{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,11,9]],"date-time":"2026-11-09T22:55:15Z","timestamp":1794264915583,"version":"4.9.0"},"reference-count":71,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[2008,5,19]],"date-time":"2008-05-19T00:00:00Z","timestamp":1211155200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/2.0"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Orphanet J Rare Dis"],"published-print":{"date-parts":[[2008,12]]},"DOI":"10.1186\/1750-1172-3-12","type":"journal-article","created":{"date-parts":[[2008,5,20]],"date-time":"2008-05-20T06:14:10Z","timestamp":1211264050000},"source":"Crossref","is-referenced-by-count":371,"title":["McCune-Albright syndrome"],"prefix":"10.1186","volume":"3","author":[{"given":"Claudia E","family":"Dumitrescu","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michael T","family":"Collins","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2008,5,19]]},"reference":[{"key":"112_CR1","first-page":"743","volume":"52","author":"DJ McCune","year":"1936","unstructured":"McCune DJ: Osteitis fibrosa cystica: the case of a nine-year-old girl who also exhibits precocious puberty, multiple pigmentation of the skin and hyperthyroidism. Am J Dis Child. 1936, 52: 743-744.","journal-title":"Am J Dis Child"},{"key":"112_CR2","doi-asserted-by":"publisher","first-page":"727","DOI":"10.1056\/NEJM193704292161701","volume":"216","author":"F Albright","year":"1937","unstructured":"Albright F, Butler AM, Hampton AO, Smith P: Syndrome characterized by osteitis fibrosa disseminata, areas, of pigmentation, and endocrine dysfunction, with precocious puberty in females: report of 5 cases. N Engl J Med. 1937, 216: 727-746.","journal-title":"N Engl J Med"},{"key":"112_CR3","doi-asserted-by":"publisher","first-page":"433","DOI":"10.1089\/thy.1997.7.433","volume":"7","author":"G Mastorakos","year":"1997","unstructured":"Mastorakos G, Mitsiades NS, Doufas AG, Koutras DA: Hyperthyroidism in McCune-Albright syndrome with a review of thyroid abnormalities sixty years after the first report. Thyroid. 1997, 7: 433-439.","journal-title":"Thyroid"},{"key":"112_CR4","doi-asserted-by":"publisher","first-page":"185","DOI":"10.1007\/BF03348702","volume":"15","author":"SI Sherman","year":"1992","unstructured":"Sherman SI, Ladenson PW: Octreotide therapy of growth hormone excess in the McCune-Albright syndrome. Journal of endocrinological investigation. 1992, 15: 185-190.","journal-title":"Journal of endocrinological investigation"},{"issue":"11","key":"112_CR5","doi-asserted-by":"publisher","first-page":"5104","DOI":"10.1210\/jc.2001-012022","volume":"87","author":"SO Akintoye","year":"2002","unstructured":"Akintoye SO, Chebli C, Booher S, Feuillan P, Kushner H, Leroith D, Cherman N, Bianco P, Wientroub S, Robey PG, Collins MT: Characterization of gsp-mediated growth hormone excess in the context of McCune-Albright syndrome. J Clin Endocrinol Metab. 2002, 87 (11): 5104-5112. 10.1210\/jc.2001-012022.","journal-title":"J Clin Endocrinol Metab"},{"key":"112_CR6","doi-asserted-by":"publisher","first-page":"806","DOI":"10.1359\/jbmr.2001.16.5.806","volume":"16","author":"MT Collins","year":"2001","unstructured":"Collins MT, Chebli C, Jones J, Kushner H, Consugar M, Rinaldo P, Wientroub S, Bianco P, Robey PG: Renal phosphate wasting in fibrous dysplasia of bone is part of a generalized renal tubular dysfunction similar to that seen in tumor-induced osteomalacia. J Bone Miner Res. 2001, 16: 806-813. 10.1359\/jbmr.2001.16.5.806.","journal-title":"J Bone Miner Res"},{"key":"112_CR7","first-page":"81","volume":"55","author":"M Danon","year":"1987","unstructured":"Danon M, Crawford JD: The McCune-Albright syndrome. Ergeb Inn Med Kinderheilkd. 