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

Year Number of Results
1992 1
1994 2
1995 3
1996 3
1997 1
1998 4
1999 1
2000 1
2002 1
2003 1
2004 1
2005 4
2006 2
2007 2
2008 1
2009 1
2011 2
2012 4
2013 4
2014 6
2015 2
2016 3
2017 3
2018 4
2019 3
2020 2
2021 2
2024 0

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56 results

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Page 1
A novel remitting leukodystrophy associated with a variant in FBP2.
Gizak A, Diegmann S, Dreha-Kulaczewski S, Wiśniewski J, Duda P, Ohlenbusch A, Huppke B, Henneke M, Höhne W, Altmüller J, Thiele H, Nürnberg P, Rakus D, Gärtner J, Huppke P. Gizak A, et al. Among authors: ohlenbusch a. Brain Commun. 2021 Mar 11;3(2):fcab036. doi: 10.1093/braincomms/fcab036. eCollection 2021. Brain Commun. 2021. PMID: 33977262 Free PMC article.
Acute onset of adult Alexander disease.
Schmidt H, Kretzschmar B, Lingor P, Pauli S, Schramm P, Otto M, Ohlenbusch A, Brockmann K. Schmidt H, et al. Among authors: ohlenbusch a. J Neurol Sci. 2013 Aug 15;331(1-2):152-4. doi: 10.1016/j.jns.2013.05.006. Epub 2013 May 23. J Neurol Sci. 2013. PMID: 23706596
Evidence of pathogenicity for the leaky splice variant c.1066-6T>G in ATM.
Schröder S, Wieland B, Ohlenbusch A, Yigit G, Altmüller J, Boltshauser E, Dörk T, Brockmann K. Schröder S, et al. Among authors: ohlenbusch a. Am J Med Genet A. 2020 Dec;182(12):2971-2975. doi: 10.1002/ajmg.a.61870. Epub 2020 Sep 11. Am J Med Genet A. 2020. PMID: 32918381
A novel ATP1A3 mutation with unique clinical presentation.
Rosewich H, Baethmann M, Ohlenbusch A, Gärtner J, Brockmann K. Rosewich H, et al. Among authors: ohlenbusch a. J Neurol Sci. 2014 Jun 15;341(1-2):133-5. doi: 10.1016/j.jns.2014.03.034. Epub 2014 Mar 25. J Neurol Sci. 2014. PMID: 24713507
GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like disease.
Henneke M, Combes P, Diekmann S, Bertini E, Brockmann K, Burlina AP, Kaiser J, Ohlenbusch A, Plecko B, Rodriguez D, Boespflug-Tanguy O, Gärtner J. Henneke M, et al. Among authors: ohlenbusch a. Neurology. 2008 Mar 4;70(10):748-54. doi: 10.1212/01.wnl.0000284828.84464.35. Epub 2007 Dec 19. Neurology. 2008. PMID: 18094336
[Vanishing white matter disease in adulthood].
Buggle F, Ciric E, Boujan T, Ohlenbusch A, Gärtner J, Grau AJ. Buggle F, et al. Among authors: ohlenbusch a. Nervenarzt. 2019 Aug;90(8):840-842. doi: 10.1007/s00115-019-0693-7. Nervenarzt. 2019. PMID: 30778629 German. No abstract available.
56 results