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- Mental disorders – epigenetic mechanisms in their etiology and pharmacotherapy
MUDr. Bc. Libor Ustohal, Ph.D., prof. MUDr. Ladislav Hosák, Ph.D., doc. MUDr. Klára Látalová, Ph.D., RNDr. Aleš Kovařík, CSc.
(1/2016, Review articles )
- Limb-girdle muscular dystrophies
doc. RNDr. Lenka Fajkusová, CSc., Mgr. Jana Zídková, Ph.D.
(2/2021, Main topic ) - Genetické příčiny epilepsií
MUDr. Katalin Štěrbová, MUDr. Petra Laššuthová, Ph.D., MUDr. Markéta Vlčková, Ph.D.
(2/2018, Main topic ) - Nové možnosti léčby vrozených neuromuskulárních onemocnění v dětském věku
MUDr. Jana Haberlová, Ph.D.
(2/2018, Main topic ) - Analysis of associated genes with neurodegenerative diseases: practical experience of neurodegenerative centers in FTN
RNDr. Eva Parobková, Ph.D., MUDr. Petr Šuhaj, Ing. Hana Šulcová, prof. MUDr. Radoslav Matěj, Ph.D.
(4/2024, Main topic )
- The utility of modern diagnostic genetic methods in clinical pediatrics
MUDr. Andrea Hladíková, Ph.D., Mgr. Dita Černá, RNDr. Alfons Balcar
(3/2016, Electronic attachment )
- Recent achievements in targeted treatment of advanced non-small cell lung cancer with rare RET, MET, BRAF and NTRK gene alterations
MUDr. Róbert Godál
(1/2021, Main topic ) - Myelodysplastic syndrome – medicine made to measure
MUDr. Eva Mikušková, doc. MUDr. Ján Staško, PhD., MUDr. Juraj Chudej, PhD., MUDr. Ľubica Váleková, PhD., MUDr. Matej Hrnčár, MUDr. Juraj Sokol, PhD., MUDr. Andrej Rosík
(6/2014, Spectrum ) - Advances in molecular monitoring and the importance of screening BCR/ABL1 mutation for Ph-positive chronic myelocytic leukemia
MUDr. Adriana Kafková, PhD., prof. MUDr. Elena Tóthová, CSc.
(1/2019, Review articles ) - FLT3mutácie u pacienta s AML: incidencia, možnosti diagnostiky a vplyv na manažment liečby
MUDr. Eva Mikušková, PhD., RNDr. Renata Lukačková, RNDr. Imrich Hikkel, PhD., Mgr. Michaela Zrubcová
(3/2018, Original articles & case reports ) - RNDr. Gabriel Minárik, PhD.
RNDr. Gabriel Minárik, PhD.
(5/2014, Main topic ) - Molecular cythogenetic in the familial cancers
Ing. Martin Čermák
(2/2015, Main topic ) - Hereditary oncological syndromes: DNA mutations and diagnostic techniques of genetic testing
RNDr. Michal Konečný, PhD., RNDr. Katarína Závodná, PhD., Mgr. Ján Markus, PhD., Mgr. Lenka Dolešová, prof. RNDr. Vanda Repiská, PhD., doc. MUDr.aniel Böhmer, PhD.1
(2/2015, Main topic ) - From molecular biology to the next-generation sequencing – genome-guided cancer therapy decisions
doc. RNDr. Zora Lasabová, CSc., prof. MUDr. Lukáš Plank, CSc.
(6/2018, Main topic )
- Genetic background of von Willebrand disease
RNDr. Jana Žolková, PhD., RNDr. Zuzana Kolková, PhD., RNDr. Dušan Loderer, PhD., Mgr. Dana Provazníková, PhD., RNDr. Ingrid Hrachovinová, PhD., MUDr. Alena Strýčková, doc. MUDr. Miroslava Dobrotová, PhD., Ing. Ingrid Škorňová, PhD., doc. RNDr. Zora Lasabová, PhD., prof. MUDr. Peter Kubisz, DrSc., prof. MUDr. Ján Staško, PhD.
(1/2021, Main topic )
- Our experience with the use of NGS in the DNA diagnosis of mitochondrial diseases
RNDr. Martina Škopková, PhD., RNDr. Daniela Gašperíková, DrSc.
(2/2024, Main topic )