Similar articles for PMID: 12959913

Year	Number of Results
1994	2
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1

Mendelian hypertension with brachydactyly as a molecular genetic lesson in regulatory physiology.

Luft FC, Toka O, Toka HR, Jordan J, Bahring S. Luft FC, et al. Am J Physiol Regul Integr Comp Physiol. 2003 Oct;285(4):R709-14. doi: 10.1152/ajpregu.00174.2003. Am J Physiol Regul Integr Comp Physiol. 2003. PMID: 12959913 Free article. Review.

2

Genetic mechanisms of hypertension.

Allison S. Allison S. Nat Rev Nephrol. 2021 Jul;17(7):437. doi: 10.1038/s41581-021-00444-0. Nat Rev Nephrol. 2021. PMID: 33990795 No abstract available.

3

Molecular genetics of human hypertension.

Luft FC. Luft FC. Curr Opin Cardiol. 2020 May;35(3):249-257. doi: 10.1097/HCO.0000000000000722. Curr Opin Cardiol. 2020. PMID: 32068615

4

Monogenic Forms of Hypertension.

Ceccato F, Mantero F. Ceccato F, et al. Endocrinol Metab Clin North Am. 2019 Dec;48(4):795-810. doi: 10.1016/j.ecl.2019.08.009. Epub 2019 Sep 19. Endocrinol Metab Clin North Am. 2019. PMID: 31655777 Review.

5

Hypertension and Brachydactyly Syndrome Associated With Vertebral Artery Malformation Caused by a PDE3A Missense Mutation.

Fan P, Zhang D, Yang KQ, Zhang QY, Luo F, Lou Y, Liu YX, Zhang HM, Song L, Cai J, Wu HY, Zhou XL. Fan P, et al. Am J Hypertens. 2020 Feb 22;33(2):190-197. doi: 10.1093/ajh/hpz151. Am J Hypertens. 2020. PMID: 31549136 Free PMC article.

6

Clinical and Molecular Perspectives of Monogenic Hypertension.

Levanovich PE, Diaczok A, Rossi NF. Levanovich PE, et al. Curr Hypertens Rev. 2020;16(2):91-107. doi: 10.2174/1573402115666190409115330. Curr Hypertens Rev. 2020. PMID: 30963979 Free PMC article. Review.

7

Renal Dysfunction Induced by Kidney-Specific Gene Deletion of Hsd11b2 as a Primary Cause of Salt-Dependent Hypertension.

Ueda K, Nishimoto M, Hirohama D, Ayuzawa N, Kawarazaki W, Watanabe A, Shimosawa T, Loffing J, Zhang MZ, Marumo T, Fujita T. Ueda K, et al. Hypertension. 2017 Jul;70(1):111-118. doi: 10.1161/HYPERTENSIONAHA.116.08966. Epub 2017 May 30. Hypertension. 2017. PMID: 28559392 Free article.

8

The importance of genetic counseling and genetic screening: a case report of a 16-year-old boy with resistant hypertension and severe hypokalemia.

Kuang ZM, Wang Y, Wang JJ, Liu JH, Zeng R, Zhou Q, Yu ZQ, Jiang L. Kuang ZM, et al. J Am Soc Hypertens. 2017 Mar;11(3):136-139. doi: 10.1016/j.jash.2017.01.012. Epub 2017 Feb 3. J Am Soc Hypertens. 2017. PMID: 28236585

9

Syndromes that Mimic an Excess of Mineralocorticoids.

Sabbadin C, Armanini D. Sabbadin C, et al. High Blood Press Cardiovasc Prev. 2016 Sep;23(3):231-5. doi: 10.1007/s40292-016-0160-5. Epub 2016 Jun 1. High Blood Press Cardiovasc Prev. 2016. PMID: 27251484 Review.

10

Clinical effects of phosphodiesterase 3A mutations in inherited hypertension with brachydactyly.

Toka O, Tank J, Schächterle C, Aydin A, Maass PG, Elitok S, Bartels-Klein E, Hollfinger I, Lindschau C, Mai K, Boschmann M, Rahn G, Movsesian MA, Müller T, Doescher A, Gnoth S, Mühl A, Toka HR, Wefeld-Neuenfeld Y, Utz W, Töpper A, Jordan J, Schulz-Menger J, Klussmann E, Bähring S, Luft FC. Toka O, et al. Hypertension. 2015 Oct;66(4):800-8. doi: 10.1161/HYPERTENSIONAHA.115.06000. Epub 2015 Aug 17. Hypertension. 2015. PMID: 26283042

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