{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,7]],"date-time":"2026-04-07T14:41:54Z","timestamp":1775572914431,"version":"3.50.1"},"reference-count":10,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2005,9,1]],"date-time":"2005-09-01T00:00:00Z","timestamp":1125532800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["International Journal of Cardiology"],"published-print":{"date-parts":[[2005,9]]},"DOI":"10.1016\/j.ijcard.2004.09.018","type":"journal-article","created":{"date-parts":[[2005,3,16]],"date-time":"2005-03-16T07:14:06Z","timestamp":1110957246000},"page":"32-34","source":"Crossref","is-referenced-by-count":5,"title":["Association of aortic arch anomalies and subclavian artery supply disruption with neurofibromatosis"],"prefix":"10.1016","volume":"104","author":[{"given":"Masao","family":"Nakagawa","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yu","family":"Osawa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Takashi","family":"Hanato","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hidetoshi","family":"Fujino","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Noriko","family":"Watanabe","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yoshihiro","family":"Takeuchi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.ijcard.2004.09.018_bib1","doi-asserted-by":"crossref","first-page":"774","DOI":"10.1016\/S1072-7515(02)01144-4","article-title":"Middle aortic syndrome: distal thoracic and abdomnal coarctation, a disorder with multiple etiologies","volume":"194","author":"Connolly","year":"2002","journal-title":"J Am Coll Surg"},{"key":"10.1016\/j.ijcard.2004.09.018_bib2","doi-asserted-by":"crossref","first-page":"108","DOI":"10.1002\/1096-8628(20001113)95:2<108::AID-AJMG4>3.0.CO;2-0","article-title":"Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1","volume":"95","author":"Lin","year":"2000","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.ijcard.2004.09.018_bib3","doi-asserted-by":"crossref","first-page":"416","DOI":"10.1259\/0007-1285-54-641-416","article-title":"An unusual case of neurofibromatosis: cystic bone lesions and coarctation of the aortic arch","volume":"54","author":"Beggs","year":"1981","journal-title":"Br J Radiol"},{"key":"10.1016\/j.ijcard.2004.09.018_bib4","first-page":"1513","article-title":"Neurofibromatosis type 1: the evolution of deep gray and white matter MR abnormalities","volume":"15","author":"Itoh","year":"1994","journal-title":"Am J Neuroradiol"},{"key":"10.1016\/j.ijcard.2004.09.018_bib5","doi-asserted-by":"crossref","first-page":"457","DOI":"10.1002\/ajmg.1320210307","article-title":"Noonan phenotype associated with neurofibromatosis","volume":"21","author":"Allanson","year":"1985","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.ijcard.2004.09.018_bib6","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1111\/j.1399-0004.1996.tb04328.x","article-title":"Neurofibromatosis\/Noonan phenotype: a variable feature of type 1 neurofibromatosis","volume":"49","author":"Colley","year":"1996","journal-title":"Clin Genet"},{"key":"10.1016\/j.ijcard.2004.09.018_bib7","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1002\/ajmg.a.20023","article-title":"Different mutations in the NF1 gene are associated with neurofibromatosis\u2013Noonan syndrome (NFNS)","volume":"119A","author":"Baralle","year":"2003","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.ijcard.2004.09.018_bib8","doi-asserted-by":"crossref","first-page":"23","DOI":"10.1007\/BF02082326","article-title":"Unusual combination of congenital heart lesions in a child with Noonan's syndrome","volume":"3","author":"Lam","year":"1982","journal-title":"Pediatr Cardiol"},{"key":"10.1016\/j.ijcard.2004.09.018_bib9","doi-asserted-by":"crossref","first-page":"903","DOI":"10.1002\/ajmg.1320230405","article-title":"Subclavian artery supply disruption sequence: hypothesis of a vascular etiology for Poland, Klippel\u2013Feil, and Moebius anomalies","volume":"23","author":"Bavinck","year":"1986","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.ijcard.2004.09.018_bib10","doi-asserted-by":"crossref","first-page":"21","DOI":"10.1016\/S0022-3476(72)80368-8","article-title":"Asymmetric crying facies: an index of other congenital anomalies","volume":"81","author":"Pape","year":"1972","journal-title":"J Pediatr"}],"container-title":["International Journal of Cardiology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0167527305001269?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0167527305001269?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,1,27]],"date-time":"2019-01-27T21:53:44Z","timestamp":1548626024000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0167527305001269"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2005,9]]},"references-count":10,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2005,9]]}},"alternative-id":["S0167527305001269"],"URL":"https:\/\/doi.org\/10.1016\/j.ijcard.2004.09.018","relation":{},"ISSN":["0167-5273"],"issn-type":[{"value":"0167-5273","type":"print"}],"subject":[],"published":{"date-parts":[[2005,9]]}}}