Annals of Pediatric Endocrinology & Metabolism

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Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes

Hyun Ah Jeong, Yoon Kyoung Park, Yeong Sang Jung, Myung-Hyun Nam, Hyo-Kyoung Nam, Kee Hyoung Lee, Young-Jun Rhie

Ann Pediatr Endocrinol Metab. 2015;20(4):230-234. Published online December 31, 2015
DOI: https://doi.org/10.6065/apem.2015.20.4.230

Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes

Hyun Ah Jeong, Yoon Kyoung Park, Yeong Sang Jung, Myung-Hyun Nam, Hyo-Kyoung Nam, Kee Hyoung Lee, Young-Jun Rhie

Annals of Pediatric Endocrinology & Metabolism. 2015;20(4):230

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Functional polymorphisms in the mineralocorticoid receptor and amirolide-sensitive sodium channel genes in a patient with sporadic pseudohypoaldosteronism

Keiko Arai, Yoshiko Nakagomi, Mitsue Iketani, Yoshie Shimura, Shin Amemiya, Kenji Ohyama, Tamotsu Shibasaki

Human Genetics. 2003;112(1):91-97

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Mineralocorticoid Receptor Polymorphisms

R.H. DeRijk, E.R. de Kloet

Encyclopedia of Stress. 2007;744-748

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Molecular characterization of the mineralocorticoid receptor in pseudohypoaldosteronism

Maria Christina Zennaro, Pascale Borensztein, Xavier Jeunemaitre, Decio Armanini, Pierre Corvol, Florent Soubrier

Steroids. 1995;60(1):164-167

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Functional Consequences of Mutations and Polymorphisms in Gonadotropin and Gonadotropin Receptor Genes

ILPO HUHTANIEMI

The Ovary. 2004;55-78

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Mutations and Polymorphisms, and Their Functional Consequences, in Gonadotropin and Gonadotropin Receptor Genes

Ilpo Huhtaniemi, Adolfo Rivero-Müller

The Ovary. 2019;127-148

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Pseudohypoaldosteronism Type 1 due to a Novel Mutation in the Mineralocorticoid Receptor Gene

Lindsey A. Loomba-Albrecht, Mato Nagel, Andrew A. Bremer

Hormone Research in Paediatrics. 2010;73(6):482-486

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Polymorphisms in androgen and estrogen receptor genes: effects on male aging

Min Jiang, Ilpo Huhtaniemi

Experimental Gerontology. 2004;39(11-12):1603-1611

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Mineralocorticoid receptor mutations are the principal cause of renal type 1 pseudohypoaldosteronism

Lucie Pujo, Jérôme Fagart, Françoise Gary, Dimitris T. Papadimitriou, Aurélie Claës, Xavier Jeunemaître, Maria-Christina Zennaro

Human Mutation. 2007;28(1):33-40

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Common functional mineralocorticoid receptor polymorphisms modulate the cortisol awakening response: Interaction with SSRIs

Melanie D. Klok, Sophie A. Vreeburg, Brenda W.J.H. Penninx, Frans G. Zitman, E. Ron de Kloet, Roel H. DeRijk

Psychoneuroendocrinology. 2011;36(4):484-494

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