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Pediatric Pulmonology
|
November 9, 2004
Trampoline use as physiotherapy for cystic fibrosis patients
A Barak, I D Wexler, O Efrati, et al.
Pediatrics
|
January 26, 1999
Clinical and genetic risk factors for cystic fibrosis-related liver disease
M Wilschanski, J Rivlin, S Cohen, et al.
Pediatric Pulmonology
|
October 3, 2000
Serum lipase levels as a diagnostic marker in cystic fibrosis patients with normal or borderline sweat tests
A Augarten, H Shmilovich, R Doolman, et al.
Pediatric Transplantation
|
September 19, 2001
Prediction of mortality and timing of referral for lung transplantation in cystic fibrosis patients
A Augarten, H Akons, M Aviram, et al.
The European Respiratory Journal
|
August 9, 2001
Nasal potential difference measurements in patients with atypical cystic fibrosis
M Wilschanski, H Famini, N Strauss-Liviatan, et al.
Clinical and Experimental Medicine
|
November 5, 2003
Serum CA 19-9 levels as a diagnostic marker in cystic fibrosis patients with borderline sweat tests
A Augarten, H Berman, M Aviram, et al.
American Journal of Respiratory and Critical Care Medicine
|
June 1, 1997
A cystic fibrosis transmembrane conductance regulator splice variant with partial penetrance associated with variable cystic fibrosis presentations
E Kerem, N Rave-Harel, A Augarten, et al.
The European Respiratory Journal
|
January 15, 2011
Chronic ataluren (PTC124) treatment of nonsense mutation cystic fibrosis
M Wilschanski, L L Miller, D Shoseyov, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 28 results.
Pediatric Pulmonology
|
November 9, 2004
Trampoline use as physiotherapy for cystic fibrosis patients
A Barak, I D Wexler, O Efrati, et al.
Pediatrics
|
January 26, 1999
Clinical and genetic risk factors for cystic fibrosis-related liver disease
M Wilschanski, J Rivlin, S Cohen, et al.
Pediatric Pulmonology
|
October 3, 2000
Serum lipase levels as a diagnostic marker in cystic fibrosis patients with normal or borderline sweat tests
A Augarten, H Shmilovich, R Doolman, et al.
Pediatric Transplantation
|
September 19, 2001
Prediction of mortality and timing of referral for lung transplantation in cystic fibrosis patients
A Augarten, H Akons, M Aviram, et al.
The European Respiratory Journal
|
August 9, 2001
Nasal potential difference measurements in patients with atypical cystic fibrosis
M Wilschanski, H Famini, N Strauss-Liviatan, et al.
Clinical and Experimental Medicine
|
November 5, 2003
Serum CA 19-9 levels as a diagnostic marker in cystic fibrosis patients with borderline sweat tests
A Augarten, H Berman, M Aviram, et al.
American Journal of Respiratory and Critical Care Medicine
|
June 1, 1997
A cystic fibrosis transmembrane conductance regulator splice variant with partial penetrance associated with variable cystic fibrosis presentations
E Kerem, N Rave-Harel, A Augarten, et al.
The European Respiratory Journal
|
January 15, 2011
Chronic ataluren (PTC124) treatment of nonsense mutation cystic fibrosis
M Wilschanski, L L Miller, D Shoseyov, et al.
Page
of 3