Stephan Zierz - Search Results

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	6

1

Muscle Carnitine Palmitoyltransferase II (CPT II) Deficiency: A Conceptual Approach.

Joshi PR, Zierz S. Joshi PR, et al. Among authors: zierz s. Molecules. 2020 Apr 13;25(8):1784. doi: 10.3390/molecules25081784. Molecules. 2020. PMID: 32295037 Free PMC article. Review.

2

Muscle Carnitine Palmitoyltransferase II Deficiency: A Review of Enzymatic Controversy and Clinical Features.

Lehmann D, Motlagh L, Robaa D, Zierz S. Lehmann D, et al. Among authors: zierz s. Int J Mol Sci. 2017 Jan 3;18(1):82. doi: 10.3390/ijms18010082. Int J Mol Sci. 2017. PMID: 28054946 Free PMC article. Review.

3

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

4

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.

5

Adolph Seeligmüller's contribution to myotonia congenita Thomsen.

Arendt C, Zierz S. Arendt C, et al. Among authors: zierz s. Neuromuscul Disord. 2020 Dec;30(12):999-1004. doi: 10.1016/j.nmd.2020.10.004. Epub 2020 Oct 20. Neuromuscul Disord. 2020. PMID: 33221127

6

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.

7

Cellular Stress in the Pathogenesis of Muscular Disorders-From Cause to Consequence.

Mensch A, Zierz S. Mensch A, et al. Among authors: zierz s. Int J Mol Sci. 2020 Aug 13;21(16):5830. doi: 10.3390/ijms21165830. Int J Mol Sci. 2020. PMID: 32823799 Free PMC article. Review.

8

Heteroplasmy and Copy Number in the Common m.3243A>G Mutation-A Post-Mortem Genotype-Phenotype Analysis.

Scholle LM, Zierz S, Mawrin C, Wickenhauser C, Urban DL. Scholle LM, et al. Among authors: zierz s. Genes (Basel). 2020 Feb 18;11(2):212. doi: 10.3390/genes11020212. Genes (Basel). 2020. PMID: 32085658 Free PMC article.

9

Response: Late-onset Pompe disease manifests in the brain.

Schneider I, Hensel O, Zierz S. Schneider I, et al. Among authors: zierz s. Mol Genet Metab Rep. 2019 Oct 16;21:100516. doi: 10.1016/j.ymgmr.2019.100516. eCollection 2019 Dec. Mol Genet Metab Rep. 2019. PMID: 31660291 Free PMC article. No abstract available.

10

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

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