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Degenerative axonopathy in a Tyrolean grey calf.
Syring C, Drögemüller C, Oevermann A, Pfister P, Henke D, Müller S, Sölkner J, Leeb T, Meylan M. Syring C, et al. Among authors: meylan m. J Vet Intern Med. 2010 Nov-Dec;24(6):1519-23. doi: 10.1111/j.1939-1676.2010.0607.x. Epub 2010 Oct 12. J Vet Intern Med. 2010. PMID: 21039865 Free article. No abstract available.
An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle.
Drögemüller C, Reichart U, Seuberlich T, Oevermann A, Baumgartner M, Kühni Boghenbor K, Stoffel MH, Syring C, Meylan M, Müller S, Müller M, Gredler B, Sölkner J, Leeb T. Drögemüller C, et al. Among authors: meylan m. PLoS One. 2011 Apr 15;6(4):e18931. doi: 10.1371/journal.pone.0018931. PLoS One. 2011. PMID: 21526202 Free PMC article.
Genetic Abnormalities in a Calf with Congenital Increased Muscular Tonus.
Wiedemar N, Riedi AK, Jagannathan V, Drögemüller C, Meylan M. Wiedemar N, et al. Among authors: meylan m. J Vet Intern Med. 2015 Sep-Oct;29(5):1418-21. doi: 10.1111/jvim.13599. Epub 2015 Aug 20. J Vet Intern Med. 2015. PMID: 26289121 Free PMC article. No abstract available.
A transposable element insertion in APOB causes cholesterol deficiency in Holstein cattle.
Menzi F, Besuchet-Schmutz N, Fragnière M, Hofstetter S, Jagannathan V, Mock T, Raemy A, Studer E, Mehinagic K, Regenscheit N, Meylan M, Schmitz-Hsu F, Drögemüller C. Menzi F, et al. Among authors: meylan m. Anim Genet. 2016 Apr;47(2):253-7. doi: 10.1111/age.12410. Epub 2016 Jan 13. Anim Genet. 2016. PMID: 26763170 Free PMC article.
[Fanconi-Bickel-Syndrom: a novel genetic disease in Original Braunvieh].
Joller S, Stettler M, Locher I, Dettwiler M, Seefried F, Meylan M, Drögemüller C. Joller S, et al. Among authors: meylan m. Schweiz Arch Tierheilkd. 2018 Mar;160(3):179-184. doi: 10.17236/sat00152. Schweiz Arch Tierheilkd. 2018. PMID: 29509141 Free article. German.
161 results