Fardella, C E
Pontificia Universidad Católica de Chile
12 papers on CoChatORCID 0000-0002-5500-4434
Most cited papers
- Verified
Case detection, diagnosis, and treatment of patients with primary aldosteronism: an Endocrine Society clinical practice guideline
Funder, J. W., Carey, R. M., Fardella, C., Gomez-Sanchez, C. E., Mantero, F., Stowasser, M., Young, W. F., & Montori, V. M. (2008) · The Journal of Clinical Endocrinology & Metabolism
Hormonal Regulation and HypertensionAdrenal Hormones and Disorders
Cited by 1,554
- Verified
Primary Hyperaldosteronism in Essential Hypertensives: Prevalence, Biochemical Profile, and Molecular Biology1
Fardella, C. E., Mosso, L., Gómez-Sánchez, C., Cortés, P., Soto, J., Gómez, L., Pinto, M., Huete, A., Oestreicher, E., Foradori, A., et al. (2000) · The Journal of Clinical Endocrinology & Metabolism
Hormonal Regulation and HypertensionRenin-Angiotensin System Studies
Cited by 463
- Verified
A possible association between primary aldosteronism and a lower β-cell function
Mosso, L. M., Carvajal, C. A., Maiz, A., Ortiz, E. H., Castillo, C. R., Artigas, R. A., & Fardella, C. E. (2007) · Journal of Hypertension
Hormonal Regulation and HypertensionPancreatic function and diabetes
Cited by 94
- Verified
Increased levels of oxidative stress, subclinical inflammation, and myocardial fibrosis markers in primary aldosteronism patients
Stehr, C. B., Mellado, R., Ocaranza, M. P., Carvajal, C. A., Mosso, L., Becerra, E., Solis, M., García, L., Lavandero, S., Jalil, J., et al. (2010) · Journal of Hypertension
Hormonal Regulation and HypertensionRenin-Angiotensin System Studies
Cited by 88
- Verified
Genetic variation in P450c11AS in Chilean patients with low renin hypertension
Fardella, C. E., Rodriguez, H., Montero, J., Zhang, G., Vignolo, P., Rojas, A., Villarroel, L., & Miller, W. L. (1996) · The Journal of Clinical Endocrinology & Metabolism
Hormonal Regulation and HypertensionRenin-Angiotensin System Studies
Cited by 77
- Verified
Deletion of amino acids Asp487-Ser488-Phe489 in human cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency.
Fardella, C. E., Zhang, L. H., Mahachoklertwattana, P., Lin, D., & Miller, W. L. (1993) · The Journal of Clinical Endocrinology & Metabolism
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 72
- Verified
Beneficial effects of mineralocorticoid receptor blockade in experimental non‐alcoholic steatohepatitis
Pizarro, M., Solís, N., Quintero, P., Barrera, F., Cabrera, D., Rojas‐de Santiago, P., Arab, J. P., Padilla, O., Roa, J. C., Moshage, H., et al. (2015) · Liver International
Liver Disease Diagnosis and TreatmentLiver physiology and pathology
Cited by 66
- Verified
Molecular biology of mineralocorticoid metabolism
Fardella, C. E., & Miller, W. L. (1996) · Annual Review of Nutrition
Hormonal Regulation and HypertensionAdrenal Hormones and Disorders
Cited by 60
- Verified
Gene conversion in the CYP11B2 gene encoding P450c11AS is associated with, but does not cause, the syndrome of corticosterone methyloxidase II deficiency.
Fardella, C. E., Hum, D. W., Rodriguez, H., Zhang, G., Barry, F. L., Ilicki, A., Bloch, C. A., & Miller, W. L. (1996) · The Journal of Clinical Endocrinology & Metabolism
Hormonal Regulation and HypertensionAdrenal Hormones and Disorders
Cited by 60
- Verified
Salt-wasting congenital adrenal hyperplasia: Detection of mutations in CYP21B gene in a Chilean population1
Fardella, C. E., Poggi, H., Pineda, P., Soto, J., Torrealba, I., Cattani, A., Oestreicher, E., & Foradori, A. (1998) · The Journal of Clinical Endocrinology & Metabolism
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 35
- Verified
Artificial mutations in P450c11AS (aldosterone synthase) can increase enzymatic activity: a model for low-renin hypertension?
Fardella, C. E., Rodriguez, H., Hum, D. W., Mellon, S. H., & Miller, W. L. (1995) · The Journal of Clinical Endocrinology & Metabolism
Hormonal Regulation and HypertensionRenin-Angiotensin System Studies
Cited by 31
- Verified
Mutations in the CYP21B gene in a Chilean population with simple virilizing congenital adrenal hyperplasia
Fardella, C. E., Poggi, H., Soto, J., Torrealba, I., Cattani, A., Ugarte, F., Cortinez, A., & Foradori, A. (2000) · Journal of Endocrinological Investigation
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 11
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