Enter your login e-mail to the account
-1.png)
Search
Search parameters
Search results
- PROTHROMBOTIC STATES AND THROMBOSIS IN HEMATOLOGIST´S VIEW
doc. MUDr. Angelika Bátorová, CSc.
(2/2006, clearly )
- Molecular genetic diagnostics of childhood muscular dystrophies
doc. RNDr. Lenka Fajkusová, CSc., Mgr. Jana Zídková, Ph.D.
(1/2022, Main topic ) - Spastic paraparesis as a clinical manifestation of severe X-linked adrenoleukodystrophy
RNDr. Anna Uhrová Mészárosová, Ph.D., MUDr. Jana Laštůvková, MUDr. Filip Cihlář, Ph.D., doc. MUDr. Alena Šantavá, CSc., MUDr. Radim Mazanec, Ph.D.
(3/2024, From the boundary of neurology ) - Hereditary spastic paraplegias: clinical and genetic aspects
MUDr. Radim Mazanec, Ph.D., Prof. MUDr. Pavel Seeman, Ph.D., RNDr. Anna Uhrová Mészárosová, Ph.D.
(6/2016, Main topic ) - Eye of tiger sign in patient with extrapyramidal syndrome – unique case report
MUDr. Martin Daniš, MUDr. Juraj Cisár, MUDr. Georgi Krastev, PhD.
(4/2020, Video case reports )
- Kabuki syndrome
MUDr. Miroslava Pozdechová, MUDr. Dominika Dóczyová, MUDr. Ivana Boďová, PhD., MUDr. Peter Švec, PhD., MUDr. Júlia Horáková, PhD., MUDr. Mária Füssiová, MUDr. RNDr. Jaroslava Adamčáková, doc. MUDr. Eva Froňková, PhD., prof. MUDr. Alexandra Kolenová, PhD.
(4/2023, Encyclopedia of rare diseases ) - Prevention of pneumococcal infection – actual situation in the world and in our country (Slovakia)
prof. MUDr. Svetozár Dluholucký, CSc.
(S3/2010, Review articles )
- Molecular-genetic analysis of hereditary breast/ovarian cancer: Results of mutation testing of BRCA1 and BRCA2 genes
doc. MUDr. Juraj Kaušitz, CSc., RNDr. Miriam Milly, PhD., RNDr. Katarína Závodná, PhD., doc. MUDr. Denisa Ilenčíková, PhD., RNDr. Michal Konečný, Ing. Ľudmila Vavrová, PhD., MUDr. Iveta Mlkvá
(2/2012, Main topic ) - Hereditary cancer syndromes
RNDr. Miriam Milly, PhD., RNDr. Michal Konečný, PhD., Ing. Ľudmila Vavrová, PhD., MUDr. Olívia Hamidová, RNDr. Katarína Závodná, PhD.1, Mgr. Lenka Dolešová
(2/2015, Main topic ) - Acute promyelocytic leukemia - pathogenesis, diagnostics, prognosis (part I.)
MUDr. Iveta Oravcová
(3/2009, Review articles )
- Congenital fibrinogen disorders with thrombotic phenotype
MUDr. Miroslava Drotárová, MUDr. Tomáš Šimurda, PhD., MUDr. Monika Brunclíková, PhD., MUDr. Kristína Mária Beláková, RNDr. Jana Žolková, PhD., Ing. Ingrid Škorňová, PhD., Prof. MUDr. Ján Staško, PhD.
(1/2023, Main topic ) - 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 )
- SPG7 and multiple sclerosis: the hidden boundary between autoimmunity and hereditary neuropathy
Mgr. Lucie Fialová, PhD., Mgr. Magdaléna Mičulková Dvořáková, MUDr. Andrea Hladíková, Ph.D., MUDr. Michal Březík, FEBO, Bc. Monika Kudrejová, prim. MUDr. Dagmar Grečmalová
(1/2025, Case reports ) - Spectrum of pathogenic variants in the NOTCH3 gene in patients with CADASIL syndrome
RNDr. Miriama Juhosová, PhD., doc. MUDr. Ján Chandoga, CSc.,, RNDr. Robert Petrovič, PhD.
(1/2024, Main topic ) - The first case of Cousin syndrome with autosomal dominant inheritance
RNDr. Katarína Skalická, PhD., MPH, Mgr. Veronika Krajčovičová, PhD., MUDr. Gabriela Hrčková, MUDr. Olívia Hamidová, MUDr. Martina Frištáková, PhD., MUDr. Milan Ilčík, MUDr. Štefan Pavlík, RNDr. Eva Štefánková, PhD., MUDr. Ľubica Tichá, PhD., MPH, prof. MUDr. Ľudmila Podracká, CSc.
(1/2024, Original articles & case reports ) - Occurrence of causal DNA variants associated with SCID congenital immune disorders in the Slovak population
Mgr. Gabriela Krasňanská, RNDr. Lenka Wachsmannová, PhD., Mgr. Marian Baldovič, PhD., Mgr. Gabriela Bľandová, Mgr. Vladimír Eliaš, RNDr. Michal Konečný, PhD.
(1/2024, Original articles & case reports )