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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1999 1
2000 2
2001 2
2002 1
2003 3
2004 6
2005 2
2006 1
2008 1
2009 1
2014 1
2024 0

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19 results

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Page 1
Long-term follow-up in patients with CCFDN syndrome.
Walter MC, Bernert G, Zimmermann U, Müllner-Eidenböck A, Moser E, Kalaydjieva L, Lochmüller H, Müller-Felber W. Walter MC, et al. Among authors: mullner eidenbock a. Neurology. 2014 Oct 7;83(15):1337-44. doi: 10.1212/WNL.0000000000000874. Epub 2014 Sep 3. Neurology. 2014. PMID: 25186864
Cellular reaction on the anterior surface of 4 types of intraocular lenses.
Müllner-Eidenböck A, Amon M, Schauersberger J, Kruger A, Abela C, Petternel V, Zidek T. Müllner-Eidenböck A, et al. J Cataract Refract Surg. 2001 May;27(5):734-40. doi: 10.1016/s0886-3350(01)00846-x. J Cataract Refract Surg. 2001. PMID: 11377905 Clinical Trial.
Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome.
Varon R, Gooding R, Steglich C, Marns L, Tang H, Angelicheva D, Yong KK, Ambrugger P, Reinhold A, Morar B, Baas F, Kwa M, Tournev I, Guerguelcheva V, Kremensky I, Lochmüller H, Müllner-Eidenböck A, Merlini L, Neumann L, Bürger J, Walter M, Swoboda K, Thomas PK, von Moers A, Risch N, Kalaydjieva L. Varon R, et al. Among authors: mullner eidenbock a. Nat Genet. 2003 Oct;35(2):185-9. doi: 10.1038/ng1243. Epub 2003 Sep 21. Nat Genet. 2003. PMID: 14517542
Refining clinical phenotypes in septo-optic dysplasia based on MRI findings.
Riedl S, Vosahlo J, Battelino T, Stirn-Kranjc B, Brugger PC, Prayer D, Müllner-Eidenböck A, Kapelari K, Blümel P, Waldhör T, Krasny J, Lebl J, Frisch H. Riedl S, et al. Among authors: mullner eidenbock a. Eur J Pediatr. 2008 Nov;167(11):1269-76. doi: 10.1007/s00431-007-0666-x. Epub 2008 Jan 30. Eur J Pediatr. 2008. PMID: 18231810
The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 gene.
Hoornaert KP, Dewinter C, Vereecke I, Beemer FA, Courtens W, Fryer A, Fryssira H, Lees M, Müllner-Eidenböck A, Rimoin DL, Siderius L, Superti-Furga A, Temple K, Willems PJ, Zankl A, Zweier C, De Paepe A, Coucke P, Mortier GR. Hoornaert KP, et al. Among authors: mullner eidenbock a. J Med Genet. 2006 May;43(5):406-13. doi: 10.1136/jmg.2005.035717. Epub 2005 Sep 9. J Med Genet. 2006. PMID: 16155195 Free PMC article.
19 results