Beata Swierczynska
- The role of CFTR/ENaC genotype in cystic fibrosis-like phenotypesBy Aleksandra Norek, Thierry Bienvenu, Sheila Scheinert, Elzbieta Kusmierek, Ewa Chrzescijanska, Ewa Sapiejka, Beata Swierczynska, Dorota Sands and Nico DerichsAleksandra Norek1Cystic Fibrosis Center, Institute of Mother and Child, Warsaw, Poland3CFTR Biomarker Center, Charite Universitätsmedizin, Berlin, GermanyThierry Bienvenu2Department of Genetics, Inserm, Paris, FranceSheila Scheinert3CFTR Biomarker Center, Charite Universitätsmedizin, Berlin, GermanyElzbieta Kusmierek4Department of Chemistry, Lodz University of Technology, Lodz, PolandEwa Chrzescijanska4Department of Chemistry, Lodz University of Technology, Lodz, PolandEwa Sapiejka5Cystic Fibrosis Center, Children Hospital "POLANKI", Gdansk, PolandBeata Swierczynska6Cystic Fibrosis Center, Children Hospital im Brudzinskiego, Bydgoszcz, PolandDorota Sands1Cystic Fibrosis Center, Institute of Mother and Child, Warsaw, PolandNico Derichs3CFTR Biomarker Center, Charite Universitätsmedizin, Berlin, Germany
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The ERS Monograph is the quarterly book series from the European Respiratory Society. Each Monograph covers a specific area of respiratory medicine, providing in-depth reviews that give clinicians at all levels a concise, comprehensive guide to symptoms, diagnosis and treatment.
The ERS Handbooks are compact guides to broad areas of the respiratory field. Launched in 2010, the series now covers adult, paediatric and sleep respiratory medicine, includes a companion volume of self-assessment questions and features the ERS Practical Handbooks.