Literature DB >> 5433633

Cystic fibrosis and hearing. Integrity of the upper respiratory tract as related to hearing sensitivity.

L L Kulczycki, G R Herer, J S Butler.   

Abstract

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Year:  1970        PMID： 5433633     DOI： 10.1177/000992287000900707

Source DB:  PubMed          Journal:  Clin Pediatr (Phila)        ISSN： 0009-9228            Impact factor:   1.168


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  5 in total

1.  Analysis of most common CFTR mutations in patients affected by nasal polyps.

Authors:  Marzena Kostuch; Janusz Klatka; Andrzej Semczuk; Jacek Wojcierowski; Lucas Kulczycki; Jan Oleszczuk
Journal:  Eur Arch Otorhinolaryngol       Date:  2005-06-17       Impact factor: 2.503

2.  Upper respiratory tract in cystic fibrosis. Ear-nose-throat survey of 50 children.

Authors:  B Taylor; J N Evans; G A Hope
Journal:  Arch Dis Child       Date:  1974-02       Impact factor: 3.791

3.  Hearing defects in cystic fibrosis.

Authors:  W Fritze; M Götz; O Stur; E Zweymüller
Journal:  Z Kinderheilkd       Date:  1973-04-04

Review 4.  Nasal polyposis, opaque paranasal sinuses and usually normal hearing: the otorhinolaryngological features of cystic fibrosis.

Authors:  T J David
Journal:  J R Soc Med       Date:  1986       Impact factor: 5.344

5.  Abnormal paranasal sinuses in patients with cystic fibrosis of the pancreas. Radiological findings.

Authors:  J Ledesma-Medina; M Z Osman; B R Girdany
Journal:  Pediatr Radiol       Date:  1980-02
  5 in total

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