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

Year Number of Results
2002 8
2003 10
2004 6
2005 13
2006 11
2007 1
2008 4
2009 5
2010 4
2011 3
2012 5
2013 8
2014 8
2015 10
2016 15
2017 9
2018 13
2019 13
2020 15
2021 7
2022 4
2023 2
2024 3
2025 0

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149 results

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Page 1
Adolph Seeligmüller (1837-1912).
Arendt C, Zierz S. Arendt C, et al. Among authors: zierz s. J Neurol. 2021 Aug;268(8):3049-3051. doi: 10.1007/s00415-020-10268-w. Epub 2020 Oct 21. J Neurol. 2021. PMID: 33084941 Free PMC article. No abstract available.
FGF-21 as a Potential Biomarker for Mitochondrial Diseases.
Scholle LM, Lehmann D, Deschauer M, Kraya T, Zierz S. Scholle LM, et al. Among authors: zierz s. Curr Med Chem. 2018;25(18):2070-2081. doi: 10.2174/0929867325666180111094336. Curr Med Chem. 2018. PMID: 29332568 Review.
A stagewise response to mitochondrial dysfunction in mitochondrial DNA maintenance disorders.
Vincent AE, Chen C, Gomes TB, Di Leo V, Laalo T, Pabis K, Capaldi R, Marusich MF, McDonald D, Filby A, Fuller A, Lehmann Urban D, Zierz S, Deschauer M, Turnbull D, Reeve AK, Lawless C. Vincent AE, et al. Among authors: zierz s. Biochim Biophys Acta Mol Basis Dis. 2024 Jun;1870(5):167131. doi: 10.1016/j.bbadis.2024.167131. Epub 2024 Mar 21. Biochim Biophys Acta Mol Basis Dis. 2024. PMID: 38521420 Free article.
Basilar artery thrombosis during sexual intercourse.
Posa A, Mueller T, Ungurs O, Kornhuber M, Zierz S. Posa A, et al. Among authors: zierz s. J Clin Neurosci. 2020 Apr;74:238-240. doi: 10.1016/j.jocn.2020.01.071. Epub 2020 Jan 22. J Clin Neurosci. 2020. PMID: 31982277
Energetic depression caused by mitochondrial dysfunction.
Gellerich FN, Trumbeckaite S, Müller T, Deschauer M, Chen Y, Gizatullina Z, Zierz S. Gellerich FN, et al. Among authors: zierz s. Mol Cell Biochem. 2004 Jan-Feb;256-257(1-2):391-405. doi: 10.1023/b:mcbi.0000009885.34498.e6. Mol Cell Biochem. 2004. PMID: 14977198 Review.
Hot-spot KIF5A mutations cause familial ALS.
Brenner D, Yilmaz R, Müller K, Grehl T, Petri S, Meyer T, Grosskreutz J, Weydt P, Ruf W, Neuwirth C, Weber M, Pinto S, Claeys KG, Schrank B, Jordan B, Knehr A, Günther K, Hübers A, Zeller D, Kubisch C, Jablonka S, Sendtner M, Klopstock T, de Carvalho M, Sperfeld A, Borck G, Volk AE, Dorst J, Weis J, Otto M, Schuster J, Del Tredici K, Braak H, Danzer KM, Freischmidt A, Meitinger T, Strom TM, Ludolph AC, Andersen PM, Weishaupt JH; German ALS network MND-NET. Brenner D, et al. Brain. 2018 Mar 1;141(3):688-697. doi: 10.1093/brain/awx370. Brain. 2018. PMID: 29342275 Free PMC article.
Bi-allelic truncating mutations in VWA1 cause neuromyopathy.
Deschauer M, Hengel H, Rupprich K, Kreiß M, Schlotter-Weigel B, Grimmel M, Admard J, Schneider I, Alhaddad B, Gazou A, Sturm M, Vorgerd M, Balousha G, Balousha O, Falna M, Kirschke JS, Kornblum C, Jordan B, Kraya T, Strom TM, Weis J, Schöls L, Schara U, Zierz S, Riess O, Meitinger T, Haack TB. Deschauer M, et al. Among authors: zierz s. Brain. 2021 Mar 3;144(2):574-583. doi: 10.1093/brain/awaa418. Brain. 2021. PMID: 33459760
149 results