1987, 55: 81-115.","journal-title":"Ergeb Inn Med Kinderheilkd"},{"key":"112_CR8","doi-asserted-by":"publisher","first-page":"853","DOI":"10.1515\/JPEM.2007.20.8.853","volume":"20","author":"A Diaz","year":"2007","unstructured":"Diaz A, Danon M, Crawford J: McCune-Albright syndrome and disorders due to activating mutations of GNAS1. J Pediatr Endocrinol Metab. 2007, 20: 853-880.","journal-title":"J Pediatr Endocrinol Metab"},{"key":"112_CR9","doi-asserted-by":"publisher","first-page":"789","DOI":"10.1016\/S0022-3476(99)70302-1","volume":"134","author":"JM Kirk","year":"1999","unstructured":"Kirk JM, Brain CE, Carson DJ, Hyde JC, Grant DB: Cushing's syndrome caused by nodular adrenal hyperplasia in children with McCune-Albright syndrome. The Journal of pediatrics. 1999, 134: 789-792. 10.1016\/S0022-3476(99)70302-1.","journal-title":"The Journal of pediatrics"},{"key":"112_CR10","doi-asserted-by":"publisher","first-page":"509","DOI":"10.1016\/S0022-3476(05)80943-6","volume":"123","author":"A Shenker","year":"1993","unstructured":"Shenker A, Weinstein LS, Moran A, Pescovitz OH, Charest NJ, Boney CM, Van Wyk JJ, Merino MJ, Feuillan PP, Spiegel AM: Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein GS. J Pediatr. 1993, 123: 509-518. 10.1016\/S0022-3476(05)80943-6.","journal-title":"J Pediatr"},{"key":"112_CR11","first-page":"777","volume":"33","author":"LJH Lichtenstein","year":"1942","unstructured":"Lichtenstein LJH: Fibrous dysplasia of bone: a condition affecting one, several or many bones, graver cases of which may present abnormal pigmentation of skin, premature sexual development, hyperthyroidism or still other extraskeletal abnormalities. Arch Path. 1942, 33: 777-816.","journal-title":"Arch Path"},{"key":"112_CR12","doi-asserted-by":"publisher","first-page":"509","DOI":"10.1016\/B978-012286551-0\/50023-3","volume-title":"Pediatric Bone: Biology and Disease","author":"P Bianco","year":"2003","unstructured":"Bianco P, Robey PG, Wientroub S: Fibrous dysplasia. Pediatric Bone: Biology and Disease. Edited by: Glorieux FH, Pettifor J, Juppner H. 2003, New York, NY: Academic Press, Elsevier, 509-539."},{"issue":"Suppl 2","key":"112_CR13","doi-asserted-by":"publisher","first-page":"P99","DOI":"10.1359\/jbmr.06s219","volume":"21","author":"MT Collins","year":"2006","unstructured":"Collins MT: Spectrum and natural history of fibrous dysplasia of bone. J Bone Miner Res. 2006, 21 (Suppl 2): P99-P104. 10.1359\/jbmr.06s219.","journal-title":"J Bone Miner Res"},{"key":"112_CR14","first-page":"415","volume-title":"Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism","author":"MT Collins","year":"2006","unstructured":"Collins MT, Bianco P: Fibrous dysplasia. Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism. Edited by: Favus MJ. 2006, Washington, D.C.: American Society for Bone and Mineral Research, 415-418. 6","edition":"6"},{"key":"112_CR15","doi-asserted-by":"publisher","first-page":"119","DOI":"10.1097\/00060793-199904000-00006","volume":"6","author":"MT Collins","year":"1999","unstructured":"Collins MT, Shenker A: McCune-Albright syndrome: new insights. Curr Opin in Endocrinol and Diabetes. 1999, 6: 119-125. 10.1097\/00060793-199904000-00006.","journal-title":"Curr Opin in Endocrinol and Diabetes"},{"key":"112_CR16","first-page":"441","volume-title":"Bone Tumors","author":"HD Dorfman","year":"1998","unstructured":"Dorfman HD, Czerniak B: Fibroosseous Lesions. Bone Tumors. Edited by: Dorfman HD, Czerniak B. 1998, St. Louis, MO: Mosby, 441-491."},{"key":"112_CR17","doi-asserted-by":"publisher","first-page":"1468","DOI":"10.1359\/jbmr.070511","volume":"22","author":"ES Hart","year":"2007","unstructured":"Hart ES, Kelly MH, Brillante B, Chen CC, Ziran N, Lee JS, Feuillan P, Leet AI, Kushner H, Robey PG, Collins MT: Onset, progression, and plateau of skeletal lesions in fibrous dysplasia and the relationship to functional outcome. J Bone Miner Res. 2007, 22: 1468-1474. 