{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,19]],"date-time":"2026-10-19T17:40:55Z","timestamp":1792431655487,"version":"4.5.0"},"reference-count":65,"publisher":"Springer Science and Business Media LLC","issue":"12","license":[{"start":{"date-parts":[[2016,8,6]],"date-time":"2016-08-06T00:00:00Z","timestamp":1470441600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"},{"start":{"date-parts":[[2016,8,6]],"date-time":"2016-08-06T00:00:00Z","timestamp":1470441600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"funder":[{"DOI":"10.13039\/100000862","name":"Doris Duke Charitable Foundation","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100000862","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["NIH U54HG006504"],"award-info":[{"award-number":["NIH U54HG006504"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000072","name":"National Institute of Dental and Craniofacial Research","doi-asserted-by":"publisher","award":["Division of Intramural Research"],"award-info":[{"award-number":["Division of Intramural Research"]}],"id":[{"id":"10.13039\/100000072","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000072","name":"National Institute of Dental and Craniofacial Research","doi-asserted-by":"publisher","award":["Division of Intramural Research"],"award-info":[{"award-number":["Division of Intramural Research"]}],"id":[{"id":"10.13039\/100000072","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000072","name":"National Institute of Dental and Craniofacial Research","doi-asserted-by":"publisher","award":["Division of Intramural Research"],"award-info":[{"award-number":["Division of Intramural Research"]}],"id":[{"id":"10.13039\/100000072","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Osteoporos Int"],"published-print":{"date-parts":[[2016,12]]},"DOI":"10.1007\/s00198-016-3702-8","type":"journal-article","created":{"date-parts":[[2016,8,6]],"date-time":"2016-08-06T08:56:21Z","timestamp":1470473781000},"page":"3615-3626","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":59,"title":["Cutaneous skeletal hypophosphatemia syndrome: clinical spectrum, natural history, and treatment"],"prefix":"10.1007","volume":"27","author":[{"given":"D.","family":"Ovejero","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Y. H.","family":"Lim","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A. M.","family":"Boyce","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R. I.","family":"Gafni","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E.","family":"McCarthy","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"T. A.","family":"Nguyen","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"L. F.","family":"Eichenfield","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C. M. C.","family":"DeKlotz","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"L. C.","family":"Guthrie","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"L. L.","family":"Tosi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P. S.","family":"Thornton","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"K. A.","family":"Choate","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M. T.","family":"Collins","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2016,8,6]]},"reference":[{"issue":"2","key":"3702_CR1","doi-asserted-by":"publisher","first-page":"397","DOI":"10.1093\/hmg\/ddt429","volume":"23","author":"YH Lim","year":"2014","unstructured":"Lim YH et al (2014) Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemia. Hum Mol Genet 23(2):397\u2013407","journal-title":"Hum Mol Genet"},{"key":"3702_CR2","doi-asserted-by":"publisher","unstructured":"Lim YH, Ovejero D, Derrick KM; Yale Center for Mendelian Genomics, Collins MT, Choate KA (2016) Cutaneous skeletal hypophosphatemia syndrome (CSHS) is a multilineage somatic mosaic RASopathy. J Am Acad Dermatol 75(2):420\u2013427. doi: 10.1016\/j.jaad.2015.11.012","DOI":"10.1016\/j.jaad.2015.11.012"},{"issue":"1","key":"3702_CR3","doi-asserted-by":"publisher","first-page":"56","DOI":"10.1016\/S0022-3476(77)80444-7","volume":"91","author":"LC Aschinberg","year":"1977","unstructured":"Aschinberg LC et al (1977) Vitamin D-resistant rickets associated with epidermal nevus syndrome: demonstration of a phosphaturic substance in the dermal lesions. J Pediatr 91(1):56\u201360","journal-title":"J Pediatr"},{"issue":"1","key":"3702_CR4","doi-asserted-by":"publisher","first-page":"2","DOI":"10.1002\/jbmr.1805","volume":"28","author":"DW Dempster","year":"2013","unstructured":"Dempster DW et al (2013) Standardized nomenclature, symbols, and units for bone histomorphometry: a 2012 update of the report of the ASBMR Histomorphometry Nomenclature Committee. J Bone Miner Res 28(1):2\u201317","journal-title":"J Bone Miner Res"},{"issue":"9","key":"3702_CR5","doi-asserted-by":"publisher","first-page":"1335","DOI":"10.1359\/jbmr.1997.12.9.1335","volume":"12","author":"SA Kuznetsov","year":"1997","unstructured":"Kuznetsov SA et al (1997) Single-colony derived strains of human marrow stromal fibroblasts form bone after transplantation in vivo. J Bone Miner Res 12(9):1335\u201347","journal-title":"J Bone Miner Res"},{"issue":"3","key":"3702_CR6","doi-asserted-by":"publisher","first-page":"307","DOI":"10.1111\/j.1365-2133.1981.tb00954.x","volume":"104","author":"EE Castilla","year":"1981","unstructured":"Castilla EE, da Graca Dutra M, Orioli-Parreiras IM (1981) Epidemiology of congenital pigmented naevi: I. Incidence rates and relative frequencies. Br J Dermatol 104(3):307\u201315","journal-title":"Br J Dermatol"},{"issue":"Suppl 1","key":"3702_CR7","doi-asserted-by":"publisher","first-page":"S188","DOI":"10.4103\/2230-8210.119567","volume":"17","author":"S Aggarwal","year":"2013","unstructured":"Aggarwal S et al (2013) Hypophosphatemic rickets associated with giant hairy nevus. Indian J Endocrinol Metab 17(Suppl 1):S188\u201390","journal-title":"Indian J Endocrinol Metab"},{"issue":"1","key":"3702_CR8","doi-asserted-by":"publisher","first-page":"E132","DOI":"10.1210\/jc.2013-2813","volume":"99","author":"E Avitan-Hersh","year":"2014","unstructured":"Avitan-Hersh E et al (2014) Postzygotic HRAS mutation causing both keratinocytic epidermal nevus and thymoma and associated with bone dysplasia and hypophosphatemia due to elevated FGF23. J Clin Endocrinol Metab 99(1):E132\u20136","journal-title":"J Clin Endocrinol Metab"},{"issue":"1","key":"3702_CR9","doi-asserted-by":"publisher","first-page":"225","DOI":"10.1111\/j.1365-2133.2006.07313.x","volume":"155","author":"J Bouthors","year":"2006","unstructured":"Bouthors J et al (2006) Phacomatosis pigmentokeratotica associated with hypophosphataemic rickets, pheochromocytoma and multiple basal cell carcinomas. Br J Dermatol 155(1):225\u20136","journal-title":"Br J Dermatol"},{"issue":"10","key":"3702_CR10","doi-asserted-by":"crossref","first-page":"7","DOI":"10.5070\/D333M6Z610","volume":"15","author":"M