Publications by authors named "Malgorzata Szperl"

Claim this Profile
P
Pathogenic variants in plakophilin-2 gene (PKP2) are associated with better survival in arrhythmogenic right ventricular cardiomyopathy.
Elżbieta K Biernacka, Karolina Borowiec, Maria Franaszczyk, Małgorzata Szperl, Alessandra Rampazzo

J Appl Genet· December 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification novel LQT syndrome-associated variants in Polish population and genotype-phenotype correlations in eight families.
Małgorzata Szperl, Urszula Kozicka, Agnieszka Kosiec, Piotr Kukla, Marta Roszczynko

J Appl Genet· November 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Andersen-Tawil syndrome: Clinical presentation and predictors of symptomatic arrhythmias - Possible role of polymorphisms K897T in KCNH2 and H558R in SCN5A gene.
Michalina Krych, Elżbieta Katarzyna Biernacka, Joanna Ponińska, Piotr Kukla, Artur Filipecki, Małgorzata Szperl

J Cardiol· November 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Titin Truncating Variants in Dilated Cardiomyopathy - Prevalence and Genotype-Phenotype Correlations.
Maria Franaszczyk, Przemyslaw Chmielewski, Grazyna Truszkowska, Piotr Stawinski, Ewa Michalak, Malgorzata Szperl

PLoS One· August 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
GROWTH RATE OF PARAGANGLIOMAS RELATED TO GERMLINE MUTATIONS OF THE SDHX GENES.
Ilona Michałowska, Jarosław B Ćwikła, Wojciech Michalski, Lucjan S Wyrwicz, Aleksander Prejbisz, Małgorzata Szperl

Endocr Pract· March 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel life-threatening mutation in long QT2 syndrome.
Elżbieta Biernacka, Małgorzata Szperl, Agnieszka Kosiec, Marta Roszczynko, Piotr Hoffman

Kardiol Pol· February 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
Q
QTc prolongation in patients with hearing loss: Electrocardiographic and genetic study.
Agnieszka Sanecka, Elżbieta Katarzyna Biernacka, Małgorzata Szperl, Magdalena Sosna, Małgorzata Mueller-Malesińska

Cardiol J· December 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Evaluation of Head and Neck Paragangliomas by Computed Tomography in Patients with Pheochromocytoma-Paraganglioma Syndromes.
Ilona Michałowska, Anna Lewczuk, Jarosław Ćwikła, Aleksander Prejbisz, Urszula Swoboda-Rydz, Małgorzata Szperl

Pol J Radiol· October 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mediastinal paragangliomas related to gene mutations.
Ilona Michałowska, Jarosław Ćwikła, Aleksander Prejbisz, Paweł Kwiatek, Małgorzata Szperl

Kardiochir Torakochirurgia Pol· September 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Combination Testing Using a Single MSH5 Variant alongside HLA Haplotypes Improves the Sensitivity of Predicting Coeliac Disease Risk in the Polish Population.
Agnieszka Paziewska, Bozena Cukrowska, Michalina Dabrowska, Krzysztof Goryca, Magdalena Piatkowska, Malgorzata Szperl

PLoS One· June 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
U
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.
Ilona Michałowska, Jarosław B Ćwikła, Mariola Pęczkowska, Mariusz I Furmanek, John R Buscombe, Małgorzata Szperl

Neuroendocrinology· April 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Coexistence of Andersen-Tawil Syndrome with Polymorphisms in hERG1 Gene (K897T) and SCN5A Gene (H558R) in One Family.
Michalina Jagodzińska, Małgorzata Szperl, Joanna Ponińska, Agnieszka Kosiec, Robert Gajda

Ann Noninvasive Electrocardiol· March 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Associations of the eNOS G894T gene polymorphism with target organ damage in children with newly diagnosed primary hypertension.
Joanna Śladowska-Kozłowska, Mieczysław Litwin, Anna Niemirska, Aldona Wierzbicka, Marta Roszczynko, Małgorzata Szperl

Pediatr Nephrol· December 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pheochromocytoma presenting as takotsubo-like cardiomyopathy following delivery.
Katarzyna Jóźwik-Plebanek, Mariola Pęczkowska, Anna Klisiewicz, Kazimierz Wrzesiński, Aleksander Prejbisz, Małgorzata Szperl

Endocr Pract· December 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study.
Frederic Castinetti, Xiao-Ping Qi, Martin K Walz, Ana Luiza Maia, Gabriela Sansó, Malgorzata Szperl

Lancet Oncol· May 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Impact of genetic and clinical factors on dose requirements and quality of anticoagulation therapy in Polish patients receiving acenocoumarol: dosing calculation algorithm.
Jolanta Wolkanin-Bartnik, Hanna Pogorzelska, Małgorzata Szperl, Aleksandra Bartnik, Jacek Koziarek

Pharmacogenet Genomics· November 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Myocardial iron homeostasis in advanced chronic heart failure patients.
Przemysław Leszek, Barbara Sochanowicz, Małgorzata Szperl, Piotr Kolsut, Kamil Brzóska

Int J Cardiol· August 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Polymorphisms of angiotensin II type 1 receptor gene and those of angiotensinogen point at culprit artery in ST-segment elevation myocardial infarction.
Anna Konopka, Małgorzata Szperl, Walerian Piotrowski, Janina Stępińska

Gene· May 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Combined renin-angiotensin system gene polymorphisms and outcomes in coronary artery disease - a preliminary report.
Zofia Dzielińska, Lukasz A Małek, Marta Roszczynko, Małgorzata Szperl, Marcin Demkow

Kardiol Pol· April 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
V
Variants of the lamin A/C (LMNA) gene in non-valvular atrial fibrillation patients: a possible pathogenic role of the Thr528Met mutation.
Michal Saj, Rafal Dabrowski, Sarah Labib, Agnieszka Jankowska, Malgorzata Szperl

Mol Diagn Ther· April 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Is evaluation of complex polymorphism helpful in the assessment of prognosis after percutaneous coronary intervention. A prospective study.
Tomasz M Rywik, Małgorzata Szperl, Rafał Płoski, Przemysław Leszek, Marta Roszczynko

Kardiol Pol· January 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Expression of cellular retinoic acid-binding protein I and II (CRABP I and II) in embryonic mouse hearts treated with retinoic acid.
Emilia Stachurska, Agnieszka Loboda, Justyna Niderla-Bielińska, Małgorzata Szperl, Michał Juszyński

Acta Biochim Pol· July 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Influence of renin-angiotensin system gene polymorphisms on the risk of ST-segment-elevation myocardial infarction and association with coronary artery disease risk factors.
Anna Konopka, Małgorzata Szperl, Walerian Piotrowski, Marta Roszczynko, Janina Stępińska

Mol Diagn Ther· June 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Dilated cardiomyopathy with profound segmental wall motion abnormalities and ventricular arrhythmia caused by the R541C mutation in the LMNA gene.
Michał Saj, Agnieszka Jankowska, Michał Lewandowski, Hanna Szwed, Małgorzata Szperl

Int J Cardiol· October 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Polymorphisms of the beta-1 and beta-2 adrenergic receptors in Polish patients with idiopathic dilated cardiomyopathy.
Aleksandra Paczkowska, Małgorzata Szperl, Łukasz Małek, Łukasz Mazurkiewicz, Ewa Skóra

Kardiol Pol· March 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis