Enter your login e-mail to the account
Search
Search parameters
Search results
- Osteomalacia and rickets
MUDr. Pavol Masaryk, CSc.
(1/2009, Review articles ) - Colorectal cancer in general practice – how to identify individuals at increased risk and when to screen first degree relatives
MUDr. Tomáš Grega, Ph.D., prof. MUDr. Jan Bureš, CSc., Mgr. Ondřej Ngo, Ph.D., Ing. Monika Ambrožová, Mgr. Renata Chloupková, RNDr. Ondřej Májek, Ph.D., prof. MUDr. Miroslav Zavoral, Ph.D., doc. MUDr. Štěpán Suchánek, Ph.D.
(1/2026, Interdisciplinary consilium ) - PROSTATE CANCER
MUDr. Peter Kertes, Milan Blaško, Marián Hladík, Ján Hoffmann
(9/2007, Topic ) - Iron – friend or foe of the men?
doc. MUDr. Radana Neuwirtová, CSc., prof. MUDr. Přemysl Poňka, Ph.D.
(2/2011, Review articles ) - CHRONIC PANCREATITIS SURGERY
prof. MUDr. Juraj Pechan, CSc., MUDr. Daniel Pinďák, PhD.
(10/2006, Main topic ) - CURRENT OVERVIEW OF THE HEREDITARY METABOLIC DISORDERS
MUDr. Katarína Fabriciová
(10/2006, 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 ) - PATHOPHYSIOLOGY OF HEART FAILURE
prof. MUDr. Fedor Šimko, CSc.
(9/2006, Main topic )
- Genetics of hereditary spastic paraplegias
RNDr. Anna Uhrová Mészárosová, Ph.D., prof. MUDr. Pavel Seeman, Ph.D.
(5/2019, Main topic ) - Therapeutic advances in hereditary muscular disorders
MUDr. Stanislav Voháňka, CSc., MBA
(3/2011, Review articles ) - The role of biopsy in the diagnosis of neuromuscular disorders in the molecular biological era
prof. MUDr. Josef Zámečník, Ph.D.
(1/2022, Main topic ) - Progressive supranuclear palsy and Guam parkinsonian complex or a Canadian in the Pacific – John C. Steele (1934–2022)“
Prof. MUDr. Petr Kaňovský, CSc., FEAN , prof. MUDr. Kateřina Menšíková, Ph.D., MBA, FEAN, prof. Ing. Miroslav Strnad, CSc., DSc., RNDr. Alena Vydrová, Mgr. Pavla Dubská, Ph.D.
(5/2024, online attachment ) - Genetics of Alzheimer's Disease in Clinical Practice
MUDr. Martin Vyhnálek , Ph.D., MUDr. Emílie Vyhnálková, Ph.D., doc. MUDr. Jan Laczó, Ph.D.
(5/2019, Main topic ) - Hereditary chorea with a tendency to insanity and adult onset: 150 years since George Huntington and his disease
MUDr. Ján Necpál, MUDr. Michal Patarák, PhD.
(1/2022, online attachment ) - Vybrané primárne svalové ochorenia podmienené poruchami štruktúry a funkcie iónových kanálov a príbuzné nozologické jednotky: myotónie a paramyotónia
doc. MUDr. Egon Kurča, PhD.
(4/2005, Main topic ) - Mitochondrial syndromes with nervous system damage
MUDr. František Cibulčík, PhD.
(6/2013, Main topic ) - Familial amyloid polyneuropathy
doc. MUDr. Peter Špalek, PhD.
(6/2013, Main topic ) - Nationwide screening of Pompe disease in patients with unspecified muscle weakness, hyperCKemia, and respiratory insufficiency
MUDr. Lívie Mensová, MUDr. Olesja Parmová
(4/2018, Informations ) - Hereditárne motorické axonopatie a neuronopatie
prof. MUDr. Ľubomír Lisý, 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 ) - Cerebral amyloid angiopathy
MUDr. Veronika Vestenická, PhD., MUDr. Stanislav Šutovský, PhD., MUDr. Zuzana Čarnická, PhD., doc. MUDr. Branislav Kollár, PhD., MUDr. Pavel Šiarnik, MUDr. Lucia Krížová
(3/2015, Case reports ) - Dědičné periferní neuropatie
MUDr. Jana Haberlová, MUDr. Radim Mazanec Ph.D., MUDr. Pavel Seeman Ph.D.
