Płoski R - Search Results

1

A combination of quinidine/mexiletine reduces arrhythmia in dilated cardiomyopathy in two patients with R814W SCN5A mutation.

Zakrzewska-Koperska J, Bilińska ZT, Truszkowska GT, Franaszczyk M, Elikowski W, Warmiński G, Kalin K, Urbanek P, Bodalski R, Orczykowski M, Szumowski Ł, Płoski R, Bilińska M. Zakrzewska-Koperska J, et al. Among authors: ploski r. ESC Heart Fail. 2020 Dec;7(6):4326-4335. doi: 10.1002/ehf2.12993. Epub 2020 Oct 20. ESC Heart Fail. 2020. PMID: 33084224 Free PMC article.

2

Dilated cardiomyopathy with profound segmental wall motion abnormalities and ventricular arrhythmia caused by the R541C mutation in the LMNA gene.

Saj M, Jankowska A, Lewandowski M, Szwed H, Szperl M, Płoski R, Bilińska ZT. Saj M, et al. Among authors: ploski r. Int J Cardiol. 2010 Oct 29;144(3):e51-3. doi: 10.1016/j.ijcard.2008.12.083. Epub 2009 Jan 22. Int J Cardiol. 2010. PMID: 19167105

3

Angiotensin-converting enzyme polymorphism and completed suicide: an association in Caucasians and evidence for a link with a method of self-injury.

Fudalej S, Fudalej M, Kostrzewa G, Kuźniar P, Franaszczyk M, Wojnar M, Krajewski P, Płoski R. Fudalej S, et al. Among authors: ploski r. Neuropsychobiology. 2009;59(3):151-8. doi: 10.1159/000218077. Epub 2009 May 12. Neuropsychobiology. 2009. PMID: 19439995

4

Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption.

Gupta P, Bilinska ZT, Sylvius N, Boudreau E, Veinot JP, Labib S, Bolongo PM, Hamza A, Jackson T, Ploski R, Walski M, Grzybowski J, Walczak E, Religa G, Fidzianska A, Tesson F. Gupta P, et al. Among authors: ploski r. Basic Res Cardiol. 2010 May;105(3):365-77. doi: 10.1007/s00395-010-0085-4. Epub 2010 Feb 3. Basic Res Cardiol. 2010. PMID: 20127487 Free PMC article.

5

Dilated cardiomyopathy in the postgenomic era.

Płoski R, Bilińska ZT. Płoski R, et al. Kardiol Pol. 2009 Nov;67(11):1248-9. Kardiol Pol. 2009. PMID: 20143516 No abstract available.

6

A new c.1621 C > G, p.R541G lamin A/C mutation in a family with DCM and regional wall motion abnormalities (akinesis/dyskinesis): genotype-phenotype correlation.

Małek LA, Labib S, Mazurkiewicz L, Saj M, Płoski R, Tesson F, Bilińska ZT. Małek LA, et al. Among authors: ploski r. J Hum Genet. 2011 Jan;56(1):83-6. doi: 10.1038/jhg.2010.137. Epub 2010 Nov 18. J Hum Genet. 2011. PMID: 21085127

7

Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts.

Płoski R, Brand OJ, Jurecka-Lubieniecka B, Franaszczyk M, Kula D, Krajewski P, Karamat MA, Simmonds MJ, Franklyn JA, Gough SC, Jarząb B, Bednarczuk T. Płoski R, et al. PLoS One. 2010 Nov 25;5(11):e15512. doi: 10.1371/journal.pone.0015512. PLoS One. 2010. PMID: 21124799 Free PMC article.

8

Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population.

Kiliszek M, Franaszczyk M, Kozluk E, Lodzinski P, Piatkowska A, Broda G, Ploski R, Opolski G. Kiliszek M, et al. Among authors: ploski r. PLoS One. 2011;6(7):e21790. doi: 10.1371/journal.pone.0021790. Epub 2011 Jul 8. PLoS One. 2011. PMID: 21760908 Free PMC article.

9

[Familial thoracic aortic aneurysms and dissections (FTAAD)].

Milanowska B, Michalak E, Janaszek-Sitkowska H, Franaszczyk M, Płoski R, Bilińska ZT. Milanowska B, et al. Among authors: ploski r. Kardiol Pol. 2011;69(12):1291-7. Kardiol Pol. 2011. PMID: 22219111 Review. Polish. No abstract available.

10

Variants of the lamin A/C (LMNA) gene in non-valvular atrial fibrillation patients: a possible pathogenic role of the Thr528Met mutation.

Saj M, Dabrowski R, Labib S, Jankowska A, Szperl M, Broda G, Szwed H, Tesson F, Bilinska ZT, Ploski R. Saj M, et al. Among authors: ploski r. Mol Diagn Ther. 2012 Apr 1;16(2):99-107. doi: 10.1007/BF03256434. Mol Diagn Ther. 2012. PMID: 22413764

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