Anzahl der Publikationen: 128
Zeitschriftenartikel
Griese, Matthias ORCID: https://orcid.org/0000-0003-0113-912X; Schwerk, Nicolaus ORCID: https://orcid.org/0000-0002-5496-7749; Carlens, Julia ORCID: https://orcid.org/0000-0001-8578-864X; Wetzke, Martin ORCID: https://orcid.org/0000-0002-1462-9569; Emiralioglu, Nagehan ORCID: https://orcid.org/0000-0002-1405-8401; Kiper, Nural ORCID: https://orcid.org/0000-0003-1261-7393; Marczak, Honorata ORCID: https://orcid.org/0000-0001-7455-4362; Lange, Joanna ORCID: https://orcid.org/0000-0003-4165-6455; Krenke, Katarzyna ORCID: https://orcid.org/0000-0002-8370-784X; Ullmann, Nicola ORCID: https://orcid.org/0000-0003-1111-5690; Krikovszky, Dora ORCID: https://orcid.org/0000-0002-0937-2121; Hämmerling, Susanne ORCID: https://orcid.org/0000-0001-7998-0723; Köster, Holger ORCID: https://orcid.org/0009-0003-2211-3233 und Seidl, Elias ORCID: https://orcid.org/0000-0001-6610-3756
(2024):
Health‐related quality scores in childhood interstitial lung disease: Good agreement between patient and caregiver reports.
In: Pediatric Pulmonology, Bd. 59, Nr. 10: S. 2572-2579
[PDF, 1MB]
Yang, Xiaohua ORCID: https://orcid.org/0009-0001-4416-9962; Forstner, Maria_E.; Rothenaigner, Ina; Bullo, Marina; Şismanlar, Tugba E. ORCID: https://orcid.org/0000-0001-7284-4999; Aslan, Ayse T.; Latzin, Philipp; Hadian, Kamyar und Griese, Matthias ORCID: https://orcid.org/0000-0003-0113-912X
(2024):
Cyclosporine A in children with ABCA3 deficiency.
In: Pediatric Pulmonology
[PDF, 1MB]
Li, Yang; Seidl, Elias ORCID: https://orcid.org/0000-0001-6610-3756; Knoflach, Katrin; Gothe, Florian; Forstner, Maria Elisabeth; Michel, Katarzyna; Pawlita, Ingo; Gesenhues, Florian; Sattler, Franziska; Yang, Xiaohua; Kroener, Carolin; Reu-Hofer, Simone; Ley-Zaporozhan, Julia; Kammer, Birgit; Krüger-Stollfuß, Ingrid; Dinkel, Julien; Carlens, Julia; Wetzke, Martin; Moreno-Galdó, Antonio ORCID: https://orcid.org/0000-0002-2496-9786; Torrent-Vernetta, Alba ORCID: https://orcid.org/0000-0002-3575-2427; Lange, Joanna; Krenke, Katarzyna; Rumman, Nisreen; Mayell, Sarah; Sismanlar, Tugba; Aslan, Ayse; Regamey, Nicolas; Proesmans, Marijke; Stehling, Florian; Naehrlich, Lutz; Ayse, Kilinc; Becker, Sebastian; Koerner-Rettberg, Cordula; Plattner, Erika; Manali, Effrosyni D; Papiris, Spyridon A; Campo, Ilaria; Kappler, Matthias; Schwerk, Nicolaus und Griese, Matthias ORCID: https://orcid.org/0000-0003-0113-912X
(2023):
ABCA3-related interstitial lung disease beyond infancy.
In: Thorax, Bd. 78, Nr. 6: S. 587-595
[PDF, 4MB]
Knoflach, Katrin ORCID: https://orcid.org/0000-0002-0104-692X; Rapp, Christina Katharina; Schwerk, Nicolaus; Carlens, Julia ORCID: https://orcid.org/0000-0001-8578-864X; Wetzke, Martin; Emiralioğlu, Nagehan ORCID: https://orcid.org/0000-0002-1405-8401; Kiper, Nural; Ring, Astrid Madsen; Buchvald, Frederik; Manali, Effrosyni; Papiris, Spyros; Reu‐Hofer, Simone; Kappler, Matthias; Schieber, Alexandra; Seidl, Elias ORCID: https://orcid.org/0000-0001-6610-3756; Gothe, Florian ORCID: https://orcid.org/0000-0003-0421-6610; Robinson, Peter N. und Griese, Matthias ORCID: https://orcid.org/0000-0003-0113-912X
(2023):
Diffuse alveolar hemorrhage in children with interstitial lung disease: Determine etiologies!
