Szperl M - Search Results

1

Impact of genetic and clinical factors on dose requirements and quality of anticoagulation therapy in Polish patients receiving acenocoumarol: dosing calculation algorithm.

Wolkanin-Bartnik J, Pogorzelska H, Szperl M, Bartnik A, Koziarek J, Bilinska ZT. Wolkanin-Bartnik J, et al. Among authors: szperl m. Pharmacogenet Genomics. 2013 Nov;23(11):611-8. doi: 10.1097/FPC.0000000000000004. Pharmacogenet Genomics. 2013. PMID: 24108193

2

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: szperl m. Mol Diagn Ther. 2012 Apr 1;16(2):99-107. doi: 10.1007/BF03256434. Mol Diagn Ther. 2012. PMID: 22413764

3

Polymorphisms of the beta-1 and beta-2 adrenergic receptors in Polish patients with idiopathic dilated cardiomyopathy.

Paczkowska A, Szperl M, Małek Ł, Mazurkiewicz Ł, Skóra E, Grzybowski J, Roszczynko M, Bilińska Z, Tesson F, Ruzyłło W. Paczkowska A, et al. Among authors: szperl m. Kardiol Pol. 2009 Mar;67(3):235-41. Kardiol Pol. 2009. PMID: 19378229

4

Titin Truncating Variants in Dilated Cardiomyopathy - Prevalence and Genotype-Phenotype Correlations.

Franaszczyk M, Chmielewski P, Truszkowska G, Stawinski P, Michalak E, Rydzanicz M, Sobieszczanska-Malek M, Pollak A, Szczygieł J, Kosinska J, Parulski A, Stoklosa T, Tarnowska A, Machnicki MM, Foss-Nieradko B, Szperl M, Sioma A, Kusmierczyk M, Grzybowski J, Zielinski T, Ploski R, Bilinska ZT. Franaszczyk M, et al. Among authors: szperl m. PLoS One. 2017 Jan 3;12(1):e0169007. doi: 10.1371/journal.pone.0169007. eCollection 2017. PLoS One. 2017. PMID: 28045975 Free PMC article.

5

Next-generation sequencing for diagnosis of thoracic aortic aneurysms and dissections: diagnostic yield, novel mutations and genotype phenotype correlations.

Poninska JK, Bilinska ZT, Franaszczyk M, Michalak E, Rydzanicz M, Szpakowski E, Pollak A, Milanowska B, Truszkowska G, Chmielewski P, Sioma A, Janaszek-Sitkowska H, Klisiewicz A, Michalowska I, Makowiecka-Ciesla M, Kolsut P, Stawinski P, Foss-Nieradko B, Szperl M, Grzybowski J, Hoffman P, Januszewicz A, Kusmierczyk M, Ploski R. Poninska JK, et al. Among authors: szperl m. J Transl Med. 2016 May 4;14(1):115. doi: 10.1186/s12967-016-0870-4. J Transl Med. 2016. PMID: 27146836 Free PMC article.

6

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: szperl m. 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

7

Genetic variants in hypertensive patients with coronary artery disease and coexisting atheromatous renal artery stenosis.

Szperl M, Dzielinska Z, Roszczynko M, Malek LA, Makowiecka-Ciesla M, Demkow M, Kadziela J, Prejbisz A, Florczak E, Zielinski T, Januszewicz A, Ruzyllo W. Szperl M, et al. Med Sci Monit. 2008 Dec;14(12):CR611-6. Med Sci Monit. 2008. PMID: 19043368

8

Influence of renin-angiotensin system gene polymorphisms on the risk of ST-segment-elevation myocardial infarction and association with coronary artery disease risk factors.

Konopka A, Szperl M, Piotrowski W, Roszczynko M, Stępińska J. Konopka A, et al. Among authors: szperl m. Mol Diagn Ther. 2011 Jun 1;15(3):167-76. doi: 10.1007/BF03256407. Mol Diagn Ther. 2011. PMID: 21657802

9

Usefulness of Somatostatin Receptor Scintigraphy (Tc-[HYNIC, Tyr3]-Octreotide) and 123I-Metaiodobenzylguanidine Scintigraphy in Patients with SDHx Gene-Related Pheochromocytomas and Paragangliomas Detected by Computed Tomography.

Michałowska I, Ćwikła JB, Pęczkowska M, Furmanek MI, Buscombe JR, Michalski W, Prejbisz A, Szperl M, Malinoc A, Moczulski D, Szutkowski Z, Kawecki A, Antoniewicz J, Pęczkowski P, Lewczuk A, Otto M, Cichocki A, Bednarek-Tupikowska G, Kabat M, Janaszek-Sitkowska H, Przybyłowska K, Janas J, Neumann HP, Januszewicz A. Michałowska I, et al. Among authors: szperl m. Neuroendocrinology. 2015;101(4):321-30. doi: 10.1159/000381458. Epub 2015 Mar 13. Neuroendocrinology. 2015. PMID: 25791839

10

The C677T mutation in methylenetetrahydrofolate reductase gene, plasma homocysteine concentration and the risk of coronary artery disease.

Kadziela J, Janas J, Dzielińska Z, Szperl M, Gaździk D, Chotkowska E, Piotrowski W, Ruzyłło W. Kadziela J, et al. Among authors: szperl m. Kardiol Pol. 2003 Jul;59(7):17-26; discussion 26. Kardiol Pol. 2003. PMID: 14560345

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