Search Results - "MARKIEWICZ‐ŁOSKOT, GRAŻYNA"

Diagnostic Value of the TpTe Interval in Children with Ventricular Arrhythmias by Jaromin, Joanna, Markiewicz-Łoskot, Grażyna, Szydłowski, Lesław, Kulawik, Agnieszka

“…The changes in the period of ventricular repolarization, i.e., QT interval, QTp (Q-Tpeak) and TpTe interval (Tpeak-Tend), make it possible to assess the…”
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The Differences in the Diagnostic Profile in Children with Vasovagal Syncope between the Result of Head-Up Tilt Table Test by Kolarczyk, Ewelina, Szydłowski, Lesław, Skierska, Agnieszka, Markiewicz-Łoskot, Grażyna

“…(1) Background: The features characterizing vasovagal syncope (VVS) are an important factor in the correct evaluation of diagnostic risk stratification in…”
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The Repolarization Period during the Head-Up Tilt Test in Children with Vasovagal Syncope by Kolarczyk, Ewelina, Markiewicz-Łoskot, Grażyna, Szydłowski, Lesław

“…Electrocardiography (ECG) and the head-up tilt test (HUTT) are vital in clinical work-up in children with vasovagal syncope (VVS). Ventricular repolarization…”
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Prolongation of Electrocardiographic T Wave Parameters Recorded during the Head-Up Tilt Table Test as Independent Markers of Syncope Severity in Children by Markiewicz-Łoskot, Grażyna, Kolarczyk, Ewelina, Mazurek, Bogusław, Łoskot, Marianna, Szydłowski, Lesław

“…The head-up tilt table test (HUTT) with the upright phase is used to help determine an imbalance of the sympathetic nervous system that is related to abnormal…”
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Genetic Heterogeneity of Left‐ventricular Noncompaction Cardiomyopathy by Moric‐Janiszewska, Ewa, Markiewicz‐Łoskot, Grazyna

“…Isolated noncompaction of the ventricular myocardium (INVM) sometimes referred to as spongy myocardium is a rare, congenital and also acquired cardiomyopathy…”
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Review on the genetics of arrhythmogenic right ventricular dysplasia by Moric-Janiszewska, Ewa, Markiewicz- oskot, Gra yna

“…Arrhythmogenic right ventricular dysplasia (ARVD) is a clinical and pathologic entity whose diagnosis rests on electrocardiographic and angiographic criteria;…”
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N‐terminal Prohormone Brain Natriuretic Peptide‐proBNP Levels in Ventricular Arrhythmias in Children by Mazurek, Bogusław, Szydłowski, Lesław, Giec‐Fuglewicz, Grażyna, Markiewicz‐Łoskot, Grażyna

“…Background Ventricular arrhythmias are the most common consequences of structural and functional heart diseases, but cases with no evident pathology are also…”
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COMPLIANCE WITH MEDICAL AND NURSING RECOMMENDATIONS IN A GROUP OF PATIENTS AFTER HEART TRANSPLANTATION by Natalia Wróblewska, Grażyna Markiewicz-Łoskot

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Costs of Healthcare for Children with Inflammatory Bowel Diseases (IBD) in Poland by Markiewicz-Łoskot, Grażyna, Chlebowczyk, Wojciech, Holecki, Tomasz

“…The last two decades have seen an increase in the incidence of inflammatory bowel disease (IBD) in many regions of the world, which has had a significant…”
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The Risk of Cardiac Events and Genotype-Based Management of LQTS Patients by Markiewicz-Łoskot, Grażyna, Moric-Janiszewska, Ewa, Mazurek, Urszula

“…This review discusses the risk of cardiac events and genotype‐based management of LQTS. We describe here the genetic background of long QT syndrome and the…”
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Tpeak-Tend Interval during Pregnancy and Postpartum by Kandzia, Tomasz, Markiewicz-Łoskot, Grażyna, Binkiewicz, Przemysław

