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Hepatic steatosis in Wilson disease--Role of copper and PNPLA3 mutations.
Stättermayer AF, Traussnigg S, Dienes HP, Aigner E, Stauber R, Lackner K, Hofer H, Stift J, Wrba F, Stadlmayr A, Datz C, Strasser M, Maieron A, Trauner M, Ferenci P. Stättermayer AF, et al. Among authors: lackner k. J Hepatol. 2015 Jul;63(1):156-63. doi: 10.1016/j.jhep.2015.01.034. Epub 2015 Feb 9. J Hepatol. 2015. PMID: 25678388
Biallelic IARS Mutations Cause Growth Retardation with Prenatal Onset, Intellectual Disability, Muscular Hypotonia, and Infantile Hepatopathy.
Kopajtich R, Murayama K, Janecke AR, Haack TB, Breuer M, Knisely AS, Harting I, Ohashi T, Okazaki Y, Watanabe D, Tokuzawa Y, Kotzaeridou U, Kölker S, Sauer S, Carl M, Straub S, Entenmann A, Gizewski E, Feichtinger RG, Mayr JA, Lackner K, Strom TM, Meitinger T, Müller T, Ohtake A, Hoffmann GF, Prokisch H, Staufner C. Kopajtich R, et al. Among authors: lackner k. Am J Hum Genet. 2016 Aug 4;99(2):414-22. doi: 10.1016/j.ajhg.2016.05.027. Epub 2016 Jul 14. Am J Hum Genet. 2016. PMID: 27426735 Free PMC article.
[Management of a huge choledochal cyst diagnosed postpartally].
Bradatsch A, Kornprat P, Lackner K, Mischinger HJ. Bradatsch A, et al. Among authors: lackner k. Zentralbl Chir. 2012 Dec;137(6):549-51. doi: 10.1055/s-0032-1328003. Epub 2012 Dec 21. Zentralbl Chir. 2012. PMID: 23264195 German. No abstract available.
990 results