Current approaches for deciphering the molecular basis of combined anterior pituitary hormone deficiency in humans
High prevalence of PROP1 gene mutations in hungarian patients with childhood-onset combined anterior pituitary hormone deficiency
Pituitary Hormone Deficiency, Combined Familial
Frequent development of combined pituitary hormone deficiency in patients initially diagnosed as isolated growth hormone deficiency: a long term follow-up of patients from a single center
Long-term follow-up of combined pituitary hormone deficiency in two siblings with aProphet of Pit-1gene mutation
Combined Pituitary Hormone Deficiency in an Inbred Brazilian Kindred Associated with a Mutation in the PROP-1 Gene
Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations
Congenital combined pituitary hormone deficiency patients have better responses to gonadotrophin-induced spermatogenesis than idiopathic hypogonadotropic hypogonadism patients
The natural history of the R120C PROP1 mutation reveals a wide phenotypic variability in two untreated adult brothers with combined pituitary hormone deficiency
Combined pituitary hormone deficiency with unique pituitary dysplasia and morning glory syndrome related to a heterozygous <i>PROKR2</i> mutation