10.1359\/jbmr.070511.","journal-title":"J Bone Miner Res"},{"key":"112_CR18","doi-asserted-by":"publisher","first-page":"571","DOI":"10.1359\/JBMR.0301262","volume":"19","author":"AI Leet","year":"2004","unstructured":"Leet AI, Chebli C, Kushner H, Chen CC, Kelly MH, Brillante BA, Robey PG, Bianco P, Wientroub S, Collins MT: Fracture incidence in polyostotic fibrous dysplasia and the McCune-Albright syndrome. J Bone Miner Res. 2004, 19: 571-577. 10.1359\/JBMR.0301262.","journal-title":"J Bone Miner Res"},{"key":"112_CR19","doi-asserted-by":"publisher","first-page":"1411","DOI":"10.1002\/1097-0142(19940301)73:5<1411::AID-CNCR2820730516>3.0.CO;2-T","volume":"73","author":"P Ruggieri","year":"1994","unstructured":"Ruggieri P, Sim FH, Bond JR, Unni KK: Malignancies in fibrous dysplasia. Cancer. 1994, 73: 1411-1424. 10.1002\/1097-0142(19940301)73:5<1411::AID-CNCR2820730516>3.0.CO;2-T.","journal-title":"Cancer"},{"key":"112_CR20","first-page":"177","volume":"66","author":"P Blanco","year":"1999","unstructured":"Blanco P, Schaeverbeke T, Baillet L, Lequen L, Bannwarth B, Dehais J: Chondrosarcoma in a patient with McCune-Albright syndrome. Report of a case. Rev Rhum Engl Ed. 1999, 66: 177-179.","journal-title":"Rev Rhum Engl Ed"},{"key":"112_CR21","doi-asserted-by":"publisher","first-page":"522","DOI":"10.1007\/s002560050556","volume":"28","author":"R Lopez-Ben","year":"1999","unstructured":"Lopez-Ben R, Pitt MJ, Jaffe KA, Siegal GP: Osteosarcoma in a patient with McCune-Albright syndrome and Mazabraud's syndrome. Skeletal Radiol. 1999, 28: 522-526. 10.1007\/s002560050556.","journal-title":"Skeletal Radiol"},{"key":"112_CR22","volume-title":"Breast","author":"EF Scanlon","year":"1980","unstructured":"Scanlon EF, Burkett FE, Sener SF, Green OC, Traisman HS, Marr TJ, Victor TA, Crist ML: Breast carcinoma in a 11-year-old girl with Albright's syndrome. Breast. 1980, 6:"},{"key":"112_CR23","doi-asserted-by":"publisher","first-page":"175","DOI":"10.1007\/BF02966691","volume":"5","author":"Y Tanabeu","year":"1998","unstructured":"Tanabeu Y, Nakahara S, Mitsuyama S, Ono M, Toyoshima S: Breast Cancer in a Patient with McCune-Albright Syndrome. Breast Cancer. 1998, 5: 175-178.","journal-title":"Breast Cancer"},{"key":"112_CR24","doi-asserted-by":"publisher","first-page":"4413","DOI":"10.1210\/jc.2002-021642","volume":"88","author":"MT Collins","year":"2003","unstructured":"Collins MT, Sarlis NJ, Merino MJ, Monroe J, Crawford SE, Krakoff JA, Guthrie LC, Bonat S, Robey PG, Shenker A: Thyroid carcinoma in the McCune-Albright syndrome: contributory role of activating Gs alpha mutations. J Clin Endocrinol Metab. 2003, 88: 4413-4417. 10.1210\/jc.2002-021642.","journal-title":"J Clin Endocrinol Metab"},{"key":"112_CR25","doi-asserted-by":"publisher","first-page":"1688","DOI":"10.1056\/NEJM199112123252403","volume":"325","author":"LS Weinstein","year":"1991","unstructured":"Weinstein LS, Shenker A, Gejman PV, Merino MJ, Friedman E, Spiegel AM: Activating mutations of the stimulatory G protein in the McCune \u2013 Albright syndrome [see comments]. N Engl J Med. 1991, 325: 1688-1695.","journal-title":"N Engl J Med"},{"key":"112_CR26","doi-asserted-by":"publisher","first-page":"5152","DOI":"10.1073\/pnas.89.11.5152","volume":"89","author":"WF Schwindinger","year":"1992","unstructured":"Schwindinger WF, Francomano CA, Levine MA: Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome. Proc Natl Acad Sci USA. 1992, 89: 5152-5156. 