{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,16]],"date-time":"2026-04-16T23:40:56Z","timestamp":1776382856213,"version":"3.51.2"},"reference-count":16,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[2014,11,28]],"date-time":"2014-11-28T00:00:00Z","timestamp":1417132800000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["BMC Urol"],"published-print":{"date-parts":[[2014,12]]},"DOI":"10.1186\/1471-2490-14-96","type":"journal-article","created":{"date-parts":[[2014,11,28]],"date-time":"2014-11-28T17:34:52Z","timestamp":1417196092000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":9,"title":["A rare case of unilateral adrenal hyperplasia accompanied by hypokalaemic periodic paralysis caused by a novel dominant mutation in CACNA1S: features and prognosis after adrenalectomy"],"prefix":"10.1186","volume":"14","author":[{"given":"Bo","family":"Yang","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yuan","family":"Yang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wenling","family":"Tu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ying","family":"Shen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Qiang","family":"Dong","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2014,11,28]]},"reference":[{"key":"387_CR1","doi-asserted-by":"publisher","first-page":"1283","DOI":"10.1007\/s11255-013-0614-9","volume":"46","author":"SB Jiang","year":"2014","unstructured":"Jiang SB, Guo XD, Wang HB, Gong RZ, Xiong H, Wang Z, Zhang HY, Jin XB: A retrospective study of laparoscopic unilateral adrenalectomy for primary hyperaldosteronism caused by unilateral adrenal hyperplasia. Int Urol Nephrol. 2014, 46: 1283-1288. 10.1007\/s11255-013-0614-9.","journal-title":"Int Urol Nephrol"},{"key":"387_CR2","doi-asserted-by":"publisher","first-page":"17","DOI":"10.1186\/1472-6823-12-17","volume":"12","author":"HA Sigurjonsdottir","year":"2012","unstructured":"Sigurjonsdottir HA, Gronowitz M, Andersson O, Eggertsen R, Herlitz H, Sakinis A, Wangberg B, Johannsson G: Unilateral adrenal hyperplasia is a usual cause of primary hyperaldosteronism. Results from a Swedish screening study. BMC Endocr Disord. 2012, 12: 17-10.1186\/1472-6823-12-17.","journal-title":"BMC Endocr Disord"},{"key":"387_CR3","doi-asserted-by":"publisher","first-page":"1248","DOI":"10.1016\/j.surg.2012.08.042","volume":"152","author":"M Iacobone","year":"2012","unstructured":"Iacobone M, Citton M, Viel G, Boetto R, Bonadio I, Tropea S, Mantero F, Rossi GP, Fassina A, Nitti D, Favia G: Unilateral adrenal hyperplasia: a novel cause of surgically correctable primary hyperaldosteronism. Surgery. 2012, 152: 1248-1255. 10.1016\/j.surg.2012.08.042.","journal-title":"Surgery"},{"key":"387_CR4","first-page":"4038","volume":"81","author":"YY Huang","year":"1996","unstructured":"Huang YY, Hsu BR, Tsai JS: Paralytic myopathy-a leading clinical presentation for primary aldosteronism in Taiwan. J Clin Endocrinol Metab. 1996, 81: 4038-4041.","journal-title":"J Clin Endocrinol Metab"},{"key":"387_CR5","doi-asserted-by":"publisher","first-page":"374","DOI":"10.1002\/ajmg.1320560406","volume":"56","author":"A Elbaz","year":"1995","unstructured":"Elbaz A, Vale-Santos J, Jurkat-Rott K, Lapie P, Ophoff RA, Bady B, Links TP, Piussan C, Vila A, Monnier N, Padberg GW, Abe K, Feingold N, Guimaraes J, Wintzen AR, van der Hoeven JH, Saudubray JM, Grunfeld JP, Lenoir G, Nivet H, Echenne B, Frants RR, Fardeau M, Lehmann-Horn F, Fontaine B: Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype\/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families. Am J Hum Genet. 1995, 56: 374-380. 10.1002\/ajmg.1320560406.","journal-title":"Am J Hum Genet"},{"key":"387_CR6","doi-asserted-by":"publisher","first-page":"1091","DOI":"10.1093\/brain\/124.6.1091","volume":"124","author":"D Sternberg","year":"2001","unstructured":"Sternberg D, Maisonobe T, Jurkat-Rott K, Nicole S, Launay E, Chauveau D, Tabti N, Lehmann-Horn F, Hainque B, Fontaine B: Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A. Brain. 2001, 124: 1091-1099. 10.1093\/brain\/124.6.1091.","journal-title":"Brain"},{"key":"387_CR7","doi-asserted-by":"publisher","first-page":"267","DOI":"10.1038\/ng0394-267","volume":"6","author":"B Fontaine","year":"1994","unstructured":"Fontaine B, Vale-Santos J, Jurkat-Rott K, Reboul J, Plassart E, Rime CS, Elbaz A, Heine R, Guimar\u00e3es J, Weissenbach J, Baumann N, Fardeau M, Lehmann-Horn F: Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families. Nat Genet. 1994, 6: 267-272. 10.1038\/ng0394-267.","journal-title":"Nat Genet"},{"key":"387_CR8","doi-asserted-by":"publisher","first-page":"1932","DOI":"10.1212\/WNL.53.9.1932","volume":"53","author":"DE Bulman","year":"1999","unstructured":"Bulman DE, Scoggan KA, van Oene MD, Nicolle MW, Hahn AF, Tollar LL, Ebers GC: A novel sodium channel mutation in a family with hypokalemic periodic paralysis. Neurology. 