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Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development.
Vivante A, Kleppa MJ, Schulz J, Kohl S, Sharma A, Chen J, Shril S, Hwang DY, Weiss AC, Kaminski MM, Shukrun R, Kemper MJ, Lehnhardt A, Beetz R, Sanna-Cherchi S, Verbitsky M, Gharavi AG, Stuart HM, Feather SA, Goodship JA, Goodship TH, Woolf AS, Westra SJ, Doody DP, Bauer SB, Lee RS, Adam RM, Lu W, Reutter HM, Kehinde EO, Mancini EJ, Lifton RP, Tasic V, Lienkamp SS, Jüppner H, Kispert A, Hildebrandt F. Vivante A, et al. Among authors: lehnhardt a. Am J Hum Genet. 2015 Aug 6;97(2):291-301. doi: 10.1016/j.ajhg.2015.07.001. Epub 2015 Jul 30. Am J Hum Genet. 2015. PMID: 26235987 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