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- PRION DISEASES OF MAN (WITH EMPHASIS ON THE CREUTZFELDT-JAKOB DISEASE)
doc. MUDr. Vlastimil Mayer, DrSc.
(12/2007, Consilium ) - CYSTIC FIBROSIS
MUDr. Hana Kayserová
(3/2007, clearly ) - 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 ) - Molecular genetics of dyslipidemy
Ing. Jaroslav A. Hubáček, CSc., MUDr. Michal Vrablík, PhD.
(4/2009, Topic of the year ) - Cystic fibrosis in adults
MUDr. Libor Fila, Ph.D.
(4/2015, Review articles ) - New perspectives of the treatment of migraine
MUDr. Rudolf Kotas, Ph.D.
(3/2019, Interdisciplinary consilium )
- Violent behavior and possibilities of its modification
MUDr. Jan Vevera, MUDr. Tereza Uhrová, MUDr. Roman Jirák, CSc., MUDr. Ilja Žukov, CSc., Mgr. Pavel Stopka, Ph.D., Ing. Mgr. Vojtěch Ort
(6/2002, Review articles ) - Is pharmacogenetic prediction of therapeutic efficacy of paroxetine possible?
MUDr. Martina Čižmáriková, PhD., MUDr. Jozef Dragašek, PhD., MUDr. Zuzana Vidová, MUDr. Silvia Žofčáková, MUDr. Silvia Kitková, prof. MVDr. Ján Mojžiš, CSc.
(2/2012, Original articles & case reports ) - Pathological gambling
Mgr. Omar Šerý, Ph.D.
(4/2001, Review articles ) - Neurochemical correlates of suicidal behavior
MUDr. Michal Patarák
(3/2014, Review articles ) - CLINICAL BENEFIT OF PHARMACOGENETICS IN PSYCHIATRY
doc. MUDr. Ladislav Hosák, Ph.D.
(4/2006, Review articles )
- Therapeutic advances in hereditary muscular disorders
MUDr. Stanislav Voháňka, CSc., MBA
(3/2011, Review articles ) - Ionové kanály a epilepsia
prof. MUDr. Ľubomír Lisý, DrSc.
(4/2005, Main topic ) - RNA interferencia – nový nástroj génovej terapie
Bc. Branislav Kusenda, RNDr. Šárka Pospíšilová, Ph.D.
(2/2006, Main topic ) - GENETIKA PARKINSONOVEJ CHOROBY
MUDr. Pavel Ressner, MUDr. Katarína Kollárová, prof. MUDr. Petr Kaňovský, CSc.
(6/2007, Review articles ) - 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 ) - Familial amyloid polyneuropathy
doc. MUDr. Peter Špalek, PhD.
(6/2013, Main topic ) - Budoucí možnosti genové terapie bolesti
RNDr. Omar Šerý, Ph.D., Prof. William Didden, MD., Ph.D.
(2/2006, Main topic ) - Genetická forma humánnych prionových chorôb
MUDr. Eva Mitrová, DrSc.
(2/2006, Main topic ) - Adult-onset huntington disease phenocopies
doc. MUDr. Jan Roth, CSc., MUDr. Martin Kucharík, MUDr. Jiří Klempíř, Ph.D.
(3/2009, Review articles ) - Clinical and genetic heterogenity of dopa-responsive dystonia
MUDr. Ján Necpál
(3/2015, Video case reports ) - Pompe disease – pathogenesis, clinical features, diagnosis and enzyme replacement therapy
doc. MUDr. Peter Špalek, PhD.
(1/2009, Review articles ) - 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 ) - Trigeminal lesions
MUDr. Jolana Marková
(5/2012, Main topic ) - The significance of correct algorithm of the diagnostics and treatment of migraine in the prophylactic treatment against calcitonin gene-related peptide
MUDr. Rudolf Kotas, Ph.D., MUDr. Ondřej Slach, MUDr. František Jelínek, MUDr. Jolana Mračková, Ph.D.
(2/2022, Review articles ) - 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 ) - Pyridoxine-dependent epilepsy – new trends in diagnosis and treatment
MUDr. Lia Elstnerová, doc. RNDr. Lenka Fajkusová, CSc., MUDr. Štefania Rusnáková, doc. MUDr. Hana Ošlejšková, Ph.D., Mgr. Eva Jansová, Ph.D., Mgr. Pavla Šultesová, doc. MUDr. Dalibor Valík, Ph.D.
