Publications by authors named "Krebsova Alice"

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Current management of transition and multidisciplinary care of patients with inherited and rare cardiomyopathies in Europe: results of the European Reference Network for rare and low prevalence complex diseases of the heart.
Emanuele Monda, Elena Biagini, Nico Blom, Fabrizio Drago, Ingrid Krapels, Alice Krebsová

Eur Heart J Qual Care Clin Outcomes· November 2025

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Characterizing Sustained Arrhythmias in Patients With Arrhythmic Mitral Valve Prolapse: Insights From the SAVE-MVP collaboration.
Avi Sabbag, Nina Ajmone-Marsan, Fatima Ezzeddine, Guido Ascione, Nicolò Azzola Guicciardi, Alice Krebsová

JACC Clin Electrophysiol· November 2025

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Intragenic Deletions in a Single Family with Dilated Cardiomyopathy.
Marketa Wayhelova, Petra Peldova, Alice Krebsova, Michaela Nemcikova, Matej Sojka

Appl Clin Genet· October 2025

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Novel four-exon deletion in ryanodine receptor gene (RYR2) associated with mixed electric and structural cardiac phenotype.
Tereza Stribna, Petra Peldova, Tatiana Vosecka, Tomas Roubicek, Milos Kubanek, Alice Krebsova

Europace· September 2025

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A homozygous TRIP13 pathogenic variant associated with familiar oocyte arrest and prematurely condensed sperm chromosomes.
Michal Schweiger, André Reis, Esen Gümüslü, Alice Krebsova, Andreas Raab

Mol Cytogenet· July 2025

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Pregnancy in women with dilated cardiomyopathy genetic variants.
María Alejandra Restrepo-Córdoba, Przemyslaw Chmielewski, Grażyna Truszkowska, María Luisa Peña-Peña, Miloš Kubánek, Alice Krebsová

Rev Esp Cardiol (Engl Ed)· January 2025

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Genotype is associated with left ventricular reverse remodelling and early events in recent-onset dilated cardiomyopathy.
Milos Kubanek, Jana Binova, Lenka Piherova, Alice Krebsova, Martin Kotrc

ESC Heart Fail· December 2024

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Post-mortem genetic testing in sudden cardiac death and genetic screening of relatives at risk: lessons learned from a Czech pilot multidisciplinary study.
Pavel Votýpka, Alice Krebsová, Patricia Norambuena-Poustková, Petra Peldová, Štěpánka Pohlová Kučerová

Int J Legal Med· November 2023

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Ablation for long QT syndrome: local or global repolarization effects?
Dan Wichterle, Markéta Segeťová, Alice Krebsová

Europace· July 2023

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Isolated aneurysmal disease as an underestimated finding in individuals with JAG1 pathogenic variants.
Jotte Rodrigues Bento, Alice Krebsová, Ilse Van Gucht, Irene Valdivia Callejon, An Van Berendoncks

Hum Mutat· December 2022

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Outcomes of a multicenter study of the causes of sudden cardiac death (SCD) in the Czech Republic and primary prevention of cardiac arrest in relatives.
Kučerová Pohlová Štěpánka, Krebsová Alice, Votýpka Pavel, Peldová Petra, Kulvajtová Markéta

Soud Lek· July 2022

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Novel Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue Findings.
Ilse Van Gucht, Alice Krebsova, Birgitte Rode Diness, Steven Laga, Dave Adlam

Int J Mol Sci· July 2021

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Pigmentary retinopathy can indicate the presence of pathogenic LAMP2 variants even in somatic mosaic carriers with no additional signs of Danon disease.
Bohdan Kousal, Filip Majer, Hana Vlaskova, Lenka Dvorakova, Lenka Piherova, Alice Krebsova

Acta Ophthalmol· February 2021

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Danon disease is an underdiagnosed cause of advanced heart failure in young female patients: a LAMP2 flow cytometric study.
Jiri Gurka, Lenka Piherova, Filip Majer, Anna Chaloupka, Daniela Zakova, Alice Krebsova

ESC Heart Fail· October 2020

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Molecular autopsy and sudden cardiac death in the young.
Rücklová Kristina, Kulvajtová Markéta, Krebsová Alice, Dobiáš Martin, Petřková Jana

Soud Lek· July 2020

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Desminopathy: Novel Desmin Variants, a New Cardiac Phenotype, and Further Evidence for Secondary Mitochondrial Dysfunction.
Miloš Kubánek, Tereza Schimerová, Lenka Piherová, Andreas Brodehl, Alice Krebsová

J Clin Med· March 2020

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Alu-mediated Xq24 deletion encompassing CUL4B, LAMP2, ATP1B4, TMEM255A, and ZBTB33 genes causes Danon disease in a female patient.
Filip Majer, Bohdan Kousal, Petr Dusek, Lenka Piherova, Martin Reboun, Alice Krebsova

Am J Med Genet A· January 2020

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LAMP2 exon-copy number variations in Danon disease heterozygote female probands: Infrequent or underdetected?
Filip Majer, Lenka Piherova, Martin Reboun, Veronika Stara, Ondrej Pelak, Alice Krebsova

Am J Med Genet A· November 2018

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Corrigendum: Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: as an Important Contributor.
Elisabeth Gillis, Ajay A Kumar, Ilse Luyckx, Christoph Preuss, Elyssa Cannaerts, Alice Krebsova

Front Physiol· September 2017

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Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: as an Important Contributor.
Elisabeth Gillis, Ajay A Kumar, Ilse Luyckx, Christoph Preuss, Elyssa Cannaerts, Alice Krebsova

Front Physiol· June 2017

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Distribution of CFTR mutations in the Czech population: positive impact of integrated clinical and laboratory expertise, detection of novel/de novo alleles and relevance for related/derived populations.
Petra Křenková, Tereza Piskáčková, Andrea Holubová, Miroslava Balaščaková, Veronika Krulišová, Alice Krebsová

J Cyst Fibros· September 2013

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High positive predictive value of PAPP-A for acute coronary syndrome diagnosis in heparin-naïve patients.
Petr Hájek, Milan Macek, Martina Pešková, Marie Hladíková, Eva Hansvenclová, Alice Krebsová

J Thromb Thrombolysis· July 2012

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Influence of concomitant heparin administration on pregnancy-associated plasma protein-A levels in acute coronary syndrome with ST segment elevation.
Petr Hájek, Milan Macek, Andrej Lashkevich, Hana Klučková, Marie Hladíková, Alice Krebsová

Arch Med Sci· December 2011

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Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1-22.3.
Arjan P M de Brouwer, Hendrikus P M Kunst, Alice Krebsova, Karin van Asseldonk, André Reis

Am J Med Genet A· August 2005

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QF-PCR examination of parental and meiotic origin of trisomy 21 in Central and Eastern Europe.
Marina Machatkova, Martina Brouckova, Milada Matejckova, Alice Krebsova, Karl Sperling

J Histochem Cytochem· March 2005

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