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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2011 | 2 |
2012 | 1 |
2013 | 1 |
2014 | 2 |
2017 | 1 |
2023 | 0 |
Search Results
7 results
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Page 1
Coexistence of Gilbert syndrome with hereditary haemolytic anaemias.
J Clin Pathol. 2012 Jul;65(7):663-5. doi: 10.1136/jclinpath-2011-200580. Epub 2012 May 3.
J Clin Pathol. 2012.
PMID: 22554963
Two novel C-terminal frameshift mutations in the β-globin gene lead to rapid mRNA decay.
Rawa K, Szczesny RJ, Owczarek EP, Adamowicz-Salach A, Klukowska A, Demkow U, Plochocka D, Szczesny P, Gora M, Dziembowski A, Burzynska B.
Rawa K, et al.
BMC Med Genet. 2017 Jun 8;18(1):65. doi: 10.1186/s12881-017-0428-1.
BMC Med Genet. 2017.
PMID: 28595636
Free PMC article.
Item in Clipboard
Different statins produce highly divergent changes in gene expression profiles of human hepatoma cells: a pilot study.
Leszczynska A, Gora M, Plochocka D, Hoser G, Szkopinska A, Koblowska M, Iwanicka-Nowicka R, Kotlinski M, Rawa K, Kiliszek M, Burzynska B.
Leszczynska A, et al. Among authors: rawa k.
Acta Biochim Pol. 2011;58(4):635-9. Epub 2011 Nov 30.
Acta Biochim Pol. 2011.
PMID: 22132374
Free article.
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Cloning and functional analysis of the dpm2 and dpm3 genes from Trichoderma reesei expressed in a Saccharomyces cerevisiae dpm1Δ mutant strain.
Zembek P, Perlińska-Lenart U, Rawa K, Górka-Nieć W, Palamarczyk G, Kruszewska JS.
Zembek P, et al. Among authors: rawa k.
Biol Chem. 2011 Apr;392(6):517-27. doi: 10.1515/BC.2011.058. Epub 2011 Apr 27.
Biol Chem. 2011.
PMID: 21521073
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Feto-maternal haemorrhage assessment in a woman with a large population of red blood cells containing fetal haemoglobin.
Gielezynska A, Stachurska A, Fabijańska-Mitek J, Debska M, Burzyńska B, Rawa K, Pawlik K.
Gielezynska A, et al. Among authors: rawa k.
Ginekol Pol. 2014 Aug;85(8):614-8. doi: 10.17772/gp/1781.
Ginekol Pol. 2014.
PMID: 25219143
Free article.
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Characterization of a novel mutation in the NADH-cytochrome b5 reductase gene responsible for rare hereditary methaemoglobinaemia type I.
Rawa K, Chelmecka-Hanusiewicz L, Plochocka D, Pawinska-Wasikowska K, Balwierz W, Burzynska B.
Rawa K, et al.
Acta Haematol. 2013;130(2):122-5. doi: 10.1159/000347041. Epub 2013 Apr 13.
Acta Haematol. 2013.
PMID: 23594618
No abstract available.
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The first reported case of G6PD deficiency due to Seoul mutation in Poland.
Kaczorowska-Hac B, Burzynska B, Plochocka D, Zak-Jasinska K, Rawa K, Adamkiewicz-Drozynska E.
Kaczorowska-Hac B, et al. Among authors: rawa k.
Ann Hematol. 2014 May;93(5):879-80. doi: 10.1007/s00277-013-1899-6.
Ann Hematol. 2014.
PMID: 24022758
Free PMC article.
No abstract available.
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