(5/2010, Review articles ) - Ideopathic generalized epilepsies
doc. MUDr. Hana Ošlejšková, Ph.D., MUDr. Štefánia Aulická
(4/2014, Review articles ) - Spinal muscular atrophy – diagnostics, therapy, research
RNDr. Petra Hedvičáková, MUDr. Jana Haberlová, Ph.D., MUDr. Alžběta Slabá, MUDr. Tereza Doušová
(6/2016, Main topic ) - Juvenile form of Huntington's disease
doc. MUDr. Jan Roth, CSc.
(3/2012, Main topic ) - Parkinsonian syndrome and extrapyramidal symptoms in neurodegenerative diseases associated with disorders of iron metabolism
MUDr. Petra Bártová, Ph.D.
(3/2012, Main topic ) - Genetic causes of parkinsonism with focus on spinocerebellar ataxias
MUDr. Matej Škorvánek, doc. MUDr. Peter Valkovič, PhD.
(3/2012, Main topic ) - Komorbidita epileptických záchvatov
h. doc. MUDr. Vladimír Donáth, PhD.
(5/2005, Main topic ) - Dravet syndrome: severe myoclonic epilepsy in infancy
doc. RNDr. Lenka Fajkusová, CSc., doc. MUDr. Hana Ošlejšková, Ph.D., MUDr. Ondřej Horák, MUDr. Pavlína Danhofer, Mgr. Jana Pavloušková
(1/2015, Review articles ) - Pompe disease – case report of the juvenile form
MUDr. Katarína Okáľová, PhD., Mgr. Slavomíra Mattošová, doc. MUDr. Ján Chandoga CSc., MUDr. Viera Holecová
(1/2015, Case reports ) - The molecular genetic and biochemical aspects of neurogenetic disorders; (Diseases caused by molecular genetic pathology of structural constituents of nervous system – part 1)
doc. MUDr. Ján Chandoga, CSc.1, MUDr. Petra Jungová, RNDr. Katarína Kolejáková, Ph.D., RNDr. Robert Petrovič, PhD., MUDr. Juraj Štofko, MBA
(4/2013, Review articles ) - Primární bolesti hlavy – léčba dnes a zítra
MUDr. Jolana Marková , MUDr. Rudolf Kotas, Ph.D.
(3/2018, Review articles ) - New perspectives of the treatment of migraine
MUDr. Rudolf Kotas, Ph.D.
(3/2017, Review articles ) - 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 ) - Familial hemiplegic migraine
MUDr. Jiří Mastík
(6/2010, Review articles ) - Molekulárno-genetické a biochemické aspekty niektorých dedičných neurologických ochorení Ochorenia podmienené molekulárno-genetickými patológiami štrukturálnych konštituentov nervového systému – 2. časť
MUDr. Petra Jungová, RNDr. Robert Petrovič, PhD., MUDr. Juraj Štofko, MBA, doc. MUDr. Ján Chandoga, CSc., RNDr. Katarína Kolejáková
(5/2013, Review articles ) - Eptinezumab – the new anti-CGRP monoclonal antibody for prophylactic treatment of migraine
MUDr. Rudolf Kotas, Ph.D.
(6/2022, Review articles ) - A case of motor and sensory neuropathy and cerebrospinal multiple sclerosis in one patient
prof. MUDr. Petr Kaňovský, CSc., MUDr. Martin Nevrlý, MUDr. Vladimíra Sládková, MUDr. Pavel Otruba, doc. MUDr. Stanislav Buřval, Ph.D., prof. MUDr. Zdeněk Lukáš, CSc.
(1/2010, Case reports ) - Migraine – from pathophysiology to monoclonal antibodies
MUDr. Rudolf Kotas, Ph.D.
(4/2019, Review articles ) - Sporadic form of late-onset transthyretin familial amyloid polyneuropathy – first case report in Slovak Republic
doc. MUDr. Peter Špalek, CSc., MUDr. Ivan Martinka, PhD., Mgr. Slavomíra Mattošová, PhD., doc. MUDr. Ján Chandoga, CSc., MUDr. Jakub Veverka
(4/2019, Events ) - Myotonic dystrophies
MUDr. Radim Mazanec, Ph.D., Mgr. Zuzana Mušová, Ph.D.