“…Pregnancy is a condition in which new cardiac arrhythmias can occur or prior undiagnosed arrhythmias may provide symptoms. The occurrence of severe ventricular…”
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Selected aspects of early postoperative care after coronary artery bypass grafting in an advanced nursing practice perspective by Wróblewska, Natalia, Markiewicz-Łoskot, Grażyna

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Age-and sex-dependent mRNA expression of KCNQ1 and HERG in patients with long QT syndrome type 1 and 2 by Moric-Janiszewska, Ewa, Glogowska-Ligus, Joanna, Paul-Samojedny, Monika, Weglarz, Ludmila, Markiewicz-Loskot, Grazyna, Szydlowski, Leslaw

“…The main goal of this study was to examine the patient age and sex dependent expression of KCNQ1 and HERG genes that encode potassium channels responsible for…”
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Isolated ventricular non-compaction: clinical study and genetic review by Markiewicz-Loskot, Grazyna, Moric-Janiszewska, Ewa, Loskot, Maria, Szydlowski, Leslaw, Weglarz, Ludmila, Hollek, Andrzej

“…Isolated non-compaction of the ventricular myocardium (INVM), sometimes referred to as 'spongy myocardium', is a congenital and exceedingly rare…”
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Challenges of Diagnosis of Long‐QT Syndrome in Children by MORIC‐JANISZEWSKA, EWA, MARKIEWICZ‐ŁOSKOT, GRAŻYNA, ŁOSKOT, MARIA, WĘGLARZ, LUDMIŁA, HOLLEK, ANDRZEJ, SZYDŁOWSKI, LESŁAW

“…We describe the clinical and genetic characteristics of the family, in which the diagnosis of LQT1 had been made. The electrocardiogram (ECG) characteristics…”
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Electrocardiographic Abnormalities in Young Athletes with Mitral Valve Prolapse by Markiewicz‐Łoskot, Grażyna, Łoskot, Maria, Moric‐Janiszewska, Ewa, Dukalska, Maria, Mazurek, BogusŁaw, Kohut, Joanna, SzydŁowski, LesŁaw

“…Background Mitral valve prolapse (MVP) is the most common primary valvular abnormality in a young population. In some individuals, MVP is silent or associated…”
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Electrocardiographic T-wave parameters in families with long QT syndrome by Markiewicz-Łoskot, Grażyna, Moric-Janiszewska, Ewa, Mazurek, Bogusław, Łoskot, Marianna, Bartusek, Mariola, Skierska, Agnieszka, Szydłowski, Lesław

“…T-wave parameters, especially the Tpeak-Tend interval (TpTe), reflect the total dispersion of repolarization, whose amplification may lead to the development…”
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Arrhythmogenic Right Ventricular Dysplasia:Clinical Study by Markiewicz‐Łoskot, Grażyna, Moric‐Janiszewska, Ewa, Łoskot, Maria, Szydłowski, Lesław, Hollek, Andrzej, Wȩglarz, Ludmiła

“…Arrhythmogenic right ventricular dysplasia (ARVD) is a complex arrhythmogenic cardiomyopathy, characterized by a partial or total replacement of the right…”
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The letter of Finsterer and Stollberger was shown to the authors who replied by Markiewicz- oskot, Gra yna, Moric-Janiszewska, Ewa, oskot, Maria, Szyd owski, Les aw, W glarz, Ludmi a, Hollek, Andrzej

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Expression of genes KCNQ1 and HERG encoding potassium ion channels Ikr, Iks in long QT syndrome by Moric-Janiszewska, Ewa, Głogowska-Ligus, Joanna, Paul-Samojedny, Monika, Smolik, Sławomir, Woźniak, Michał, Markiewicz-Łoskot, Grażyna, Mazurek, Urszula, Węglarz, Ludmiła, Szydłowski, Lesław

“…The KCNQ1 and HERG genes mutations are responsible for specific types of congenital long QT syndrome (LQT). To examine the expression of KCNQ1 and HERG genes…”
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