Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Hypokalemia and SLC12A3[original query] |
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Case-control study of the role of the Gitelman's syndrome gene in essential hypertension. Endocrine journal 2008 May 55 (2): 305-10. Aoi Noriko, Nakayama Tomohiro, Sato Naoyuki, Kosuge Kotoko, Haketa Akira, Sato Mikano, Soma Masayos |
[Mutational analysis of a thiazide-sensitive Na-Cl cotransporter (SLC12A3) gene in a Japanese population--the Iwaki Health Promotion Project]. Rinsho byori. The Japanese journal of clinical pathology 2009 Apr 57 (4): 391-6. Yasujima Minoru, Tsutaya Sho |
Genetic predictors of thiazide-induced serum potassium changes in nondiabetic hypertensive patients. Hypertension research : official journal of the Japanese Society of Hypertension 2014 Aug 37 (8): 759-64. Huang Chin-Chou, Chung Chia-Min, Hung Shuen-Iu, Leu Hsin-Bang, Lin Liang-Yu, Huang Po-Hsun, Wu Tao-Cheng, Lin Shing-Jong, Pan Wen-Harn, Chen Jaw-W |
Mutation profile and treatment of Gitelman syndrome in Chinese patients. Clinical and experimental nephrology 2016 May . Wang Fen, Shi Chuan, Cui Yunying, Li Chunyan, Tong An |
Clinical and genetic analyses of Chinese patients with Gitelman syndrome. Genetics and molecular research : GMR 2016 15 (2): . Miao M, Zhao C Q, Wang X L, Shan Z |
Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like Syndrome. Journal of Korean medical science 2016 Jan 31 (1): 47-54. Lee Jae Wook, Lee Jeonghwan, Heo Nam Ju, Cheong Hae Il, Han Jin S |
Clinical and Genetic Characteristics in Patients With Gitelman Syndrome. Kidney international reports 2019 1 4 (1): 119-125. Fujimura Junya, Nozu Kandai, Yamamura Tomohiko, Minamikawa Shogo, Nakanishi Keita, Horinouchi Tomoko, Nagano China, Sakakibara Nana, Nakanishi Koichi, Shima Yuko, Miyako Kenichi, Nozu Yoshimi, Morisada Naoya, Nagase Hiroaki, Ninchoji Takeshi, Kaito Hiroshi, Iijima Kazumo |
Type 2 diabetes mellitus caused by Gitelman syndrome-related hypokalemia: A case report. Medicine 2020 7 99 (29): e21123. He Guangyu, Gang Xiaokun, Sun Zhonghua, Wang Ping, Wang Guixia, Guo Weiyi |
Rapidly Progressing to ESRD in an Individual with Coexisting ADPKD and Masked Klinefelter and Gitelman Syndromes. Genes 2022 3 13 (3): . Peces Ramón, Peces Carlos, Mena Rocío, Cuesta Emilio, García-Santiago Fe Amalia, Ossorio Marta, Afonso Sara, Lapunzina Pablo, Nevado Juli |
Clinical Features and Unusual Heterozygous Mutations in Patients with Renal Hypokalemia. Clinical laboratory 2024 10 70 (10): . Yongjing Zhang, Zhihao Wu, Lingguang Luo, Shanshan Deng, Shaogang |
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