Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Hypertension in Pregnancy|March 6, 2019
Circulating HO-1 levels are not associated with plasma sFLT-1 and GTn HMOX1 polymorphism in preeclampsiaValeria Sandrim, Fernanda Borchers Coeli-Lacchini, Jose Eduardo Tanus-Santos, et al.
Archives of Endocrinology and Metabolism|May 19, 2026
The essential role of the redox balance in adrenal steroidogenesisJuliana Lourenço Gebenlian, Aline Faccioli Bodoni, Fernanda Borchers Coeli-Lacchini, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|February 14, 2020
USP8 Mutations and Cell Cycle Regulation in Corticotroph AdenomasClarissa Silva Martins, Renata Costa Camargo, Fernanda Borchers Coeli-Lacchini, et al.
Revista Latino-Americana De Enfermagem|August 20, 2020
Nurse empowerment through PharmacogeneticsJordana Carvalhaes de Moraes, Fernanda Daniela Dornelas Nunes, Fernanda Borchers Coeli-Lacchini, et al.
Revista Brasileira De Ginecologia E Obstetricia : Revista Da Federacao Brasileira Das Sociedades De Ginecologia E Obstetricia|June 20, 2020
Interaction Between NOS3 and HMOX1 on Antihypertensive Drug Responsiveness in PreeclampsiaValeria Cristina Sandrim, Marcelo Rizzatti Luizon, Eliane Pilan, et al.
Gene|April 11, 2013
A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiencyFernanda Borchers Coeli-Lacchini, Wendy Turatti, Paula Conde Lamparelli Elias, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|March 28, 2020
Clinical, Molecular, Functional, and Structural Characterization of CYP17A1 Mutations in Brazilian Patients with 17-Hydroxylase DeficiencyFernanda Borchers Coeli-Lacchini, Livia M Mermejo, Aline Faccioli Bodoni, et al.
European Journal of Clinical Pharmacology|January 7, 2021
Arginase II polymorphisms modify the hypotensive responses to propofol by affecting nitric oxide bioavailabilityGustavo H Oliveira-Paula, Fernanda Borchers Coeli-Lacchini, Letícia Perticarrara Ferezin, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|October 28, 2023
Accumulation of sphingosine kinase 2 protein induces malignant transformation in oral keratinocytes associated with stemness, autophagy, senescence, and proliferationLais Brigliadori Fugio, Gabriel Silva, Camila Lopes Ferraz, et al.
Clinical Endocrinology|July 25, 2014
Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defectsSabrina Soares Paulo, Fábio L Fernandes-Rosa, Wendy Turatti, et al.
Pageof 3