P. Peldová

发表

(Complex approach towards patients with hypertrophic cardiomyopathy and indications to genetic testing)

J. Kautzner, M. Macek, J. Veselka, 2020 .

(Diagnosis of laminopathy with predominant cardiac involvement during pretransplant assessment - a case report with a review of risk stratification and disease management of laminopathies)

J. Kautzner, V. Melenovský, M. Macek, 2022, Cor et Vasa.

Isolated aneurysmal disease as an underestimated finding in individuals with JAG1 pathogenic variants

M. Macek, B. Loeys, A. Van Berendoncks, 2022, Human mutation.

Constitutively active Lyn kinase causes a cutaneous small vessel vasculitis and liver fibrosis syndrome

S. Pittaluga, E. Meffre, S. Hewitt, 2022, Nature Communications.

Language and international relations: Linguistic support for other academic disciplines

Irena Headlandová Kalischová, Julia Hüttner, Piotr Twardzisz, 2020 .

Post-mortem genetic testing in sudden cardiac death and genetic screening of relatives at risk: lessons learned from a Czech pilot multidisciplinary study

J. Kautzner, P. Tomášek, Jakub Stocek, 2023, International Journal of Legal Medicine.

(Postmortem genetic testing in sudden cardiac death victims and genetic screening of relatives at risk in the Czech Republic)

J. Kautzner, P. Tomášek, M. Kulvajtová, 2023, Cor et Vasa.

(PRKAG2 syndrome as a highly arrhythmogenic eventuality in the differential diagnosis of hypertrophic cardiomyopathy - an example of two families with a confirmed causative DNA variant)

T. Roubíček, R. Polášek, P. Peldová, 2023, Cor et Vasa.

Sudden cardiac arrest in a child with Gitelman syndrome: a case report and literature review

Miroslava Balaščáková, J. Zieg, P. Kubuš, 2023, Frontiers in Pediatrics.

(Czech Association for Preventive Cardiology Expert Consensus Statement on the State of Genetic Testing for Inherited Cardiovascular Diseases)

I. Grochová, P. Votýpka, P. Peldová, 2023, Cor et Vasa.