- Aetiology and treatment of neonatal diabetes2019 | Second Faculty of Medicine
- Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes2004 | Second Faculty of Medicine
- Mutations in the gene encoding the Kir6.2 calcium channel subunit as another onset of neonatal diabetes2006 | Second Faculty of Medicine
- Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia2012 | Faculty of Medicine in Pilsen
- Sulphonylurea treatment does not improve psychomotor development in children with KCNJ11 mutations causing permanent neonatal diabetes mellitus accompanied by developmental delay and epilepsy (DEND syndrome)2007 | Second Faculty of Medicine
- Neonatal Diabetes Mellitus Caused by Activation Mutation in the Gene Encoding the Kir6.2 Subunit of Potassium Channel: Is Insulindependency Inevitably Life-long?2005 | Second Faculty of Medicine, Third Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Neonatal diabetes mellitus2007 | Second Faculty of Medicine
- Recessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis2010 | Second Faculty of Medicine
- Clinical Heterogeneity in Patients With FOXP3 Mutations Presenting With Permanent Neonatal Diabetes2009 | Second Faculty of Medicine
- Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study2018 | Second Faculty of Medicine
- Monogenic diabetes: what should we know for correct diagnosis and treatment?2020 | Second Faculty of Medicine
- Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY)2010 | Second Faculty of Medicine
- Treatment of diabetes in small children2019 | Second Faculty of Medicine
- Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents2006 | Second Faculty of Medicine, Third Faculty of Medicine
- Monogenic forms of diabetes: they are more common than we have thought so far2014 | Second Faculty of Medicine
- Paediatric diabetes subtypes in a consanguineous population: a single-centre cohort study from Kurdistan, Iraq2024 | Second Faculty of Medicine
- A description of clinician reported diagnosis of type 2 diabetes and other non-type 1 diabetes included in a large international multicentered pediatric diabetes registry (SWEET)2016 | Second Faculty of Medicine
- Monogenic forms of diabetes mellitus2007 | Second Faculty of Medicine
- Familial mild hyperglycemia associated with a novel ABCC8-V84I mutation within three generations2011 | Second Faculty of Medicine, Third Faculty of Medicine
- GATA6 mutations cause a broad phenotypic spectrum of diabetes from pancreatic agenesis to adult-onset diabetes without exocrine insufficiency2013 | Second Faculty of Medicine
- Monogenic types of diabetes mellitus2007 | Third Faculty of Medicine
- Stay in touch with the medicine and on maternity leave2008 | Second Faculty of Medicine
- Treatment for patients with monogenic diabetes2011 | Third Faculty of Medicine
- Differential diagnosis of hyperglycemia in children and adolescent2005 | Third Faculty of Medicine
- NEUROD1 reinforces endocrine cell fate acquisition in pancreatic development2023 | Central Library of Charles University
- Frameshift mutations in the insulin gene leading to prolonged molecule of insulin in two families with Maturity-Onset Diabetes of the Young2015 | Second Faculty of Medicine, Third Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- NEUROD1 Is Required for the Early alpha and beta Endocrine Differentiation in the Pancreas2021 | Faculty of Science, Central Library of Charles University
