- The role of LMNA in adipose: a novel mouse model of lipodystrophy based on the Dunnigan-type familial partial lipodystrophy mutation2009 | First Faculty of Medicine
- A mutation in the c-Fos gene associated with congenital generalized lipodystrophy2013 | Second Faculty of Medicine
- Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy2002 | Second Faculty of Medicine
- Prevalence of mutations in AGPAT2 among human lipodystrophies2003 | Second Faculty of Medicine
- Lipodystrophy related to insulin injection-often overlooked disorder2021 | Second Faculty of Medicine
- Metreleptin Robustly Increases Resting-state Brain Connectivity in Treatment-naïve Female Patients With Lipodystrophy2023 | First Faculty of Medicine
- Changes in FGF21 Serum Concentrations and Liver mRNA Expression in an Experimental Model of Complete Lipodystrophy and Insulin-Resistant Diabetes2014 | First Faculty of Medicine, Third Faculty of Medicine
- Reward Processing During Monetary Incentive Delay Task After Leptin Substitution in Lipodystrophy-an fMRI Case Series2023 | First Faculty of Medicine
- Epidermolysis bullosa simplex with progressive lipodystrophy +1Publication without faculty affiliation
- Epidermolysis bullosa simplex with progressive lipodystrophy - a new syndrome?Publication without faculty affiliation
- Autosomal recessive congenital total Lipodystrophy of the Berardinelli-Seip type: clinical features in 15 new patients1995 | Second Faculty of Medicine
- kin changes in diabetic patients2020 | Central Library of Charles University, Second Faculty of Medicine
- The origin and development of fat droplet and its role in health and illness2018 | Faculty of Medicine in Pilsen
- Skin changes in diabetic patients from a perspective of a diabetologist2007 | Second Faculty of Medicine
- Adrenocortical changes and arterial hypertension in lipoatrophic A-ZIP/F-1 mice2008 | First Faculty of Medicine
- CDG: a new case of a combined defect in the biosynthesis of N- and O-glycans2006 | Central Library of Charles University, Faculty of Medicine in Hradec Králové
- Stromal Vascular Fraction and its Role in the Management of Alopecia: A Review2019 | Third Faculty of Medicine
- Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies2011 | Second Faculty of Medicine
- Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study2008 | Second Faculty of Medicine
- Eva Seemanova 80 Years - International Medical Genetics, Prague 1971-20162019 | Second Faculty of Medicine
