Browsing by Author "247fd548-78dc-44e1-b7fc-a00a1cadc5f5"

Now showing items 1-4 of 4

    • A rational approach to the diagnosis of polycystic ovarian syndrome during adolescence Uma abordagem racional ... 
      Merino, Paulina M.; Codner Dujovne, Ethel; Cassorla Goluboff, Fernando (2011)
      Polycystic ovarian syndrome (PCOS) is a lifelong disorder characterized by hyperandrogenism and ovulatory dysfunction, with a wide spectrum of clinical symptoms and signs. Three different sets of diagnostic criteria have ...
    • Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency 
      Balasubramanian, Ravikumar; Choi, Jin Ho; Francescatto, Ludmila; Willer, Jason; Horton, Edward R.; Asimacopoulos, Eleni P.; Stankovic, Konstantina M.; Plummer, Lacey; Buck, Cassandra L.; Quinton, Richard; Nebesio, Todd D.; Mericq, Verónica; Merino, Paulina M.; Meyer, (National Academy of Sciences, 2014)
      © 2014, National Academy of Sciences. All rights reserved. Inactivating mutations in chromodomain helicase DNA binding protein 7 (CHD7) cause CHARGE syndrome, a severe multiorgan system disorder of which Isolated ...
    • Ovarian Function in Adolescents Conceived Using Assisted Reproductive Technologies 
      Merino, Paulina M.; Lopez, Patricia; Salinas, Abril; Pastene, Carolina; Ferrada Muñoz, Alex Eduardo; Cassorla Goluboff, Fernando; Codner Dujovne, Ethel (Elsevier USA, 2019)
      © 2018 North American Society for Pediatric and Adolescent Gynecology Study Objective: To compare ovarian function between adolescents conceived using assisted reproductive technology (AcART) and adolescents who were ...
    • When genetic load does not correlate with phenotypic spectrum: Lessons from the GnRH receptor (GNRHR) 
      Gianetti, Elena; Hall, Janet E.; Au, Margaret G.; Kaiser, Ursula B.; Quinton, Richard; Stewart, Jane A.; Metzger, Daniel L.; Pitteloud, Nelly; Mericq, Verónica; Merino, Paulina M.; Levitsky, Lynne L.; Izatt, Louise; Lang-Muritano, Mariarosaria; Fujimoto, Victor Y.; Dlu (2012)
      Context: A broad spectrum of GnRH-deficient phenotypes has been identified in individuals with both mono- and biallelic GNRHR mutations. Objective: The objective of the study was to determine the correlation between the ...