María Sonia Baquedano

Author

Also Known As

M. S. Baquedano, Maria Baquedano, Maria Sonia Baquedano, María Sonia Baquedano, María S Baquedano, María Sonia Baquedano, María Sonia Baquedano

Publications

593

Citations

H-Index

Concepts

All Affiliations

Garrahan Hospital Universidad de Buenos Aires Consejo Nacional de Investigaciones Científicas y Técnicas

About

María Sonia Baquedano is an author at Garrahan Hospital specializing in developmental biology, medicine, and endocrinology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	188
2	Endocrinology	3	3	188
3	Education	1	1	51
4	Public Health	1	1	102
5	Cell Biology	1	1	35

María Sonia Baquedano

Publications

460

Citations

H-Index

Page 1

	Year	Citations
Expression of Aromatase, Estrogen Receptor α and β, Androgen Receptor, and Cytochrome P-450scc in the Human Early Prepubertal Testis Esperanza Berensztein, María Sonia Baquedano, Candela R. González, Pediatric Research SpermatogenesisAndrogen ReceptorDevelopmental BiologyFertilityHormonal Receptor	2006	102
Three New SF-1 <i>(NR5A1) </i>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 Subjects Diana Mónica Warman, Mariana Costanzo, Roxana Marino, Hormone Research in Paediatrics	2010	60
Expression of the IGF System in Human Adrenal Tissues from Early Infancy to Late Puberty: Implications for the Development of Adrenarche María Sonia Baquedano, Esperanza Berensztein, Nora Saraco, Pediatric Research Adrenal GlandDevelopmental BiologyGrowth HormoneHuman GrowthAdrenal Health	2005	51
Identification and Developmental Changes of Aromatase and Estrogen Receptor Expression in Prepubertal and Pubertal Human Adrenal Tissues María Sonia Baquedano, Nora Saraco, Esperanza Berensztein, The Journal of Clinical Endocrinology & Metabolism	2007	45
Two Novel Mutations of the TSH-β Subunit Gene Underlying Congenital Central Hypothyroidism Undetectable in Neonatal TSH Screening María Sonia Baquedano, Marta Ciaccio, Noelia Dujovne, The Journal of Clinical Endocrinology & Metabolism	2010	41
Preserved Fertility in a Patient with a 46,XY Disorder of Sex Development due to a New Heterozygous Mutation in the <b><i>NR5A1/SF-1 </i></b>Gene: Evidence of 46,XY and 46,XX Gonadal Dysgenesis Phenotype Variability in Multiple Members of an Affected Kindred Marta Ciaccio, Mariana Costanzo, Gabriela Guercio, Hormone Research in Paediatrics	2012	35
Role of IGFs and Insulin in the Human Testis During Postnatal Activation: Differentiation of Steroidogenic Cells Esperanza Berensztein, María Sonia Baquedano, Carolina Pepe, Pediatric Research Developmental BiologyGrowth HormoneHuman GrowthPostnatal ActivationDevelopmental Endocrinology	2008	35
The cytochrome P450 aromatase lacking exon 5 is associated with a phenotype of nonclassic aromatase deficiency and is also present in normal human steroidogenic tissues Carolina Pepe, Nora Saraco, María Sonia Baquedano, Clinical Endocrinology	2007	35
Unique Dominant Negative Mutation in the N-Terminal Mitochondrial Targeting Sequence of StAR, Causing a Variant Form of Congenital Lipoid Adrenal Hyperplasia María Sonia Baquedano, Gabriela Guercio, Roxana Marino, The Journal of Clinical Endocrinology & Metabolism	2012	20
A Novel Missense Mutation in the<i>HSD3B2</i>Gene, Underlying Nonsalt-Wasting Congenital Adrenal Hyperplasia. New Insight Into the Structure-Function Relationships of 3β-Hydroxysteroid Dehidrogenase Type II María Sonia Baquedano, Marta Ciaccio, Roxana Marino, The Journal of Clinical Endocrinology & Metabolism	2014	13

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