{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,3,31]],"date-time":"2022-03-31T04:06:11Z","timestamp":1648699571277},"reference-count":11,"publisher":"Springer Science and Business Media LLC","issue":"4","license":[{"start":{"date-parts":[[2010,11,19]],"date-time":"2010-11-19T00:00:00Z","timestamp":1290124800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Sleep Breath"],"published-print":{"date-parts":[[2011,12]]},"DOI":"10.1007\/s11325-010-0438-0","type":"journal-article","created":{"date-parts":[[2010,11,23]],"date-time":"2010-11-23T00:23:30Z","timestamp":1290471810000},"page":"875-878","source":"Crossref","is-referenced-by-count":1,"title":["Congenital central hypoventilation syndrome due to PHOX2B mutation in a Saudi child: a case report"],"prefix":"10.1007","volume":"15","author":[{"given":"Muslim Mohammed","family":"Al Saadi","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2010,11,19]]},"reference":[{"key":"438_CR1","doi-asserted-by":"crossref","first-page":"72","DOI":"10.1378\/chest.127.1.72","volume":"127","author":"H Trang","year":"2005","unstructured":"Trang H, Dehan M, Beaufils F, Zaccaria I, Amiel J, Gaultier C (2005) The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype. Chest 127:72\u201379","journal-title":"Chest"},{"key":"438_CR2","doi-asserted-by":"crossref","first-page":"421","DOI":"10.1086\/428366","volume":"76","author":"D Trochet","year":"2005","unstructured":"Trochet D, O\u2019Brien LM, Gozal D, Trang H, Nordenskj\u00f6ld A, Laudier B, Svensson PJ, Uhrig S, Cole T, Munnich A, Gaultier C, Lyonnet S, Amiel J (2005) PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndrome. Am J Hum Genet 76:421\u2013426","journal-title":"Am J Hum Genet"},{"key":"438_CR3","doi-asserted-by":"crossref","first-page":"1139","DOI":"10.1164\/rccm.200602-305OC","volume":"174","author":"EM Berry-Kravis","year":"2006","unstructured":"Berry-Kravis EM, Zhou L, Rand CM, Weese-Mayer DE (2006) Congenital central hypoventilation syndrome: pHOX2B mutations and phenotype. Am J Respir Crit Care Med 174:1139\u20131144","journal-title":"Am J Respir Crit Care Med"},{"key":"438_CR4","doi-asserted-by":"crossref","first-page":"88","DOI":"10.1164\/ajrccm.171.1.950","volume":"171","author":"DE Weese-Mayer","year":"2005","unstructured":"Weese-Mayer DE, Berry-Kravis EM, Zhou L (2005) Adult identified with congenital central hypoventilation syndrome: mutation in PHOX2b gene and late-onset CHS. Am J Respir Crit Care Med 171:88","journal-title":"Am J Respir Crit Care Med"},{"key":"438_CR5","doi-asserted-by":"crossref","first-page":"923","DOI":"10.1164\/rccm.200605-607CR","volume":"174","author":"NA Antic","year":"2006","unstructured":"Antic NA, Malow BA, Lange N, McEvoy RD, Olson AL, Turkington P, Windisch W, Samuels M, Stevens CA, Berry-Kravis EM, Weese-Mayer DE (2006) PHOX2B mutation confirmed congenital central hypoventilation syndrome: presentation in adulthood. Am J Respir Crit Care Med 174:923\u2013927","journal-title":"Am J Respir Crit Care Med"},{"key":"438_CR6","doi-asserted-by":"crossref","first-page":"894","DOI":"10.1002\/elps.200600383","volume":"28","author":"CC Hung","year":"2007","unstructured":"Hung CC, Su YN, Tsao PN, Chen PC, Lin SJ, Lin CH, Mu SC, Liu CA, Chang YC, Lin WL, Hsieh WS, Hsu SM (2007) Unequal crossover recombination-population screening for PHOX2B gene polyalanine polymorphism using CE. Electrophoresis 28:894\u2013899","journal-title":"Electrophoresis"},{"key":"438_CR7","doi-asserted-by":"crossref","first-page":"459","DOI":"10.1038\/ng1130","volume":"33","author":"J Amiel","year":"2003","unstructured":"Amiel J, Laudier B, Atti\u00e9-Bitach T, Trang H, de Pontual L, Gener B, Trochet D, Etchevers H, Ray P, Simonneau M, Vekemans M, Munnich A, Gaultier C, Lyonnet S (2003) Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Nat Genet 33:459\u2013461","journal-title":"Nat Genet"},{"key":"438_CR8","doi-asserted-by":"crossref","first-page":"267","DOI":"10.1002\/ajmg.a.20527","volume":"123","author":"DE Weese-Mayer","year":"2003","unstructured":"Weese-Mayer DE, Berry-Kravis EM, Zhou L (2003) Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b. Am J Med Genet A 123:267\u2013278","journal-title":"Am J Med Genet A"},{"key":"438_CR9","doi-asserted-by":"crossref","first-page":"182","DOI":"10.1016\/j.prrv.2004.04.009","volume":"5","author":"ML Chen","year":"2004","unstructured":"Chen ML, Keens TG (2004) Congenital central hypoventilation syndrome: not just another rare disorder. Paediatr Respir Rev 5:182\u2013189","journal-title":"Paediatr Respir Rev"},{"key":"438_CR10","doi-asserted-by":"crossref","first-page":"906","DOI":"10.1164\/rccm.200707-1079OC","volume":"177","author":"D Trochet","year":"2008","unstructured":"Trochet D, de Pontual L, Straus C, Gozal D, Trang H, Landrieu P, Munnich A, Lyonnet S, Gaultier C, Amiel J (2008) PHOX2B germline and somatic mutations in late-onset central hypoventilation syndrome. Am J Respir Crit Care Med 177:906\u2013911","journal-title":"Am J Respir Crit Care Med"},{"issue":"4","key":"438_CR11","doi-asserted-by":"crossref","first-page":"601","DOI":"10.1016\/j.jsmc.2008.08.006","volume":"3","author":"M Hiren","year":"2008","unstructured":"Hiren M, Raanan A (2008) Central alveolar hypoventilation syndromes. Sleep Med Clin 3(4):601\u2013615","journal-title":"Sleep Med Clin"}],"container-title":["Sleep and Breathing"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s11325-010-0438-0.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s11325-010-0438-0\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s11325-010-0438-0","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,6,1]],"date-time":"2019-06-01T13:44:08Z","timestamp":1559396648000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s11325-010-0438-0"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2010,11,19]]},"references-count":11,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2011,12]]}},"alternative-id":["438"],"URL":"https:\/\/doi.org\/10.1007\/s11325-010-0438-0","relation":{},"ISSN":["1520-9512","1522-1709"],"issn-type":[{"value":"1520-9512","type":"print"},{"value":"1522-1709","type":"electronic"}],"subject":[],"published":{"date-parts":[[2010,11,19]]}}}