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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

Review 3. 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

4. Ear disease is not a common complication in cystic fibrosis.

Authors: M Cipolli; M Canciani; M Cavazzani; P Uras; P Zampieri; G Mastella
Journal: Eur J Pediatr Date: 1993-03 Impact factor: 3.183

5. Functional Impacts of Aminoglycoside Treatment on Speech Perception and Extended High-Frequency Hearing Loss in a Pediatric Cystic Fibrosis Cohort.

Authors: Chelsea M Blankenship; Lisa L Hunter; M Patrick Feeney; Madison Cox; Lindsey Bittinger; Angela C Garinis; Li Lin; Gary McPhail; John P Clancy
Journal: Am J Audiol Date: 2021-01-19 Impact factor: 1.636

5 in total