Cabanillas","year":"2009","unstructured":"Cabanillas M et al (2009) Epidermal nevus syndrome associated with polyostotic fibrous dysplasia, CNS lipoma, and aplasia cutis. Dermatol Online J 15(10):7","journal-title":"Dermatol Online J"},{"issue":"6","key":"3702_CR11","doi-asserted-by":"publisher","first-page":"994","DOI":"10.1016\/S0022-3476(86)80283-9","volume":"109","author":"DE Carey","year":"1986","unstructured":"Carey DE et al (1986) Hypophosphatemic rickets\/osteomalacia in linear sebaceous nevus syndrome: a variant of tumor-induced osteomalacia. J Pediatr 109(6):994\u20131000","journal-title":"J Pediatr"},{"issue":"1","key":"3702_CR12","doi-asserted-by":"publisher","first-page":"93","DOI":"10.1515\/JPEM.2005.18.1.93","volume":"18","author":"YY Chou","year":"2005","unstructured":"Chou YY et al (2005) Hypophosphatemic rickets associated with epidermal nevus syndrome and giant hairy nevus. J Pediatr Endocrinol Metab 18(1):93\u20135","journal-title":"J Pediatr Endocrinol Metab"},{"issue":"2","key":"3702_CR13","first-page":"125","volume":"11","author":"OO de Morais","year":"2013","unstructured":"de Morais OO et al (2013) Phacomatosis pigmentokeratotica\u2014a patient with hypophosphatemic rickets. Skinmed 11(2):125\u20138","journal-title":"Skinmed"},{"issue":"12","key":"3702_CR14","first-page":"881","volume":"57","author":"JL Feldmann","year":"1990","unstructured":"Feldmann JL et al (1990) Solomon\u2019s syndrome associated with fibrous dysplasia of bone and vitamin-resistant rickets. Rev Rhum Mal Osteoartic 57(12):881\u20134","journal-title":"Rev Rhum Mal Osteoartic"},{"issue":"5","key":"3702_CR15","doi-asserted-by":"publisher","first-page":"430","DOI":"10.1007\/s12098-012-0802-0","volume":"80","author":"G Gathwala","year":"2013","unstructured":"Gathwala G et al (2013) Giant congenital melanocytic nevi: a rare association with hypophosphatemic rickets. Indian J Pediatr 80(5):430\u20131","journal-title":"Indian J Pediatr"},{"issue":"1","key":"3702_CR16","doi-asserted-by":"publisher","first-page":"109","DOI":"10.1016\/S0190-9622(08)81813-0","volume":"29","author":"JR Goldblum","year":"1993","unstructured":"Goldblum JR, Headington JT (1993) Hypophosphatemic vitamin D-resistant rickets and multiple spindle and epithelioid nevi associated with linear nevus sebaceus syndrome. J Am Acad Dermatol 29(1):109\u201311","journal-title":"J Am Acad Dermatol"},{"issue":"2","key":"3702_CR17","doi-asserted-by":"publisher","first-page":"67","DOI":"10.1002\/ajmg.a.30915","volume":"139","author":"CL Heike","year":"2005","unstructured":"Heike CL et al (2005) Skeletal changes in epidermal nevus syndrome: does focal bone disease harbor clues concerning pathogenesis? Am J Med Genet A 139(2):67\u201377","journal-title":"Am J Med Genet A"},{"issue":"3","key":"3702_CR18","doi-asserted-by":"publisher","first-page":"233","DOI":"10.1002\/ajmg.a.30599","volume":"134","author":"WH Hoffman","year":"2005","unstructured":"Hoffman WH et al (2005) Elevated fibroblast growth factor-23 in hypophosphatemic linear nevus sebaceous syndrome. Am J Med Genet A 134(3):233\u20136","journal-title":"Am J Med Genet A"},{"issue":"4","key":"3702_CR19","doi-asserted-by":"publisher","first-page":"578","DOI":"10.1302\/0301-620X.85B4.13483","volume":"85","author":"HS Hosalkar","year":"2003","unstructured":"Hosalkar HS et al (2003) Linear sebaceous naevus syndrome and resistant rickets. J Bone Joint Surg Br 85(4):578\u201383","journal-title":"J Bone Joint Surg