A. Lindblad (Gothenburg, Sweden), B. Assael (Verona, Italy)
Anatomopathological bronchopulmonary peculiarities in children with cystic fibrosis
S. Sciuca, O. Turcu, V. Petrovici, E. Chioroglo (Chisinau, Republic Of Moldova)
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Children with cystic fibrosis are MBL deficient or not?
I. Ciuca, I. Popa, Z. Popa, L. Pop, A. Rosca, S. Turcu (Timisoara, Romania)
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Neutrophil elastase in children with chronic lung diseases
Y. Gorinova, O. Simonova, E. Vasilieva (Moscow, Russian Federation)
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Correlation between inflammatory and oxidation markers in adults with cystic fibrosis
E. Acosta, F. Espíldora, G. Olveira, C. Olveira, A. Dorado, E. Casado, V. Alonso, J. L. De la Cruz (Málaga, Spain)
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Whether low frequency of hepatobiliary abnormalities in cystic fibrosis patients is associated with anti-inflammatory treatment?
A. Pukhalsky, G. Shmarina, D. Pukhalskaya, L. Perederko (Moscow, Russian Federation)
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Exercise tolerance in adults with cystic fibrosis
I. Peres Claro, E. Fragoso, C. Lopes, M. Felizardo, P. Azevedo, J. Valenca, R. Sotto-Mayor, A. Bugalho de Almeida (Lisbon, Portugal)
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Hypomagnesaemia in patients with cystic fibrosis (CF) in R. Macedonia
T. Jakovska, S. Fustik, L. Spirevska (Skopje, Fyrom)
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Physical aerobic training program in children with cystic fibrosis
A. C. Oliveira, R. Mesquita, J. Oliveira, N. Damasceno, L. Sampaio (São Paulo – SP, Brazil)
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Efficiency of west airway clearance system in combination with autogenic drainage physiotherapy technique in adult CF patients during lung exacerbation
A. Scherbakova (Moscow, Russian Federation)
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Retrograde scientometric analysis of the scientific impact of cystic fibrosis
S. Falahkohan, D. Groneberg, C. Scutaru, A. Fischer, D. Quarcoo, B. Kloft (Berlin, Germany)
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Multiple breath washout (MBW) using an ultrasonic flow sensor (USFS) – hygienic aspects
S. Fuchs, M. Waltner-Romen, M. Gappa, H. Ellemunter (Hannover, Germany; Innsbruck, Austria)
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Totally implantable venous access devices in patients with cystic fibrosis
G. Thalhammer, E. Eber, B. Oberwaldner, D. Dacar, M. Zach (Graz, Austria)
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A 5-year retrospective study of totally implatable ports in CF patients
E. De Wachter, I. De Schutter, T. De Backer, A. Malfroot (Brussels, Belgium)
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A three-year follow-up of nasal polyposis in children and adolescents with cystic fibrosis
S. Weber, G. Ferrari (Botucatu/SP, Brazil)
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