10.1073\/pnas.89.11.5152.","journal-title":"Proc Natl Acad Sci USA"},{"key":"112_CR27","doi-asserted-by":"publisher","first-page":"120","DOI":"10.1359\/jbmr.2000.15.1.120","volume":"15","author":"P Bianco","year":"2000","unstructured":"Bianco P, Riminucci M, Majolagbe A, Kuznetsov SA, Collins MT, Mankani MH, Corsi A, Bone HG, Wientroub S, Spiegel AM, Fisher LW, Robey PG: Mutations of the GNAS1 gene, stromal cell dysfunction, and osteomalacic changes in non-McCune-Albright fibrous dysplasia of bone. J Bone Miner Res. 2000, 15: 120-128. 10.1359\/jbmr.2000.15.1.120.","journal-title":"J Bone Miner Res"},{"key":"112_CR28","doi-asserted-by":"publisher","first-page":"691","DOI":"10.1111\/j.1365-2559.2007.02676.x","volume":"50","author":"BD Idowu","year":"2007","unstructured":"Idowu BD, Al-Adnani M, O'Donnell P, Yu L, Odell E, Diss T, Gale RE, Flanagan AM: A sensitive mutation-specific screening technique for GNAS1 mutations in cases of fibrous dysplasia: the first report of a codon 227 mutation in bone. Histopathology. 2007, 50: 691-704. 10.1111\/j.1365-2559.2007.02676.x.","journal-title":"Histopathology"},{"issue":"Suppl 2","key":"112_CR29","doi-asserted-by":"publisher","first-page":"P125","DOI":"10.1359\/jbmr.06s224","volume":"21","author":"M Riminucci","year":"2006","unstructured":"Riminucci M, Saggio I, Robey PG, Bianco P: Fibrous dysplasia as a stem cell disease. J Bone Miner Res. 2006, 21 (Suppl 2): P125-131. 10.1359\/jbmr.06s224.","journal-title":"J Bone Miner Res"},{"key":"112_CR30","doi-asserted-by":"publisher","first-page":"219","DOI":"10.1359\/JBMR.041111","volume":"20","author":"MT Collins","year":"2005","unstructured":"Collins MT, Kushner H, Reynolds JC, Chebli C, Kelly MH, Gupta A, Brillante B, Leet AI, Riminucci M, Robey PG, Bianco P, Wientroub S, Chen CC: An instrument to measure skeletal burden and predict functional outcome in fibrous dysplasia of bone. J Bone Miner Res. 2005, 20: 219-226. 10.1359\/JBMR.041111.","journal-title":"J Bone Miner Res"},{"key":"112_CR31","doi-asserted-by":"publisher","first-page":"155","DOI":"10.1097\/00009957-200305000-00001","volume":"12","author":"E Ippolito","year":"2003","unstructured":"Ippolito E, Bray EW, Corsi A, De Maio F, Exner UG, Robey PG, Grill F, Lala R, Massobrio M, Pinggera O, Riminucci M, Snela S, Zambakidis C, Bianco P: Natural history and treatment of fibrous dysplasia of bone: a multicenter clinicopathologic study promoted by the European Pediatric Orthopaedic Society. Journal of pediatric orthopaedics. 2003, 12: 155-177. 10.1097\/00009957-200305000-00001.","journal-title":"Journal of pediatric orthopaedics"},{"key":"112_CR32","volume-title":"Osteoporos Int","author":"MH Kelly","year":"2007","unstructured":"Kelly MH, Brillante B, Collins MT: Pain in fibrous dysplasia of bone: age-related changes and the anatomical distribution of skeletal lesions. Osteoporos Int. 2007"},{"key":"112_CR33","doi-asserted-by":"publisher","first-page":"249","DOI":"10.1002\/(SICI)1096-9896(199901)187:2<249::AID-PATH222>3.0.CO;2-J","volume":"187","author":"M Riminucci","year":"1999","unstructured":"Riminucci M, Liu B, Corsi A, Shenker A, Spiegel AM, Robey PG, Bianco P: The histopathology of fibrous dysplasia of bone in patients with activating mutations of the Gs alpha gene: site-specific patterns and recurrent histological hallmarks. The Journal of pathology. 1999, 187: 249-258. 10.1002\/(SICI)1096-9896(199901)187:2<249::AID-PATH222>3.0.CO;2-J.","journal-title":"The Journal of pathology"},{"key":"112_CR34","doi-asserted-by":"publisher","first-page":"1235","DOI":"10.1359\/jbmr.2003.18.7.1235","volume":"18","author":"A Corsi","year":"2003","unstructured":"Corsi A, Collins MT, Riminucci M, Howell PG, Boyde A, Robey PG, Bianco P: Osteomalacic and hyperparathyroid changes in fibrous dysplasia of bone: core biopsy studies and clinical correlations. J Bone Miner Res. 2003, 18: 1235-1246. 