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

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

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64 results

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Page 1
Perspectives for Primary Ciliary Dyskinesia.
Bukowy-Bieryllo Z, Witt M, Zietkiewicz E. Bukowy-Bieryllo Z, et al. Among authors: witt m. Int J Mol Sci. 2022 Apr 8;23(8):4122. doi: 10.3390/ijms23084122. Int J Mol Sci. 2022. PMID: 35456939 Free PMC article.
Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders--updated European recommendations.
Dequeker E, Stuhrmann M, Morris MA, Casals T, Castellani C, Claustres M, Cuppens H, des Georges M, Ferec C, Macek M, Pignatti PF, Scheffer H, Schwartz M, Witt M, Schwarz M, Girodon E. Dequeker E, et al. Among authors: witt m. Eur J Hum Genet. 2009 Jan;17(1):51-65. doi: 10.1038/ejhg.2008.136. Epub 2008 Aug 6. Eur J Hum Genet. 2009. PMID: 18685558 Free PMC article.
Recent advances in primary ciliary dyskinesia genetics.
Kurkowiak M, Ziętkiewicz E, Witt M. Kurkowiak M, et al. Among authors: witt m. J Med Genet. 2015 Jan;52(1):1-9. doi: 10.1136/jmedgenet-2014-102755. Epub 2014 Oct 28. J Med Genet. 2015. PMID: 25351953 Free PMC article. Review.
Access to medicines for rare diseases: beating the drum for primary ciliary dyskinesia.
Crowley S, Azevedo I, Boon M, Bush A, Eber E, Haarman E, Karadag B, Kötz K, Leigh M, Moreno-Galdó A, Mussaffi H, Nielsen KG, Omran H, Papon JF, Pohunek P, Priftis K, Rindlisbacher B, Santamaria F, Valiulis A, Witt M, Yiallouros P, Zivkovic Z, Kuehni CE, Lucas JS. Crowley S, et al. Among authors: witt m. ERJ Open Res. 2020 Sep 14;6(3):00377-2020. doi: 10.1183/23120541.00377-2020. eCollection 2020 Jul. ERJ Open Res. 2020. PMID: 32964005 Free PMC article.
64 results