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

Year Number of Results
1993 2
1994 2
1995 1
1996 2
1997 1
1998 2
1999 2
2000 2
2001 2
2002 6
2003 3
2004 7
2005 3
2006 6
2007 6
2008 6
2009 2
2010 3
2011 2
2012 10
2013 6
2014 8
2015 7
2016 8
2017 7
2018 11
2019 9
2020 9
2021 7
2022 4
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Search Results

133 results
Results by year
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Page 1
Congenital disorders of glycosylation: Still "hot" in 2020.
Ondruskova N, Cechova A, Hansikova H, Honzik T, Jaeken J. Ondruskova N, et al. Among authors: hansikova h. Biochim Biophys Acta Gen Subj. 2021 Jan;1865(1):129751. doi: 10.1016/j.bbagen.2020.129751. Epub 2020 Sep 28. Biochim Biophys Acta Gen Subj. 2021. PMID: 32991969 Review.
Mitophagy in Huntington's disease.
Šonský I, Vodička P, Vodičková Kepková K, Hansíková H. Šonský I, et al. Among authors: hansikova h. Neurochem Int. 2021 Oct;149:105147. doi: 10.1016/j.neuint.2021.105147. Epub 2021 Jul 28. Neurochem Int. 2021. PMID: 34329735 Free article. Review.
Biogenesis of eukaryotic cytochrome c oxidase.
Stiburek L, Hansikova H, Tesarova M, Cerna L, Zeman J. Stiburek L, et al. Among authors: hansikova h. Physiol Res. 2006;55 Suppl 2:S27-41. Physiol Res. 2006. PMID: 17298220 Free article. Review.
Oral D-galactose supplementation in PGM1-CDG.
Wong SY, Gadomski T, van Scherpenzeel M, Honzik T, Hansikova H, Holmefjord KSB, Mork M, Bowling F, Sykut-Cegielska J, Koch D, Hertecant J, Preston G, Jaeken J, Peeters N, Perez S, Nguyen DD, Crivelly K, Emmerzaal T, Gibson KM, Raymond K, Abu Bakar N, Foulquier F, Poschet G, Ackermann AM, He M, Lefeber DJ, Thiel C, Kozicz T, Morava E. Wong SY, et al. Among authors: hansikova h. Genet Med. 2017 Nov;19(11):1226-1235. doi: 10.1038/gim.2017.41. Epub 2017 Jun 15. Genet Med. 2017. PMID: 28617415 Free PMC article. Clinical Trial.
Sideroblastic anemia associated with multisystem mitochondrial disorders.
Tesarova M, Vondrackova A, Stufkova H, Veprekova L, Stranecky V, Berankova K, Hansikova H, Magner M, Galoova N, Honzik T, Vodickova E, Stary J, Zeman J. Tesarova M, et al. Among authors: hansikova h. Pediatr Blood Cancer. 2019 Apr;66(4):e27591. doi: 10.1002/pbc.27591. Epub 2018 Dec 26. Pediatr Blood Cancer. 2019. PMID: 30588737
Fatal neonatal nephrocutaneous syndrome in 18 Roma children with EGFR deficiency.
Mazurova S, Tesarova M, Zeman J, Stranecky V, Hansikova H, Baxova A, Giertlova M, Lastuvkova J, Chovanova V, Rusnakova S, Knapkova M, Minarik G, Honzik T, Magner M. Mazurova S, et al. Among authors: hansikova h. J Dermatol. 2020 Jun;47(6):663-668. doi: 10.1111/1346-8138.15317. Epub 2020 Apr 6. J Dermatol. 2020. PMID: 32250467
Genetic defects of cytochrome c oxidase assembly.
Pecina P, Houstková H, Hansíková H, Zeman J, Houstek J. Pecina P, et al. Among authors: hansikova h. Physiol Res. 2004;53 Suppl 1:S213-23. Physiol Res. 2004. PMID: 15119951 Free article. Review.
133 results