Mutations in STK11 gene in Czech Peutz-Jeghers patients

por Vasovčák, Peter, Puchmajerová, Alena, Roubalík, Jan, Křepelová, Anna
Publicado 2009

Multiple primary malignancies and subtle mucocutaneous lesions associated with a novel PTEN gene mutation in a patient with Cowden syndrome: Case report

por Vasovčák, Peter, Šenkeříková, Mária, Hatlová, Jana, Křepelová, Anna
Publicado 2011

Molecular Genetic Analysis of 103 Sporadic Colorectal Tumours in Czech Patients

por Vasovcak, Peter, Pavlikova, Kristyna, Sedlacek, Zdenek, Skapa, Petr, Kouda, Martin, Hoch, Jiri, Krepelova, Anna
Publicado 2011

CHEK2(p.I157T) Mutation Is Associated with Increased Risk of Adult-Type Ovarian Granulosa Cell Tumors

por Švajdler, Peter, Vasovčák, Peter, Švajdler, Marián, Šedivcová, Monika, Urbán, Veronika, Michal, Michal, Mezencev, Roman
Publicado 2022

Ventricular fibrillation and arrhythmia associated with cardiac fibromas involving both ventricles in a 1.5-year-old girl

por Farkaš, Daniel, Pisarčíková, Mária, Vasovčák, Peter, Crhová, Anna, Ginelliová, Alžbeta, Mistríková, Lucia, Fröhlichová, Lucia, Farkašová Iannaccone, Silvia
Publicado 2023