Příběh sv. Starosty: Legenda, historie a endokrinní kontext jednoho zázraku

Avendaño A, Paradisi I, Cammarata-Scalisi F, Callea M. 5-𝛂-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review. Hormones (Athens) 2018; 17(2): 197–204. 

Bertelloni S, Scaramuzzo RT, Parrini D, et al. Early diagnosis of 5alpha-reductase deficiency in newborns. Sex Dev 2007; 1(3): 147–51.  

Galli-Tsinopoulou A, Serbis A, Kotanidou EP, et al. 46,XY disorder of sex development due to 17-beta hydroxysteroid dehydrogenase type 3 deficiency in an infant of Greek origin. J Clin Res Pediatr Endocrinol 2018; 10(1): 74–78.  

Houk CP, Hughes IA, Ahmed SF, Lee PA; Writing Committee for the International Intersex Consensus Conference Participants. Summary of consensus sta tement on intersex disorders and their management. International Intersex Consensus Conference. Pediatrics 2006; 118(2): 753–7.  

Jakouběová V. Podmalba na skle Ukřižování svaté Starosty. Dostupné na: https://www.muzeum-turnov.cz/prosinec-top-exponat/

Nascimento RLP, de Andrade Mesquita IM, Gondim R, et al. Gender identity in patients with 5-alpha reductase deficiency raised as females. J Pediatr Urol 2018; 14(5): 419.e1–419.e6.  

Rosler A. 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population. Pediatr Endocrinol Rev 2006; 3: 455–461.