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

Year Number of Results
1970 1
1986 1
1988 3
1991 5
1992 3
1993 5
1994 4
1995 4
1996 7
1997 5
1999 1
2000 1
2005 1
2011 1
2015 2
2016 1
2017 1
2024 0

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45 results

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Page 1
Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1.
Strickland AV, Schabhüttl M, Offenbacher H, Synofzik M, Hauser NS, Brunner-Krainz M, Gruber-Sedlmayr U, Moore SA, Windhager R, Bender B, Harms M, Klebe S, Young P, Kennerson M, Garcia AS, Gonzalez MA, Züchner S, Schule R, Shy ME, Auer-Grumbach M. Strickland AV, et al. Among authors: offenbacher h. J Neurol. 2015 Sep;262(9):2124-34. doi: 10.1007/s00415-015-7727-2. Epub 2015 Jun 24. J Neurol. 2015. PMID: 26100331 Free PMC article.
Susac's syndrome: clinical course and epidemiology in a Central European population.
Seifert-Held T, Langner-Wegscheider BJ, Komposch M, Simschitz P, Franta C, Teuchner B, Offenbacher H, Otto F, Sellner J, Rauschka H, Fazekas F. Seifert-Held T, et al. Among authors: offenbacher h. Int J Neurosci. 2017 Sep;127(9):776-780. doi: 10.1080/00207454.2016.1254631. Epub 2016 Nov 11. Int J Neurosci. 2017. PMID: 27788613
Phenotypes of the N88S Berardinelli-Seip congenital lipodystrophy 2 mutation.
Auer-Grumbach M, Schlotter-Weigel B, Lochmüller H, Strobl-Wildemann G, Auer-Grumbach P, Fischer R, Offenbacher H, Zwick EB, Robl T, Hartl G, Hartung HP, Wagner K, Windpassinger C; Austrian Peripheral Neuropathy Study Group. Auer-Grumbach M, et al. Among authors: offenbacher h. Ann Neurol. 2005 Mar;57(3):415-24. doi: 10.1002/ana.20410. Ann Neurol. 2005. PMID: 15732094
45 results