- Pyridoxine-dependent Epilepsy - Case Reports2017 | Faculty of Medicine in Pilsen
- Pyridoxine use in children with epilepsy: a pharmacist's point of view2016 | Faculty of Pharmacy in Hradec Králové
- treatment of mild hyperhomocysteinemia with fixed combination of folate, cyanocobalamin and pyridoxin2006 | First Faculty of Medicine
- Selected questions and answers from the Drug Information Centre: How high doses of pyridoxine are possible to administer during pregnancy?1998 | Faculty of Pharmacy in Hradec Králové
- New mutation in erythroid-specific delta-aminolevulinate synthase as the cause of X-linked sideroblastic anemia responsive to pyridoxine2011 | Faculty of Medicine in Hradec Králové
- Proconvulsant effects induced by pyridoxine in young rats1998 | Third Faculty of Medicine
- Vliv Kardioprotektinu (fixní kombinace folátu, vitaminu B12 a pyridoxinu) na mírnou hyperhomocysteinemiiPublication without faculty affiliation
- Cystathionine beta-synthase deficiency in the E-HOD registry-part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis2021 | First Faculty of Medicine, Faculty of Mathematics and Physics
- Pyridoxamine decreases the risk of progression of renl failure in patient with diabetic nephropathy. Commentary on: Am.J.Nephrol 27,2007,s.605-6142008 | First Faculty of Medicine
- Homocysteinemia in Czech Population of Juvenile Hypertonic and Normotonic Patients2003 | Third Faculty of Medicine
- Enzymatic diagnosis of homocystinuria by determination of cystathionine-beta-synthase activity in plasma using LC-MS/MS2015 | First Faculty of Medicine
- New ionophores for vitamin B1 and vitamin B6 potentiometric sensors for multivitaminic control2008 | Central Library of Charles University
- Pregnancy nausea and vomiting2023 | Third Faculty of Medicine
- Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency2017 | First Faculty of Medicine
- Chaperone therapy for homocystinuria: the rescue of CBS mutations by heme arginate2015 | First Faculty of Medicine
- Neurodegenerative diseases in the view od free radicals2017 | Third Faculty of Medicine
- Ancient origin of the CTH alelle carrying the c. 200C > T (p.T67I) variant in patients with cystathioninuria2010 | First Faculty of Medicine
- ESPGHAN/ESPEN/ESPR/CSPEN guidelines on pediatric parenteral nutrition: Vitamins2018 | First Faculty of Medicine, Second Faculty of Medicine
- Cystathionine beta-Synthase Mutations: Effect of Mutation Topology on Folding and Activity2010 | First Faculty of Medicine
- Mixed ligand palladium(II) complexes of oxalate and malonate with vitamin-B-6 molecules: synthesis, crystal structure and kinetics2003 | Faculty of Science
- West syndrome model: seek and you will find1997 | Third Faculty of Medicine
- Determination of cystathionine beta-synthase activity in human plasma by LC-MS/MS: potential use in diagnosis of CBS deficiency2011 | First Faculty of Medicine
- Disorders of Sulfur Amino Acid Metabolism2022 | First Faculty of Medicine
- Age-Specific N-Methyl-D-Aspartate - Induced Seizures: Perspectives for the West Syndrome Model1999 | Third Faculty of Medicine
- Cystathionine β-Synthase (CBS) Deficiency: Genetics2018 | First Faculty of Medicine
- Recent therapeutic approaches to cystathionine beta-synthase-deficient homocystinuria2023 | First Faculty of Medicine
- Impaired heme binding and aggregation of mutant cystathionine beta-synthase subunits in homocystinuria2001 | First Faculty of Medicine
- Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines2015 | First Faculty of Medicine
- Potential pharmacological chaperones for cystathionine beta-synthase-deficient homocystinuria2018 | First Faculty of Medicine
- Diversity of cystathionine beta-synthase haplotypes bearing the most common homocystinuria mutation c.833T>C: a possible role for gene conversion2007 | First Faculty of Medicine