Editor-in-Chief Emeritus
B.S.Kaganov, Corr. Member of RAS
Editor-in-Chief
A.V.Gorelov, Corr. Member of RAS
Deputy Editors-in-Chief
A.I.Kamilov, Prof. (Uzbekistan)
M.Katz, Prof. (Israel)
D.V.Pechkurov, Prof. (Russia)
K.A.Uzakbaev, Prof. (Kyrgyzstan)
Secretary
N.G.Kolosova, PhD (Russia)
E.V.Mikhaylova, PhD, prof.(Russia)
S.V.Nikolaeva, PhD (Russia)
B.S.Kaganov, Corr. Member of RAS
Editor-in-Chief
A.V.Gorelov, Corr. Member of RAS
Deputy Editors-in-Chief
A.I.Kamilov, Prof. (Uzbekistan)
M.Katz, Prof. (Israel)
D.V.Pechkurov, Prof. (Russia)
K.A.Uzakbaev, Prof. (Kyrgyzstan)
Secretary
N.G.Kolosova, PhD (Russia)
E.V.Mikhaylova, PhD, prof.(Russia)
S.V.Nikolaeva, PhD (Russia)
2022 - volume 17 issue 3
Original Articles
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Effectiveness of neonatal screening for cystic fibrosis in the Russian Federation
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Epidemiological role of chronic lung infection caused by Achromobacter in patients with cystic fibrosis
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Microbiological monitoring of chronic lung infection caused by Achromobacter spp. in patients with cystic fibrosis
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COVID-19 in children and adolescents with cystic fibrosis
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Effect of respiratory tract infections on the costs of cystic fibrosis therapy
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Diagnostic role of calprotectin determination in children with cystic fibrosis
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Risk factors for chronic rhinosinusitis with nasal polyps in children with cystic fibrosis
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Health status of cystic fibrosis patients with liver cirrhosis and after liver transplantation
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Health status of twins with cystic fibrosis and F508del/R334W genotype: opportunities of targeted therapy
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Selection of CFTR modulators for children with the W1282R variant
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Importance of breastfeeding maintenance in children with cystic fibrosis
Clinical Case Reports
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Difficulties associated with differential diagnosis between cystic fibrosis and primary ciliary dyskinesia
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Phenotypic manifestations of the CFTR c.3140-16T>A (3272-16T>A) variant in homozygous state in a child with cystic fibrosis
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Clinical characteristics of the pathogenic variant L138ins of the CFTR gene in patients with cystic fibrosis
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Pancreatitis in children with cystic fibrosis and preserved pancreatic exocrine function
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Congenital concomitant pathology of the pancreas: cystic fibrosis, pancreatitis, and diabetes
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Efficacy of lumacaftor/ivacaftor in a child with severe cystic fibrosis
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Tailored approach to the treatment of pulmonary mycobacteriosis in patients with cystic fibrosis
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