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

Year Number of Results
2002 1
2005 2
2007 1
2009 1
2011 2
2012 4
2013 4
2014 4
2015 1
2016 2
2017 3
2018 4
2019 3
2020 2
2021 2
2024 0

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30 results

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Page 1
[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.
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
Clinical utility gene card for: Zellweger syndrome spectrum.
Rosewich H, Waterham H, Poll-The BT, Ohlenbusch A, Gärtner J. Rosewich H, et al. Among authors: ohlenbusch a. Eur J Hum Genet. 2015 Aug;23(8):1111-. doi: 10.1038/ejhg.2014.250. Epub 2014 Nov 19. Eur J Hum Genet. 2015. PMID: 25407003 Free PMC article. No abstract available.
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
RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection.
Henneke M, Diekmann S, Ohlenbusch A, Kaiser J, Engelbrecht V, Kohlschütter A, Krätzner R, Madruga-Garrido M, Mayer M, Opitz L, Rodriguez D, Rüschendorf F, Schumacher J, Thiele H, Thoms S, Steinfeld R, Nürnberg P, Gärtner J. Henneke M, et al. Among authors: ohlenbusch a. Nat Genet. 2009 Jul;41(7):773-5. doi: 10.1038/ng.398. Epub 2009 Jun 14. Nat Genet. 2009. PMID: 19525954
A unique chromosomal in-frame deletion identified among seven XP-C patients.
Schubert S, Rieper P, Ohlenbusch A, Seebode C, Lehmann J, Gratchev A, Emmert S. Schubert S, et al. Among authors: ohlenbusch a. Photodermatol Photoimmunol Photomed. 2016 Sep;32(5-6):276-283. doi: 10.1111/phpp.12251. Epub 2016 Jul 27. Photodermatol Photoimmunol Photomed. 2016. PMID: 27387384
The expanding clinical and genetic spectrum of ATP1A3-related disorders.
Rosewich H, Ohlenbusch A, Huppke P, Schlotawa L, Baethmann M, Carrilho I, Fiori S, Lourenço CM, Sawyer S, Steinfeld R, Gärtner J, Brockmann K. Rosewich H, et al. Among authors: ohlenbusch a. Neurology. 2014 Mar 18;82(11):945-55. doi: 10.1212/WNL.0000000000000212. Epub 2014 Feb 12. Neurology. 2014. PMID: 24523486
30 results