Sinonasal manifestations of cystic fibrosis: A correlation between genotype and phenotype?

Journal of Cystic Fibrosis

Volumn 13, Issue 4, 2014, Pages 442-448

  Berkhout, M C ^a   Van Rooden, C J ^a   Rijntjes, E ^a   Fokkens, W J ^b   El Bouazzaoui, L H ^a   Heijerman, H G M ^a  

^a HAGA HOSPITAL   (Netherlands)

^b ACADEMIC MEDICAL CENTER   (Netherlands)

Author keywords

Cystic fibrosis; Genotype; Nasal polyps; Rhinosinusitis

Indexed keywords

ADULT; ARTICLE; COMPUTER ASSISTED TOMOGRAPHY; CONTROLLED STUDY; CYSTIC FIBROSIS; ENDOSCOPY; FEMALE; FRONTAL SINUS; GENOTYPE PHENOTYPE CORRELATION; HUMAN; MAJOR CLINICAL STUDY; MALE; MAXILLARY SINUS; MUTATION; NOSE DISEASE; NOSE POLYP; OBSERVATIONAL STUDY; OSTEITIS; PARANASAL SINUS; PREVALENCE; PROSPECTIVE STUDY; QUALITY OF LIFE; QUESTIONNAIRE; RHINOSINUSITIS; SPHENOID SINUS; COMPLICATION; GENETICS; METABOLISM; NUCLEOTIDE SEQUENCE; PARANASAL SINUS DISEASES; PHENOTYPE;

CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; DNA;

ADULT; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; DNA; DNA MUTATIONAL ANALYSIS; ENDOSCOPY; FEMALE; HUMANS; MALE; MUTATION; PARANASAL SINUS DISEASES; PHENOTYPE; QUALITY OF LIFE; QUESTIONNAIRES; TOMOGRAPHY, X-RAY COMPUTED;

EID: 84902319967     PISSN: 15691993     EISSN: 18735010     Source Type: Journal    
DOI: 10.1016/j.jcf.2013.10.011     Document Type: Article

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