10.1359\/jbmr.2003.18.7.1235.","journal-title":"J Bone Miner Res"},{"key":"112_CR35","doi-asserted-by":"publisher","first-page":"532","DOI":"10.1067\/mpd.2003.153","volume":"142","author":"TS Hannon","year":"2003","unstructured":"Hannon TS, Noonan K, Steinmetz R, Eugster EA, Levine MA, Pescovitz OH: Is McCune-Albright syndrome overlooked in subjects with fibrous dysplasia of bone?. J Pediatr. 2003, 142: 532-538. 10.1067\/mpd.2003.153.","journal-title":"J Pediatr"},{"key":"112_CR36","unstructured":"Center for Genetic Testing. [ http:\/\/www.sfh-lab.com ]"},{"key":"112_CR37","unstructured":"Genome Diagnostics. [ http:\/\/www.umcutrecht.nl\/subsite\/genome-diagnostics\/DNA-diagnostics\/Gene-Tests.htm ]"},{"key":"112_CR38","doi-asserted-by":"publisher","first-page":"1164","DOI":"10.1111\/j.1556-4029.2007.00512.x","volume":"52","author":"RW Byard","year":"2007","unstructured":"Byard RW: Forensic considerations in cases of neurofibromatosis \u2013 an overview. Journal of forensic sciences. 2007, 52: 1164-1170. 10.1111\/j.1556-4029.2007.00512.x.","journal-title":"Journal of forensic sciences"},{"key":"112_CR39","doi-asserted-by":"publisher","first-page":"842","DOI":"10.7326\/0003-4819-144-11-200606060-00010","volume":"144","author":"A Theos","year":"2006","unstructured":"Theos A, Korf BR: Pathophysiology of neurofibromatosis type 1. Annals of internal medicine. 2006, 144: 842-849.","journal-title":"Annals of internal medicine"},{"key":"112_CR40","doi-asserted-by":"publisher","first-page":"1670","DOI":"10.1056\/NEJMoa020742","volume":"347","author":"JS Lee","year":"2002","unstructured":"Lee JS, FitzGibbon E, Butman JA, Dufresne CR, Kushner H, Wientroub S, Robey PG, Collins MT: Normal vision despite narrowing of the optic canal in fibrous dysplasia. N Engl J Med. 2002, 347: 1670-1676. 10.1056\/NEJMoa020742.","journal-title":"N Engl J Med"},{"key":"112_CR41","doi-asserted-by":"crossref","first-page":"1011","DOI":"10.1227\/01.NEU.0000254440.02736.E3","volume":"59","author":"CM Cutler","year":"2006","unstructured":"Cutler CM, Lee JS, Butman JA, FitzGibbon EJ, Kelly MH, Brillante BA, Feuillan P, Robey PG, DuFresne CR, Collins MT: Long-term outcome of optic nerve encasement and optic nerve decompression in patients with fibrous dysplasia: risk factors for blindness and safety of observation. Neurosurgery. 2006, 59: 1011-1017. discussion 1017\u20131018","journal-title":"Neurosurgery"},{"key":"112_CR42","doi-asserted-by":"publisher","first-page":"1596","DOI":"10.1210\/jcem-71-6-1596","volume":"71","author":"PP Feuillan","year":"1990","unstructured":"Feuillan PP, Shawker T, Rose SR, Jones J, Jeevanram RK, Nisula BC: Thyroid abnormalities in the McCune-Albright syndrome: ultrasonography and hormone studies. J Clin Endocrinol Metab. 1990, 71: 1596-1601.","journal-title":"J Clin Endocrinol Metab"},{"key":"112_CR43","doi-asserted-by":"publisher","first-page":"683","DOI":"10.1172\/JCI18399","volume":"112","author":"M Riminucci","year":"2003","unstructured":"Riminucci M, Collins MT, Fedarko NS, Cherman N, Corsi A, White KE, Waguespack S, Gupta A, Hannon T, Econs MJ, Bianco P, Gehron Robey P: FGF-23 in fibrous dysplasia of bone and its relationship to renal phosphate wasting. J Clin Invest. 2003, 112: 683-692.","journal-title":"J Clin Invest"},{"key":"112_CR44","doi-asserted-by":"publisher","first-page":"1949","DOI":"10.1359\/jbmr.2002.17.11.1949","volume":"17","author":"L Terpstra","year":"2002","unstructured":"Terpstra L, Rauch F, Plotkin H, Travers R, Glorieux FH: Bone mineralization in polyostotic fibrous dysplasia: histomorphometric analysis. J Bone Miner Res. 2002, 17: 1949-1953. 10.1359\/jbmr.2002.17.11.1949.","journal-title":"J Bone Miner Res"},{"issue":"Suppl 2","key":"112_CR45","doi-asserted-by":"publisher","first-page":"P110","DOI":"10.1359\/jbmr.06s221","volume":"21","author":"FH Glorieux","year":"2006","unstructured":"Glorieux FH, Rauch F: Medical therapy of children with fibrous dysplasia. J Bone Miner Res. 2006, 21 (Suppl 2): P110-113. 