Br"},{"issue":"12","key":"3702_CR20","doi-asserted-by":"publisher","first-page":"1557","DOI":"10.1001\/archderm.1997.03890480077011","volume":"133","author":"R Ivker","year":"1997","unstructured":"Ivker R, Resnick SD, Skidmore RA (1997) Hypophosphatemic vitamin D-resistant rickets, precocious puberty, and the epidermal nevus syndrome. Arch Dermatol 133(12):1557\u201361","journal-title":"Arch Dermatol"},{"issue":"6","key":"3702_CR21","first-page":"611","volume":"42","author":"M John","year":"2005","unstructured":"John M, Shah NS (2005) Hypophosphatemic rickets with epidermal nevus syndrome. Indian Pediatr 42(6):611\u20132","journal-title":"Indian Pediatr"},{"issue":"1","key":"3702_CR22","doi-asserted-by":"publisher","first-page":"48","DOI":"10.1111\/j.1525-1470.2005.22111.x","volume":"22","author":"ES Kishida","year":"2005","unstructured":"Kishida ES et al (2005) Epidermal nevus syndrome associated with adnexal tumors, spitz nevus, and hypophosphatemic vitamin D-resistant rickets. Pediatr Dermatol 22(1):48\u201354","journal-title":"Pediatr Dermatol"},{"issue":"6","key":"3702_CR23","doi-asserted-by":"publisher","first-page":"1056","DOI":"10.1359\/jbmr.1998.13.6.1056","volume":"13","author":"GL Klein","year":"1998","unstructured":"Klein GL et al (1998) Congenital linear sebaceous nevus syndrome. J Bone Miner Res 13(6):1056\u20137","journal-title":"J Bone Miner Res"},{"issue":"2","key":"3702_CR24","doi-asserted-by":"publisher","first-page":"120","DOI":"10.1007\/BF00975318","volume":"5","author":"R Moorjani","year":"1976","unstructured":"Moorjani R, Shaw DG (1976) Feuerstein and Mims syndrome with resistant rickets. Pediatr Radiol 5(2):120\u20132","journal-title":"Pediatr Radiol"},{"issue":"9","key":"3702_CR25","doi-asserted-by":"crossref","first-page":"14","DOI":"10.5070\/D311M6X0BQ","volume":"16","author":"AI Moreira","year":"2010","unstructured":"Moreira AI et al (2010) Epidermal nevus syndrome associated with hypophosphatemic rickets. Dermatol Online J 16(9):14","journal-title":"Dermatol Online J"},{"issue":"5","key":"3702_CR26","doi-asserted-by":"publisher","first-page":"861","DOI":"10.1007\/s00467-011-2086-4","volume":"27","author":"R Narazaki","year":"2012","unstructured":"Narazaki R et al (2012) Linear nevus sebaceous syndrome with hypophosphatemic rickets with elevated FGF-23. Pediatr Nephrol 27(5):861\u20133","journal-title":"Pediatr Nephrol"},{"issue":"2","key":"3702_CR27","doi-asserted-by":"publisher","first-page":"103","DOI":"10.1007\/s004310051027","volume":"158","author":"JL Olivares","year":"1999","unstructured":"Olivares JL et al (1999) Epidermal naevus syndrome and hypophosphataemic rickets: description of a patient with central nervous system anomalies and review of the literature. Eur J Pediatr 158(2):103\u20137","journal-title":"Eur J Pediatr"},{"issue":"3","key":"3702_CR28","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1177\/014107689308600324","volume":"86","author":"EM O\u2019Neill","year":"1993","unstructured":"O\u2019Neill EM (1993) Linear sebaceous naevus syndrome with oncogenic rickets and diffuse pulmonary angiomatosis. J R Soc Med 86(3):177\u20138","journal-title":"J R Soc Med"},{"issue":"9","key":"3702_CR29","doi-asserted-by":"publisher","first-page":"1167","DOI":"10.1001\/archderm.1994.01690090091013","volume":"130","author":"AP Oranje","year":"1994","unstructured":"Oranje AP et al (1994) Solomon\u2019s epidermal nevus syndrome (type: linear nevus sebaceus) and hypophosphatemic vitamin D-resistant rickets. Arch Dermatol 