Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Susanne Hämmerling"'
Autor:
Julian Berges, Simon Y. Graeber, Susanne Hämmerling, Yin Yu, Arne Krümpelmann, Mirjam Stahl, Stephanie Hirtz, Heike Scheuermann, Marcus A. Mall, Olaf Sommerburg
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2023)
Rationale: Lumacaftor/ivacaftor was approved for the treatment of patients with cystic fibrosis who are homozygous for F508del aged 2 years and older following positive results from phase three trials. However, the improvement in CFTR function associ
Externí odkaz:
https://doaj.org/article/6c73e53185be46f1bc745000132421e9
Autor:
Pia Maier, Sumathy Jeyaweerasinkam, Janina Eberhard, Lina Soueidan, Susanne Hämmerling, Dirk Kohlmüller, Patrik Feyh, Gwendolyn Gramer, Sven F. Garbade, Georg F. Hoffmann, Jürgen G. Okun, Olaf Sommerburg
Publikováno v:
International Journal of Neonatal Screening, Vol 10, Iss 1, p 5 (2024)
Newborn screening (NBS) for cystic fibrosis (CF) based on pancreatitis-associated protein (PAP) has been performed for several years. While some influencing factors are known, there is currently a lack of information on the influence of seasonal temp
Externí odkaz:
https://doaj.org/article/e0c6ae699db647dfb9155aa3279b50db
Autor:
Olaf Sommerburg, Susanne Hämmerling, S. Philipp Schneider, Jürgen Okun, Claus-Dieter Langhans, Patricia Leutz-Schmidt, Mark O. Wielpütz, Werner Siems, Simon Y. Gräber, Marcus A. Mall, Mirjam Stahl
Publikováno v:
Antioxidants, Vol 10, Iss 3, p 483 (2021)
Rationale: Cystic fibrosis (CF), caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, leads to impaired pancreatic function and therefore reduced intestinal absorption of lipids and fat-soluble vitamins especial
Externí odkaz:
https://doaj.org/article/be35b711a4b64940872bfe40649354f3
Autor:
Simon Y. Graeber, Diane M. Renz, Mirjam Stahl, Sophia T. Pallenberg, Olaf Sommerburg, Lutz Naehrlich, Julian Berges, Martha Dohna, Felix C. Ringshausen, Felix Doellinger, Constanze Vitzthum, Jobst Röhmel, Christine Allomba, Susanne Hämmerling, Sandra Barth, Claudia Rückes-Nilges, Mark O. Wielpütz, Gesine Hansen, Jens Vogel-Claussen, Burkhard Tümmler, Marcus A. Mall, Anna-Maria Dittrich
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 206:311-320
Autor:
Olaf Sommerburg, Margit Happich, Georg F. Hoffmann, Jürgen G. Okun, Dirk Kohlmüller, Marcus A. Mall, Mirjam Stahl, Susanne Hämmerling, Martina U. Muckenthaler, Gwendolyn Gramer, Andreas E. Kulozik
Publikováno v:
Journal of Cystic Fibrosis. 21:422-433
Background Previous studies suggest that PAP-based CF protocols are suitable for newborn screening (NBS) for cystic fibrosis (CF) when newborns designated as CFSPID should not be detected. However, there are still discussions about the performance of
Autor:
Christoph Seitz, Hans-Ulrich Kauczor, Simon Y. Graeber, Eva Steinke, Mark O. Wielpütz, Monika Eichinger, Olaf Sommerburg, Cornelia Joachim, Susanne Hämmerling, Mirjam Stahl, Marcus A. Mall
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 204:943-953
Rationale: Previous cross-sectional studies have demonstrated that chest magnetic resonance imaging (MRI) is sensitive to detect early lung disease in infants and preschool children with cystic fib...
Autor:
Olaf Sommerburg, Cornelia Joachim, Mirjam Stahl, Mark O. Wielpütz, Susanne Hämmerling, Monika Eichinger, Marcus A. Mall, Hans-Ulrich Kauczor, Eva Steinke, Christoph Seitz
Publikováno v:
Cystic fibrosis.
Autor:
Susanne Hämmerling, Kerstin Blessing, Marcus A. Mall, Olaf Sommerburg, Cornelia Joachim, Mirjam Stahl, Philipp Latzin
Publikováno v:
Respiration. 87:357-363
Background: Cystic fibrosis (CF) lung disease starts in the first months of life often before the onset of clinical symptoms. Multiple breath washout (MBW) detects abnormal lung function in infants and young children in the laboratory setting. Object
Publikováno v:
Pediatric pulmonology. 52(7)
Hemoptysis is rare in children and adolescents. We describe an 11-year-old girl who presented with hemoptysis, cough, and exertional dyspnea. Radiologic and bronchoscopic assessment revealed a pedunculated mass in the right main stem bronchus with a
Autor:
Monika Eichinger, Mark O. Wielpütz, Olaf Sommerburg, Mirjam Stahl, Susanne Hämmerling, Simon Gräber, Marcus A. Mall
Publikováno v:
7.3 Cystic Fibrosis.