- Neuronal ceroid lipofuscinosis with cardiac involvement2019 | Faculty of Medicine in Pilsen
- Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis.2009 | First Faculty of Medicine
- Study of sleep architecture in neuronal ceroid lipofuscinosis (NCL)Publication without faculty affiliation
- Diagnosis of neuronal ceroid lipofuscinosis type 2 (CLN2 disease): Expert recommendations for early detection and laboratory diagnosis2016 | First Faculty of Medicine
- Juvenil neuronal ceroid lipofuscinosisPublication without faculty affiliation
- Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease)2016 | First Faculty of Medicine
- The NCLs: Evolution of the Concept and Classification2011 | First Faculty of Medicine
- Autosomal dominant adult neuronal ceroid lipofuscinosis: a novel form of NCL with granular osmiophilic deposits without palmitoyl protein thioesterase 1 deficiency2003 | First Faculty of Medicine
- Autosomal dominant adult neuronal ceroid lipofuscinosis: a novel form of NCL with granular osmiophilic deposits without palmitoyl protein thioesterase 1 deficiency2003 | Faculty of Physical Education and Sport
- Neuronal ceroid lipofuscinosis. Closing chapter of a long story (An overview)2000 | First Faculty of Medicine
- Expression and lysosomal targeting of CLN7, a major facilitator superfamily transporter associated with variant late-infantile neuronal ceroid lipofuscinosis2010 | First Faculty of Medicine
- Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis.2009 | Publication without faculty affiliation
- Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis2011 | First Faculty of Medicine
- Juvenille neuronal ceroid lipofuscinosis CLN 3 (Bastten, Vogt-Spielmeyer) A Report of a casePublication without faculty affiliation
- Neuronal ceroid-lipofuscinoses in the Czech Republic. III. Electrophysiological findings1998 | Second Faculty of Medicine
- Neuronal ceroid lipofuscinosis in the Czech Republic: Analysis of 57 cases. Report of the 'Prague NCL group'.1997 | Faculty of Physical Education and Sport
- NCL Nomenclature and Classification2011 | First Faculty of Medicine
- NCL Diagnosis and Algorithms2011 | First Faculty of Medicine
- Autosomal-dominant adult neuronal ceroid lipofuscinosis caused by duplication in DNAJC5 initially missed by Sanger and whole-exome sequencing2020 | First Faculty of Medicine
- CLN52011 | First Faculty of Medicine
- Morphological Diagnostic and Pathological Considerations2011 | First Faculty of Medicine
- CLN72011 | First Faculty of Medicine
- CLN22011 | First Faculty of Medicine
- Follow-up study of subunit c of mitochondrial ATP synthase (SCMAS) in Batten disease and in unrelated lysosomal disorders1997 | First Faculty of Medicine
- Cerebellar dysfunction in a family harboring the PSEN1 mutation co-segregating with a Cathepsin D variant p.A58V2013 | First Faculty of Medicine
- Bioinformatic perspectives in the neuronal ceroid lipofuscinoses2013 | First Faculty of Medicine
- Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion2018 | First Faculty of Medicine
- Enhanced expression of manganese-dependent superoxide dismutase in human and sheep CLN6 tissues2003 | First Faculty of Medicine
- Enhanced expression of manganese-dependent superoxide dismutase in human and sheep CLN6 tissues2003 | Faculty of Physical Education and Sport
- Genetics and Pathophysiology of Neurodegeneration with Brain Iron Accumulation (NBIA)2013 | First Faculty of Medicine