Fardella CE - Search Results

1

Aldosterone promotes autoimmune damage by enhancing Th17-mediated immunity.

Herrada AA, Contreras FJ, Marini NP, Amador CA, González PA, Cortés CM, Riedel CA, Carvajal CA, Figueroa F, Michea LF, Fardella CE, Kalergis AM. Herrada AA, et al. Among authors: fardella ce. J Immunol. 2010 Jan 1;184(1):191-202. doi: 10.4049/jimmunol.0802886. Epub 2009 Nov 30. J Immunol. 2010. PMID: 19949098

2

[11 beta-hydroxysteroid dehydrogenase type 2 activity in Chilean patients with hypertension].

Mosso L, Carvajal C, Campino C, Rojas A, González A, Barraza A, Montero J, Fardella C. Mosso L, et al. Rev Med Chil. 2002 Nov;130(11):1201-8. Rev Med Chil. 2002. PMID: 12587501 Spanish.

3

Two homozygous mutations in the 11 beta-hydroxysteroid dehydrogenase type 2 gene in a case of apparent mineralocorticoid excess.

Carvajal CA, Gonzalez AA, Romero DG, González A, Mosso LM, Lagos ET, Hevia Mdel P, Rosati MP, Perez-Acle TO, Gomez-Sanchez CE, Montero JA, Fardella CE. Carvajal CA, et al. Among authors: fardella ce. J Clin Endocrinol Metab. 2003 Jun;88(6):2501-7. doi: 10.1210/jc.2002-021909. J Clin Endocrinol Metab. 2003. PMID: 12788846

4

Primary aldosteronism and hypertensive disease.

Mosso L, Carvajal C, González A, Barraza A, Avila F, Montero J, Huete A, Gederlini A, Fardella CE. Mosso L, et al. Among authors: fardella ce. Hypertension. 2003 Aug;42(2):161-5. doi: 10.1161/01.HYP.0000079505.25750.11. Epub 2003 Jun 9. Hypertension. 2003. PMID: 12796282

5

Congenital lipoid adrenal hyperplasia caused by a novel splicing mutation in the gene for the steroidogenic acute regulatory protein.

González AA, Reyes ML, Carvajal CA, Tobar JA, Mosso LM, Baquedano P, Solar A, Venegas A, Fardella CE. González AA, et al. Among authors: fardella ce. J Clin Endocrinol Metab. 2004 Feb;89(2):946-51. doi: 10.1210/jc.2003-030345. J Clin Endocrinol Metab. 2004. PMID: 14764819

6

Novel intronic mutation of MEN1 gene causing familial isolated primary hyperparathyroidism.

Carrasco CA, González AA, Carvajal CA, Campusano C, Oestreicher E, Arteaga E, Wohllk N, Fardella CE. Carrasco CA, et al. Among authors: fardella ce. J Clin Endocrinol Metab. 2004 Aug;89(8):4124-9. doi: 10.1210/jc.2003-032101. J Clin Endocrinol Metab. 2004. PMID: 15292357

7

[Free urinary cortisol is elevated in patients with low-renin essential hypertension].

Krall P, Mosso L, Carvajal C, Rojas A, Fardella C. Krall P, et al. Rev Med Chil. 2004 Sep;132(9):1053-9. doi: 10.4067/s0034-98872004000900005. Rev Med Chil. 2004. PMID: 15543761 Spanish.

8

Biochemical and genetic characterization of 11 beta-hydroxysteroid dehydrogenase type 2 in low-renin essential hypertensives.

Carvajal CA, Romero DG, Mosso LM, González AA, Campino C, Montero J, Fardella CE. Carvajal CA, et al. Among authors: fardella ce. J Hypertens. 2005 Jan;23(1):71-7. doi: 10.1097/00004872-200501000-00015. J Hypertens. 2005. PMID: 15643127

9

[Microsatellite marker AGAT of the mineralocorticoid receptor gene is associated with plasma renin activity in patients with essential hypertension].

Muñoz-Brauning CR, Carvajal CA, Mosso LM, Valdivia G, Fardella CE. Muñoz-Brauning CR, et al. Among authors: fardella ce. Rev Med Chil. 2005 Dec;133(12):1415-23. doi: 10.4067/s0034-98872005001200002. Epub 2006 Jan 27. Rev Med Chil. 2005. PMID: 16446868 Free article. Spanish.

10

New splicing mutation of MEN1 gene affecting the translocation of menin to the nucleus.

Tala HP, Carvajal CA, González AA, Garrido JL, Tobar J, Solar A, Campino C, Arteaga E, Fardella CE. Tala HP, et al. Among authors: fardella ce. J Endocrinol Invest. 2006 Nov;29(10):888-93. doi: 10.1007/BF03349192. J Endocrinol Invest. 2006. PMID: 17185897

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