{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,30]],"date-time":"2026-03-30T08:07:42Z","timestamp":1774858062310,"version":"3.50.1"},"reference-count":30,"publisher":"Springer Science and Business Media LLC","issue":"4","license":[{"start":{"date-parts":[[2010,9,15]],"date-time":"2010-09-15T00:00:00Z","timestamp":1284508800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Eur Arch Otorhinolaryngol"],"published-print":{"date-parts":[[2011,4]]},"DOI":"10.1007\/s00405-010-1382-0","type":"journal-article","created":{"date-parts":[[2010,9,14]],"date-time":"2010-09-14T14:52:16Z","timestamp":1284475936000},"page":"519-524","source":"Crossref","is-referenced-by-count":18,"title":["Prevalence of rhinosinusitis among atypical cystic fibrosis patients"],"prefix":"10.1007","volume":"268","author":[{"given":"Tal","family":"Marshak","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Y.","family":"Rivlin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L.","family":"Bentur","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"O.","family":"Ronen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"N.","family":"Uri","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2010,9,15]]},"reference":[{"key":"1382_CR1","doi-asserted-by":"crossref","first-page":"1308","DOI":"10.1056\/NEJM199310283291804","volume":"329","author":"The Cystic Fibrosis Genotype\u2013Phenotype Consortium","year":"1993","unstructured":"The Cystic Fibrosis Genotype\u2013Phenotype Consortium (1993) Correlation between genotype and phenotype in patients with cystic fibrosis. N Engl J Med 329:1308\u20131313","journal-title":"N Engl J Med"},{"key":"1382_CR2","doi-asserted-by":"crossref","first-page":"1229","DOI":"10.1164\/ajrccm.154.5.8912731","volume":"154","author":"PB Davis","year":"1996","unstructured":"Davis PB, Drumm M, Konstan MW (1996) State of the art\u2014cystic fibrosis. Am J Respir Crit Care Med 154:1229\u20131256","journal-title":"Am J Respir Crit Care Med"},{"key":"1382_CR3","doi-asserted-by":"crossref","first-page":"262","DOI":"10.1002\/ajmg.a.10886","volume":"116","author":"LL Kulczycki","year":"2003","unstructured":"Kulczycki LL, Kostuch M, Bellanti JA (2003) A clinical perspective of cystic fibrosis and new genetics finding: relationship of CFTR mutations to genotype\u2013phenotype manifestations. Am J Med Genet A 116:262\u2013267","journal-title":"Am J Med Genet A"},{"issue":"3","key":"1382_CR4","doi-asserted-by":"crossref","first-page":"597","DOI":"10.1016\/S0025-7125(05)70243-1","volume":"84","author":"JE Mickle","year":"2000","unstructured":"Mickle JE, Cutting GR (2000) Genotype\u2013phenotype relationships in cystic fibrosis. Med Clin N Am 84(3):597\u2013607","journal-title":"Med Clin N Am"},{"key":"1382_CR5","doi-asserted-by":"crossref","first-page":"439","DOI":"10.1056\/NEJMe020070","volume":"347","author":"Editorials","year":"2002","unstructured":"Editorials (2002) What is cystic fibrosis? N Engl J Med 347:439\u2013442","journal-title":"N Engl J Med"},{"key":"1382_CR6","doi-asserted-by":"crossref","first-page":"487","DOI":"10.1056\/NEJM199702133360707","volume":"336","author":"RC Stern","year":"1997","unstructured":"Stern RC (1997) The diagnosis of cystic fibrosis. N Engl J Med 336:487\u2013491","journal-title":"N Engl J Med"},{"issue":"Suppl 43","key":"1382_CR7","first-page":"2","volume":"96","author":"C Wallis","year":"2003","unstructured":"Wallis C (2003) Atypical cystic fibrosis\u2014diagnostic and management dilemmas. J R Soc Med 96(Suppl 43):2\u201310","journal-title":"J R Soc Med"},{"key":"1382_CR8","doi-asserted-by":"crossref","first-page":"1133","DOI":"10.5858\/2003-127-1133-CCICFS","volume":"127","author":"E Lyon","year":"2003","unstructured":"Lyon E, Miller C (2003) Current challenges in cystic fibrosis screening. Arch Pathol Lab Med 127:1133\u20131139","journal-title":"Arch Pathol Lab Med"},{"issue":"5","key":"1382_CR9","doi-asserted-by":"crossref","first-page":"619","DOI":"10.1016\/j.ijporl.2008.01.010","volume":"72","author":"D Babinski","year":"2008","unstructured":"Babinski D, Trawinska-Bartnicka M (2008) Rhinosinusitis in cystic fibrosis: not