Bartter syndrome type 3 in an elderly complicated with adrenocorticotropin-deficiency-Reference-Cited by-同舟云学术

Bartter syndrome type 3 in an elderly complicated with adrenocorticotropin-deficiency

Published:2014 Issue:9 Volume:61 Page:855-860
ISSN:0918-8959
Container-title:Endocrine Journal
language:en
Short-container-title:Endocr J

Author:

Tamagawa Eri¹,Inaba Hidefumi¹,Ota Takayuki¹,Ariyasu Hiroyuki¹,Kawashima Hiromichi¹,Wakasaki Hisao¹,Furuta Hiroto¹,Nishi Masahiro¹,Nakao Taisei¹,Kaito Hiroshi²,Iijima Kazumoto²,Nakanishi Koichi³,Yoshikawa Norishige³,Akamizu Takashi¹

Affiliation:

1. The First Department of Medicine, Wakayama Medical University, Wakayama, Japan

2. Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan

3. Department of Pediatrics, Wakayama Medical University, Wakayama, Japan

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.jstage.jst.go.jp/article/endocrj/61/9/61_EJ14-0125/_pdf

Reference22 articles.

1. 1. Bartter FC, Pronove P, Gill JR, MacCardle RC (1962) Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis: a new syndrome. Am J Med 33: 811-828.

2. 2. Simon DB, Karet FE, Hamdan JM, DiPietro A, Sanjad SA (1996) Bartter’s syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2. Nat Genet 13: 183-188.

3. 3. Simon DB, Karet FE, Rodriguez-Soriano J, Hamdan JH, DiPietro A, et al. (1996) Genetic heterogeneity of Bartter’s syndrome revealed by mutations in the K⁺ channel, ROMK. Nat Genet 14: 152-156.

4. 4. Simon DB, Bindra RS, Mansfield TA, Nelson-Williams C, Mendonca E, et al. (1997) Mutations in the chloride channel gene, CLCNKB, cause Bartter’s syndrome type III. Nat Genet 17: 171-178.

5. 5. Birkenhäger R, Otto E, Schurmann MJ, Vollmer M, Ruf EM, et al. (2001) Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure. Nat Genet 29: 310-314.

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