https://scholars.lib.ntu.edu.tw/handle/123456789/514970
標題: | Response to letter to the editor: “Adrenalectomy completely cured hypertension in familial hyperaldosteronism type I patients with somatic KCNJ5 mutation” | 作者: | Lin, Yu-Fang Peng, Kang-Yung Chang, Chia-Hui Hu, Ya-Hui VIN-CENT WU SHIH-CHIEH CHUEH |
公開日期: | 2020 | 出版社: | Endocrine Society | 卷: | 105 | 期: | 5 | 起(迄)頁: | dgz110 | 來源出版物: | Journal of Clinical Endocrinology and Metabolism | URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85082542566&doi=10.1210%2fclinem%2fdgz110&partnerID=40&md5=f0c141dba9b578055ccbc8f37e651ea9 https://scholars.lib.ntu.edu.tw/handle/123456789/514970 |
ISSN: | 0021-972X | DOI: | 10.1210/clinem/dgz110 | SDG/關鍵字: | aldosterone; renin; G protein coupled inwardly rectifying potassium channel; KCNJ5 protein, human; adrenalectomy; aldosterone blood level; biochemical analysis; biochemical composition; clinical feature; familial disease; human; hyperaldosteronism; hypertension; KCNJ5 gene; Letter; outcome assessment; phenotypic variation; plasma renin activity; postoperative period; prediction; priority journal; somatic mutation; treatment response; adrenalectomy; genetics; mutation; adrenal tumor; familial hyperaldosteronism type I; gene; mutational analysis; phenotype; primary hyperaldosteronism; surgical patient; treatment outcome; treatment response; Adrenalectomy; G Protein-Coupled Inwardly-Rectifying Potassium Channels; Humans; Hyperaldosteronism; Hypertension; Mutation |
顯示於: | 醫學系 |
在 IR 系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。