Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Human Immunology|September 25, 2012
TYK2 rs34536443 polymorphism is associated with a decreased susceptibility to endometriosis-related infertilityCarla Peluso, Denise M Christofolini, Cecília S Goldman, et al.
Human Immunology|January 7, 2012
The possible role of genetic variants in autoimmune-related genes in the development of endometriosisBianca Bianco, Gustavo M André, Fábia L Vilarino, et al.
Genetic Testing and Molecular Biomarkers|August 9, 2011
Genetic variants in fibrinolytic system-related genes in infertile women with and without endometriosisAriel Brandes, Denise M Christofolini, Camila M Cavalheiro, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|September 12, 2018
Kisspeptin/GPR54 System: What Do We Know About Its Role in Human Reproduction?Camila M Trevisan, Erik Montagna, Renato de Oliveira, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|March 21, 2015
AMH and AMHR2 polymorphisms and AMH serum level can predict assisted reproduction outcomes: a cross-sectional studyCarla Peluso, Fernando L A Fonseca, Guilherme G Gastaldo, et al.
International Braz J Urol : Official Journal of the Brazilian Society of Urology|May 12, 2011
Chromosomal and molecular abnormalities in a group of Brazilian infertile men with severe oligozoospermia or non-obstructive azoospermia attending an infertility serviceFernanda A Mafra, Denise M Christofolini, Bianca Bianco, et al.
American Journal of Medical Genetics. Part A|April 17, 2025
Compound Heterozygous Variants in ZSWIM7 Gene Linked to Infertility and Its Role in Gonadal DevelopmentDenise M Christofolini, Guilherme Pinn, Thainá Vilella, et al.
Archives of Medical Research|December 11, 2013
Aberrant telomerase expression in the endometrium of infertile women with deep endometriosisFernanda A Mafra, Denise M Christofolini, Viviane Cavalcanti, et al.
Fertility and Sterility|February 21, 2012
Genetic association study of polymorphisms FOXP3 and FCRL3 in women with endometriosisCaio P Barbosa, Juliana S Teles, Tatiana G Lerner, et al.
Arquivos Brasileiros De Cardiologia|July 1, 2009
22q11.2 deletion in patients with conotruncal heart defect and del22q syndrome phenotypeSintia Iole Nogueira Belangero, Fernanda T S Bellucco, Leslie Domenici Kulikowski, et al.
Pageof 4