Expression of Aromatase, Estrogen Receptor α and β, Androgen Receptor, and Cytochrome P-450scc in the Human Early Prepubertal Testis

Esperanza Berensztein, María Sonia Baquedano, Candela R. González, +5

Pediatric Research

SpermatogenesisAndrogen ReceptorDevelopmental BiologyFertilityHormonal Receptor +12

Hypothalamic-Pituitary-Ovarian Axis during Infancy, Early and Late Prepuberty in an Aromatase-Deficient Girl Who Is a Compound Heterocygote for Two New Point Mutations of the CYP19 Gene

Alicia Belgorosky, Carolina Pepe, Roxana Marino, +4

The Journal of Clinical Endocrinology & Metabolism

Three New SF-1 <i>(NR5A1) </i>Gene Mutations in Two Unrelated Families with Multiple Affected Members: Within-Family Variability in 46,XY Subjects and Low Ovarian Reserve in Fertile 46,XX Subjects

Diana Mónica Warman, Mariana Costanzo, Roxana Marino, +13

Hormone Research in Paediatrics

Expression of the IGF System in Human Adrenal Tissues from Early Infancy to Late Puberty: Implications for the Development of Adrenarche

María Sonia Baquedano, Esperanza Berensztein, Nora Saraco, +4

Pediatric Research

Adrenal GlandDevelopmental BiologyGrowth HormoneHuman GrowthAdrenal Health +12

Identification and Developmental Changes of Aromatase and Estrogen Receptor Expression in Prepubertal and Pubertal Human Adrenal Tissues

María Sonia Baquedano, Nora Saraco, Esperanza Berensztein, +6

The Journal of Clinical Endocrinology & Metabolism

Decrease in the Expression of the 3β-Hydroxysteroid Dehydrogenase Gene in Human Adrenal Tissue during Prepuberty and Early Puberty: Implications for the Mechanism of Adrenarche

Andrea Dardis, Nora Saraco, Marco A. Rivarola, +1

Pediatric Research

Adrenal GlandDevelopmental BiologyEndocrine MechanismMedicine3β-Hydroxysteroid Dehydrogenase Gene +11

Five New Cases of 46,XX Aromatase Deficiency: Clinical Follow-Up From Birth to Puberty, a Novel Mutation, and a Founder Effect

Roxana Marino, Natalia Pérez Garrido, Mariana Costanzo, +12

The Journal of Clinical Endocrinology & Metabolism

Preserved Fertility in a Patient with a 46,XY Disorder of Sex Development due to a New Heterozygous Mutation in the <b><i>NR5A1/SF-1 </i></b>Gene: Evidence of 46,XY and 46,XX Gonadal Dysgenesis Phenotype Variability in Multiple Members of an Affected Kindred

Marta Ciaccio, Mariana Costanzo, Gabriela Guercio, +13

Hormone Research in Paediatrics

Role of IGFs and Insulin in the Human Testis During Postnatal Activation: Differentiation of Steroidogenic Cells

Esperanza Berensztein, María Sonia Baquedano, Carolina Pepe, +5

Pediatric Research

Developmental BiologyGrowth HormoneHuman GrowthPostnatal ActivationDevelopmental Endocrinology +7

The cytochrome P450 aromatase lacking exon 5 is associated with a phenotype of nonclassic aromatase deficiency and is also present in normal human steroidogenic tissues

Carolina Pepe, Nora Saraco, María Sonia Baquedano, +7

Clinical Endocrinology