(4/2012, Main topic ) - Hereditary neuropathy
MUDr. Tomáš Nedělka, MUDr. Radim Mazanec, Ph.D., MUDr. Veronika Potočková, MUDr. Dana Šafka Brožková, Ph.D., MUDr. Petra Laššuthová, Ph.D., RNDr. Jana Neupauerová, MUDr. Jana Haberlová, Ph.D.
(2/2015, Review articles ) - Genetic aspects of „idiopathic“ epilepsies
doc. RNDr. Lenka Fajkusová, CSc., doc. MUDr. Robert Kuba, Ph.D., MUDr. Štefania Rusnáková, doc. MUDr. Hana Ošlejšková, Ph.D., Mgr. Pavla Šultesová, Mgr. Eva Jansová, Mgr. Marie Chovančíková, Ph.D.
(2/2012, Review articles )
- Hereditárna pankreatitída u 17-ročného pacienta
MUDr. Iveta Čierna, PhD., MUDr. Vladimír Cingel
(3/2011, Case reports ) - Martin s bolesťami brucha a krvácaním z nosa
prof. MUDr. László Kovács, DrSc., MPH, MUDr. Anna Hlavatá, PhD., doc. MUDr. Denisa Ilenčíková, PhD., RNDr. Milan Škorvaga, PhD., MUDr. Eva Pálová, MUDr. Gabriela Magyarová
(3/2011, Genetics Daily ) - Gilbert‘s syndrome – a disease, risk factor, but also an evolutionary advantage?
MUDr. Iveta Čierna, PhD., RNDr. Katarína Hlinková, MUDr. Gabriela Nagyová, Mgr. Michaela Čižmárová, Mgr. Slavka Požgayová
(3/2015, Review articles ) - Ciliopathies and polycystic kidney disease
prof. MUDr. László Kovács, DrSc., MPH, doc. MUDr. Denisa Ilenčíková, PhD., MUDr. Gabriela Nagyová, Mgr. Adriána Krajčiová
(4/2012, Review articles ) - ACTUAL TRENDS IN PREVENTION AND TREATMENT OF TYPE 1 DIABETES MELLITUS
MUDr. Stanislava Koloušková, CSc., MUDr. Pavla Mendlová
(4/2007, Review articles ) - Marfan syndrome – clinical experiences
MUDr. Andrea Hladíková, Ph.D., MUDr. Eva Šilhánová, Ing. Petra Cibulková
(3/2014, Original articles & Case reports ) - New perspectives in cytogenetics and classification of pediatric acute lymphoblastic leukemia
Mgr. Anita Vaská, Mgr. Ágnes Baranyaiová, RNDr. Katarína Skalická, PhD., doc. MUDr. Alexandra Kolenová, PhD.
(2/2017, Review articles ) - Thomas, who had head as a rock...
prof. MUDr. László Kovács, DrSc., MPH, doc. MUDr. Ľudmila Košťálová, CSc., doc. MUDr. Denisa Ilenčíková, PhD., MUDr. Júlia Horáková, PhD., MUDr. Anna Hlavatá, PhD., MPH
(6/2013, Case reports ) - Angelman syndrome, cause of epilepsy in infants
doc. MUDr. Pavol Sýkora, CSc., MUDr. Lucia Švecová, MUDr. Miriam Kolníková, MUDr. Alžbeta Vicenová
(6/2014, Original articles & Case reports ) - 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 ) - FOLIC ACID AND CONGENITAL ANOMALIES
prof. MUDr. László Kovács, DrSc., MPH, MUDr. Lucia Šabová
(1/2008, Review articles ) - A rare cause of severe obesity in 4 years old boy
doc. MUDr. Ľudmila Košťálová, CSc., MUDr. Zuzana Pribilincová, CSc., MUDr. Eva Vitáriušová, PhD., MUDr. Anna Hlavatá, PhD., MPH, RNDr. Emil Polák, PhD., MUDr. Mária Poprocká, prof. MUDr. Ľudevít Kádaši, DrSc.