a simple story. Int J Pediatr Otorhinolaryngol 72(5):619\u2013624","journal-title":"Int J Pediatr Otorhinolaryngol"},{"key":"1382_CR10","doi-asserted-by":"crossref","first-page":"589","DOI":"10.1016\/S0022-3476(98)70344-0","volume":"132","author":"BJ Rosenstien","year":"1998","unstructured":"Rosenstien BJ, Cutting GR (1998) The diagnosis of cystic fibrosis: a consensus statement. J Pediatr 132:589\u2013595","journal-title":"J Pediatr"},{"key":"1382_CR11","doi-asserted-by":"crossref","first-page":"481","DOI":"10.1002\/1099-0496(200012)30:6<481::AID-PPUL8>3.0.CO;2-N","volume":"30","author":"C Gysin","year":"2000","unstructured":"Gysin C, Alothman GA, Papsin BC (2000) Sinonasal disease in cystic fibrosis: clinical characteristics, diagnosis, and management. Pediatr Pulmonol 30:481\u2013489","journal-title":"Pediatr Pulmonol"},{"key":"1382_CR12","doi-asserted-by":"crossref","first-page":"1005","DOI":"10.1097\/00005537-199608000-00018","volume":"106","author":"VG Gentile","year":"1996","unstructured":"Gentile VG, Isaacson G (1996) Patterns of sinusitis in cystic fibrosis. Laryngoscope 106:1005\u20131009","journal-title":"Laryngoscope"},{"key":"1382_CR13","doi-asserted-by":"crossref","first-page":"51","DOI":"10.1385\/CRIAI:21:1:51","volume":"21","author":"GK Mak","year":"2001","unstructured":"Mak GK, Henig NR (2001) Sinus disease in cystic fibrosis. Clin Rev Allergy Immunol 21:51\u201364","journal-title":"Clin Rev Allergy Immunol"},{"key":"1382_CR14","doi-asserted-by":"crossref","first-page":"623","DOI":"10.1067\/mhn.2002.125602","volume":"126","author":"JA Stankiewicz","year":"2002","unstructured":"Stankiewicz JA, Chow JM (2002) Nasal endoscopy and the definition and diagnosis of chronic rhinosinusitis. Otolaryngol Head Neck Surg 126:623\u2013627","journal-title":"Otolaryngol Head Neck Surg"},{"issue":"3","key":"1382_CR15","doi-asserted-by":"crossref","first-page":"216","DOI":"10.1053\/srin.2000.18071","volume":"15","author":"RR Casiano","year":"2000","unstructured":"Casiano RR (2000) Treatment of acute and chronic rhinosinusitis. Semin Respir Infect 15(3):216\u2013226","journal-title":"Semin Respir Infect"},{"key":"1382_CR16","first-page":"183","volume":"31","author":"VJ Lund","year":"1993","unstructured":"Lund VJ, Mackay IS (1993) Staging in rhinosinusitis. Rhinology 31:183\u2013184","journal-title":"Rhinology"},{"issue":"193","key":"1382_CR17","first-page":"205","volume":"29","author":"GJ Nishioka","year":"1996","unstructured":"Nishioka GJ, Cook PR (1996) Paranasal sinus disease in patients with cystic fibrosis. Otolaryngol Clin N Am 29(193):205\u2013210","journal-title":"Otolaryngol Clin N Am"},{"key":"1382_CR18","doi-asserted-by":"crossref","first-page":"95","DOI":"10.1183\/09031936.04.00097503","volume":"24","author":"D McShane","year":"2004","unstructured":"McShane D, Davies JC, Wodehouse T, Bush A, Geddes D, Alton EWFW (2004) Normal nasal mucociliary clearance in CF children: evidence against a CFTR-related defect. Eur Respir J 24:95\u2013100","journal-title":"Eur Respir J"},{"key":"1382_CR19","doi-asserted-by":"crossref","first-page":"1814","DOI":"10.1001\/jama.284.14.1814","volume":"284","author":"X Wang","year":"2000","unstructured":"Wang X, Moylan B, Leopold DA, Kim J, Rubentein RC, Togias A, Proud D, Zeitlin PL, Cutting GR (2000) Mutations in the gene responsible for cystic fibrosis and predisposition to chronic rhinosinusitis in the general population. JAMA 284:1814\u20131819","journal-title":"JAMA"},{"key":"1382_CR20","doi-asserted-by":"crossref","first-page":"E13","DOI":"10.1542\/peds.109.1.e13","volume":"109","author":"V Raman","year":"2002","unstructured":"Raman V, Clary R, Siegrist KL, Zehnbauer B, Chatila TA (2002) Increased prevalence of mutations in the cystic fibrosis transmembrane conductance regulator in children with chronic rhinosinusitis. Pediatrics 109:E13","journal-title":"Pediatrics"},{"key":"1382_CR21","doi-asserted-by":"crossref","first-page":"839","DOI":"10.1097\/00005537-200405000-00009","volume":"114","author":"A Coste","year":"2004","unstructured":"Coste A, Girodon E, Louis S, Pruliere-Escabasse V, Goosens M, Peynegre