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Lilia Baldazzi Selected Research

Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency

5/2020Correction: Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations.
5/2014Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations.

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Lilia Baldazzi Research Topics

Disease

3Congenital Adrenal Hyperplasia (Hyperplasia, Congenital Adrenal)
01/2020 - 01/2017
2Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency
05/2020 - 05/2014
2Congenital Hypothyroidism (Cretinism)
01/2013 - 11/2009
1Hyperandrogenism
09/2019
1XX Disorders of Sex Development 46 (Female Pseudohermaphroditism)
09/2019
146,XY Disorder of Sex Development (Male Pseudohermaphroditism)
01/2018
1Rare Diseases (Rare Disease)
01/2017
1Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
05/2014
1Hypothyroidism
11/2009
1Hypogonadism (Hypergonadotropic Hypogonadism)
08/2006
1Gonadoblastoma
06/2005

Drug/Important Bio-Agent (IBA)

3Oxidoreductases (Dehydrogenase)IBA
01/2020 - 01/2017
2Steroid 11-beta-Hydroxylase (11 beta-Hydroxylase)IBA
05/2020 - 05/2014
2EnzymesIBA
01/2020 - 09/2019
2Mixed Function Oxygenases (Monooxygenases)IBA
01/2020 - 09/2019
2Steroid 21-Hydroxylase (21 Hydroxylase)IBA
01/2020 - 09/2019
2Thyrotropin Receptors (Thyrotropin Receptor)IBA
01/2013 - 11/2009
1steroidogenic acute regulatory proteinIBA
01/2020
1Cholesterol Side-Chain Cleavage Enzyme (CYP11A1)IBA
01/2020
1Hydroxysteroid DehydrogenasesIBA
01/2020
1Proteins (Proteins, Gene)FDA Link
01/2020
1Steroid 17-alpha-Hydroxylase (17 alpha Hydroxylase)IBA
01/2020
1Aromatase deficiencyIBA
09/2019
1AndrogensIBA
09/2019
1Steroidogenic Factor 1IBA
01/2018
1SaltsIBA
01/2017
1Thyrotropin (Thyroid-Stimulating Hormone)FDA Link
11/2009
1Hormones (Hormone)IBA
11/2009
1LHRH Receptors (Gonadotropin-Releasing Hormone Receptor)IBA
08/2006

Therapy/Procedure

1Therapeutics
01/2017
1Castration
06/2005