1. DNA damage signalling barrier, oxidative stress and treatment‐relevant DNA repair factor alterations during progression of human prostate cancer. Issue 6 (3rd March 2016) Authors: Kurfurstova, Daniela; Bartkova, Jirina; Vrtel, Radek; Mickova, Alena; Burdova, Alena; Majera, Dusana; Mistrik, Martin; Kral, Milan; Santer, Frederic R.; Bouchal, Jan; Bartek, Jiri Journal: Molecular oncology Issue: Volume 10:Issue 6(2016:Jun.) Page Start: 879 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Familial atypical parkinsonism with rare variant in VPS35 and FBXO7 genes: A case report. Issue 46 (November 2016) Authors: Bartonikova, Tereza; Mensikova, Katerina; Mikulicova, Lenka; Vodicka, Radek; Vrtel, Radek; Godava, Marek; Vastik, Miroslav; Kaiserova, Michaela; Otruba, Pavel; Dolinova, Iva; Nevrly, Martin; Kanovsky, Petr Other Names: Tusconi. Massimo section editor. Journal: Medicine Issue: Volume 95:Issue 46(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Familial atypical parkinsonism with rare variant in VPS35 and FBXO7 genes: A case report. Issue 46 (November 2016) Authors: Bartonikova, Tereza; Mensikova, Katerina; Mikulicova, Lenka; Vodicka, Radek; Vrtel, Radek; Godava, Marek; Vastik, Miroslav; Kaiserova, Michaela; Otruba, Pavel; Dolinova, Iva; Nevrly, Martin; Kanovsky, Petr Editors: Tusconi., Massimo Journal: Medicine Issue: Volume 95:Issue 46(2016) Page Start: e5398 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Fetal heart rhabdomyomatosis: a single-center experience. (4th March 2021) Authors: Pavlicek, Jan; Klaskova, Eva; Kapralova, Sabina; Prochazka, Martin; Vrtel, Radek; Gruszka, Tomas; Kacerovsky, Marian Journal: Journal of maternal-fetal & neonatal medicine Issue: Volume 34:Number 5(2021) Page Start: 701 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Mutational analysis of TSC1 and TSC2 genes in Tuberous Sclerosis Complex patients from Greece. Issue 1 (December 2017) Authors: Avgeris, Socratis; Fostira, Florentia; Vagena, Andromachi; Ninios, Yiannis; Delimitsou, Angeliki; Vodicka, Radek; Vrtel, Radek; Youroukos, Sotirios; Stravopodis, Dimitrios; Vlassi, Metaxia; Astrinidis, Aristotelis; Yannoukakos, Drakoulis; Voutsinas, Gerassimos Journal: Scientific reports Issue: Volume 7:Issue 1(2017) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