Items where Author is "Lohse, Peter"

Article

Kroener, Carolin and Wittmann, Thomas and Reu, Simone and Teusch, Veronika and Klemme, Mathias and Rauch, Daniela and Hengst, Meike and Kappler, Matthias and Cobanoglu, Nazan and Sismanlar, Tugba and Aslan, Ayse T. and Campo, Ilaria and Proesmans, Marijke and Schaible, Thomas and Terheggen-Lagro, Susanne and Regamey, Nicolas and Eber, Ernst and Seidenberg, Juergen and Schwerk, Nicolaus and Aslanidis, Charalampos and Lohse, Peter and Brasch, Frank and Zarbock, Ralf and Griese, Matthias (2017) Lung disease caused by ABCA3 mutations. THORAX, 72 (3). pp. 213-220. ISSN 0040-6376, 1468-3296

Wittmann, Thomas and Frixel, Sabrina and Hoeppner, Stefanie and Schindlbeck, Ulrike and Schams, Andrea and Kappler, Matthias and Hegermann, Jan and Wrede, Christoph and Liebisch, Gerhard and Vierzig, Anne and Zacharasiewicz, Angela and Kopp, Matthias Volkmar and Poets, Christian F. and Baden, Winfried and Hartl, Dominik and van Kaam, Anton H. and Lohse, Peter and Aslanidis, Charalampos and Zarbock, Ralf and Griese, Matthias (2016) Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3. MOLECULAR MEDICINE, 22. ISSN 1076-1551, 1528-3658

Griese, Matthias and Lorenz, Elke and Hengst, Meike and Schams, Andrea and Wesselak, Traudl and Rauch, Daniela and Wittmann, Thomas and Kirchberger, Valerie and Escribano, Amparo and Schaible, Thomas and Baden, Winfried and Schulze, Johannes and Krude, Heiko and Aslanidis, Charalampos and Schwerk, Nicolaus and Kappler, Matthias and Hartl, Dominik and Lohse, Peter and Zarbock, Ralf (2016) Surfactant proteins in pediatric interstitial lung disease. PEDIATRIC RESEARCH, 79 (1). pp. 34-41. ISSN 0031-3998, 1530-0447

Kleinlein, Barbara and Griese, Matthias and Liebisch, Gerhard and Krude, Heiko and Lohse, Peter and Aslanidis, Charalampos and Schmitz, Gerd and Peters, Jochen and Holzinger, Andreas (2011) Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasis. ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 96 (6). F453-F456. ISSN 1359-2998

Fischereder, Michael and Schneeberger, Helmut and Lohse, Peter and Kraemer, Bernhard K. and Schloendorff, Detlef and Land, Walter (2001) Increased rate of renal transplant failure in patients with the G20210A mutation of the prothrombin gene. AMERICAN JOURNAL OF KIDNEY DISEASES, 38 (5). pp. 1061-1064. ISSN 0272-6386