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

Year Number of Results
2002 1
2004 1
2005 1
2006 2
2007 3
2009 1
2010 4
2011 4
2012 5
2013 3
2014 1
2015 1
2016 4
2017 1
2018 1
2019 2
2020 3
2021 2
2022 3
2023 1
2024 0

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41 results

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Page 1
Types of congenital nonsyndromic ichthyoses.
Pinkova B, Buckova H, Borska R, Fajkusova L. Pinkova B, et al. Among authors: fajkusova l. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2020 Dec;164(4):357-365. doi: 10.5507/bp.2020.050. Epub 2020 Oct 21. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2020. PMID: 33087941 Free article. Review.
Malignant hyperthermia in Czechia and Slovakia.
Klincová M, Štěpánková D, Schröderová I, Klabusayová E, Ošťádalová E, Valášková I, Fajkusová L, Zídková J, Gaillyová R, Štourač P. Klincová M, et al. Among authors: fajkusova l. Br J Anaesth. 2022 Aug;129(2):e41-e43. doi: 10.1016/j.bja.2022.04.029. Epub 2022 Jun 17. Br J Anaesth. 2022. PMID: 35718563 Free article. No abstract available.
Genetic findings in Czech patients with limb girdle muscular dystrophy.
Zídková J, Kramářová T, Kopčilová J, Réblová K, Haberlová J, Mazanec R, Voháňka S, Gřegořová A, Langová M, Honzík T, Šoukalová J, Ošlejšková H, Solařová P, Vyhnálková E, Fajkusová L. Zídková J, et al. Among authors: fajkusova l. Clin Genet. 2023 Nov;104(5):542-553. doi: 10.1111/cge.14407. Epub 2023 Aug 1. Clin Genet. 2023. PMID: 37526466
CAPN3 c.1746-20C>G variant is hypomorphic for LGMD R1 calpain 3-related.
Mroczek M, Inashkina I, Stavusis J, Zayakin P, Khrunin A, Micule I, Kenina V, Zdanovica A, Zídková J, Fajkusová L, Limborska S, van der Kooi AJ, Brusse E, Leonardis L, Maver A, Pajusalu S, Õunap K, Puusepp S, Dobosz P, Sypniewski M, Burnyte B, Lace B. Mroczek M, et al. Among authors: fajkusova l. Hum Mutat. 2022 Oct;43(10):1347-1353. doi: 10.1002/humu.24421. Epub 2022 Jun 22. Hum Mutat. 2022. PMID: 35731190
Next-generation sequencing in children with epilepsy: The importance of precise genotype-phenotype correlation.
Horák O, Burešová M, Kolář S, Španělová K, Jeřábková B, Gaillyová R, Česká K, Réblová K, Šoukalová J, Zídková J, Fajkusová L, Ošlejšková H, Rektor I, Danhofer P. Horák O, et al. Among authors: fajkusova l. Epilepsy Behav. 2022 Mar;128:108564. doi: 10.1016/j.yebeh.2022.108564. Epub 2022 Jan 19. Epilepsy Behav. 2022. PMID: 35065395
Inherited ichthyoses: molecular causes of the disease in Czech patients.
Borská R, Pinková B, Réblová K, Bučková H, Kopečková L, Němečková J, Puchmajerová A, Malíková M, Hermanová M, Fajkusová L. Borská R, et al. Among authors: fajkusova l. Orphanet J Rare Dis. 2019 May 2;14(1):92. doi: 10.1186/s13023-019-1076-7. Orphanet J Rare Dis. 2019. PMID: 31046801 Free PMC article.
Bending of DNA duplexes with mutation motifs.
Růžička M, Souček P, Kulhánek P, Radová L, Fajkusová L, Réblová K. Růžička M, et al. Among authors: fajkusova l. DNA Res. 2019 Aug 1;26(4):341-352. doi: 10.1093/dnares/dsz013. DNA Res. 2019. PMID: 31230075 Free PMC article.
Cardio-ankle vascular index in heterozygous familial hypercholesterolemia.
Soska V, Dobsak P, Dusek L, Shirai K, Jarkovsky J, Novakova M, Brhel P, Stastna J, Fajkusova L, Freiberger T, Yambe T. Soska V, et al. Among authors: fajkusova l. J Atheroscler Thromb. 2012;19(5):453-61. doi: 10.5551/jat.9639. Epub 2012 Jan 12. J Atheroscler Thromb. 2012. PMID: 22659529 Free article.
41 results