Zobrazeno 1 - 10
of 162
pro vyhledávání: '"Acquired Gitelman syndrome"'
Autor:
Gu, Xiangchen1, Su, Zheling1, Chen, Min1, Xu, Yanqiu1 xuyanqiu6@medmail.com.cn, Wang, Yi1 dryiwang@126.com
Publikováno v:
Nephrology. Aug2017, Vol. 22 Issue 8, p652-655. 4p.
Autor:
Kim, Yong Kyun, Song, Ho Cheol, Kim, Wan-Young, Yoon, Hye Eun, Choi, Yeong-Jin, Ki, Chang-Seok, Park, Cheol-Whee, Yang, Chul Woo, Kim, Jin, Kim, Yong-Soo, Choi, Eui Jin, Bang, Byung Kee
Publikováno v:
In American Journal of Kidney Diseases 2008 52(6):1163-1167
Publikováno v:
Rhode Island Medical Journal. Nov2018, Vol. 101 Issue 9, p36-38. 3p.
Publikováno v:
Indian Journal of Nephrology. Jul/Aug2015, Vol. 25 Issue 4, p246-247. 2p.
Publikováno v:
Cureus
Gitelman syndrome is an inherited renal disorder characterized by hypomagnesemia, hypokalemia, hypocalciuria and metabolic alkalosis linked to the genes encoding the thiazide sensitive NaCl cotransporter (NCCT) located on the distal convoluted tubule
Autor:
Mishima, Eikan, Mori, Takayasu, Sohara, Eisei, Uchida, Shinichi, Abe, Takaaki, Ito, Sadayoshi
Publikováno v:
CEN Case Reports; Nov2017, Vol. 6 Issue 2, p180-184, 5p
Autor:
Ramirez Botana, Leonardo R.
Publikováno v:
Journal of the American Society of Nephrology; October 2024, Vol. 35 Issue: 10, Number 10 Supplement 10
Akademický článek
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Autor:
Masab M; Internal Medicine, West Virginia University, Morgantown, USA., Goyal A; Internal Medicine, Einstein Medical Center, Philadelphia, USA., Abrol S; Dentistry, Smilekraft Clinic, Dharamshala, IND., Rangaswami J; Internal Medicine, Einstein Medical Center, Philadelphia, USA.
Publikováno v:
Cureus [Cureus] 2019 Jan 20; Vol. 11 (1), pp. e3923. Date of Electronic Publication: 2019 Jan 20.
Publikováno v:
CEN Case Reports
Gitelman syndrome (GS) is an autosomal recessive, salt-losing renal tubulopathy caused by mutations in the SLC12A3 gene; however, it can also be acquired in patients with autoimmune disease, especially in those with Sjögren’s syndrome. Differentia