10.1359\/jbmr.06s221.","journal-title":"J Bone Miner Res"},{"key":"112_CR46","doi-asserted-by":"publisher","first-page":"552","DOI":"10.1007\/BF03348018","volume":"20","author":"MM Hammami","year":"1997","unstructured":"Hammami MM, Hussain SS, Vencer LJ, Butt A, al-Zahrani A: Primary hyperparathyroidism-associated polyostotic fibrous dysplasia: absence of McCune-Albright syndrome mutations. J Endocrinol Invest. 1997, 20: 552-558.","journal-title":"J Endocrinol Invest"},{"key":"112_CR47","doi-asserted-by":"publisher","first-page":"752","DOI":"10.1111\/j.1532-5415.2007.01161.x","volume":"55","author":"A Barone","year":"2007","unstructured":"Barone A, Giusti A, Pioli G, Girasole G, Razzano M, Pizzonia M, Palummeri E, Bianchi G: Secondary hyperparathyroidism due to hypovitaminosis D affects bone mineral density response to alendronate in elderly women with osteoporosis: a randomized controlled trial. Journal of the American Geriatrics Society. 2007, 55: 752-757. 10.1111\/j.1532-5415.2007.01161.x.","journal-title":"Journal of the American Geriatrics Society"},{"key":"112_CR48","doi-asserted-by":"publisher","first-page":"809","DOI":"10.1007\/BF03347375","volume":"29","author":"A Giusti","year":"2006","unstructured":"Giusti A, Barone A, Razzano M, Pizzonia M, Oliveri M, Palummeri E, Pioli G: High prevalence of secondary hyperparathyroidism due to hypovitaminosis D in hospitalized elderly with and without hip fracture. Journal of endocrinological investigation. 2006, 29: 809-813.","journal-title":"Journal of endocrinological investigation"},{"key":"112_CR49","doi-asserted-by":"publisher","first-page":"579","DOI":"10.1185\/030079905X41435","volume":"21","author":"JY Reginster","year":"2005","unstructured":"Reginster JY: The high prevalence of inadequate serum vitamin D levels and implications for bone health. Current medical research and opinion. 2005, 21: 579-586. 10.1185\/030079905X41435.","journal-title":"Current medical research and opinion"},{"key":"112_CR50","doi-asserted-by":"publisher","first-page":"213","DOI":"10.1007\/s00774-005-0674-8","volume":"24","author":"S Hashemipour","year":"2006","unstructured":"Hashemipour S, Larijani B, Adibi H, Sedaghat M, Pajouhi M, Bastan-Hagh MH, Soltani A, Javadi E, Shafaei AR, Baradar-Jalili R, Hossein-Nezhad A: The status of biochemical parameters in varying degrees of vitamin D deficiency. Journal of bone and mineral metabolism. 2006, 24: 213-218. 10.1007\/s00774-005-0674-8.","journal-title":"Journal of bone and mineral metabolism"},{"issue":"Suppl 2","key":"112_CR51","doi-asserted-by":"publisher","first-page":"P105","DOI":"10.1359\/jbmr.06s220","volume":"21","author":"RP Stanton","year":"2006","unstructured":"Stanton RP: Surgery for fibrous dysplasia. J Bone Miner Res. 2006, 21 (Suppl 2): P105-109. 10.1359\/jbmr.06s220.","journal-title":"J Bone Miner Res"},{"issue":"Suppl 2","key":"112_CR52","doi-asserted-by":"publisher","first-page":"P114","DOI":"10.1359\/jbmr.06s222","volume":"21","author":"RD Chapurlat","year":"2006","unstructured":"Chapurlat RD: Medical therapy in adults with fibrous dysplasia of bone. J Bone Miner Res. 2006, 21 (Suppl 2): P114-119. 10.1359\/jbmr.06s222.","journal-title":"J Bone Miner Res"},{"key":"112_CR53","doi-asserted-by":"publisher","first-page":"953","DOI":"10.1016\/S0140-6736(94)90069-8","volume":"343","author":"D Liens","year":"1994","unstructured":"Liens D, Delmas PD, Meunier PJ: Long-term effects of intravenous pamidronate in fibrous dysplasia of bone. Lancet. 1994, 343: 953-954. 