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- Combination therapy by psychiatric drugs for chronic pain syndrome
MUDr. Gabriela Vrbová
(3/2014, Original articles & case reports )
- Neurologické projevy poruch metabolizmu lipidů
doc. MUDr. Ivanka Vlachová
(1/2005, Main topic ) - Subcortical band heterotopia of the cerebral cortex with pharmacoresistant epilepsy
prof. MUDr. Petr Kaňovský, CSc., doc. MUDr. Robert Kuba, Ph.D., doc. MUDr. Stanislav Buřval, Ph.D., MUDr. Milan Labonek, MUDr. Marta Neklanová, MUDr. Jindřiška Burešová, prof. MUDr. Roman Herzig, Ph.D.
(1/2012, Case reports ) - Development of quadriparesis after delirium: simple routine or diagnostic challenge?
MUDr. Eva Gödöllová, MUDr. Julia Travkina, MUDr. Katarína Surmajová, MUDr. Tatiana Hučeková
(1/2021, Case reports )
- Most common genetic syndromes associated with congenital heart defects
MUDr. Michaela Lapšová, doc. MUDr. Peter Olejník, PhD.
(6/2023, Encyclopedia of rare diseases ) - Prevention of infective endocarditis in children
MUDr. Pavol Kunovský, CSc., MBA
(6/2013, Review articles ) - New born child with congenital epidermolysis bullosa (case report)
MUDr. Katarína Soršáková Trnovská, PhD., doc. MUDr. Dušan Buchvald, PhD., MUDr. Zuzana Velická, CSc.
(1/2019, Original articles & Case reports ) - Hirschsprung’s disease
MUDr. Miroslava Fuňáková, MUDr. Mária Jursová, MUDr. Rastislav Králik, doc. MUDr. Ján Trnka, CSc
(4/2014, Original articles & Case reports ) - During childhood unrecognized congenital heart defect in patient with Turner syndrome, and its implications
doc. MUDr. Jiřina Zapletalová, Ph.D., MUDr. Eva Klásková, MUDr. Zbyněk Tüdös, Ph.D., MUDr. Sabina Kaprálová
(5/2015, Electronic attachment ) - Rare case of nasal obstruction in 13-month old child – case report
doc. MUDr. Pavel Doležal, CSc., mim. prof., MUDr. Lucia Majáková, MUDr. Samuel Kunzo, MUDr. Ivona Klochanová, MUDr. Andrea Jovankovičová
(6/2015, Original articles & Case reports ) - Gastroschisis: not quite easy to diagnose in a newborn
MUDr. Kateřina Konopásková, MUDr. Alena Kokešová, Ph.D, MUDr. Dagmar Heroldová, MUDr. Mahulena Mojžíšová, doc. MUDr. Michal Rygl, Ph.D.
(6/2015, Electronic attachment ) - Conotruncal cardiac anomalies and 22q11.2 microdeletion syndrome (DiGeorge syndrome)
MUDr. Veronika Krasňanová, doc. MUDr. Ľubica Kováčiková, PhD., MUDr. Peter Škrak, PhD., MUDr. Zuzana Hrubšová, MUDr. Rudolf Poruban, PhD.
(1/2024, Review articles ) - Tetralogy of Fallot
MUDr. Mária Bartová, doc. MUDr. Peter Olejník, PhD.
(4/2021, Review articles ) - Nevi of skin in children. I. Pigmented nevi
doc. MUDr. Tibor Danilla, CSc., PhDr. Viera Tereková, PhD.
(4/2015, Review articles ) - DiGeorge syndrome (22q11.2 microdeletion syndrome) with congenital heart defect
MUDr. Veronika Krasňanová, doc. MUDr. Ľubica Kováčiková, PhD., doc. MUDr. Peter Čižnár, PhD., MUDr. Daniela Šubová
(5/2019, Review articles ) - Pseudoarthrosis and its solution in children and adolescent
MUDr. Martina Frištáková, PhD., MUDr. Paulína Kubičková, MUDr. Jana Bevilaqua, MUDr. Matúš Halas
(5/2023, Review articles ) - Adult patient with chronic inflammatory bowel disease and inborn error of immunity: hematopoietic stem cell transplantation as an option for curative treatment
MUDr. Veronika Dobšinská, MUDr. Peter Švec, PhD., MUDr. Júlia Horáková, PhD., MUDr. Róbert Ostró, MUDr. Miroslava Pozdechová, MUDr. Ivana Boďová, PhD., doc. MUDr. Peter Čižnár, CSc., RNDr. Michal Konečný, PhD., MUDr. Iveta Čierna, PhD., MUDr. RNDr. Jaroslava Adamčáková, MUDr. Mária Füssiová, MUDr. Tomáš Sýkora, PhD., prof. MUDr. Alexandra Kolenová, PhD.
(6/2022, Original articles & Case reports )
- Albright hereditary osteodystrophy
MUDr. Denisa Kacerovská, Ph.D., doc. MUDr. Dmitry V. Kazakov, Ph.D., Mgr. Jana Němcová, RNDr. Tomáš Vaněček, Ph.D., prof. MUDr. Michal Michal
(2/2010, Interdisciplinary consilium )
- New fibrinogen variants in patients with congenital fibrinogen disorders
MUDr. Miroslava Drotárová, MUDr. Tomáš Šimurda, PhD., MPH, MUDr. Monika Brunclíková, PhD., MUDr. Kristína Mária Beláková, RNDr. Jana Žolková, PhD., doc. Ing. Ingrid Škorňová, PhD., Prof. MUDr. Ján Staško, PhD., doc. MUDr. Juraj Sokol, PhD., MBA
(1/2025, Main topic ) - Afibrinogenaemia and dysfibrinogenaemias
doc. MUDr. Ján Staško, PhD., prof. MUDr. Peter Kubisz, DrSc., MUDr. Tomáš Šimurda, MUDr. Miroslava Dobrotová, PhD.
(2/2015, Review articles ) - Hemorrhagic-thrombotic complications of patients with congenital hypoproconvertinaemia (FVII defect) – case report
MUDr. Alena Strýčková, doc. MUDr. Miroslava Dobrotová, PhD., RNDr. Jana Žolková, PhD., MUDr. Tomáš Šimurda, PhD., MUDr. Martin Jozef Péč, prof. MUDr. Marián Mokáň, DrSc., FRCP Edin., prof. MUDr. Ján Staško, PhD.
(1/2021, Main topic ) - Hereditary thrombophilic platelet defects
MUDr. Lenka Bartošová, PhD., MUDr. Ivana Plameňová, PhD., MUDr. Jela Ivanková, prof. MUDr. Peter Kubisz, DrSc.
(1/2011, Main topic ) - XXI. Slovenský angiologický kongres spojený so 6. kurzom Central European Vascular Forum
(S3/2013, Supplement )
- Current options for covering the open neural tube defect in fetal surgery
MUDr. Miroslava Kohútková, MUDr. Marek Dráb, PhD., doc. MUDr. František Horn, PhD.
(3-4e/2024, Review articles )
- Perioperative characteristics of adults with congenital heart defects
doc. MUDr. Ľubica Kováčiková, PhD., MUDr. Zuzana Hrubšová, MUDr. Peter Škrak, PhD.
(1/2020, Review articles )
- Termination of pregnancy due to genetic indication in the region of Eastern Bohemia
MUDr. Martin Schwarz, Ph.D., MBA, MDDr. Lenka Šodková, Ph.D., MUDr. Eva Míšová, Ph.D., MBA
(2/2025, Main topic )