(3/2006, Review articles ) - Clinical and genetic heterogenity of dopa-responsive dystonia
MUDr. Ján Necpál
(3/2015, Video case reports ) - Classic form of Huntington’s disease manifested by asymmetric Parkinson’s syndrome with rigidity responding to levodopa
doc. MUDr. Irena Rektorová, Ph.D., MUDr. Věra Zelená, Mgr. Zuzana Fanfrdlová,
(1/2009, Video case reports ) - Rare diseases and the Orphanet
MUDr. Gabriela Hrčková
(2/2021, Main topic ) - Orphan drugs in treatment of rare neuromuscular disorders
doc. MUDr. Peter Špalek, PhD.
(2/2021, Main topic ) - Spinal muscular atrophy and its differential diagnosis. A patient's case report and his journey to diagnosis
MUDr. Olesja Parmová, Ph.D.
(2/2025, Case reports ) - 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 ) - 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 ) - Family with hereditary transthyretin amyloidosis – case report
MUDr. Tomáš Bauer
(5/2022, Case reports ) - Kennedy's disease (bulbar and spinal muscular atrophy)
MUDr. Petr Ridzoň
(6/2016, Main topic ) - Late manifestation of Pompe disease
MUDr. Tomáš Kalous
(4/2014, Case reports ) - Hereditary motor neuropathies
MUDr. Radim Mazanec, Ph.D., MUDr. Veronika Potočková, MUDr. Petra Laššuthová, Ph.D., RNDr. Jana Neupauerová, MUDr. Daniel Baumgartner, MUDr. Dana Šafka-Brožková, Ph.D., Prof. MUDr. Pavel Seeman, Ph.D.
(6/2016, Main topic ) - 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 ) - AUTOSOMÁLNĚ RECESIVNÍ A X-VÁZANÉ ATAXIE
MUDr. Alena Zumrová, Ph.D.
(5/2007, Main topic ) - AUTOSOMÁLNĚ DOMINANTNÍ SPINOCEREBELÁRNÍ ATAXIE
MUDr. Alena Zumrová, Ph.D.
(5/2007, Main topic ) - Gene-based therapy for neuromuscular diseases
MUDr. Aneta Podsedníková, MUDr. Lenka Juříková, Ph.D.
(2/2026, Main topic ) - Spinal muscular atrophy – diagnostics, therapy, research
RNDr. Petra Hedvičáková, MUDr. Jana Haberlová, Ph.D., MUDr. Alžběta Slabá, MUDr. Tereza Doušová
(6/2016, Main topic ) - Novel therapeutic options in hereditary neurodegenerative cerebellar ataxias
doc. MUDr. Martina Bočková, Ph.D., MUDr. Tomáš Boušek, MUDr. Jaroslava Paulasová Schwabová, Ph.D., doc. MUDr. Martin Vyhnálek, Ph.D.
(2/2026, Trends in neuropharmacotherapy ) - Transthyretin-related hereditory amyloidosis and its neurological manifestations
MUDr. Jana Laštovičková
(2/2011, Case reports ) - Juvenile form of Huntington's disease
doc. MUDr. Jan Roth, CSc.
(3/2012, Main topic ) - Patient with myopathy… or not?
MUDr. Jana Junkerová, MUDr. Eva Kovalová, MUDr. Martin Sabela
(1/2024, Case reports ) - 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 ) - K problematike neurodegeneratívnych ochorení
prof. MUDr. Pavel Varsik, DrSc., prof. MUDr. Jozef Černáček, DrSc., MUDr. Zoltán Goldenberg, prof. MUDr. Pavol Traubner, Ph.D.
(1/2002, Review articles ) - Periferní neuropatie u dětí
MUDr. Josef Kraus, CSc. , MUDr. Ivana Perníková, Marie Brožová
(3/2018, Main topic ) - 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 ) - The importance of monitoring asymptomatic carriers of the TTR gene mutation in hereditary transthyretin amyloidosis – a neurologist´s perspective
MUDr. Ivan Martinka, PhD., MUDr. Alexandra Mražíková
(6/2025, Review articles ) - Genetická heterogenita a fenotypová variabilita tzv. asociovaných príznakov u neurodegeneratívnych ochorení. Pes cavus
prof. MUDr. Pavel Varsik, DrSc., MUDr. Zoltán Goldenberg, MUDr. Pavol Kučera, PhD., MUDr. Darina Buranová, PhD., prof. MUDr. Pavel Traubner, PhD.
