{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T14:39:09Z","timestamp":1787755149090,"version":"build-2784847793"},"reference-count":24,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JBJS Case Connector"],"published-print":{"date-parts":[[2017,3,8]]},"abstract":"<jats:sec>\n                    <jats:title>Case:<\/jats:title>\n                    <jats:p>A 16-year-old girl with Pompe disease underwent surgery for scoliosis. She had been able to walk without any assistance, and kept her balance by swinging her waist. Therefore, we performed posterior selective spinal correction and fusion to avoid any adverse effects on walking ability that could occur with immobilization of the lumbosacral spine. After surgery, she was highly satisfied with her ability to perform the activities of daily living.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion:<\/jats:title>\n                    <jats:p>For nonambulatory patients with scoliosis and Pompe disease, long fusion from the upper thoracic spine to the pelvis is generally required. However, in ambulatory patients, in order to maintain the ability to walk, selective spinal fusion is an alternative.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.2106\/jbjs.cc.16.00137","type":"journal-article","created":{"date-parts":[[2017,2,25]],"date-time":"2017-02-25T16:44:11Z","timestamp":1488041051000},"page":"e15","source":"Crossref","is-referenced-by-count":4,"title":["Selective Spinal Fusion for Neuromuscular Scoliosis in a Patient with Pompe Disease"],"prefix":"10.2106","volume":"7","author":[{"given":"Atsushi","family":"Tanida","sequence":"first","affiliation":[{"name":"Department of Orthopedic Surgery (A.T., S.T., T.M., and H.N.) and Division of Child Neurology (A.N. and Y.M.), Faculty of Medicine, Tottori University, Tottori, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shinji","family":"Tanishima","sequence":"additional","affiliation":[{"name":"Department of Orthopedic Surgery (A.T., S.T., T.M., and H.N.) and Division of Child Neurology 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Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hideki","family":"Nagashima","sequence":"additional","affiliation":[{"name":"Department of Orthopedic Surgery (A.T., S.T., T.M., and H.N.) and Division of Child Neurology (A.N. and Y.M.), Faculty of Medicine, Tottori University, Tottori, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"issue":"1","key":"bib1-20230712","doi-asserted-by":"crossref","first-page":"e39","DOI":"10.1542\/peds.2007-2222","article-title":"Early detection of Pompe disease by newborn screening is feasible: results from the Taiwan screening program","volume":"122","author":"Chien","year":"2008","journal-title":"Pediatrics."},{"issue":"9813","key":"bib2-20230712","doi-asserted-by":"crossref","first-page":"335","DOI":"10.1016\/S0140-6736(11)61266-X","article-title":"Neonatal screening for lysosomal storage disorders: feasibility and incidence from a nationwide study in 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