Belgorosky, Alicia
Consejo Nacional de Investigaciones Científicas y Técnicas · Garrahan Hospital
7 papers on CoChatORCID 0000-0002-4234-400X
Most cited papers
- Verified
Steroid 21‐hydroxylase gene mutational spectrum in 454 Argentinean patients: genotype–phenotype correlation in a large cohort of patients with congenital adrenal hyperplasia
Marino, R., Ramirez, P., Galeano, J., Perez Garrido, N., Rocco, C., Ciaccio, M., Warman, D. M., Guercio, G., Chaler, E., Maceiras, M., et al. (2011) · Clinical Endocrinology
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 98
- Verified
Decrease in the expression of the 3β-hydroxysteroid dehydrogenase gene in human adrenal tissue during prepuberty and early puberty: implications for the mechanism of adrenarche
Dardis, A., Saraco, N., Rivarola, M. A., & Belgorosky, A. (1999) · Pediatric Research
Adrenal Hormones and DisordersSexual Differentiation and Disorders
Cited by 45
- Verified
Progressive Decrease in Serum Sex Hormone-Binding Globulin from Infancy to Late Prepuberty in Boys
BELGOROSKY, A., & RIVAROLA, M. A. (1986) · The Journal of Clinical Endocrinology & Metabolism
Hormonal and reproductive studiesHypothalamic control of reproductive hormones
Cited by 42
- Verified
Two Novel Mutations of the TSH-β Subunit Gene Underlying Congenital Central Hypothyroidism Undetectable in Neonatal TSH Screening
Baquedano, M. S., Ciaccio, M., Dujovne, N., Herzovich, V., Longueira, Y., Warman, D. M., Rivarola, M. A., & Belgorosky, A. (2010) · The Journal of Clinical Endocrinology & Metabolism
Thyroid Disorders and TreatmentsGenomics and Rare Diseases
Cited by 41
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Progressive Increase in Nonsex Hormone-Binding Globulin-Bound Testosterone and Estradiol From Infancy to Late Prepuberty in Girls*
BELGOROSKY, A., & RIVAROLA, M. A. (1988) · The Journal of Clinical Endocrinology & Metabolism
Hypothalamic control of reproductive hormonesHormonal and reproductive studies
Cited by 36
- Verified
Ehlers–Danlos Syndrome: Molecular and Clinical Characterization of TNXA/TNXB Chimeras in Congenital Adrenal Hyperplasia
Marino, R., Garrido, N. P., Ramirez, P., Notaristéfano, G., Moresco, A., Touzon, M. S., Vaiani, E., Finkielstain, G., Obregón, M. G., Balbi, V., et al. (2021) · The Journal of Clinical Endocrinology & Metabolism
Connective tissue disorders researchSexual Differentiation and Disorders
Cited by 23
- Verified
Unique dominant negative mutation in the N-terminal mitochondrial targeting sequence of StAR, causing a variant form of congenital lipoid adrenal hyperplasia
Baquedano, M. S., Guercio, G., Marino, R., Berensztein, E., Costanzo, M., Bailez, M., Vaiani, E., Maceiras, M., Ramirez, P., Chaler, E., et al. (2013) · The Journal of Clinical Endocrinology & Metabolism
Adrenal Hormones and DisordersSexual Differentiation and Disorders
Cited by 19
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