(2/2015, Original articles & Case reports ) - CONGENITAL HYPOTHYROIDISM
prof. MUDr. Olga Hníková, CSc.
(3/2005, Review articles ) - Sotos syndrome or functional (hormone-making) pituitary microadenoma as a cause of excessive growth in an 11-year-old girl?
MUDr. Alžbeta Lencsésová, MUDr. Ľubica Tichá, PhD., MUDr. Ľudmila Trejbalová, MUDr. Michaela Pietrzyková, prof. MUDr. Ľudmila Podracká, CSc.
(6/2017, Original articles & Case reports ) - Klinický obraz familiárne nízkeho vzrastu u pacientky s kostnou dyspláziou pri Léri-Weillovom syndróme
MUDr. Zuzana Pribilincová, CSc.
(4/2010, Case reports )
- 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 ) - Treatment of patients with low-risk myelodysplastic syndrome
prof. MUDr. Elena Tóthová, CSc., MUDr. Adriana Kafková, PhD.
(6/2014, Spectrum ) - Systemic treatment of malignant melanoma
MUDr. Iveta Andrezálová Vochyanová
(3/2013, Main topic ) - Changes in the new WHO classification of tumors of the central nervous system in 2016
MUDr. Marián Švajdler ml., MUDr. Boris Rychlý, PhD., doc. MUDr. Andrej Šteňo, PhD., MPH
(5/2016, Main topic ) - mTOR inhibitors in the treatment of advanced renal cell carcinoma
MUDr. Radovan Barilla, PhD., MUDr. Zuzana Syčová-Milá
(1/2009, Review articles ) - The polymorphisms of DNA-repair genes in pathogenesis of NHL
prof. MUDr. Elena Tóthová, CSc., MUDr. Adriana Kafková, PhD., RNDr. Lucia Klimčáková, PhD., prof. RNDr. Ján Šalagovič, CSc.
(6/2013, Review articles ) - Chromosomal rearrangements in lung adenocarcinoma – new treatment options
RNDr. Katarína Hlinková
(3/2014, Review articles ) - Molecular markers of targeted therapy in oncology malignancies
RNDr. Katarína Hlinková
(2/2010, Review articles ) - Lynch syndrome – novelties in diagnostics and therapy
MUDr. Denisa Ilenčíková, RNDr. Zdena Bartošová, CSc., prof. MUDr. Pavel Babál, CSc.
(2/2010, Review articles ) - Hereditary form of malignant melanoma associated with mutations in CDKN2A gene
doc. MUDr. Juraj Kaušitz, CSc., RNDr. Zdena Bartošová, CSc., RNDr. Miriam Milly, PhD., RNDr. Michal Konečný, PhD., RNDr. Katarína Závodná, PhD., RNDr. Eva Weismanová, PhD.
(2/2010, Review articles ) - Hereditary breast ovarian cancer: molecular-genetic analysis of BRCA genes
doc. MUDr. Juraj Kaušitz, CSc., RNDr. Zdena Bartošová, CSc., RNDr. Miriam Milly, PhD., RNDr. Michal Konečný, PhD., RNDr. Katarína Závodná, PhD., RNDr. Eva Weismanová, PhD.
(2/2010, Review articles ) - Treatment of ALK-rearranged non-small cell lung cancer
MUDr. Zuzana Pribulová
(6/2015, Main topic ) - Prophylactic procedures in women with gene mutations BRCA1 and BRCA2
doc. MUDr. Vladimír Bella, PhD.
(2/2012, Main topic ) - 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 ) - Diagnosis of chronic myeloid leukemia
MUDr. Ľudmila Demitrovičová, MUDr. Lucia Copáková, MUDr. Eva Mikušková, Mgr. Michaela Leitnerová
(2/2012, Topic of the year ) - The current view of the familial adenomatous polyposis (FAP)
MUDr. Vladimír Holec, doc. RNDr. Vladimír Zajac, CSc., Mgr. Zuzana Adamčíková, Ing. Mgr. Katarína Hainová, RNDr. Soňa Čierniková, PhD., Viola Števurková
(2/2012, Review articles ) - Myelodysplastic syndrome – classification, pathophysiology
prof. MUDr. Elena Tóthová, CSc.
