- Partial hypogonadotropic hypogonadism associated with the Leu266Arg and Gln106Arg mutation of the gonadotropin-releasing hormone receptor2009 | Faculty of Medicine in Pilsen, First Faculty of Medicine
- Coding sequence analysis of GNRHR and GPR54 in patients with congenital and adult-onset forms of hypogonadotropic hypogonadism2006 | Faculty of Medicine in Pilsen, First Faculty of Medicine
- Genetics of hypogonadotropic hypogonadism2000 | Faculty of Medicine in Pilsen
- Partial hypogonadotropic hypogonadism associated with the Leu266Arg and Gln106Arg mutation of the gonadotropin-releasing hormone receptor2009 | Faculty of Medicine in Pilsen
- Coding sequence analysis of GNRHR and GPR54 in patients with congenital and adult-onset forms of hypogonadotropic hypogonadism2006 | Faculty of Medicine in Pilsen
- Prevalence, phenotypic spectrum, and modes of inheritance of gonadotropin-releasing hormone receptor mutations in idiopathic hypogonadotropic hypogonadism.2001 | Faculty of Medicine in Pilsen
- Hypogonadotropic hypogonadism: spermatogenesis induction in young males, multidisciplinar cooperation.2002 | Central Library of Charles University, Second Faculty of Medicine
- Hypogonadotropic hypogonadism in a homozygous MC4R mutation carrier and the effect of sibutramine treatment on body weight and obesity-related health risks2011 | Third Faculty of Medicine
- Kal gene novel mutations in idiopathic hypogonadotropic hypogonadism (IHH): genotype-phenotype correlations2000 | Faculty of Medicine in Pilsen
- Partial hypogonadotropic hypogonadism due to a compound heterozygous mutatio of the gonadotropin releasing hormone receptor gene2000 | Faculty of Medicine in Pilsen
- Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C2021 | Central Library of Charles University
- A boy with adrenal insufficiency and DAX-1 gene defect2001 | Third Faculty of Medicine
- Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosaPublication without faculty affiliation
- The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics2001 | Faculty of Medicine in Pilsen
- Micropenis2014 | Second Faculty of Medicine
- Prader-Willi syndrome2011 | Faculty of Medicine in Hradec Králové