{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,27]],"date-time":"2026-10-27T17:24:54Z","timestamp":1793121894153,"version":"4.5.0"},"reference-count":29,"publisher":"SAGE Publications","issue":"3","license":[{"start":{"date-parts":[[2009,10,12]],"date-time":"2009-10-12T00:00:00Z","timestamp":1255305600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Child Neurol"],"published-print":{"date-parts":[[2010,3]]},"abstract":"<jats:p>Niemann-Pick disease type C is a rare, genetic disease associated with impaired intracellular lipid trafficking and progressive neurological symptoms. Miglustat slowed disease progression in a 12-month randomized trial in juveniles and adults with Niemann-Pick disease type C, and in a parallel, noncontrolled study in affected children. Here, the authors report the open-label extension to the pediatric study. Patients aged 4 to 12 years received open-label miglustat (dose adjusted for body surface area) for an initial 12 months, during a further 12-month extension, and a long-term, continued extension phase. Efficacy assessments included horizontal saccadic eye movement, swallowing, and ambulation. Ten children completed 24 months\u2019 treatment. Horizontal saccadic eye movement, ambulation, and swallowing were stabilized at 24 months. Analysis of key parameters of disease progression showed disease stability in 8 of 10 patients (80%). Miglustat stabilized neurological disease progression in pediatric patients with Niemann-Pick disease type C, with comparable safety and tolerability to that observed in adults and juveniles.<\/jats:p>","DOI":"10.1177\/0883073809344222","type":"journal-article","created":{"date-parts":[[2009,10,12]],"date-time":"2009-10-12T21:54:08Z","timestamp":1255384448000},"page":"300-305","source":"Crossref","is-referenced-by-count":140,"title":["Long-Term Miglustat Therapy in Children With Niemann-Pick Disease Type C"],"prefix":"10.1177","volume":"25","author":[{"given":"Marc C.","family":"Patterson","sequence":"first","affiliation":[{"name":"Department of Neurology, Mayo Clinic, Rochester, Minnesota,"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Darleen","family":"Vecchio","sequence":"additional","affiliation":[{"name":"Department of Neurology, Columbia University, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Elizabeth","family":"Jacklin","sequence":"additional","affiliation":[{"name":"Willink Biochemical Genetics Unit, Royal Manchester Children's Hospital, Manchester, United Kingdom"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Larry","family":"Abel","sequence":"additional","affiliation":[{"name":"Department of Optometry and Vision Sciences, University of Melbourne, Victoria, Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Harbajan","family":"Chadha-Boreham","sequence":"additional","affiliation":[{"name":"Actelion Pharmaceuticals Ltd, Allschwil, Switzerland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Cecile","family":"Luzy","sequence":"additional","affiliation":[{"name":"Actelion Pharmaceuticals Ltd, Allschwil, Switzerland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ruben","family":"Giorgino","sequence":"additional","affiliation":[{"name":"Actelion Pharmaceuticals Ltd, Allschwil, Switzerland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"James E.","family":"Wraith","sequence":"additional","affiliation":[{"name":"Willink Biochemical Genetics Unit, Royal Manchester Children's Hospital, Manchester, United Kingdom"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2009,10,12]]},"reference":[{"key":"atypb1","doi-asserted-by":"publisher","DOI":"10.1001\/jama.281.3.249"},{"key":"atypb2","doi-asserted-by":"publisher","DOI":"10.1086\/302620"},{"issue":"1","key":"atypb3","first-page":"118","volume":"58","author":"Vanier MT","year":"1996","journal-title":"Am J Hum Genet"},{"key":"atypb4","doi-asserted-by":"publisher","DOI":"10.1086\/324068"},{"key":"atypb5","doi-asserted-by":"publisher","DOI":"10.1126\/science.290.5500.2298"},{"key":"atypb6","unstructured":"Patterson MC, Vanier MT, Suzuki K., et al. Niemann-Pick disease type C: a lipid trafficking disorder. In: Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Vogelstein B, eds. The Metabolic and Molecular Bases of Inherited Disease. New York: McGraw-Hill; 2001:3611-3633."},{"key":"atypb7","doi-asserted-by":"publisher","DOI":"10.1016\/j.bbalip.2004.08.008"},{"key":"atypb8","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-2275(20)39414-1"},{"key":"atypb9","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-3476(71)80151-8"},{"key":"atypb10","doi-asserted-by":"publisher","DOI":"10.1093\/jnen\/60.1.49"},{"key":"atypb11","doi-asserted-by":"publisher","DOI":"10.1016\/j.bbalip.2004.08.011"},{"key":"atypb12","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.39.8.1040"},{"key":"atypb13","doi-asserted-by":"publisher","DOI":"10.1034\/j.1399-0004.2003.00147.x"},{"key":"atypb14","doi-asserted-by":"publisher","DOI":"10.1023\/A:1021259403196"},{"key":"atypb15","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1988.tb03460.x"},{"key":"atypb16","doi-asserted-by":"publisher","DOI":"10.1007\/BF00685003"},{"key":"atypb17","doi-asserted-by":"publisher","DOI":"10.1007\/s10545-006-0384-7"},{"key":"atypb18","doi-asserted-by":"publisher","DOI":"10.1620\/tjem.209.263"},{"key":"atypb19","doi-asserted-by":"publisher","DOI":"10.1002\/mds.21779"},{"key":"atypb20","doi-asserted-by":"publisher","DOI":"10.1001\/jama.1996.03540070057031"},{"key":"atypb21","doi-asserted-by":"publisher","DOI":"10.1016\/S0021-9258(17)37202-2"},{"key":"atypb22","doi-asserted-by":"publisher","DOI":"10.1016\/S0960-9822(01)00396-7"},{"key":"atypb23","doi-asserted-by":"publisher","DOI":"10.1016\/S1474-4422(07)70194-1"},{"key":"atypb24","volume-title":"Presented at: 58th Annual Meeting of the American Society of Human Genetics","author":"Patterson MC"},{"key":"atypb25","doi-asserted-by":"publisher","DOI":"10.1007\/s10545-007-0630-y"},{"key":"atypb26","doi-asserted-by":"publisher","DOI":"10.1007\/s10545-008-0923-9"},{"key":"atypb27","doi-asserted-by":"publisher","DOI":"10.1016\/j.jns.2006.05.054"},{"key":"atypb28","doi-asserted-by":"publisher","DOI":"10.1196\/annals.1325.041"},{"key":"atypb29","doi-asserted-by":"publisher","DOI":"10.1212\/01.wnl.0000345040.01917.9d"}],"container-title":["Journal of Child Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/0883073809344222","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/0883073809344222","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,4,29]],"date-time":"2026-04-29T20:35:03Z","timestamp":1777494903000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.sagepub.com\/doi\/10.1177\/0883073809344222"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2009,10,12]]},"references-count":29,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2010,3]]}},"alternative-id":["10.1177\/0883073809344222"],"URL":"https:\/\/doi.org\/10.1177\/0883073809344222","relation":{},"ISSN":["0883-0738","1708-8283"],"issn-type":[{"value":"0883-0738","type":"print"},{"value":"1708-8283","type":"electronic"}],"subject":[],"published":{"date-parts":[[2009,10,12]]}}}