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

Year Number of Results
2014 1
2015 1
2016 1
2017 2
2018 2
2019 2
2020 6
2021 6
2022 0
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20 results
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Page 1
Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management.
Simurda T, Asselta R, Zolkova J, Brunclikova M, Dobrotova M, Kolkova Z, Loderer D, Skornova I, Hudecek J, Lasabova Z, Stasko J, Kubisz P. Simurda T, et al. Among authors: loderer d. Diagnostics (Basel). 2021 Nov 19;11(11):2140. doi: 10.3390/diagnostics11112140. Diagnostics (Basel). 2021. PMID: 34829490 Free PMC article. Review.
Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype.
Simurda T, Brunclikova M, Asselta R, Caccia S, Zolkova J, Kolkova Z, Loderer D, Skornova I, Hudecek J, Lasabova Z, Stasko J, Kubisz P. Simurda T, et al. Among authors: loderer d. Int J Mol Sci. 2020 Jun 29;21(13):4616. doi: 10.3390/ijms21134616. Int J Mol Sci. 2020. PMID: 32610551 Free PMC article. Review.
Establishment of PANDA - a new human pancreatic ductal adenocarcinoma cell line with 3D cell culture technology.
Zahumenska R, Kalman M, Marcinek J, Mersakova S, Kertys M, Pindura M, Palkoci B, Kycina R, Vojtko M, Chromec T, Dumortier HM, Skovierova H, Novakova S, Mitruskova B, Kapralik I, Loderer D, Grendar M, Brany D, Mokry J, Bouvet M, Valasek MA, Janik J, Plank L, Laca L, Halasova E, Strnadel J. Zahumenska R, et al. Among authors: loderer d. Neoplasma. 2021 Nov 25:210924N1360. doi: 10.4149/neo_2021_210924N1360. Online ahead of print. Neoplasma. 2021. PMID: 34818028
20 results