130(9):1167\u201371","journal-title":"Arch Dermatol"},{"issue":"12","key":"3702_CR30","first-page":"969","volume":"108","author":"AM Pierini","year":"1981","unstructured":"Pierini AM, Ortonne JP, Floret D (1981) Cutaneous manifestations of McCune-Albright syndrome: report of a case (author\u2019s transl). Ann Dermatol Venereol 108(12):969\u201376","journal-title":"Ann Dermatol Venereol"},{"issue":"5","key":"3702_CR31","doi-asserted-by":"publisher","first-page":"1074","DOI":"10.1046\/j.1365-2133.2003.05273.x","volume":"148","author":"A Saraswat","year":"2003","unstructured":"Saraswat A et al (2003) Phakomatosis pigmentokeratotica associated with hypophosphataemic vitamin D-resistant rickets: improvement in phosphate homeostasis after partial laser ablation. Br J Dermatol 148(5):1074\u20136","journal-title":"Br J Dermatol"},{"issue":"8","key":"3702_CR32","doi-asserted-by":"publisher","first-page":"1577","DOI":"10.1007\/s00467-010-1485-2","volume":"25","author":"SK Sethi","year":"2010","unstructured":"Sethi SK, Hari P, Bagga A (2010) Elevated FGF-23 and parathormone in linear nevus sebaceous syndrome with resistant rickets. Pediatr Nephrol 25(8):1577\u20138","journal-title":"Pediatr Nephrol"},{"issue":"11\u201312","key":"3702_CR33","first-page":"1063","volume":"24","author":"E Shahgholi","year":"2011","unstructured":"Shahgholi E et al (2011) Congenital rhabdomyosarcoma, central precocious puberty, hemihypertrophy and hypophosphatemic rickets associated with epidermal nevus syndrome. J Pediatr Endocrinol Metab 24(11\u201312):1063\u20136","journal-title":"J Pediatr Endocrinol Metab"},{"issue":"6","key":"3702_CR34","doi-asserted-by":"publisher","first-page":"452","DOI":"10.1016\/0887-8994(91)90030-O","volume":"7","author":"CC Shieh","year":"1991","unstructured":"Shieh CC, Wang PJ (1991) Giant nevocellular nevi with rickets and brainstem tumor. Pediatr Neurol 7(6):452\u20134","journal-title":"Pediatr Neurol"},{"issue":"6 Pt 1","key":"3702_CR35","doi-asserted-by":"publisher","first-page":"855","DOI":"10.1016\/S0022-3476(87)80204-4","volume":"111","author":"F Skovby","year":"1987","unstructured":"Skovby F, Svejgaard E, Moller J (1987) Hypophosphatemic rickets in linear sebaceous nevus sequence. J Pediatr 111(6 Pt 1):855\u20137","journal-title":"J Pediatr"},{"issue":"3","key":"3702_CR36","doi-asserted-by":"publisher","first-page":"278","DOI":"10.1159\/000246861","volume":"189","author":"N Stosiek","year":"1994","unstructured":"Stosiek N et al (1994) Extensive linear epidermal nevus associated with hemangiomas of bones and vitamin-D-resistant rickets. Dermatology 189(3):278\u201382","journal-title":"Dermatology"},{"issue":"7","key":"3702_CR37","doi-asserted-by":"publisher","first-page":"566","DOI":"10.1111\/jpc.12472","volume":"50","author":"D Sukkhojaiwaratkul","year":"2014","unstructured":"Sukkhojaiwaratkul D, Mahachoklertwattana P, Poomthavorn P (2014) Epidermal nevus syndrome with hypophosphatemic rickets in a young girl. J Paediatr Child Health 50(7):566\u20139","journal-title":"J Paediatr Child Health"},{"issue":"2","key":"3702_CR38","first-page":"247","volume":"39","author":"A Tokatli","year":"1997","unstructured":"Tokatli A, Coskun T, Ozalp I (1997) Hypophosphatemic vitamin-D resistant rickets associated with epidermal nevus syndrome. A case report. Turk J Pediatr 39(2):247\u201351","journal-title":"Turk J Pediatr"},{"issue":"4","key":"3702_CR39","doi-asserted-by":"publisher","first-page":"432","DOI":"10.1111\/j.0736-8046.2004.21402.x","volume":"21","author":"H