Pathophysiology, diagnosis, and treatment of mineralocorticoid disorders.

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2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年學術文章

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2014年學術文章

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2014年學術文章

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name

Pathophysiology, diagnosis, and treatment of mineralocorticoid disorders.

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Item

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Pathophysiology, diagnosis, and treatment of mineralocorticoid disorders.

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prefLabel

Pathophysiology, diagnosis, and treatment of mineralocorticoid disorders.

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P1476

Pathophysiology, diagnosis, and treatment of mineralocorticoid disorders.

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P2093

Steven B Magill

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P2860

Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor

Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure

A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin

Mutations in the CYP11B1 gene causing congenital adrenal hyperplasia and hypertension cluster in exons 6, 7, and 8

A novel splice-site mutation in the gamma subunit of the epithelial sodium channel gene in three pseudohypoaldosteronism type 1 families

Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I

Kelch-like 3 and Cullin 3 regulate electrolyte homeostasis via ubiquitination and degradation of WNK4

Molecular basis for hypertension in the "type II variant" of apparent mineralocorticoid excess

Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency

A de novo missense mutation of the beta subunit of the epithelial sodium channel causes hypertension and Liddle syndrome, identifying a proline-rich segment critical for regulation of channel activity

P304

1083-1119

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P31

scholarly article

P356

10.1002/CPHY.C130042

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P433

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P478

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P577

2014-07-01T00:00:00Z

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P698

24944031

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