Browsing by Author "López, Pamela"

Now showing items 1-2 of 2

    • Clinical features and possible founder mutation of the 8bp duplication mutation in the SLC4A11 gene causing ... 
      Romero, Pablo T.; Donoso, Rodrigo; López, Pamela; Miranda, Ana; Rodríguez, Leandro; Chrzanowsky, Dominique; Asenjo, Maria S.; Burgos, Gonzalo; Villegas, Pablo; Desir, Julie; Moya, Graciela; Herrera, Luisa M. (Taylor and Francis Ltd, 2019)
      Background: Corneal Dystrophy and Perceptive Deafness (CDPD) or Harboyan syndrome is an autosomal recessive rare disorder, characterized by congenital corneal opacities and progressive sensorineural hearing loss, which ...
    • Relationship of cortisol levels and genetic polymorphisms to antidepressant response to placebo and fluoxetine ... 
      Ventura Juncá, Raúl; Symon Maturana, Adriana; López, Pamela; Fiedler Temer, Jenny; Rojas Castillo, María Graciela; Heskia Vergara, Cristóbal; Lara, Pamela; Marín, Felipe; Guajardo, Viviana; Araya, A. Verónica; Sasso Aguirre, Jaime Alfredo; Herrera Cisterna, Luisa (BioMed Central, 2014)
      Background: Increased cortisol levels and genetic polymorphisms have been related to both major depressive disorder and antidepressant treatment outcome. The aim of this study is to evaluate the relationship between circadian ...