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Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation.
Knoblauch H, Geier C, Adams S, Budde B, Rudolph A, Zacharias U, Schulz-Menger J, Spuler A, Yaou RB, Nürnberg P, Voit T, Bonne G, Spuler S. Knoblauch H, et al. Among authors: budde b. Ann Neurol. 2010 Jan;67(1):136-40. doi: 10.1002/ana.21839. Ann Neurol. 2010. PMID: 20186852
Noncompaction of the ventricular myocardium is associated with a de novo mutation in the beta-myosin heavy chain gene.
Budde BS, Binner P, Waldmüller S, Höhne W, Blankenfeldt W, Hassfeld S, Brömsen J, Dermintzoglou A, Wieczorek M, May E, Kirst E, Selignow C, Rackebrandt K, Müller M, Goody RS, Vosberg HP, Nürnberg P, Scheffold T. Budde BS, et al. PLoS One. 2007 Dec 26;2(12):e1362. doi: 10.1371/journal.pone.0001362. PLoS One. 2007. PMID: 18159245 Free PMC article.
A new Fgf10 mutation in the mouse leads to atrophy of the harderian gland and slit-eye phenotype in heterozygotes: a novel model for dry-eye disease?
Puk O, Esposito I, Söker T, Löster J, Budde B, Nürnberg P, Michel-Soewarto D, Fuchs H, Wolf E, Hrabé de Angelis M, Graw J. Puk O, et al. Among authors: budde b. Invest Ophthalmol Vis Sci. 2009 Sep;50(9):4311-8. doi: 10.1167/iovs.09-3451. Epub 2009 Apr 30. Invest Ophthalmol Vis Sci. 2009. PMID: 19407009
Mutations of KIF14 cause primary microcephaly by impairing cytokinesis.
Moawia A, Shaheen R, Rasool S, Waseem SS, Ewida N, Budde B, Kawalia A, Motameny S, Khan K, Fatima A, Jameel M, Ullah F, Akram T, Ali Z, Abdullah U, Irshad S, Höhne W, Noegel AA, Al-Owain M, Hörtnagel K, Stöbe P, Baig SM, Nürnberg P, Alkuraya FS, Hahn A, Hussain MS. Moawia A, et al. Among authors: budde b. Ann Neurol. 2017 Oct;82(4):562-577. doi: 10.1002/ana.25044. Epub 2017 Oct 14. Ann Neurol. 2017. PMID: 28892560
82 results