(1/2014, Spectrum ) - Ras genes of metastatic colorectal carcinoma
RNDr. Katarína Hlinková
(4/2014, Review articles ) - The importance of biological therapy in malignant tumor of unknown primary origin
MUDr. Róbert Godál
(4/2013, Main topic ) - CORRELATION OF CHIMERISM AFTER ALLOGENEIC HAEMATOPOLETIC CELL TRANSPLANTATION WITH GvHD OCCURRENCE AND RELAPSE
MUDr. Miriam Ladická, MUDr. Monika Krivošíková, Mgr. Ivana Shawkatová, prof. MUDr. Milan Buc, DrSc., MUDr. Eva Bojtárová, PhD., RNDr. Mária Kušíková, MUDr. Branislav Czako, doc. MUDr. Martin Mistrík, MUDr. Sabína Šufliarska, doc. RNDr. Katarína Kozlíková, CSc.
(4/2006, Original articles ) - Bioptická diagnostika myeloproliferatívnych neoplázií
MUDr. Juraj Marcinek, PhD., prof. MUDr. Lukáš Plank, CSc.
(2/2018, Spectrum ) - Publikujeme v zahraničí
(4/2013, Information & comments ) - Nové perspektívy v liečbe pokročilého a metastatického HR+ HER2- karcinómu prsníka
MUDr. Miroslava Malejčíková, MUDr. Silvia Jurišová
(2/2018, Review articles ) - New research and therapeutic targets in molecular genetics of tumors − our research potential
RNDr. Alena Gábelová, CSc., Mgr. Miroslav Chovanec, PhD., RNDr. Ján Sedlák, DrSc., Mgr. Lucia Kučerová, PhD., RNDr. Božena Smolková, PhD., Mgr. Viera Kajabová, PhD., RNDr. Ivana Fridrichová, CSc.
(1/2015, Main topic ) - Hereditary forms of breast cancer
MUDr. Vladimír Bella, PhD.
(2/2009, Review articles ) - Increased production of HE4 by tumour tissues and its importance of measurement in patients with malignant tumours
MUDr. Jaroslav Weissensteiner, doc. Mgr. Eva Babušíková, PhD.
(1/2015, Review articles ) - Zriedkavý nádor hrudníka: malígny pleurálny mezotelióm
MUDr. Lucia Denková, MUDr. František Sándor, PhD., FCCP
(3/2018, Main topic ) - Polycytémia vera – súčasný pohľad na diagnostiku a liečbu
MUDr. Antónia Hatalová, PhD., MUDr. Jana Malinová, doc. MUDr. Martin Mistrík, PhD., prof. MUDr. Angelika Bátorová, CSc.
(3/2018, Spectrum ) - Genetic perspectives in prediction of cytostatic toxicity
prof. MUDr. László Kovács, DrSc., MPH, MUDr. Sabína Šufliarska, MUDr. Alica Dzurenková, doc. MUDr. Beáta Mladosievičová, CSc., RNDr. Gabriel Minárik, PhD.
(4/2009, 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 ) - The treatment of ALK-positive NSCLC ceritinib – view panel of experts Purpose: To find out the opinion of the Panel of experts on the effectiveness and
doc. MUDr. Peter Beržinec, CSc., MUDr. Peter Kasan
(6/2015, Information & comments ) - Role of stem cells in tumor initiation, metastasis formation and their use in cancer therapy
doc. Ing. Čestmír Altaner, DrSc., Ing. Veronika Altanerová, CSc.
(1/2010, Review articles ) - Molecular pathology of selected types of ovarian cancer
doc. MUDr. Karol Kajo, PhD.
(5/2014, Main topic ) - Pheochromocytoma and paraganglioma
MUDr. Mária Rečková
(2/2013, Main topic ) - Current possibilities of immunotherapy in the treatment of malignant melanoma
MUDr. Iveta Andrezálová Vochyanová
(4/2016, Main topic ) - Targeted terapy of gastric cancer
MUDr. Vanda Ušáková, PhD.
