RNDr. Iveta Valášková, Ph.D.

2019

• Generation of two Duchenne muscular dystrophy patient-specific induced pluripotent stem cell lines DMD02 and DMD03 (MUNIi001-A and MUNIi003-A)

  JELÍNKOVÁ Šárka MARKOVÁ Lenka PEŠL Martin VALÁŠKOVÁ Iveta MAKATUROVÁ Eva JUŘÍKOVÁ Lenka VONDRÁČEK Petr LACAMPAGNE Alain DVOŘÁK Petr MELI Albano ROTREKL Vladimír

  Article in Periodical

  STEM CELL RESEARCH, year: 2019, volume: 40, edition: OCT 2019, DOI

• Molecular analysis confirmed common ancestor of 10 Czech families with long QT syndrome carrying C926T-KCNQ1 variant

  SYNKOVÁ Iva VALÁŠKOVÁ Iveta GAILLYOVÁ Renata NOVOTNÝ Tomáš BÉBAROVÁ Markéta ANDRŠOVÁ Irena FLORIANOVA A. VÍT Pavel NAVRATIL R.

  Conference abstract

  Year: 2019, type: Conference abstract

• Mutace T309I asociovaná se syndromem dlouhého QT typu 1: akumulace IKs jako mechanismus ochrany srdce proti arytmii

  BÉBAROVÁ Markéta SYNKOVÁ Iva ANDRŠOVÁ Irena BAIAZITOVA Larisa ŠVECOVÁ Olga HOŠEK Jan PÁSEK Michal VÍT Pavel VALÁŠKOVÁ Iveta GAILLYOVÁ Renata NAVRÁTIL Rostislav NOVOTNÝ Tomáš

  Conference abstract

  Year: 2019, type: Conference abstract

• 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

• Novorozenecký screening cystické fibrózy a diagnostika CFSPID.

  BARTOŠOVÁ Jana ZEMKOVÁ D. HOLUBOVÁ Andrea GAILLYOVÁ Renata VALÁŠKOVÁ Iveta HOLČÍKOVÁ Alena MALÁ Miriam SKALICKÁ Veronika

  Article in Periodical

  Česko-slovenská pediatrie, year: 2019, volume: 74, edition: 7

• 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

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

• 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

2016

• Clonal cytogenetics changes in progression of multiple myeloma to extramedullary relapse and plasmocellular leukemia: a case report

  SMETANA Jan KUGLÍK Petr GREŠLIKOVÁ Henrieta KUPSKÁ Renata NĚMEC Pavel MIKULÁŠOVÁ Aneta VALÁŠKOVÁ Iveta OPPELT Jan ALMÁŠI Martina KREJČÍ Marta ADAM Zdeněk POUR Luděk HÁJEK Roman

  Article in Periodical

  International Journal of Clinical and Experimental Pathology, year: 2016, volume: 9, edition: 1