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Anzahl der Publikationen: 5
Zeitschriftenartikel
Kröner, Carolin; Wittmann, Thomas; Reu, Simone; Teusch, Veronika; Klemme, Mathias; Rauch, Daniela; Hengst, Meike; Kappler, Matthias; Cobanoglu, Nazan; Sismanlar, Tugba; Aslan, Ayse T.; Campo, Ilaria; Prösmans, Marijke; Schaible, Thomas; Terheggen-Lagro, Susanne; Regamey, Nicolas; Eber, Ernst; Seidenberg, Jürgen; Schwerk, Nicolaus; Aslanidis, Charalampos; Lohse, Peter; Brasch, Frank; Zarbock, Ralf und Griese, Matthias
(2017):
Lung disease caused by ABCA3 mutations.
In: Thorax, Bd. 72, Nr. 3: S. 213-220
[PDF, 538kB]
Wittmann, Thomas; Frixel, Sabrina; Höppner, Stefanie; Schindlbeck, Ulrike; Schams, Andrea; Kappler, Matthias; Hegermann, Jan; Wrede, Christoph; Liebisch, Gerhard; Vierzig, Anne; Zacharasiewicz, Angela; Kopp, Matthias Volkmar; Poets, Christian F.; Baden, Winfried; Hartl, Dominik; Kaam, Anton H. van; Lohse, Peter; Aslanidis, Charalampos; Zarbock, Ralf und Griese, Matthias
(2016):
Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3.
In: Molecular Medicine, Bd. 22
[PDF, 1MB]
Griese, Matthias; Lorenz, Elke; Hengst, Meike; Schams, Andrea; Wesselak, Traudl; Rauch, Daniela; Wittmann, Thomas; Kirchberger, Valerie; Escribano, Amparo; Schaible, Thomas; Baden, Winfried; Schulze, Johannes; Krude, Heiko; Aslanidis, Charalampos; Schwerk, Nicolaus; Kappler, Matthias; Hartl, Dominik; Lohse, Peter und Zarbock, Ralf
(2016):
Surfactant proteins in pediatric interstitial lung disease.
In: Pediatric Research, Bd. 79, Nr. 1: S. 34-41
Wittmann, Thomas; Schindlbeck, Ulrike; Höppner, Stefanie; Kinting, Susanna; Frixel, Sabrina; Kröner, Carolin; Liebisch, Gerhard; Hegermann, Jan; Aslanidis, Charalampos; Brasch, Frank; Reu, Simone; Lasch, Peter; Zarbock, Ralf und Griese, Matthias
(2016):
Tools to explore ABCA3 mutations causing interstitial lung disease.
In: Pediatric Pulmonology, Bd. 51, Nr. 12: S. 1284-1294
Kleinlein, Barbara; Griese, Matthias; Liebisch, Gerhard; Krude, Heiko; Lohse, Peter; Aslanidis, Charalampos; Schmitz, Gerd; Peters, Jochen und Holzinger, Andreas
(November 2011):
Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasis.
In: Archives of disease in childhood. Fetal and neonatal edition, Bd. 96, Nr. 6:
F453-F456
[PDF, 196kB]