{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,25]],"date-time":"2026-05-25T08:04:35Z","timestamp":1779696275590,"version":"3.53.1"},"reference-count":13,"publisher":"Scientific Scholar","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Indian J Nucl Med"],"published-print":{"date-parts":[[2019]]},"DOI":"10.4103\/ijnm.ijnm_57_19","type":"journal-article","created":{"date-parts":[[2019,6,20]],"date-time":"2019-06-20T08:06:01Z","timestamp":1561017961000},"page":"209","source":"Crossref","is-referenced-by-count":3,"title":["Fibrodysplasia ossificans progressiva \u2013 A rare genetic disorder and the role of Technetium-99m methylene diphosphonate bone scan"],"prefix":"10.25259","volume":"34","author":[{"given":"Nitin","family":"Gupta","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ankur","family":"Pruthi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Suneel","family":"Kumar","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ritu","family":"Verma","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"EthelShangne","family":"Belho","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"10894","reference":[{"key":"key-10.4103\/0972-3919.260760-1","first-page":"264","volume-title":"Myositis ossificans progressiva (Munchmeyer's disease).Brief review with report of two cases treated with corticosteroids and observed for 16 years","author":"Illingworth","year":"1971","journal-title":"Arch Dis Child"},{"key":"key-10.4103\/0972-3919.260760-2","first-page":"201","volume-title":"The genetics of fibrodysplasia ossificans progressiva","author":"Shore","year":"2005","journal-title":"Clin Rev Bone Miner Metab"},{"key":"key-10.4103\/0972-3919.260760-3","first-page":"555","volume-title":"Overexpression of an osteogenic morphogen in fibrodysplasia ossificans progressiva","author":"Shafritz","year":"1996","journal-title":"N Engl J Med"},{"key":"key-10.4103\/0972-3919.260760-4","first-page":"76","volume-title":"Fibrodysplasia ossificans progressiva.The clinical features and natural history of 34 patients","author":"Connor","year":"1982","journal-title":"J Bone Joint Surg Br"},{"key":"key-10.4103\/0972-3919.260760-5","first-page":"183","volume-title":"The phenotype of fibrodysplasia ossificans progressiva","author":"Kaplan","year":"2005","journal-title":"Clin Rev Bone Miner Metab"},{"key":"key-10.4103\/0972-3919.260760-6","first-page":"215","volume-title":"The natural history of heterotopic ossification in patients who have fibrodysplasia ossificans progressiva.A study of forty-four patients","author":"Cohen","year":"1993","journal-title":"J Bone Joint Surg Am"},{"key":"key-10.4103\/0972-3919.260760-7","first-page":"e654","volume-title":"Iatrogenic harm caused by diagnostic errors in fibrodysplasia ossificans progressiva","author":"Kitterman","year":"2005","journal-title":"Pediatrics"},{"key":"key-10.4103\/0972-3919.260760-8","first-page":"433","volume-title":"A Bizarre bone scan of fibrodysplasia ossificans progressiva","author":"Chuang","year":"2018","journal-title":"Clin Nucl Med"},{"key":"key-10.4103\/0972-3919.260760-9","first-page":"616","volume-title":"Diagnostic features of fibrodysplasia (myositis) ossificans progressiva on bone scan","author":"Tulchinsky","year":"2007","journal-title":"Clin Nucl Med"},{"key":"key-10.4103\/0972-3919.260760-10","first-page":"290","volume-title":"Fibrodysplasia ossificance progressiva: A familial presentation","author":"Pawar","year":"2015","journal-title":"Indian J Nucl Med","ISSN":"https:\/\/id.crossref.org\/issn\/0972-3919","issn-type":"print"},{"key":"key-10.4103\/0972-3919.260760-11","first-page":"153","volume-title":"Fibrodysplasia ossificans progressiva: CT appearance","author":"Reinig","year":"1986","journal-title":"Radiology"},{"key":"key-10.4103\/0972-3919.260760-12","first-page":"1379","volume-title":"Developmental anomalies of the cervical spine in patients with fibrodysplasia ossificans progressiva are distinctly different from those in patients with klippel-feil syndrome: Clues from the BMP signaling pathway","author":"Schaffer","year":"1976","journal-title":"Spine (Phila Pa"},{"key":"key-10.4103\/0972-3919.260760-13","first-page":"7","volume-title":"Fibrodysplasia (myositis) ossificans progressiva.Clinical lessons from a rare disease","author":"Smith","year":"1998","journal-title":"Clin Orthop Relat Res"}],"container-title":["Indian Journal of Nuclear Medicine"],"original-title":[],"language":"en","deposited":{"date-parts":[[2026,5,25]],"date-time":"2026-05-25T07:35:21Z","timestamp":1779694521000},"score":1,"resource":{"primary":{"URL":"https:\/\/ijnm.co.in\/fibrodysplasia-ossificans-progressiva-a-rare-genetic-disorder-and-the-role-of-technetium-99m-methylene-diphosphonate-bone-scan\/"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019]]},"references-count":13,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2019]]}},"alternative-id":["260760"],"URL":"https:\/\/doi.org\/10.4103\/ijnm.ijnm_57_19","relation":{},"ISSN":["0972-3919"],"issn-type":[{"value":"0972-3919","type":"print"}],"subject":[],"published":{"date-parts":[[2019]]}}}