediatr Nephrol. 2011. PMID: 21181208 Free PMC article. Review.
Neurological involvement in children with E. coli O104:H4-induced hemolytic uremic syndrome.
Bauer A, Loos S, Wehrmann C, Horstmann D, Donnerstag F, Lemke J, Hillebrand G, Löbel U, Pape L, Haffner D, Bindt C, Ahlenstiel T, Melk A, Lehnhardt A, Kemper MJ, Oh J, Hartmann H. Bauer A, et al. Among authors: lehnhardt a. Pediatr Nephrol. 2014 Sep;29(9):1607-15. doi: 10.1007/s00467-014-2803-x. Epub 2014 Mar 25. Pediatr Nephrol. 2014. PMID: 24664191
21 results