{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,11]],"date-time":"2025-09-11T17:52:03Z","timestamp":1757613123247,"version":"3.44.0"},"reference-count":4,"publisher":"BMJ","issue":"4","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["Pract Neurol"],"accepted":{"date-parts":[[2019,2,18]]},"published-print":{"date-parts":[[2019,8]]},"DOI":"10.1136\/practneurol-2019-002204","type":"journal-article","created":{"date-parts":[[2019,4,4]],"date-time":"2019-04-04T17:34:51Z","timestamp":1554399291000},"page":"321-325","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":3,"title":["Proximal muscle weakness"],"prefix":"10.1136","volume":"19","author":[{"given":"Paloma","family":"Gonzalez-Perez","sequence":"first","affiliation":[{"name":"Department of Neurology, Harvard Medical School, Massachusetts General Hospital, Boston, Massachusetts, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Matthew","family":"Torre","sequence":"additional","affiliation":[{"name":"Department of Pathology, Harvard Medical School, Brigham Women\u2019s Hospital, Boston, Massachusetts, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jeffrey","family":"Helgager","sequence":"additional","affiliation":[{"name":"Department of Pathology, Harvard Medical School, Brigham Women\u2019s Hospital, Boston, Massachusetts, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anthony A.","family":"Amato","sequence":"additional","affiliation":[{"name":"Department of Neurology, Harvard Medical School, Brigham Women\"s Hospital, Boston, Massachusetts, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[2019,4,4]]},"reference":[{"key":"2025090410453715000_19.4.321.1","doi-asserted-by":"crossref","unstructured":"Gr\u00fcnert SC . Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency. Orphanet J Rare Dis 2014;9.doi:10.1186\/s13023-014-0117-5","DOI":"10.1186\/s13023-014-0117-5"},{"key":"2025090410453715000_19.4.321.2","doi-asserted-by":"crossref","first-page":"1425","DOI":"10.4103\/0366-6999.183423","article-title":"Skeletal muscle magnetic resonance imaging of the lower limbs in late-onset lipid storage myopathy with electron transfer flavoprotein dehydrogenase gene mutations","volume":"129","author":"Liu","year":"2016","journal-title":"Chin Med J"},{"key":"2025090410453715000_19.4.321.3","unstructured":"Amato AA , Russell JA . Neuromuscular disorders. 2nd Edn. McGraw-Hill Education, 2016: 758\u201372."},{"key":"2025090410453715000_19.4.321.4","doi-asserted-by":"crossref","first-page":"283","DOI":"10.1016\/j.nmd.2010.01.010","article-title":"162nd ENMC international workshop: disorders of muscle lipid metabolism in adults 28\u201330 November 2008, Bussum, the Netherlands","volume":"20","author":"Lafor\u00eat","year":"2010","journal-title":"Neuromuscul Disord"}],"container-title":["Practical Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/practneurol-2019-002204","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,9,4]],"date-time":"2025-09-04T17:45:43Z","timestamp":1757007943000},"score":1,"resource":{"primary":{"URL":"https:\/\/pn.bmj.com\/lookup\/doi\/10.1136\/practneurol-2019-002204"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,4,4]]},"references-count":4,"journal-issue":{"issue":"4","published-online":{"date-parts":[[2019,7,11]]},"published-print":{"date-parts":[[2019,8]]}},"alternative-id":["10.1136\/practneurol-2019-002204"],"URL":"https:\/\/doi.org\/10.1136\/practneurol-2019-002204","relation":{},"ISSN":["1474-7758","1474-7766"],"issn-type":[{"type":"print","value":"1474-7758"},{"type":"electronic","value":"1474-7766"}],"subject":[],"published":{"date-parts":[[2019,4,4]]}}}