{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T00:39:43Z","timestamp":1760834383242,"version":"build-2065373602"},"reference-count":16,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2019,6,1]],"date-time":"2019-06-01T00:00:00Z","timestamp":1559347200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2019,6,1]],"date-time":"2019-06-01T00:00:00Z","timestamp":1559347200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2019,6,1]],"date-time":"2019-06-01T00:00:00Z","timestamp":1559347200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2019,6,1]],"date-time":"2019-06-01T00:00:00Z","timestamp":1559347200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2019,6,1]],"date-time":"2019-06-01T00:00:00Z","timestamp":1559347200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2019,6,1]],"date-time":"2019-06-01T00:00:00Z","timestamp":1559347200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2019,6,1]],"date-time":"2019-06-01T00:00:00Z","timestamp":1559347200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","jocn-journal.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of Clinical Neuroscience"],"published-print":{"date-parts":[[2019,6]]},"DOI":"10.1016\/j.jocn.2019.03.067","type":"journal-article","created":{"date-parts":[[2019,4,5]],"date-time":"2019-04-05T12:46:13Z","timestamp":1554468373000},"page":"4-5","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":2,"special_numbering":"C","title":["Familial, long-term pollakisuria as initial manifestation of HSP4 due to the SPAST variant c.683-2A>C"],"prefix":"10.1016","volume":"64","author":[{"given":"Josef","family":"Finsterer","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Salma M.","family":"Wakil","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Franco","family":"Laccone","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.jocn.2019.03.067_b0005","unstructured":"Hedera P. Hereditary Spastic Paraplegia Overview. 2000 Aug 15 [updated 2018 Sep 27]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews\u00ae [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018. Available from http:\/\/www.ncbi.nlm.nih.gov\/books\/NBK1509\/"},{"key":"10.1016\/j.jocn.2019.03.067_b0010","doi-asserted-by":"crossref","first-page":"3331","DOI":"10.1093\/brain\/awy285","article-title":"SPATAX network. Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex","volume":"141","author":"Parodi","year":"2018","journal-title":"Brain"},{"issue":"5","key":"10.1016\/j.jocn.2019.03.067_b0015","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0036505","article-title":"Transcriptional and post-transcriptional regulation of SPAST, the gene most frequently mutated in hereditary spastic paraplegia","volume":"7","author":"Henson","year":"2012","journal-title":"PLoS ONE"},{"key":"10.1016\/j.jocn.2019.03.067_b0020","article-title":"Clinical and genetic study of hereditary spastic paraplegia in Canada","volume":"3","author":"Chrestian","year":"2016","journal-title":"Neurol Genet"},{"issue":"8","key":"10.1016\/j.jocn.2019.03.067_b0025","doi-asserted-by":"crossref","DOI":"10.3390\/brainsci8080153","article-title":"JASPAC: Japan Spastic Paraplegia Research Consortium","volume":"8","author":"Koh","year":"2018","journal-title":"Brain Sci"},{"issue":"1","key":"10.1016\/j.jocn.2019.03.067_b0030","doi-asserted-by":"crossref","first-page":"36","DOI":"10.1186\/s13024-018-0269-1","article-title":"Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China","volume":"13","author":"Dong","year":"2018","journal-title":"Mol Neurodegener"},{"key":"10.1016\/j.jocn.2019.03.067_b0035","doi-asserted-by":"crossref","first-page":"18","DOI":"10.1016\/j.jns.2017.10.010","article-title":"Clinical and molecular characterization of hereditary spastic paraplegias: a next-generation sequencing panel approach","volume":"383","author":"Burguez","year":"2017","journal-title":"J Neurol Sci"},{"key":"10.1016\/j.jocn.2019.03.067_b0040","doi-asserted-by":"crossref","first-page":"92","DOI":"10.1016\/j.jns.2017.07.011","article-title":"Spastic