(5/2014, Review articles ) - ABC transporters: multidrug resistance and different types of human diseases
prof. MUDr. Stanislav Špánik, CSc., doc. MUDr. Viera Lehotská, PhD., MUDr. Katarína Rauová, RNDr. Eva Weismanová, PhD., RNDr. Ľubomír Horváth, CSc., Mgr. Ján Markus, PhD., MUDr. Ladislav Sopko
(1/2012, Review articles ) - Genetic counseling as part of genetic analysis
RNDr. Zdena Bartošová, CSc., RNDr. Michal Konečný, PhD., doc. MUDr. Denisa Ilenčíková, PhD., MUDr. Olívia Hamidová
(2/2015, 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 ) - 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 ) - Molecular pathology of diffuse large B-cell lymphoma – a review
prof. MUDr. Lukáš Plank, CSc., MUDr. Tomáš Balhárek, PhD., MUDr. Jozef Mičák
(2/2015, Spectrum ) - New perspectives in cytogenetics and classification of pediatric acute lymphoblastic leukemia
Mgr. Anita Vaská, Mgr. Ágnes Baranyaiová, RNDr. Katarína Skalická, PhD., doc. MUDr. Alexandra Kolenová, PhD.
(1/2017, Review articles ) - Actual therapeutic strategy of patients with non small cell lung cancer with EML4-ALK rearrangement
MUDr. Juraj Mazal, MUDr. Michal Urda, RNDr. Anna Farkašová, PhD.
(1/2017, Review articles ) - Recent applications of massive parallel sequencing in cancer diagnosis and treatment
RNDr. Regína Lohajová Behulová, PhD., Mgr. Romana Valenčíková, PhD., Mgr. Lukáš Šebest, PhD., Mgr. Lenka Dolešová, PhD., Mgr. Tomáš Slamka, Mgr. Eva Krascsenitsová, PhD.
(3/2022, Original articles ) - Chronic lymphocytic leukemia – genetics
MUDr. Lucia Copáková, RNDr. Michaela Leitnerová, RNDr. Barbora Piačková
(2/2014, Oncohematology Review ) - Molecular pathology of prostate carcinoma (part 1)
MUDr. Katarína Macháleková, doc. MUDr. Karol Kajo, PhD, Mgr. Petra Tilandyová, RNDr. Zora Lasabová, PhD., MUDr. Roman Tomaškin
(3/2009, Review articles ) - SHOX2 gene methylation as a diagnostic marker of lung cancer
RNDr. Michal Konečný, PhD., Mgr. Lenka Dolešová, doc. RNDr. Iveta Waczulíková, PhD., doc. MUDr. Ivan Majer, CSc., Mgr. Ján Markus, PhD.1, MUDr. Helena Novosadová
(2/2016, Original articles & case reports ) - SIGNIFICANCE OF GENE EXPRESSION PROFILING FOR PREDICTION OF PROGNOSIS AND THERAPY RESPONSE IN BREAST CARCINOMA
prof. MUDr. Lukáš Plank, CSc., doc. MUDr. Karol Kajo, PhD.
(4/2008, Review articles ) - Prognostické faktory pri chronickej lymfocytovej leukémii
MUDr. Ľudmila Demitrovičová, PhD.
(4/2018, Review articles )
- ALLERGY – SYSTEMIC DISEASE WITH TOPICAL MANIFESTATIOS
MUDr. Václava Gutová
(1/2007, Interdisciplinary overviews ) - Hereditárne ichtyózy – nová klasifikácia a pokroky v diagnostike a liečbe
doc. MUDr. Dušan Buchvald, PhD., MUDr. Zuzana Rajczyová
(3/2018, Review articles ) - 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 )
- Genetic background and management in patients with factor XIII deficiency – our experience
MUDr. Ivana Plameňová, PhD., MBA, RNDr. Jana Žolková, PhD., doc. MUDr. Juraj Sokol, PhD., prof. MUDr. Ján Staško, PhD.
(1/2021, Main topic ) - Genetic background sticky platelet syndrome in patients with abortion
prof. MUDr. Peter Kubisz, DrSc., MUDr. Juraj Chudej, PhD., MUDr. Juraj Sokol, PhD., RNDr. Mária Škereňová, RNDr. Jela Ivanková, prof.MUDr. Ján Staško, PhD.
(2/2016, Main topic )
- 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 )