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The Journal of Clinical Endocrinology and Metabolism|November 22, 2014
Five new cases of 46,XX aromatase deficiency: clinical follow-up from birth to puberty, a novel mutation, and a founder effectRoxana Marino, Natalia Perez Garrido, Mariana Costanzo, et al.Clinical Endocrinology|May 26, 2011
Steroid 21-hydroxylase gene mutational spectrum in 454 Argentinean patients: genotype-phenotype correlation in a large cohort of patients with congenital adrenal hyperplasiaRoxana Marino, Pablo Ramirez, Jesica Galeano, et al.The Biochemical Journal|February 3, 2023
GLI1 interaction with p300 modulates SDF1 expression in cancer-associated fibroblasts to promote pancreatic cancer cells migrationRenzo E Vera, María J Lamberti, Luciana L Almada, et al.Hormone Research in Paediatrics|September 24, 2010
Three new SF-1 (NR5A1) 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 subjectsDiana Monica Warman, Mariana Costanzo, Roxana Marino, et al.Hormone Research in Paediatrics|August 22, 2012
Preserved fertility in a patient with a 46,XY disorder of sex development due to a new heterozygous mutation in the NR5A1/SF-1 gene: evidence of 46,XY and 46,XX gonadal dysgenesis phenotype variability in multiple members of an affected kindredMarta Ciaccio, Mariana Costanzo, Gabriela Guercio, et al.Pageof 14