Vidaurri-de la Cruz","year":"2004","unstructured":"Vidaurri-de la Cruz H et al (2004) Epidermal nevus syndromes: clinical findings in 35 patients. Pediatr Dermatol 21(4):432\u20139","journal-title":"Pediatr Dermatol"},{"issue":"2","key":"3702_CR40","doi-asserted-by":"publisher","first-page":"102","DOI":"10.1007\/BF01991909","volume":"154","author":"AC Yu","year":"1995","unstructured":"Yu AC et al (1995) Epidermal naevus syndrome associated with polyostotic fibrous dysplasia and central precocious puberty. Eur J Pediatr 154(2):102\u20134","journal-title":"Eur J Pediatr"},{"issue":"1","key":"3702_CR41","doi-asserted-by":"publisher","first-page":"72","DOI":"10.1159\/000070948","volume":"207","author":"M Zutt","year":"2003","unstructured":"Zutt M et al (2003) Schimmelpenning-Feuerstein-Mims syndrome with hypophosphatemic rickets. Dermatology 207(1):72\u20136","journal-title":"Dermatology"},{"issue":"5","key":"3702_CR42","doi-asserted-by":"publisher","first-page":"371","DOI":"10.1111\/j.1365-2230.1989.tb02589.x","volume":"14","author":"MH Rustin","year":"1989","unstructured":"Rustin MH et al (1989) Polyostotic fibrous dysplasia associated with extensive linear epidermal naevi. Clin Exp Dermatol 14(5):371\u20135","journal-title":"Clin Exp Dermatol"},{"key":"3702_CR43","first-page":"491","volume":"113","author":"JN Bouwes Bavinck","year":"1985","unstructured":"Bouwes Bavinck JN, van de Kamp JJP (1985) Organoid naevus phakomatosis: Schimmelpenning-Feuerstein-Mims syndrome. Br J Dermatol 113:491\u2013492","journal-title":"Br J Dermatol"},{"issue":"2","key":"3702_CR44","first-page":"143","volume":"112","author":"F Camacho Martinez","year":"1985","unstructured":"Camacho Martinez F, Moreno Gimenez JC (1985) Epidermal nevus syndrome (of Solomon, Fretzin and Dewald). Ann Dermatol Venereol 112(2):143\u20137","journal-title":"Ann Dermatol Venereol"},{"issue":"2","key":"3702_CR45","first-page":"184","volume":"79","author":"G Grun","year":"1972","unstructured":"Grun G, Didier MF (1972) Albright\u2019s syndrome (apropos of 2 cases). Bull Soc Fr Dermatol Syphiligr 79(2):184\u20135","journal-title":"Bull Soc Fr Dermatol Syphiligr"},{"issue":"5","key":"3702_CR46","doi-asserted-by":"publisher","first-page":"298","DOI":"10.1016\/S0901-5027(05)80520-X","volume":"22","author":"I Kaplan","year":"1993","unstructured":"Kaplan I, Metzker A, Calderon S (1993) Epidermal nevus syndrome with maxillary involvement. Int J Oral Maxillofac Surg 22(5):298\u2013300","journal-title":"Int J Oral Maxillofac Surg"},{"issue":"4","key":"3702_CR47","doi-asserted-by":"publisher","first-page":"606","DOI":"10.1007\/s003300050444","volume":"8","author":"C Muhle","year":"1998","unstructured":"Muhle C et al (1998) Skeletal involvement and follow-up in linear nevus sebaceous syndrome. Eur Radiol 8(4):606\u20138","journal-title":"Eur Radiol"},{"issue":"3","key":"3702_CR48","doi-asserted-by":"publisher","first-page":"145","DOI":"10.1097\/01.ten.0000218513.86979.d7","volume":"16","author":"O Sanmaneechai","year":"2006","unstructured":"Sanmaneechai O, Wisuthsarewong W, Sawathiparnich P (2006) Epidermal nevus syndrome presenting as hypophosphatemic rickets. Endocrinologist 16(3):145\u2013149","journal-title":"Endocrinologist"},{"issue":"3","key":"3702_CR49","doi-asserted-by":"publisher","first-page":"242","DOI":"10.1001\/archneur.1969.00480150032003","volume":"21","author":"GI Sugarman","year":"1969","unstructured":"Sugarman GI, Reed WB (1969) Two