Płoski R - Search Results

1

A Novel DSP Truncating Variant in a Family with Episodic Myocardial Injury in the Course of Arrhythmogenic Cardiomyopathy-A Possible Role of a Low Penetrance NLRP3 Variant.

Chmielewski P, Truszkowska GT, Kukla P, Zakrzewska-Koperska J, Śpiewak M, Stępień-Wojno M, Bilińska M, Lutyńska A, Płoski R, Bilińska ZT. Chmielewski P, et al. Among authors: ploski r. Diagnostics (Basel). 2020 Nov 16;10(11):955. doi: 10.3390/diagnostics10110955. Diagnostics (Basel). 2020. PMID: 33207704 Free PMC article.

2

Coexisting polymorphisms of P2Y12 and CYP2C19 genes as a risk factor for persistent platelet activation with clopidogrel.

Malek LA, Kisiel B, Spiewak M, Grabowski M, Filipiak KJ, Kostrzewa G, Huczek Z, Ploski R, Opolski G. Malek LA, et al. Among authors: ploski r. Circ J. 2008 Jul;72(7):1165-9. doi: 10.1253/circj.72.1165. Circ J. 2008. PMID: 18577829 Free article.

3

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

4

Influence of C3435T multidrug resistance gene-1 (MDR-1) polymorphism on platelet reactivity and prognosis in patients with acute coronary syndromes.

Spiewak M, Małek ŁA, Kostrzewa G, Kisiel B, Serafin A, Filipiak KJ, Płoski R, Opolski G. Spiewak M, et al. Among authors: ploski r. Kardiol Pol. 2009 Aug;67(8):827-34. Kardiol Pol. 2009. PMID: 19784880

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

Cytochrome P450 2C19 polymorphism, suboptimal reperfusion and all-cause mortality in patients with acute myocardial infarction.

Małek LA, Przyłuski J, Spiewak M, Kłopotowski M, Kostrzewa G, Kruk M, Płoski R, Witkowski A, Rużyłło W. Małek LA, et al. Among authors: ploski r. Cardiology. 2010;117(2):81-7. doi: 10.1159/000320093. Epub 2010 Oct 6. Cardiology. 2010. PMID: 20924183

7

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

8

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

9

LMNA mutations in Polish patients with dilated cardiomyopathy: prevalence, clinical characteristics, and in vitro studies.

Saj M, Bilinska ZT, Tarnowska A, Sioma A, Bolongo P, Sobieszczanska-Malek M, Michalak E, Golen D, Mazurkiewicz L, Malek L, Walczak E, Fidzianska A, Grzybowski J, Przybylski A, Zielinski T, Korewicki J, Tesson F, Ploski R. Saj M, et al. Among authors: ploski r. BMC Med Genet. 2013 May 23;14:55. doi: 10.1186/1471-2350-14-55. BMC Med Genet. 2013. PMID: 23702046 Free PMC article.

10

Does p.Q247X in TRIM63 cause human hypertrophic cardiomyopathy?

Ploski R, Pollak A, Müller S, Franaszczyk M, Michalak E, Kosinska J, Stawinski P, Spiewak M, Seggewiss H, Bilinska ZT. Ploski R, et al. Circ Res. 2014 Jan 17;114(2):e2-5. doi: 10.1161/CIRCRESAHA.114.302662. Circ Res. 2014. PMID: 24436435

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