Nikkila H - Search Results

1

Possible association but no linkage of the HSD11B2 gene encoding the kidney isozyme of 11beta-hydroxysteroid dehydrogenase to hypertension in Black people.

White PC, Agarwal AK, Li A, Nikkila H, Pratt JH, Caulfield M, Clark A, McTernan C, Stewart PM. White PC, et al. Among authors: nikkila h. Clin Endocrinol (Oxf). 2001 Aug;55(2):249-52. doi: 10.1046/j.1365-2265.2001.01314.x. Clin Endocrinol (Oxf). 2001. PMID: 11531933

2

Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenase.

Mune T, Rogerson FM, Nikkilä H, Agarwal AK, White PC. Mune T, et al. Among authors: nikkila h. Nat Genet. 1995 Aug;10(4):394-9. doi: 10.1038/ng0895-394. Nat Genet. 1995. PMID: 7670488

3

CA-Repeat polymorphism in intron 1 of HSD11B2 : effects on gene expression and salt sensitivity.

Agarwal AK, Giacchetti G, Lavery G, Nikkila H, Palermo M, Ricketts M, McTernan C, Bianchi G, Manunta P, Strazzullo P, Mantero F, White PC, Stewart PM. Agarwal AK, et al. Among authors: nikkila h. Hypertension. 2000 Aug;36(2):187-94. doi: 10.1161/01.hyp.36.2.187. Hypertension. 2000. PMID: 10948076 Clinical Trial.

4

Genetic analysis of 11 beta-hydroxysteroid dehydrogenase.

White PC, Obeid J, Agarwal AK, Tannin GM, Nikkila H. White PC, et al. Among authors: nikkila h. Steroids. 1994 Feb;59(2):111-5. doi: 10.1016/0039-128x(94)90086-8. Steroids. 1994. PMID: 8191538 Review.

5

Defects in the HSD11 gene encoding 11 beta-hydroxysteroid dehydrogenase are not found in patients with apparent mineralocorticoid excess or 11-oxoreductase deficiency.

Nikkilä H, Tannin GM, New MI, Taylor NF, Kalaitzoglou G, Monder C, White PC. Nikkilä H, et al. J Clin Endocrinol Metab. 1993 Sep;77(3):687-91. doi: 10.1210/jcem.77.3.8370690. J Clin Endocrinol Metab. 1993. PMID: 8370690

6

Nikkila H, McMillan DR, Nunez BS, Pascoe L, Curnow KM, White PC. Nikkila H, et al. Mol Endocrinol. 2000 Sep;14(9):1351-64. doi: 10.1210/mend.14.9.0511. Mol Endocrinol. 2000. PMID: 10976914

7

Associations between aldosterone synthase gene polymorphism and the adrenocortical function in males.

Hautanena A, Lankinen L, Kupari M, Jänne OA, Adlercreutz H, Nikkilä H, White PC. Hautanena A, et al. Among authors: nikkila h. J Intern Med. 1998 Jul;244(1):11-8. doi: 10.1046/j.1365-2796.1998.00308.x. J Intern Med. 1998. PMID: 9698019 Free article.

8

Associations between human aldosterone synthase (CYP11B2) gene polymorphisms and left ventricular size, mass, and function.

Kupari M, Hautanen A, Lankinen L, Koskinen P, Virolainen J, Nikkila H, White PC. Kupari M, et al. Among authors: nikkila h. Circulation. 1998 Feb 17;97(6):569-75. doi: 10.1161/01.cir.97.6.569. Circulation. 1998. PMID: 9494027

9

Higher cerebrospinal fluid angiotensin-converting enzyme levels in neuroleptic-treated than in drug-free patients with schizophrenia.

Wahlbeck K, Ahokas A, Miettinen K, Nikkilä H, Rimón R. Wahlbeck K, et al. Among authors: nikkila h. Schizophr Bull. 1998;24(3):391-7. doi: 10.1093/oxfordjournals.schbul.a033334. Schizophr Bull. 1998. PMID: 9718631

10

Distinct biopsychosocial profiles emerge among nonpatients.

Ahlberg J, Suvinen TI, Rantala M, Lindholm H, Nikkilä H, Savolainen A, Nissinen M, Kaarento K, Sarna S, Könönen M. Ahlberg J, et al. Among authors: nikkila h. J Psychosom Res. 2002 Dec;53(6):1077-81. doi: 10.1016/s0022-3999(02)00349-5. J Psychosom Res. 2002. PMID: 12479989

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