10.1016\/S0140-6736(94)90069-8.","journal-title":"Lancet"},{"key":"112_CR54","doi-asserted-by":"publisher","first-page":"4569","DOI":"10.1210\/jc.2003-030050","volume":"88","author":"H Plotkin","year":"2003","unstructured":"Plotkin H, Rauch F, Zeitlin L, Munns C, Travers R, Glorieux FH: Effect of pamidronate treatment in children with polyostotic fibrous dysplasia of bone. J Clin Endocrinol Metab. 2003, 88: 4569-4575. 10.1210\/jc.2003-030050.","journal-title":"J Clin Endocrinol Metab"},{"key":"112_CR55","first-page":"75","volume":"19","author":"B Chan","year":"2006","unstructured":"Chan B, Zacharin M: Pamidronate treatment of polyostotic fibrous dysplasia: failure to prevent expansion of dysplastic lesions during childhood. J Pediatr Endocrinol Metab. 2006, 19: 75-80.","journal-title":"J Pediatr Endocrinol Metab"},{"issue":"3","key":"112_CR56","doi-asserted-by":"crossref","first-page":"531","DOI":"10.2106\/00004623-200403000-00011","volume":"86-A","author":"AI Leet","year":"2004","unstructured":"Leet AI, Magur E, Lee JS, Wientroub S, Robey PG, Collins MT: Fibrous dysplasia in the spine: prevalence of lesions and association with scoliosis. J Bone Joint Surg Am. 2004, 86-A (3): 531-537.","journal-title":"J Bone Joint Surg Am"},{"key":"112_CR57","doi-asserted-by":"publisher","first-page":"2100","DOI":"10.1210\/jc.2006-2350","volume":"92","author":"P Feuillan","year":"2007","unstructured":"Feuillan P, Calis K, Hill S, Shawker T, Robey PG, Collins MT: Letrozole Treatment of Precocious Puberty in Girls with the McCune-Albright Syndrome: A Pilot Study. J Clin Endocrinol Metab. 2007, 92: 2100-2106. 10.1210\/jc.2006-2350.","journal-title":"J Clin Endocrinol Metab"},{"key":"112_CR58","first-page":"243","volume-title":"Sexual precocity: etiology, diagnosis and management","author":"PP Feuillan","year":"1993","unstructured":"Feuillan PP: Treatment of sexual precocity in girls with the McCune-Albright syndrome. Sexual precocity: etiology, diagnosis and management. Edited by: Grave GD, Cutler GB. 1993, New York: Raven Press, 243-251."},{"key":"112_CR59","doi-asserted-by":"publisher","first-page":"60","DOI":"10.1016\/S0022-3476(03)00128-8","volume":"143","author":"EA Eugster","year":"2003","unstructured":"Eugster EA, Rubin SD, Reiter EO, Plourde P, Jou HC, Pescovitz OH: Tamoxifen treatment for precocious puberty in McCune-Albright syndrome: a multicenter trial. The Journal of pediatrics. 2003, 143: 60-66. 10.1016\/S0022-3476(03)00128-8.","journal-title":"The Journal of pediatrics"},{"issue":"Suppl 4","key":"112_CR60","first-page":"429","volume":"4","author":"V Congedo","year":"2007","unstructured":"Congedo V, Celi FS: Thyroid disease in patients with McCune-Albright syndrome. Pediatr Endocrinol Rev. 2007, 4 (Suppl 4): 429-433.","journal-title":"Pediatr Endocrinol Rev"},{"key":"112_CR61","doi-asserted-by":"publisher","first-page":"2960","DOI":"10.1210\/jc.2005-2661","volume":"91","author":"SO Akintoye","year":"2006","unstructured":"Akintoye SO, Kelly MH, Brillante B, Cherman N, Turner S, Butman JA, Robey PG, Collins MT: Pegvisomant for the treatment of gsp-mediated growth hormone excess in patients with McCune-Albright syndrome. J Clin Endocrinol Metab. 2006, 91: 2960-2966. 10.1210\/jc.2005-2661.","journal-title":"J Clin Endocrinol Metab"},{"issue":"Suppl 4","key":"112_CR62","first-page":"453","volume":"4","author":"P Chanson","year":"2007","unstructured":"Chanson P, Salenave S, Orcel P: McCune-Albright syndrome in adulthood. Pediatr Endocrinol Rev. 2007, 4 (Suppl 4): 453-462.","journal-title":"Pediatr Endocrinol Rev"},{"key":"112_CR63","doi-asserted-by":"publisher","first-page":"4957","DOI":"10.1210\/jc.2006-0561","volume":"91","author":"F Galland","year":"2006","unstructured":"Galland F, Kamenicky P, Affres H, Reznik Y, Pontvert D, Le Bouc Y, Young J, Chanson P: McCune-Albright syndrome and acromegaly: effects of hypothalamopituitary radiotherapy and\/or pegvisomant in somatostatin analog-resistant patients. J Clin Endocrinol Metab. 