(3/2004, Case reports ) - Friedreich ataxia – what we have learned in 160 years
prof. MUDr. Martin Vališ, Ph.D., FEAN, MUDr. Simona Halúsková, MUDr. David Matyáš, MUDr. Pavlína Hemerková
(4/2024, Review articles ) - Can I drive a truck? – very late-onset Friedreich's ataxia
MUDr. Kristýna Janotová, MUDr. Zdeněk Kunáš, doc. MUDr. Svatopluk Ostrý, Ph.D.
(3/2025, Trends in neuropharmacotherapy ) - Muscular dystrophy of adult age
MUDr. Petr Ridzoň, MUDr. Kateřina Matějová, MUDr. Adéla Škvorová
(3/2019, Main topic ) - Familial hemiplegic migraine
MUDr. Jiří Mastík
(6/2010, Review articles ) - Deep brain stimulation in dystonia
doc. MUDr. Robert Jech, Ph.D.
(5/2013, Main topic ) - 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 ) - MONOGENNĚ PODMÍNĚNÉ FORMY PARKINSONOVY NEMOCI
doc. MUDr. Jan Roth, CSc.
(3/2007, Review articles ) - The late-onset form of Pompe disease
MUDr. Radka Mišurová, MUDr. Věra Malinová
(4/2021, Case reports ) - 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 ) - 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 ) - Charcot-Marie-Toothdisease as the most common inherited neuropathy: a case report from our department
MUDr. Alžbeta Hlucháňová, MUDr. Michal Kozmon, doc. MUDr. Pavol Kučera, PhD., MUDr. Mário Lazar
(2/2020, Case reports ) - Metabolic myopathies
MUDr. Hana Kolářová, Ph.D.,, doc. RNDr. MUDr. Pavel Ješina, Ph.D.
(1/2022, Main topic ) - Hereditary neuropathies in childhood
Prof. MUDr. Pavel Seeman, Ph.D.
(1/2022, Main topic )
- Neuromuscular diseases in childhood
MUDr. Dana Šišková
(5/2013, Review articles ) - Atopic dermatitis – theory and practical guidelines
MUDr. Zuzana Nevoralová, Ph.D.
(4/2017, Review articles ) - 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 ) - 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 ) - 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 ) - Juvenile retinoschisis
MUDr. Klára Hodálová, MUDr. Daniel Havalda, MUDr. Beáta Bušányová, PhD., MBA, doc. MUDr. Dana Tomčíková, PhD., MHA, prof. MUDr. Anton Gerinec, CSc.
(1/2022, Original articles & Case reports ) - Periodic fever syndromes – PFAPA syndrome
prof. MUDr. László Kovács, DrSc., MPH, MUDr. Anna Hlavatá, PhD., Ing. Ema Paulovičová, Mgr. Marian Baldovič, MUDr. Tomáš Dallos, PhD.
(3/2009, Original articles ) - Prolonged fever and fever of unknown origin in children
prof. MUDr. László Kovács, DrSc., MPH
(1/2009, Review articles ) - Edemas – causes and differential diagnosis
prof. MUDr. Ľudmila Podracká, CSc., prof. MUDr. László Kovács, DrSc., MPH
(6/2013, Review articles ) - Neurologic symptoms of mitochondrial diseases
doc. MUDr. Pavol Sýkora, CSc., MUDr. Miriam Kolníková
(6/2009, Review articles ) - Od retardace růstu k transplantaci ledviny
MUDr. Andrea Konečná, prof. MUDr. Zdeněk Doležel, CSc., MUDr. Dana Dostálková
(2/2018, Original articles & Case reports ) - Hereditary fructose intolerance
MUDr. Katarína Brennerová, PhD., Tatiana Martinkovičová, Ing. Anna Šalingová, Doc. MUDr. Vladimír Bzdúch, CSc.
(5/2022, Review articles ) - 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 ) - Diferenciálna diagnostika café-au-lait makúl
MUDr. Zuzana Novaresio, MUDr. Anna Hlavatá, PhD., MPH
(3/2018, Review articles ) - THE PROBLEM OF NATAL AND NEONATAL TEETH
MUDr. Romana Ivančaková, CSc., Ana Lucía Seminario, DDS, MDS
(1/2004, 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 ) - Nephrocalcinosis – etiology, diagnostics, treatment
MUDr. Dagmar Urbanová, PhD., prof. MUDr. Ľudmila Podracká, CSc.
