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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 11
2021
Schuch, Luise A.; Forstner, Maria; Rapp, Christina K.; Li, Yang; Smith, Desiree E. C.; Mendes, Marisa I.; Delhommel, Florent; Sattler, Michael; Emiralioglu, Nagehan; Taskiran, Ekim Z.; Orhan, Diclehan; Kiper, Nural; Rohlfs, Meino; Jeske, Tim; Hastreiter, Maximilian; Gerstlauer, Michael; Torrent-Vernetta, Alba; Moreno-Galdo, Antonio; Kammer, Birgit; Brasch, Frank; Reu-Hofer, Simone und Griese, Matthias
(2021):
FARS1-related disorders caused by bi-allelic mutations in cytosolic phenylalanyl-tRNA synthetase genes: Look beyond the lungs!
In: Clinical Genetics, Bd. 99, Nr. 6: S. 789-801
2020
Prenzel, Freerk; Harfst, Jacqueline; Schwerk, Nicolaus; Ahrens, Frank; Rietschel, Ernst; Schmitt-Groh, Sabina; Rubak, Sune M. L.; Poplawska, Krystyna; Baden, Winfried; Vogel, Mandy; Hollizeck, Sebastian; Ley-Zaporozhan, Julia; Brasch, Frank; Reu, Simone und Griese, Matthias
(2020):
Lymphocytic interstitial pneumonia and follicular bronchiolitis in children: A registry-based case series.
In: Pediatric Pulmonology, Bd. 55, Nr. 4: S. 909-917
2018
Hengst, Meike; Naehrlich, Lutz; Mahavadi, Poornima; Grosse-Onnebrink, Jörg; Terheggen-Lagro, Suzanne; Skanke, Lars Hosoien; Schuch, Luise A.; Brasch, Frank; Günther, Andreas; Reu, Simone; Ley-Zaporozhan, Julia und Griese, Matthias
(2018):
Hermansky-Pudlak syndrome type 2 manifests with fibrosing lung disease early in childhood.
In: Orphanet Journal of Rare Diseases
13:42
[PDF, 2MB]
Xu, Zhiwen; Lo, Wing-Sze; Beck, David B.; Schuch, Luise A.; Olahova, Monika; Kopajtich, Robert; Chong, Yeeting E.; Alston, Charlotte L.; Seidl, Elias; Zhai, Liting; Lau, Ching-Fun; Timchak, Donna; LeDuc, Charles A.; Borczuk, Alain C.; Teich, Andrew F.; Juusola, Jane; Sofeso, Christina; Müller, Christoph; Pierre, Germaine; Hilliard, Tom; Turnpenny, Peter D.; Wagner, Matias; Kappler, Matthias; Brasch, Frank; Bouffard, John Paul; Nangle, Leslie A.; Yang, Xiang-Lei; Zhang, Mingjie; Taylor, Robert W.; Prokisch, Holger; Griese, Matthias; Chung, Wendy K. und Schimmel, Paul
(2018):
Bi-allelic Mutations in Phe-tRNA Synthetase Associated with a Multi-system Pulmonary Disease Support Non-translational Function.
In: American Journal of Human Genetics, Bd. 103, Nr. 1: S. 100-114
2017
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]
2016
Rauch, Daniela; Wetzke, Martin; Reu, Simone; Wesselak, Waltraud; Schams, Andrea; Hengst, Meike; Kammer, Birgit; Ley-Zaporozhan, Julia; Kappler, Matthias; Proesmans, Marijke; Lange, Joanna; Escribano, Amparo; Kerem, Eitan; Ahrens, Frank; Brasch, Frank; Schwerk, Nicolaus und Griese, Matthias
(2016):
Persistent Tachypnea of Infancy Usual and Aberrant.
In: American Journal of Respiratory and Critical Care Medicine, Bd. 193, Nr. 4: S. 438-447
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
2015
Griese, Matthias; Irnstetter, Armin; Hengst, Meike; Burmester, Helen; Nagel, Felicitas; Ripper, Jan; Feilcke, Maria; Pawlita, Ingo; Gothe, Florian; Kappler, Matthias; Schams, Andrea; Wesselak, Traudl; Rauch, Daniela; Wittmann, Thomas; Lohse, Peter; Brasch, Frank und Kröner, Carolin
(2015):
Categorizing diffuse parenchymal lung disease in children.
In: Orphanet Journal of Rare Diseases
10:122
[PDF, 988kB]
2013
Griese, Matthias; Haug, Melanie; Hartl, Dominik; Teusch, Veronika; Gloeckner-Pagel, Judith und Brasch, Frank
(2013):
Hypersensitivity pneumonitis: lessons for diagnosis and treatment of a rare entity in children.
In: Orphanet Journal of Rare Diseases
8:121
[PDF, 1MB]
2011
Griese, Matthias; Ripper, Jan; Sibbersen, Anke; Lohse, Pia; Lohse, Peter; Brasch, Frank; Schams, Andrea; Pamir, Asli; Schaub, Bianca; Muensterer, Oliver J.; Schoen, Carola; Gloeckner-Pagel, Judith; Nicolai, Thomas; Reiter, Karl und Hector, Andreas
(2011):
Long-term follow-up and treatment of congenital alveolar proteinosis.
In: BMC Pediatrics
11:72
[PDF, 2MB]
2009
Griese, Matthias; Haug, Melanie; Brasch, Frank; Freihorst, Achim; Lohse, Peter; Kries, Rüdiger von; Zimmermann, Theodor und Hartl, Dominik
(2009):
Incidence and classification of pediatric diffuse parenchymal lung diseases in Germany.
In: Orphanet Journal of Rare Diseases
4:26
[PDF, 347kB]