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- PRIMARY IMMUNE DEFICIENCIES, DIAGNOSIS AND THERAPY
MUDr. Peter Čižnár, CSc.
(3/2006, Main topic ) - Evolokumab pro léčbu familiární hypercholesterolémie
prof. MUDr. Vladimír Bláha, CSc.
(4/2018, Drugs & drug classes ) - Hereditary disorders of purine metabolism associated with renal impairment
prof. MUDr. László Kovács, DrSc., MPH, RNDr. Katarína Hlinková, MUDr. Gabriela Nagyová, Mgr. Michaela Čižmárová, MUDr. Anna Hlavatá, PhD., MPH
(3/2015, Interdisciplinary consilium )
- Syndrómy naliehajúcich génov s neurobehaviorálnou symptomatológiou
MUDr. Darina Ďurovčíková CSc., RNDr. Iveta Černáková, PhD., RNDr. Robert Petrovič, Mgr. Ján Futas
(2/2006, Main topic ) - X-viazaná adrenoleukodystrofia – najčastejšia dedičná metabolická porucha peroxizómov
doc. MUDr. Ján Chandoga, CSc., RNDr. Robert Petrovič, Mgr. Ján Futas, MUDr. Darina Ďurovčíková, CSc., MUDr. Juraj Štofko, PhD., MUDr. Stanislav Jančo, CSc., MUDr. Mária Brezinová, prof. MUDr. Peter Turčáni, PhD.
(2/2006, Main topic ) - Treatable inherited metabolic disorders with extrapyramidal manifestation in children
Doc. MUDr. Miriam Kolníková, PhD., MUDr. Dominika Kovárová, MUDr. Patrícia Balážová, MUDr. Silvia Radová
(2/2022, Main topic ) - Treatable lysosomal storage disorders with movement disorder manifestations
MUDr. Alexandra Lacková, Doc. MUDr. Matej Škorvánek, PhD.
(2/2022, Main topic ) - Glycogen storage disease type II (GSD II, Pompe disease). Current diagnostic and therapeutic options. Clinical case report
MUDr. Věra Malinová
(5/2010, Review articles ) - Pokroky v léčbě dědičných metabolických poruch s neurologickou symptomatologií
doc. MUDr. Martin Magner, Ph.D., MUDr. Hana Kolářová, doc. MUDr. Tomáš Honzík, Ph.D.
(2/2018, Main topic ) - Rhabdomyolysis
doc. MUDr. Peter Špalek, PhD.
(4/2012, Main topic )
- B12 vitamin metabolism disorders
MUDr. Katarína Fabriciová, MUDr. Darina Behúlová, PhD., RNDr. Jozefína Škodová, MUDr. Darina Holešová, MUDr. Mária Ostrožlíková, Ing. Katarína Schmidtová, doc. MUDr. Viktor Kožich, PhD.
(4/2012, Review articles ) - DIFFERENTIAL DIAGNOSTICS OF HYPOGLYCEMIA IN NEWBORN PERIOD AND CHILDHOOD
prof. MUDr. Ľudmila Podracká, CSc., MUDr. Juliana Ferenczová, PhD.
(3/2008, DIFFERENTIAL DIAGNOSIS ) - Hereditary disorders of purine metabolism associated with renal impairment
prof. MUDr. László Kovács, DrSc., MPH, RNDr. Katarína Hlinková, MUDr. Gabriela Nagyová, Mgr. Michaela Čižmárová, MUDr. Anna Hlavatá, PhD., MPH
(6/2015, Review articles ) - Late onset of inherited urea cycle disorder – ornithine transcarbamoylase deficiency
prof. MUDr. Zdeněk Doležel, CSc., MUDr. RNDr. Pavel Ješina, Ph.D., MUDr. Jiří Štarha, Ph.D., doc. MUDr. Tomáš Honzík, Ph.D., MUDr. Jan Papež, MUDr. Petr Jabandžiev, doc. MUDr. Dagmar Procházková, Ph.D.
(6/2016, Original articles & Case reports ) - DIFFERENTIAL DIAGNOSIS OF HYPERGLYCEMIA IN CHILDREN AND ADOLESCENTS
MUDr. Štěpánka Průhová, Ph.D., prof. MUDr. Jan Lebl, CSc.
(6/2005, Review articles ) - Hyperammonemia
MUDr. Claudia Šebová, doc. MUDr. Vladimír Bzdúch, CSc.
(6/2019 ) - Treatable inherited metabolic disorders with extrapyramidal manifestation in children
Doc. MUDr. Miriam Kolníková, PhD., MUDr. Dominika Kovárová, MUDr. Patrícia Balážová, MUDr. Silvia Radová
(3/2022, Original articles & Case reports )
- Acrodermatitis enteropathica and metabolic disorders that resemble its cutaneous features
MUDr. Zuzana Kardošová, PhD., doc. MUDr. Dušan Buchvald, PhD.
(2/2019, Review articles )
- Pathology of folic acid nad pregnancy
MUDr. Michal Koucký
(3/2011, Current pharmacotherapy )
- Neurodegeneration and lysosomal storage disorders
MUDr. Katarína Juríčková, PhD., MUDr. Anna Hlavatá, PhD., MPH
(1/2024, Main topic )