(6/2022, Guidelines )
- Genetically determined renal diseases that a urologist does or may encounter in the practice
MUDr. Jiří Kladenský
(3/2019, From the frontier of urology ) - Parapelvic renal cysts
doc. MUDr. Jana Reiterová, Ph.D.
(4/2023, From the frontier of urology )
- Cytogenetic and molecular cytogenetic methods in hemato-oncology
Mgr. Petra Nováková, MUDr. Denisa Ilenčíková, PhD.
(2/2010, Review articles ) - Systemic amyloidosis
MUDr. Lenka Zahradová, Ph.D.
(6/2016, Spectrum ) - 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 ) - Prophylactic procedures in women with gene mutations BRCA1 and BRCA2
doc. MUDr. Vladimír Bella, PhD.
(2/2012, Main topic ) - Gastric cancer – the view of the gastroenterologist
MUDr. Boris Pekárek, PhD., MUDr. Ľuboš Žitňan, MUDr. Michal Makovník, MUDr. Juraj Májek, PhD.
(3/2011, Review articles ) - SYSTEMIC THERAPY OF NEUROENDOCRINE TUMORS
MUDr. Tomáš Šálek
(4/2006, Review articles ) - 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 ) - GASTRIC CANCER
MUDr. Tomáš Šálek
(2/2007, Review articles ) - METASTATIC CARCINOMA OF THE PARATHYROID GLAND – RARE CAUSE OF PRIMARY HYPERPARATHYREOSIS
MUDr. Katarína Macháleková, MUDr. Pavol Povinec, PhD., MUDr. Peter Kentoš, MUDr. Mikuláš Pura, MUDr. Peter Szépe, MUDr. Ondrej Bencúr, MUDr. Peter Vaňuga, PhD.
(5/2008, Original articles ) - Hereditary forms of breast cancer
MUDr. Vladimír Bella, PhD.
(2/2009, Review articles ) - Histopathology of bone tumors
prof. MUDr. Štefan Galbavý, DrSc.
(2/2011, Review articles ) - Pheochromocytoma and paraganglioma
MUDr. Mária Rečková
(2/2013, Main topic ) - Current trends in the surgical treatment of thyroid tumors
MUDr. Róbert Králik, PhD., prof. MUDr. Štefan Durdík, PhD., MHA
(5/2015, Main topic ) - CHEMOPREVENTION OF BREAST CANCER
prof. MUDr. Ľudovít M. Jurga, DrSc., prof. MUDr. Myrón Malý, CSc.
(5/2007, 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 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 ) - 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 ) - 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 ) - ADVANCES IN NEUROBLASTOMA DIAGNOSTICS AND TREATMENT
MUDr. Viera Bajčiová, CSc., MUDr. Pavel Mazánek, prof. MUDr. Jaroslav Šterba, PhD.,, doc. RNDr. Petr Kuglík, CSc., doc. RNDr. Renata Veselská, PhD.
(4/2008, Review articles )
- Hereditárne ichtyózy – nová klasifikácia a pokroky v diagnostike a liečbe
doc. MUDr. Dušan Buchvald, PhD., MUDr. Zuzana Rajczyová
(3/2018, Review articles ) - Urticaria – part II.: Overview of different types of urticaria
doc. MUDr. Tibor Danilla, CSc., MUDr. Michaela Petrovajová,
(2/2012, Review articles ) - Genetic background of skin tumors
MUDr. Zuzana Murárová, PhD.
(3/2024, Topic of the year ) - Morbus Bourneville-Pringle
MUDr. Martina Škvarlová, MUDr. Klára Martinásková PhD, MUDr. Beáta Nagyová, MUDr. Marta Koleničová
(1/2010, Original articles & case reports )
- 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 ) - Bleeding thrombocytopathies
doc. MUDr. Ján Staško, PhD., prof. MUDr. Peter Kubisz, DrSc., MUDr. Juraj Sokol, MUDr. Lucia Stančiaková, Ing. Ingrid Škorňová
(2/2013, Review articles )
- Anaesthesia for Charcot-Marie-Tooth disease – case report
doc. MUDr. Jozef Firment, PhD., MUDr. Bc. Peter Firment
(1/2012, Case reports )
- 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 )