{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T23:42:35Z","timestamp":1790206955913,"version":"4.1.0"},"reference-count":14,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2019,2,1]],"date-time":"2019-02-01T00:00:00Z","timestamp":1548979200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"funder":[{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"crossref","award":["81471295"],"award-info":[{"award-number":["81471295"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"crossref","award":["81671075"],"award-info":[{"award-number":["81671075"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":["clinicalkey.jp","jocn-journal.com","clinicalkey.com","clinicalkey.es","clinicalkey.com.au","clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of Clinical Neuroscience"],"published-print":{"date-parts":[[2019,2]]},"DOI":"10.1016\/j.jocn.2018.10.040","type":"journal-article","created":{"date-parts":[[2018,10,22]],"date-time":"2018-10-22T18:46:18Z","timestamp":1540233978000},"page":"164-166","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":16,"special_numbering":"C","title":["Familial amyloid polyneuropathy with chronic paroxysmal dry cough in Mainland China: A Chinese family with a proven heterozygous missense mutation c.349G&gt;T in the transthyretin gene"],"prefix":"10.1016","volume":"60","author":[{"given":"Zhenhua","family":"Yuan","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lina","family":"Guo","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xixi","family":"Liu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xuewen","family":"Xiao","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bin","family":"Jiao","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Junling","family":"Wang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xinxiang","family":"Yan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Beisha","family":"Tang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lu","family":"Shen","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"issue":"Suppl 1","key":"10.1016\/j.jocn.2018.10.040_b0005","doi-asserted-by":"crossref","first-page":"71","DOI":"10.3109\/13506129.2012.673184","article-title":"Clinical features of TTR-FAP in Portugal","volume":"19","author":"Conceicao","year":"2012","journal-title":"Amyloid"},{"key":"10.1016\/j.jocn.2018.10.040_b0010","doi-asserted-by":"crossref","first-page":"282","DOI":"10.3109\/13506129909007341","article-title":"Usefulness of MALDI\/TOF mass spectrometry of immunoprecipitated serum variant transthyretin in the diagnosis of familial amyloid polyneuropathy","volume":"6","author":"Tachibana","year":"1999","journal-title":"Amyloid"},{"key":"10.1016\/j.jocn.2018.10.040_b0015","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1016\/j.jns.2007.10.011","article-title":"Transthyretin Ala97Ser in Chinese-Taiwanese patients with familial amyloid polyneuropathy: genetic studies and phenotype expression","volume":"267","author":"Liu","year":"2008","journal-title":"J Neurol Sci"},{"key":"10.1016\/j.jocn.2018.10.040_b0020","doi-asserted-by":"crossref","first-page":"532","DOI":"10.1212\/WNL.0b013e3181ec7fda","article-title":"Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97Ser","volume":"75","author":"Yang","year":"2010","journal-title":"Neurology"},{"key":"10.1016\/j.jocn.2018.10.040_b0025","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0141935","article-title":"The temporal profiles of changes in nerve excitability indices in familial amyloid polyneuropathy","volume":"10","author":"Lai","year":"2015","journal-title":"PLoS ONE"},{"key":"10.1016\/j.jocn.2018.10.040_b0030","doi-asserted-by":"crossref","first-page":"272","DOI":"10.1002\/ana.24438","article-title":"Sudomotor innervation in transthyretin amyloid neuropathy: pathology and functional correlates","volume":"78","author":"Chao","year":"2015","journal-title":"Ann Neurol"},{"key":"10.1016\/j.jocn.2018.10.040_b0035","doi-asserted-by":"crossref","first-page":"4911","DOI":"10.1007\/s12035-017-0694-0","article-title":"A missense variant p.Ala117Ser in the transthyretin gene of a Han Chinese family with familial amyloid polyneuropathy","volume":"556","author":"Chen","year":"2018","journal-title":"Mol Neurobiol"},{"key":"10.1016\/j.jocn.2018.10.040_b0040","doi-asserted-by":"crossref","first-page":"195","DOI":"10.1001\/archneurol.2010.261","article-title":"Mass spectrometric-based proteomic analysis of amyloid neuropathy type in nerve tissue","volume":"68","author":"Klein","year":"2011","journal-title":"Arch Neurol"},{"key":"10.1016\/j.jocn.2018.10.040_b0045","doi-asserted-by":"crossref","first-page":"632","DOI":"10.1086\/377591","article-title":"A locus for hereditary sensory neuropathy with cough and gastroesophageal reflux on chromosome 3p22-p24","volume":"73","author":"Kok","year":"2003","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.jocn.2018.10.040_b0050","doi-asserted-by":"crossref","first-page":"1905","DOI":"10.1212\/01.WNL.0000125287.98456.23","article-title":"Chronic cough due to Thr124Met mutation in the peripheral myelin protein zero (MPZ gene)","volume":"62","author":"Baloh","year":"2004","journal-title":"Neurology"},{"key":"10.1016\/j.jocn.2018.10.040_b0055","doi-asserted-by":"crossref","first-page":"88","DOI":"10.1016\/j.jns.2008.06.027","article-title":"Hereditary motor and sensory neuropathy with proximal dominancy in the lower extremities, urinary disturbance, and paroxysmal dry cough","volume":"273","author":"Miura","year":"2008","journal-title":"J Neurol Sci"},{"key":"10.1016\/j.jocn.2018.10.040_b0060","doi-asserted-by":"crossref","first-page":"269","DOI":"10.1590\/0004-282X20140014","article-title":"Clinical and neurophysiologic characterization of an European family with hereditary sensory neuropathy, paroxysmal cough and gastroesophageal reflux","volume":"72","author":"Barros","year":"2014","journal-title":"Arq Neuropsiquiatr"},{"key":"10.1016\/j.jocn.2018.10.040_b0065","doi-asserted-by":"crossref","first-page":"265","DOI":"10.1590\/0004-282X20140031","article-title":"Neuropathy and cough may not be a fortuitous association","volume":"72","author":"Marques","year":"2014","journal-title":"Arq Neuropsiquiatr"},{"key":"10.1016\/j.jocn.2018.10.040_b0070","doi-asserted-by":"crossref","first-page":"1086","DOI":"10.1016\/S1474-4422(11)70246-0","article-title":"Familial amyloid polyneuropathy","volume":"10","author":"Plante-Bordeneuve","year":"2011","journal-title":"Lancet Neurol"}],"container-title":["Journal of Clinical Neuroscience"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0967586818314280?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0967586818314280?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,1,6]],"date-time":"2019-01-06T05:42:18Z","timestamp":1546753338000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0967586818314280"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,2]]},"references-count":14,"alternative-id":["S0967586818314280"],"URL":"https:\/\/doi.org\/10.1016\/j.jocn.2018.10.040","relation":{},"ISSN":["0967-5868"],"issn-type":[{"value":"0967-5868","type":"print"}],"subject":[],"published":{"date-parts":[[2019,2]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Familial amyloid polyneuropathy with chronic paroxysmal dry cough in Mainland China: A Chinese family with a proven heterozygous missense mutation c.349G>T in the transthyretin gene","name":"articletitle","label":"Article Title"},{"value":"Journal of Clinical Neuroscience","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jocn.2018.10.040","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2018 Elsevier Ltd. All rights reserved.","name":"copyright","label":"Copyright"}]}}