All Stories

  1. Underdiagnosis of central precocious puberty in boys with loss-of-function mutations of MKRN3
  2. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty
  3. Causes, diagnosis, and treatment of central precocious puberty
  4. Time Course of Central Precocious Puberty Development Caused by an MKRN3 Gene Mutation: A Prismatic Case
  5. 12. Approach to the Patient With Hypogonadotropic Hypogonadism
  6. New Causes of Central Precocious Puberty: The Role of Genetic Factors
  7. Approach to the Patient With Hypogonadotropic Hypogonadism
  8. Kisspeptin and Clinical Disorders
  9. Insulin-like growth factor system on adrenocortical tumorigenesis
  10. Disorders of Sex Development and Hypogonadism: Genetics, Mechanism, and Therapies
  11. Genetics basis for GnRH-dependent pubertal disorders in humans
  12. Nonsense Mutations inFGF8Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency
  13. The Role of Prokineticins in the Pathogenesis of Hypogonadotropic Hypogonadism
  14. Role of Kisspeptin/GPR54 System in Human Reproductive Axis
  15. The neurokinin B pathway in human reproduction
  16. Insights learned from L457(3.43)R, an activating mutant of the human lutropin receptor
  17. An Inhibin B and Estrogen-Secreting Adrenocortical Carcinoma Leading to Selective FSH Suppression
  18. Familial Hyperestrogenism in Both Sexes: Clinical, Hormonal, and Molecular Studies of Two Siblings
  19. Mutações ativadoras do gene do receptor do hormônio luteinizante em meninos com testotoxicose
  20. Naturally Occurring Mutations of the Luteinizing Hormone Receptor Gene Affecting Reproduction