unusual neurocutaneous disorders with facial cutaneous signs. Arch Neurol 21(3):242\u20137","journal-title":"Arch Neurol"},{"issue":"3","key":"3702_CR50","doi-asserted-by":"publisher","first-page":"204","DOI":"10.1111\/j.1525-1470.1994.tb00587.x","volume":"11","author":"S Shpall","year":"1994","unstructured":"Shpall S et al (1994) Risk of malignant transformation of congenital melanocytic nevi in blacks. Pediatr Dermatol 11(3):204\u20138","journal-title":"Pediatr Dermatol"},{"issue":"8","key":"3702_CR51","doi-asserted-by":"publisher","first-page":"1998","DOI":"10.1038\/jid.2013.24","volume":"133","author":"L Groesser","year":"2013","unstructured":"Groesser L et al (2013) Phacomatosis pigmentokeratotica is caused by a postzygotic HRAS mutation in a multipotent progenitor cell. J Invest Dermatol 133(8):1998\u20132003","journal-title":"J Invest Dermatol"},{"issue":"7","key":"3702_CR52","doi-asserted-by":"publisher","first-page":"783","DOI":"10.1038\/ng.2316","volume":"44","author":"L Groesser","year":"2012","unstructured":"Groesser L et al (2012) Postzygotic HRAS and KRAS mutations cause nevus sebaceous and Schimmelpenning syndrome. Nat Genet 44(7):783\u2013U211","journal-title":"Nat Genet"},{"issue":"4","key":"3702_CR53","doi-asserted-by":"publisher","first-page":"249","DOI":"10.1136\/jmedgenet-2011-100637","volume":"49","author":"C Hafner","year":"2012","unstructured":"Hafner C et al (2012) Keratinocytic epidermal nevi are associated with mosaic RAS mutations. J Med Genet 49(4):249\u2013253","journal-title":"J Med Genet"},{"issue":"9","key":"3702_CR54","doi-asserted-by":"publisher","first-page":"2229","DOI":"10.1038\/jid.2013.70","volume":"133","author":"VA Kinsler","year":"2013","unstructured":"Kinsler VA et al (2013) Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRAS. J Investig Dermatol 133(9):2229\u20132236","journal-title":"J Investig Dermatol"},{"key":"3702_CR55","unstructured":"Boyce AM, Collins MT (1993) Fibrous dysplasia\/McCune-Albright syndrome. In: Pagon RA et al (ed) GeneReviews(R). Seattle (WA)"},{"issue":"11","key":"3702_CR56","doi-asserted-by":"publisher","first-page":"1248","DOI":"10.1038\/ng1868","volume":"38","author":"B Lorenz-Depiereux","year":"2006","unstructured":"Lorenz-Depiereux B et al (2006) DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis. Nat Genet 38(11):1248\u201350","journal-title":"Nat Genet"},{"issue":"6","key":"3702_CR57","doi-asserted-by":"publisher","first-page":"931","DOI":"10.1359\/jbmr.070304","volume":"22","author":"JL Geller","year":"2007","unstructured":"Geller JL et al (2007) Cinacalcet in the management of tumor-induced osteomalacia. J Bone Miner Res 22(6):931\u20137","journal-title":"J Bone Miner Res"},{"issue":"4","key":"3702_CR58","doi-asserted-by":"publisher","first-page":"1587","DOI":"10.1172\/JCI72829","volume":"124","author":"TO Carpenter","year":"2014","unstructured":"Carpenter TO et al (2014) Randomized trial of the anti-FGF23 antibody KRN23 in X-linked hypophosphatemia. J Clin Invest 124(4):1587\u201397","journal-title":"J Clin Invest"},{"issue":"4","key":"3702_CR59","doi-asserted-by":"publisher","first-page":"899","DOI":"10.1002\/jbmr.1810","volume":"28","author":"S Wohrle","year":"2013","unstructured":"Wohrle S et al (2013) Pharmacological inhibition of fibroblast growth factor (FGF) receptor signaling ameliorates FGF23-mediated hypophosphatemic rickets. J Bone Miner Res 28(4):899\u2013911","journal-title":"J Bone Miner