1999, 53: 1932-1936. 10.1212\/WNL.53.9.1932.","journal-title":"Neurology"},{"key":"387_CR9","doi-asserted-by":"crossref","first-page":"1179","DOI":"10.1681\/ASN.V871179","volume":"8","author":"ID Weiner","year":"1997","unstructured":"Weiner ID, Wingo CS: Hypokalemia-consequences, causes, and correction. J Am Soc Nephrol. 1997, 8: 1179-1188.","journal-title":"J Am Soc Nephrol"},{"key":"387_CR10","doi-asserted-by":"publisher","first-page":"211","DOI":"10.4103\/0972-2327.112469","volume":"16","author":"AK Kayal","year":"2013","unstructured":"Kayal AK, Goswami M, Das M, Jain R: Clinical and biochemical spectrum of hypokalemic paralysis in North: East India. Ann Indian Acad Neurol. 2013, 16: 211-217. 10.4103\/0972-2327.112469.","journal-title":"Ann Indian Acad Neurol"},{"key":"387_CR11","doi-asserted-by":"publisher","first-page":"321","DOI":"10.1111\/j.1469-7793.1999.00321.x","volume":"520","author":"JA Morrill","year":"1999","unstructured":"Morrill JA, Cannon SC: Effects of mutations causing hypokalaemic periodic paralysis on the skeletal muscle L-type Ca2+ channel expressed in Xenopus laevis oocytes. J Physiol. 1999, 520: 321-336. 10.1111\/j.1469-7793.1999.00321.x.","journal-title":"J Physiol"},{"key":"387_CR12","doi-asserted-by":"publisher","first-page":"9549","DOI":"10.1073\/pnas.97.17.9549","volume":"97","author":"K Jurkat-Rott","year":"2000","unstructured":"Jurkat-Rott K, Mitrovic N, Hang C, Kouzmekine A, Iaizzo P, Herzog J, Lerche H, Nicole S, Vale-Santos J, Chauveau D, Fontaine B, Lehmann-Horn F: Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current. Proc Natl Acad Sci U S A. 2000, 97: 9549-9554. 10.1073\/pnas.97.17.9549.","journal-title":"Proc Natl Acad Sci U S A"},{"key":"387_CR13","doi-asserted-by":"publisher","first-page":"203","DOI":"10.1007\/s00109-005-0638-4","volume":"83","author":"Q Wang","year":"2005","unstructured":"Wang Q, Liu M, Xu C, Tang Z, Liao Y, Du R, Li W, Wu X, Wang X, Liu P, Zhang X, Zhu J, Ren X, Ke T, Wang Q, Yang J: Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family. J Mol Med (Berl). 2005, 83: 203-208. 10.1007\/s00109-005-0638-4.","journal-title":"J Mol Med (Berl)"},{"key":"387_CR14","doi-asserted-by":"publisher","first-page":"6813","DOI":"10.4076\/1757-1626-2-6813","volume":"2","author":"P Kotsaftis","year":"2009","unstructured":"Kotsaftis P, Savopoulos C, Agapakis D, Ntaios G, Tzioufa V, Papadopoulos V, Fahantidis E, Hatzitolios A: Hypokalemia induced myopathy as first manifestation of primary hyperaldosteronism - an elderly patient with unilateral adrenal hyperplasia: a case report. Cases J. 2009, 2: 6813-10.4076\/1757-1626-2-6813.","journal-title":"Cases J"},{"key":"387_CR15","doi-asserted-by":"publisher","first-page":"9","DOI":"10.1186\/1750-1172-5-9","volume":"5","author":"L Amar","year":"2010","unstructured":"Amar L, Plouin PF, Steichen O: Aldosterone-producing adenoma and other surgically correctable forms of primary aldosteronism. Orphanet J Rare Dis. 2010, 5: 9-10.1186\/1750-1172-5-9.","journal-title":"Orphanet J Rare Dis"},{"key":"387_CR16","doi-asserted-by":"publisher","first-page":"1080","DOI":"10.1212\/01.wnl.0000237527.27595.87","volume":"67","author":"HY Ng","year":"2006","unstructured":"Ng HY, Lin SH, Hsu CY, Tsai YZ, Chen HC, Lee CT: Hypokalemic paralysis due to Gitelman syndrome: a family study. Neurology. 2006, 67: 1080-1082. 10.1212\/01.wnl.0000237527.27595.87.","journal-title":"Neurology"}],"container-title":["BMC Urology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1186\/1471-2490-14-96.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1186\/1471-2490-14-96\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1186\/1471-2490-14-96","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"},{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1186\/1471-2490-14-96.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,9,2]],"date-time":"2021-09-02T06:44:33Z","timestamp":1630565073000},"score":1,"resource":{"primary":{"URL":"https:\/\/bmcurol.biomedcentral.com\/articles\/10.1186\/1471-2490-14-96"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,11,28]]},"references-count":16,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2014,12]]}},"alternative-id":["387"],"URL":"https:\/\/doi.org\/10.1186\/1471-2490-14-96","relation":{},"ISSN":["1471-2490"],"issn-type":[{"value":"1471-2490","type":"electronic"}],"subject":[],"published":{"date-parts":[[2014,11,28]]},"assertion":[{"value":"1 May 2014","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"20 November 2014","order":2,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"28 November 2014","order":3,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}}],"article-number":"96"}}