R, Escudier E (2004) Atypical sinusitis in adult must lead to looking for cystic fibrosis and primary ciliary dyskinesia. Laryngoscope 114:839\u2013843","journal-title":"Laryngoscope"},{"issue":"11","key":"1382_CR22","doi-asserted-by":"crossref","first-page":"1209","DOI":"10.1001\/archotol.1996.01890230055011","volume":"122","author":"TT Kingdom","year":"1996","unstructured":"Kingdom TT, Lee KC, FitzSimmons SC, Cropp GJ (1996) Clinical characteristic and genotype analysis of patients with cystic fibrosis and nasal polyposis requiring surgery. Arch Otolaryngol Head Neck Surg 122(11):1209\u20131213","journal-title":"Arch Otolaryngol Head Neck Surg"},{"key":"1382_CR23","doi-asserted-by":"crossref","first-page":"1412","DOI":"10.1164\/ajrccm.159.5.9712056","volume":"159","author":"MB Jorissen","year":"1999","unstructured":"Jorissen MB, Boeck K, Cuppens H (1999) Genotype\u2013phenotype correlation for the paranasal sinuses in cystic fibrosis. Am J Respir Crit Care Med 159:1412\u20131416","journal-title":"Am J Respir Crit Care Med"},{"key":"1382_CR24","first-page":"194","volume":"34","author":"I Gaudemar De","year":"1996","unstructured":"De Gaudemar I, Contencin P, Van Den Abeele T, Munck A, Cropp J (1996) Is nasal polyposis a direct manifestation of genetic mutation or a complication of chronic infection? Rhinology 34:194\u2013197","journal-title":"Rhinology"},{"key":"1382_CR25","doi-asserted-by":"crossref","first-page":"40","DOI":"10.1378\/chest.121.1.40","volume":"121","author":"G Henriksson","year":"2002","unstructured":"Henriksson G, Westrin K, Karpati F, Wikstrom A-C, Stierna P, Hjelte L (2002) Nasal polyps in cystic fibrosis, clinical endoscopic study with nasal lavage fluid analysis. Chest 121:40\u201347","journal-title":"Chest"},{"key":"1382_CR26","first-page":"491","volume":"5","author":"H Blau","year":"2003","unstructured":"Blau H, Livne M, Mussaffi M (2003) Cystic fibrosis in adults: a changing scene. IMAJ 5:491\u2013495","journal-title":"IMAJ"},{"key":"1382_CR27","first-page":"94","volume":"2","author":"Y Lotem","year":"2000","unstructured":"Lotem Y, Barak A, Mussaffi H, Shohat M, Wilschanski M, Sivan Y, Blau H (2000) Reaching the diagnosis of cystic fibrosis\u2014the limits of the spectrum. IMAJ 2:94\u201398","journal-title":"IMAJ"},{"key":"1382_CR28","doi-asserted-by":"crossref","first-page":"1215","DOI":"10.1378\/chest.126.4.1215","volume":"126","author":"M Gilljam","year":"2004","unstructured":"Gilljam M, Ellis L, Corey M, Zielenski J, Durie P, Tullis A (2004) Clinical manifestation of cystic fibrosis among patients with diagnosis in adulthood. Chest 126:1215\u20131222","journal-title":"Chest"},{"key":"1382_CR29","doi-asserted-by":"crossref","unstructured":"Nishioka GJ, Cook PR (1996) Paranasal sinus disease in patients with cystic fibrosis. Otolaryngol Clin N Am 29:193\u2013205","DOI":"10.1016\/S0030-6665(20)30426-6"},{"issue":"1","key":"1382_CR30","doi-asserted-by":"crossref","first-page":"7","DOI":"10.1016\/j.jcf.2004.12.002","volume":"4","author":"E Kerem","year":"2005","unstructured":"Kerem E, Conway S, Elborn S, Heijerman H (2005) Standards of care for patients with cystic fibrosis: a European consensus. J Cyst Fibros 4(1):7\u201326","journal-title":"J Cyst Fibros"}],"container-title":["European Archives of Oto-Rhino-Laryngology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00405-010-1382-0.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s00405-010-1382-0\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00405-010-1382-0","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,11,9]],"date-time":"2021-11-09T22:25:02Z","timestamp":1636496702000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s00405-010-1382-0"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2010,9,15]]},"references-count":30,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2011,4]]}},"alternative-id":["1382"],"URL":"https:\/\/doi.org\/10.1007\/s00405-010-1382-0","relation":{},"ISSN":["0937-4477","1434-4726"],"issn-type":[{"value":"0937-4477","type":"print"},{"value":"1434-4726","type":"electronic"}],"subject":[],"published":{"date-parts":[[2010,9,15]]}}}