{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T20:36:20Z","timestamp":1786653380414,"version":"build-2736575974"},"reference-count":15,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Ann Indian Acad Neurol"],"published-print":{"date-parts":[[2016]]},"DOI":"10.4103\/0972-2327.176861","type":"journal-article","created":{"date-parts":[[2016,2,17]],"date-time":"2016-02-17T08:08:28Z","timestamp":1455696508000},"page":"201","source":"Crossref","is-referenced-by-count":0,"title":["Coexistence of central nucleus, cores, and rods: Diagnostic relevance"],"prefix":"10.4103","volume":"19","author":[{"given":"Gayathri","family":"Narayanappa","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sathiyabama","family":"Dhinakaran","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"RashmiSanthosh","family":"Kumar","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ravindra","family":"Thakkar","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"key-10.4103\/0972-2327.176861-1","first-page":"527","volume-title":"Congenital myopathies at their molecular dawning","author":"Goebel","year":"2003","journal-title":"Muscle Nerve"},{"key":"key-10.4103\/0972-2327.176861-2","first-page":"555","volume-title":"Common origin of rods, cores, miniature cores, and focal loss of cross-striations","author":"Bethlem","year":"1978","journal-title":"Arch Neurol"},{"key":"key-10.4103\/0972-2327.176861-3","first-page":"395","volume-title":"Myopathy with pathological features of both centronuclear myopathy and multicore disease","author":"Fitzsimons","year":"1982","journal-title":"J Neurol Sci"},{"key":"key-10.4103\/0972-2327.176861-4","first-page":"1689","volume-title":"A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathy","author":"Scacheri","year":"2000","journal-title":"Neurology"},{"key":"key-10.4103\/0972-2327.176861-5","first-page":"338","volume-title":"Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene","author":"Jungbluth","year":"2007","journal-title":"Neuromuscular Disord"},{"key":"key-10.4103\/0972-2327.176861-6","first-page":"281","volume-title":"Congenital myopathies \u2014 a comprehensive update of recent advancements","author":"Sharma","year":"2009","journal-title":"Acta Neurol Scand"},{"key":"key-10.4103\/0972-2327.176861-7","first-page":"277","volume-title":"A fatal congenital myopathy with severe type I fiber atrophy, central nuclei and multicores","author":"Lee","year":"1981","journal-title":"J Neurol Sci"},{"key":"key-10.4103\/0972-2327.176861-8","first-page":"311","volume-title":"Cytopathology of an unusual case of centronuclear myopathy.Light- and electron-microscopic investigations","author":"H\u00fclsmann","year":"1981","journal-title":"J Neurol Sci"},{"key":"key-10.4103\/0972-2327.176861-9","doi-asserted-by":"crossref","unstructured":"Vallat J.M, de Lumley L, Loubet A, Leboutet MJ, Corvisier N, Umdenstock R. Coexistence of minicores, and rods in the same muscle biopsy. A new example of mixed congenital myopathy. Acta Neuropathol 1982;58:229-32.","DOI":"10.1007\/BF00690806"},{"key":"key-10.4103\/0972-2327.176861-10","first-page":"371","volume-title":"Congenital nonprogressive myopathy: Central core disease and nemaline myopathy in one family","author":"Afifi","year":"1965","journal-title":"Neurology"},{"key":"key-10.4103\/0972-2327.176861-11","first-page":"1470","volume-title":"Central core disease is due to RYR1 mutations in more than 90% of patients","author":"Wu","year":"2006","journal-title":"Brain"},{"key":"key-10.4103\/0972-2327.176861-12","first-page":"410","volume-title":"Ryanodine receptor mutations in malignant hyperthermia and central core disease","author":"McCarthy","year":"2000","journal-title":"Hum Mutat"},{"key":"key-10.4103\/0972-2327.176861-13","first-page":"433","volume-title":"What's new in congenital myopathies?","author":"North","year":"2008","journal-title":"Neuromuscul Disord"},{"key":"key-10.4103\/0972-2327.176861-14","first-page":"2599","volume-title":"An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptor","author":"Monnier","year":"2000","journal-title":"Hum Mol Genet"},{"key":"key-10.4103\/0972-2327.176861-15","first-page":"165","volume-title":"Congenital myopathies: An update","author":"Nance","year":"2012","journal-title":"Curr Neurol Neurosci Rep"}],"container-title":["Annals of Indian Academy of Neurology"],"original-title":[],"language":"en","deposited":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T19:36:13Z","timestamp":1786649773000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.4103\/0972-2327.176861"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016]]},"references-count":15,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2016]]}},"alternative-id":["176861"],"URL":"https:\/\/doi.org\/10.4103\/0972-2327.176861","relation":{},"ISSN":["0972-2327"],"issn-type":[{"value":"0972-2327","type":"print"}],"subject":[],"published":{"date-parts":[[2016]]}}}