Masaryk University

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    2024

    1. KOŠKOVÁ, Olga, Jaroslav ŠTĚRBA, Renata FABEROVÁ, Petra POKORNÁ, Martin ŠTĚRBA, Petr MARCIÁN, Zdeňka RÁČILOVÁ, Michaela RICHTROVÁ, Linda MORAVCOVÁ and Libor STREIT. Multioborový přístup k léčbě vaskulárních anomálií. In XLII. Kongres plastické chirurgie, Špindlerův Mlýn. 2024.

      Type of participation: active participation (giving a lecture, organization, etc.)

      Changed by: MUDr. Olga Košková, Ph.D., učo 136078. Changed: 12/9/2024 16:31.
    2. KOŠKOVÁ, Olga, Petr MARCIÁN, Jaroslav ŠTĚRBA, Renata FABEROVÁ, Anna SEEHOFNEROVÁ, Zdeňka RÁČILOVÁ, Petra POKORNÁ, Michaela RICHTROVÁ and Martin ŠTĚRBA. Use of 3D printing in pre-surgical planning in severe cases of pediatric patients with vascular anomalies. In ISSVA World Congress 2024: The Latest in Vascular Anomalies. Madrid, Spain. 2024.

      Type of participation: active participation (giving a lecture, organization, etc.)
      International impact: yes

      Changed by: MUDr. Olga Košková, Ph.D., učo 136078. Changed: 21/7/2024 09:03.

    2023

    1. KOŠKOVÁ, Olga, Jaroslav ŠTĚRBA, Renata FABEROVÁ, Petra POKORNÁ, Martin ŠTĚRBA, P MARCIÁN, Dominika MATYSKOVÁ, Anna SEEHOFNEROVÁ and Michaela RICHTROVÁ. Moderní přístupy v léčbě cévních anomálií u dětí. In XL. KONGRES PLASTICKÉ CHIRURGIE, Praha,. 2023.

      Type of participation: active participation (giving a lecture, organization, etc.)

      Changed by: MUDr. Hana Harazim, Ph.D., učo 175411. Changed: 18/4/2024 08:51.
    2. HONZÍKOVÁ, Klára, Renata FABEROVÁ, Jaroslav ŠTĚRBA, Martin ŠTĚRBA and Olga KOŠKOVÁ. Nové terapeutické možnosti rozsáhlých venózních malformací. In KONFERENCE DĚTSKÉ DERMATOLOGIE, Brno. 2023.
      Changed by: MUDr. Olga Košková, Ph.D., učo 136078. Changed: 17/4/2024 19:55.
    3. ŠTĚRBA, Martin, Petra POKORNÁ, Renata FABEROVÁ, Blanka PINKOVÁ, Jarmila SKOTÁKOVÁ, Anna SEEHOFNEROVÁ, Jan BLATNÝ, Lucia JANIGOVÁ, Olga KOŠKOVÁ, Hana PÁLOVÁ, Michal MAHDAL, Lukáš PAZOUREK, Petr JABANDŽIEV, Ondřej SLABÝ, Peter MÚDRY and Jaroslav ŠTĚRBA. Targeted treatment of severe vascular malformations harboring PIK3CA and TEK mutations with alpelisib is highly effective with limited toxicity. Scientific reports. BERLIN: NATURE PORTFOLIO, 2023, vol. 13, No 1, p. 1-9. ISSN 2045-2322. Available from: https://dx.doi.org/10.1038/s41598-023-37468-4.
      URL
      RIV/00216224:14110/23:00131299 Article in a journal. English. Germany.
      Štěrba, Martin (203 Czech Republic, belonging to the institution) -- Pokorná, Petra (203 Czech Republic, belonging to the institution) -- Faberová, Renata (203 Czech Republic, belonging to the institution) -- Pinková, Blanka (203 Czech Republic, belonging to the institution) -- Skotáková, Jarmila (203 Czech Republic, belonging to the institution) -- Seehofnerová, Anna (203 Czech Republic, belonging to the institution) -- Blatný, Jan (203 Czech Republic, belonging to the institution) -- Janigová, Lucia (703 Slovakia, belonging to the institution) -- Košková, Olga (203 Czech Republic, belonging to the institution) -- Pálová, Hana (203 Czech Republic, belonging to the institution) -- Mahdal, Michal (203 Czech Republic, belonging to the institution) -- Pazourek, Lukáš (203 Czech Republic, belonging to the institution) -- Jabandžiev, Petr (203 Czech Republic, belonging to the institution) -- Slabý, Ondřej (203 Czech Republic, belonging to the institution) -- Múdry, Peter (203 Czech Republic, guarantor, belonging to the institution) -- Štěrba, Jaroslav (203 Czech Republic, belonging to the institution)
      Keywords in English: vascular malformations; PIK3CA and TEK mutations; alpelisib; targeted treatment
      International impact: yes
      Reviewed: yes

      Changed by: Mgr. Eva Dubská, učo 77638. Changed: 8/4/2024 10:23.

    2021

    1. PAPEŽ, Jan, Jiří ŠTARHA, Pavel ZERHAU, Denisa PAVLOVSKÁ, Marta JEŽOVÁ, Tomáš JUŘENČÁK, Kateřina SLABÁ, Martin ŠTĚRBA, Arpád KEREKES, Tomáš MERTA, Terézia HALUŠKOVÁ, Hana PÁLOVÁ, Ondřej SLABÝ, Jaroslav ŠTĚRBA and Petr JABANDŽIEV. Spindle Cell Hemangioma and Atypically Localized Juxtaglomerular Cell Tumor in a Patient with Hereditary BRIP1 Mutation: A Case Report. Genes. Basel: MDPI, 2021, vol. 12, No 2, p. 1-8. ISSN 2073-4425. Available from: https://dx.doi.org/10.3390/genes12020220.
      URL
      RIV/00216224:14110/21:00120086 Article in a journal. English. Switzerland.
      Papež, Jan (203 Czech Republic, belonging to the institution) -- Štarha, Jiří (203 Czech Republic, belonging to the institution) -- Zerhau, Pavel (203 Czech Republic, belonging to the institution) -- Pavlovská, Denisa (203 Czech Republic, belonging to the institution) -- Ježová, Marta (203 Czech Republic, belonging to the institution) -- Juřenčák, Tomáš (203 Czech Republic, belonging to the institution) -- Slabá, Kateřina (203 Czech Republic, belonging to the institution) -- Štěrba, Martin (203 Czech Republic, belonging to the institution) -- Kerekes, Arpád (703 Slovakia, belonging to the institution) -- Merta, Tomáš (203 Czech Republic, belonging to the institution) -- Halušková, Terézia (703 Slovakia, belonging to the institution) -- Pálová, Hana (203 Czech Republic, belonging to the institution) -- Slabý, Ondřej (203 Czech Republic, belonging to the institution) -- Štěrba, Jaroslav (203 Czech Republic, belonging to the institution) -- Jabandžiev, Petr (203 Czech Republic, guarantor, belonging to the institution)
      Keywords in English: juxtaglomerular cell tumor; reninoma; spindle cell hemangioendothelioma; kidney; hypertension; children
      International impact: yes
      Reviewed: yes

      Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 21/2/2022 09:18.
Displayed: 19/9/2024 09:26