MUDr. Irena Andršová, Ph.D.

2019

• Mutation R591C associated with long QT syndrome type 1: clinical, genetic, and functional analysis

  ŠVECOVÁ Olga BÉBAROVÁ Markéta BAIAZITOVA Larisa POLICAROVÁ Marcela HOŠEK Jan ANDRŠOVÁ Irena VALÁŠKOVÁ Iveta SYNKOVÁ Iva GAILLYOVÁ Renata VÍT Pavel NOVOTNÝ Tomáš

  Conference abstract

  Year: 2019, type: Conference abstract

• Targeted resequencing of genes associated with long QT syndrome in Czech patients: two newly identified likely pathogenic variants in previously investigated patient with negative results

  SYNKOVÁ Iva OSTADALOVA E. VALÁŠKOVÁ Iveta GAILLYOVÁ Renata NOVOTNÝ Tomáš ANDRŠOVÁ Irena FLORIANOVA A. VIT P.

  Conference abstract

  Year: 2019, type: Conference abstract

2018

• Automation bias in medicine: The influence of automated diagnoses on interpreter accuracy and uncertainty when reading electrocardiograms

  BOND Raymond R. NOVOTNÝ Tomáš ANDRŠOVÁ Irena KOC Lumír ŠIŠÁKOVÁ Martina FINLAY Dewar GULDENRING Daniel MCLAUGHLIN James PEACE Aaron MCGILLIGAN Victoria LESLIE Stephen J. WANG Hui MALIK Marek

  Article in Periodical

  JOURNAL OF ELECTROCARDIOLOGY, year: 2018, volume: 51, edition: 6, DOI

• Hypersensitivity to material and environmental burden as a possible cause of late complications of cardiac implantable electronic devices

  MAŇOUSEK Jan ANDRŠOVÁ Irena STEJSKAL Vera VLAŠÍNOVÁ Jitka SEPŠI Milan KUTA Jan KLÁNOVÁ Jana MAZÍK Michal JARKOVSKÝ Jiří ŠNAJDROVÁ Lenka BENEŠOVÁ Klára NOVOTNÝ Tomáš ZADÁKOVÁ Andrea ŠPINAR Jindřich

  Article in Periodical

  EP Europace, year: 2018, volume: 20, edition: 9, DOI

2017

• „Founder“ mutace asociované se syndromem dlouhého QT: Česká republika versus svět

  BÉBAROVÁ Markéta ANDRŠOVÁ Irena VALÁŠKOVÁ Iveta SYNKOVÁ Iva GAILLYOVÁ Renata VÍT Pavel NOVOTNÝ Tomáš

  Appeared in Conference without Proceedings

  Year: 2017, type: Appeared in Conference without Proceedings

• Higher incidence of hypotension episodes in women during the sub-acute phase of ST elevation myocardial infarction and relationship to covariates

  KALA Petr NOVOTNÝ Tomáš ANDRŠOVÁ Irena BENEŠOVÁ Klára HOLICKÁ Mária JARKOVSKÝ Jiří HNATKOVA Katerina KOC Lumír MIKOLÁŠKOVÁ Monika NOVÁKOVÁ Tereza ONDRÚŠ Tomáš PŘÍVAROVÁ Lenka ŠPINAR Jindřich MALIK Marek

  Article in Periodical

  Plos one, year: 2017, volume: 12, edition: 3, DOI

• Klinické a genetické charakteristiky mutace T309I-Kv7.1 asociované se syndromem dlouhého QT

  ŠATKOVÁ Júlia BÉBAROVÁ Markéta ANDRŠOVÁ Irena VALÁŠKOVÁ Iveta SYNKOVÁ Iva GAILLYOVÁ Renata VÍT Pavel NOVOTNÝ Tomáš

  Appeared in Conference without Proceedings

  Year: 2017, type: Appeared in Conference without Proceedings

• T309I-Kv7.1 mutation as a feasible founder LQT1 mutation: clinical, genetic and biophysical analysis

  BÉBAROVÁ Markéta VEJMĚLEK Adam HOŠEK Jan ANDRŠOVÁ Irena VALÁŠKOVÁ Iveta GAILLYOVÁ Renata VÍT Pavel NOVOTNÝ Tomáš

  Conference abstract

  Year: 2017, type: Conference abstract

• The role of computerized diagnostic proposals in the interpretation of the 12-lead electrocardiogram by cardiology and non-cardiology fellows

  NOVOTNÝ Tomáš BOND Raymond ANDRŠOVÁ Irena KOC Lumír ŠIŠÁKOVÁ Martina FINLAY Dewar GULDENRING Daniel ŠPINAR Jindřich MALIK Marek

  Article in Periodical

  International Journal of Medical Informatics, year: 2017, volume: 101, edition: MAY 2017, DOI

2016

• Mutace T309I jako možná „founder„ mutace syndromu dlouhého intervalu QT typu I

  BÉBAROVÁ Markéta VEJMĚLEK Adam HOŠEK Jan ANDRŠOVÁ Irena VALÁŠKOVÁ Iveta GAILLYOVÁ Renata VÍT Pavel NOVOTNÝ Tomáš

  Conference abstract

  Year: 2016, type: Conference abstract