paraplegia type 4: a novel SPAST splice site donor mutation and expansion of the phenotype variability","volume":"380","author":"Kawarai","year":"2017","journal-title":"J Neurol Sci"},{"key":"10.1016\/j.jocn.2019.03.067_b0045","doi-asserted-by":"crossref","first-page":"1276","DOI":"10.1038\/sj.ejhg.5201924","article-title":"A multi-exonic SPG4 duplication underlies sex-dependent penetrance of hereditary spastic paraplegia in a large Brazilian pedigree","volume":"15","author":"Mitne-Neto","year":"2007","journal-title":"Eur J Hum Genet"},{"key":"10.1016\/j.jocn.2019.03.067_b0050","doi-asserted-by":"crossref","first-page":"17","DOI":"10.1186\/1471-2377-10-17","article-title":"Unique spectrum of SPAST variants in Estonian HSP patients: presence of benign missense changes but lack of exonic rearrangements","volume":"10","author":"Braschinsky","year":"2010","journal-title":"BMC Neurol"},{"key":"10.1016\/j.jocn.2019.03.067_b0055","doi-asserted-by":"crossref","first-page":"2471","DOI":"10.1093\/brain\/awv178","article-title":"Hereditary spastic paraplegia SPG4: what is known and not known about the disease","volume":"138","author":"Solowska","year":"2015","journal-title":"Brain"},{"key":"10.1016\/j.jocn.2019.03.067_b0060","doi-asserted-by":"crossref","first-page":"1191","DOI":"10.1002\/dneu.22640","article-title":"Spastin interacts with CRMP5 to promote neurite outgrowth by controlling the microtubule dynamics","volume":"78","author":"Ji","year":"2018","journal-title":"Dev Neurobiol"},{"key":"10.1016\/j.jocn.2019.03.067_b0065","doi-asserted-by":"crossref","first-page":"681","DOI":"10.1136\/jnnp-2017-315796","article-title":"Truncating mutations in SPAST patients are associated with a high rate of psychiatric comorbidities in hereditary spastic paraplegia","volume":"88","author":"Chelban","year":"2017","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"10.1016\/j.jocn.2019.03.067_b0070","first-page":"187","article-title":"[Spastic paraplegia caused by a novel mutation in the spastin gene (1207C -->G, P361R) - clinical features of a patient without family history]","volume":"60","author":"Machino","year":"2008","journal-title":"Brain Nerve"},{"key":"10.1016\/j.jocn.2019.03.067_b0075","article-title":"Urinary symptoms, quality of life, and patient satisfaction in genetic and sporadic hereditary spastic paraplegia","author":"Schneider","year":"2018","journal-title":"J Neurol"},{"key":"10.1016\/j.jocn.2019.03.067_b0080","doi-asserted-by":"crossref","first-page":"329","DOI":"10.1177\/0883073818756680","article-title":"Association of early-onset spasticity and risk for cognitive impairment with mutations at amino acid 499 in SPAST","volume":"33","author":"Gillespie","year":"2018","journal-title":"J Child Neurol"}],"container-title":["Journal of Clinical Neuroscience"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0967586819303819?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0967586819303819?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,18]],"date-time":"2025-10-18T21:18:16Z","timestamp":1760822296000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0967586819303819"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,6]]},"references-count":16,"alternative-id":["S0967586819303819"],"URL":"https:\/\/doi.org\/10.1016\/j.jocn.2019.03.067","relation":{},"ISSN":["0967-5868"],"issn-type":[{"type":"print","value":"0967-5868"}],"subject":[],"published":{"date-parts":[[2019,6]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Familial, long-term pollakisuria as initial manifestation of HSP4 due to the SPAST variant c.683-2A>C","name":"articletitle","label":"Article Title"},{"value":"Journal of Clinical Neuroscience","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jocn.2019.03.067","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2019 Elsevier Ltd. All rights reserved.","name":"copyright","label":"Copyright"}]}}