2006, 91: 4957-4961. 10.1210\/jc.2006-0561.","journal-title":"J Clin Endocrinol Metab"},{"key":"112_CR64","doi-asserted-by":"publisher","first-page":"234","DOI":"10.7326\/0003-4819-77-2-234","volume":"77","author":"U Ehrig","year":"1972","unstructured":"Ehrig U, Wilson DR: Fibrous dysplasia of bone and primary hyperparathyroidism. Ann Intern Med. 1972, 77: 234-238.","journal-title":"Ann Intern Med"},{"key":"112_CR65","doi-asserted-by":"publisher","first-page":"556","DOI":"10.1097\/00003072-199207000-00005","volume":"17","author":"WD Leslie","year":"1992","unstructured":"Leslie WD, Reinhold C, Rosenthall L, Tau C, Glorieux FH: Panostotic fibrous dysplasia. A new craniotubular dysplasia. Clinical nuclear medicine. 1992, 17: 556-560. 10.1097\/00003072-199207000-00005.","journal-title":"Clinical nuclear medicine"},{"key":"112_CR66","first-page":"235","volume":"6","author":"PP Feuillan","year":"1997","unstructured":"Feuillan PP: McCune-Albright syndrome. Curr Ther Endocrinol Metab. 1997, 6: 235-239.","journal-title":"Curr Ther Endocrinol Metab"},{"issue":"Suppl 2","key":"112_CR67","first-page":"561","volume":"19","author":"C Defilippi","year":"2006","unstructured":"Defilippi C, Chiappetta D, Marzari D, Mussa A, Lala R: Image diagnosis in McCune-Albright syndrome. J Pediatr Endocrinol Metab. 2006, 19 (Suppl 2): 561-570.","journal-title":"J Pediatr Endocrinol Metab"},{"key":"112_CR68","doi-asserted-by":"publisher","first-page":"154","DOI":"10.1016\/S0168-8278(00)80202-0","volume":"32","author":"ES Silva","year":"2000","unstructured":"Silva ES, Lumbroso S, Medina M, Gillerot Y, Sultan C, Sokal EM: Demonstration of McCune-Albright mutations in the liver of children with high gammaGT progressive cholestasis. Journal of hepatology. 2000, 32: 154-158. 10.1016\/S0168-8278(00)80202-0.","journal-title":"Journal of hepatology"},{"key":"112_CR69","doi-asserted-by":"publisher","first-page":"727","DOI":"10.1089\/thy.1999.9.727","volume":"9","author":"D Zimmerman","year":"1999","unstructured":"Zimmerman D: Fetal and neonatal hyperthyroidism. Thyroid. 1999, 9: 727-733.","journal-title":"Thyroid"},{"key":"112_CR70","doi-asserted-by":"publisher","first-page":"258","DOI":"10.1159\/000246379","volume":"192","author":"RA Schwartz","year":"1996","unstructured":"Schwartz RA, Spicer MS, Leevy CB, Ticker JB, Lambert WC: Cutaneous fibrous dysplasia: an incomplete form of the McCune-Albright syndrome. Dermatology (Basel, Switzerland). 1996, 192: 258-261.","journal-title":"Dermatology (Basel, Switzerland)"},{"key":"112_CR71","first-page":"969","volume":"108","author":"AM Pierini","year":"1981","unstructured":"Pierini AM, Ortonne JP, Floret D: [Cutaneous manifestations of McCune-Albright syndrome: report of a case (author's transl)]. Annales de dermatologie et de venereologie. 1981, 108: 969-976.","journal-title":"Annales de dermatologie et de venereologie"}],"container-title":["Orphanet Journal of Rare Diseases"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1186\/1750-1172-3-12.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1186\/1750-1172-3-12\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1186\/1750-1172-3-12.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,18]],"date-time":"2023-05-18T12:23:41Z","timestamp":1684412621000},"score":1,"resource":{"primary":{"URL":"https:\/\/ojrd.biomedcentral.com\/articles\/10.1186\/1750-1172-3-12"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,5,19]]},"references-count":71,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2008,12]]}},"alternative-id":["112"],"URL":"https:\/\/doi.org\/10.1186\/1750-1172-3-12","relation":{},"ISSN":["1750-1172"],"issn-type":[{"value":"1750-1172","type":"electronic"}],"subject":[],"published":{"date-parts":[[2008,5,19]]},"article-number":"12"}}