nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A systematic Cochrane Review of correctors (specific therapies for class II CFTR mutations) for cystic fibrosis [1]
|
Southern, K.W. |
|
2019 |
30 |
C |
p. 25-26 |
artikel |
2 |
Bronchopulmonary dysplasia: Pathophysiology and potential anti-inflammatory therapies
|
Papagianis, Paris C. |
|
2019 |
30 |
C |
p. 34-41 |
artikel |
3 |
Clinical pulmonary function testing in Duchenne muscular dystrophy
|
Mayer, Oscar Henry |
|
2019 |
30 |
C |
p. 9-12 |
artikel |
4 |
Diagnosis, management and pathophysiology of central sleep apnea in children
|
McLaren, Anya T. |
|
2019 |
30 |
C |
p. 49-57 |
artikel |
5 |
Duchenne Muscular Dystrophy longitudinal pulmonary assessment and management
|
Mayer, Oscar Henry |
|
2019 |
30 |
C |
p. 1 |
artikel |
6 |
Early onset children’s interstitial lung diseases: Discrete entities or manifestations of pulmonary dysmaturity?
|
Bush, Andrew |
|
2019 |
30 |
C |
p. 65-71 |
artikel |
7 |
Management of paediatric empyema by video-assisted thoracoscopic surgery (VATS) versus chest drain with fibrinolysis: Systematic review and meta-analysis
|
Pacilli, Maurizio |
|
2019 |
30 |
C |
p. 42-48 |
artikel |
8 |
Pulmonary function and clinical correlation in DMD
|
Mayer, Oscar H. |
|
2019 |
30 |
C |
p. 13-15 |
artikel |
9 |
Question 13: Can we predict the need for lung transplantation in children with cystic fibrosis?
|
Piper, Nick |
|
2019 |
30 |
C |
p. 30-33 |
artikel |
10 |
Question 3: What are the indications for and challenges in performing polysomnography in infants?
|
Cielo, Christopher M. |
|
2019 |
30 |
C |
p. 27-29 |
artikel |
11 |
Respiratory support for infants with bronchiolitis, a narrative review of the literature
|
Franklin, Donna |
|
2019 |
30 |
C |
p. 16-24 |
artikel |
12 |
Sleep disordered breathing in Duchenne muscular dystrophy
|
Sawnani, Hemant |
|
2019 |
30 |
C |
p. 2-8 |
artikel |
13 |
The child with an incessant dry cough
|
Galway, Niamh C. |
|
2019 |
30 |
C |
p. 58-64 |
artikel |