Res"},{"issue":"2","key":"3702_CR60","doi-asserted-by":"publisher","first-page":"65","DOI":"10.1007\/s11914-013-0144-5","volume":"11","author":"AM Boyce","year":"2013","unstructured":"Boyce AM, Bhattacharyya N, Collins MT (2013) Fibrous dysplasia and fibroblast growth factor-23 regulation. Curr Osteoporos Rep 11(2):65\u201371","journal-title":"Curr Osteoporos Rep"},{"issue":"11","key":"3702_CR61","doi-asserted-by":"publisher","first-page":"1731","DOI":"10.1359\/jbmr.080609","volume":"23","author":"SA Kuznetsov","year":"2008","unstructured":"Kuznetsov SA et al (2008) Age-dependent demise of GNAS-mutated skeletal stem cells and \u201cnormalization\u201d of fibrous dysplasia of bone. J Bone Miner Res 23(11):1731\u201340","journal-title":"J Bone Miner Res"},{"issue":"4","key":"3702_CR62","doi-asserted-by":"publisher","first-page":"547","DOI":"10.1083\/jcb.201009094","volume":"192","author":"F Rodier","year":"2011","unstructured":"Rodier F, Campisi J (2011) Four faces of cellular senescence. J Cell Biol 192(4):547\u201356","journal-title":"J Cell Biol"},{"issue":"21","key":"3702_CR63","doi-asserted-by":"publisher","first-page":"1408","DOI":"10.1056\/NEJM199411243312103","volume":"331","author":"AS Paller","year":"1994","unstructured":"Paller AS et al (1994) Genetic and clinical mosaicism in a type of epidermal nevus. N Engl J Med 331(21):1408\u201315","journal-title":"N Engl J Med"},{"issue":"6","key":"3702_CR64","doi-asserted-by":"publisher","first-page":"715","DOI":"10.1111\/j.1525-1470.2011.01655.x","volume":"28","author":"R Chantorn","year":"2011","unstructured":"Chantorn R, Shwayder T (2011) Phacomatosis pigmentokeratotica: a further case without extracutaneous anomalies and review of the condition. Pediatr Dermatol 28(6):715\u20139","journal-title":"Pediatr Dermatol"},{"issue":"7092","key":"3702_CR65","doi-asserted-by":"publisher","first-page":"424","DOI":"10.1038\/nature04869","volume":"441","author":"RJ Shaw","year":"2006","unstructured":"Shaw RJ, Cantley LC (2006) Ras, PI(3)K and mTOR signalling controls tumour cell growth. Nature 441(7092):424\u201330","journal-title":"Nature"}],"container-title":["Osteoporosis International"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00198-016-3702-8.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s00198-016-3702-8\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00198-016-3702-8.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,8,19]],"date-time":"2023-08-19T15:09:39Z","timestamp":1692457779000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s00198-016-3702-8"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,8,6]]},"references-count":65,"journal-issue":{"issue":"12","published-print":{"date-parts":[[2016,12]]}},"alternative-id":["3702"],"URL":"https:\/\/doi.org\/10.1007\/s00198-016-3702-8","relation":{},"ISSN":["0937-941X","1433-2965"],"issn-type":[{"value":"0937-941X","type":"print"},{"value":"1433-2965","type":"electronic"}],"subject":[],"published":{"date-parts":[[2016,8,6]]},"assertion":[{"value":"9 December 2015","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"6 July 2016","order":2,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"6 August 2016","order":3,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}},{"order":1,"name":"Ethics","group":{"name":"EthicsHeading","label":"Compliance with ethical standards"}},{"value":"The authors declare that they have no conflict of interest.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Conflicts of interest"}}]}}