In: Pediatric Pulmonology, Bd. 58, Nr. 4: S. 1106-1121
[PDF, 1MB]
Griese, Matthias; Kappler, Matthias; Stehling, Florian; Schulze, Johannes; Baden, Winfried; Koerner-Rettberg, Cordula; Carlens, Julia; Prenzel, Freerk; Nährlich, Lutz; Thalmeier, Andreas; Sebah, Daniela; Kronfeld, Kai; Rock, Hans; Ruckes, Christian; Olivier, Margarete; Zielen, Stefan; Bagheri-Potthof, Azadeh; Thome, Ulrich; Gebhardt, Julia; Mehl, Anna; Lau, Susanne Gabriele; Philipp, Utz; Kopp, Matthias; Stichtenoth, Guido; Sommerburg, Olaf; Stahl, Mirjam; Kitz, Richard; Rietschel, Christoph; Stock, Philippe; Ahrens, Frank; Hebestreit, Helge; Segerer, Florian; Brinkmann, Folke; Anne, Schlegtendal; Eismann, Claudia; Neuner, Dörthe; Witt, Sabine; Hengst, Meike; Feilcke, Maria; Babl, Jürgen; Stauffer, Gabriele; Nickolay, Tanja; Gorbulev, Stanislav; Anthony, Gisela; Stöhr, Linda; Vieweg, Laura; Strenge-Hesse, Anke; Wetzke, Martin; Seidl, Elias und Schwerk, Nicolaus
(23. Juli 2022):
Randomized controlled phase 2 trial of hydroxychloroquine in childhood interstitial lung disease.
In: Orphanet Journal of Rare Diseases, Bd. 17
[PDF, 942kB]
Raedler, Johannes; Hoelz, Hannes; Zschoke, Anna; Loeffler-Ragg, Judith; Paolini, Marco; Ley-Zaporozhan, Julia und Griese, Matthias
(7. Juli 2022):
Do Not Miss Acute Diffuse Panbronchiolitis for Tree-in-Bud:
Case Series of a Rare Lung Disease.
In: Do Not Miss Acute Diffuse Panbronchiolitis for Tree-in-Bud: Case Series of a Rare Lung Disease, Bd. 12, Nr. 1653
[PDF, 2MB]
Griese, Matthias; Panagiotou, Panagiota; Manali, Effrosyni D.; Stahl, Mirjam; Schwerk, Nicolaus; Costa, Vanessa; Douros, Konstantinos; Kallieri, Maria; Urbantat, Ruth Maria; von Bernuth, Horst; Kolilekas, Lykourgos; Morais, Lurdes; Ramos, Ana; Landwehr, Kerstin; Knoflach, Katrin; Gothe, Florian; Reiter, Karl; Papaevangelou, Vassiliki; Kaditis, Athanasios G.; Kanaka-Gantenbein, Christina und Papiris, Spyros A.
(17. März 2022):
Autoimmune PAP (aPAP) in children.
In: ERJ Open Research: S. 1-6
[PDF, 1MB]
Griese, Matthias; Schwerk, Nicolaus; Carlens, Julia; Wetzke, Martin; Emiralioglu, Nagehan; Kiper, Nural; Lange, Joanna; Krenke, Katarzyna und Seidl, Elias
(2022):
Minimal important difference in childhood interstitial lung diseases.
In: Thorax, Bd. 78, Nr. 5: S. 476-483
[PDF, 1MB]
Seidl, Elias; Schwerk, Nicolaus; Carlens, Julia; Wetzke, Martin; Cunningham, Steve; Emiralioglu, Nagehan; Kiper, Nural; Lange, Joanna; Krenke, Katarzyna; Ullmann, Nicola; Krikovszky, Dora; Maqhuzu, Phillen; Griese, Charlotte A.; Schwarzkopf, Larissa und Griese, Matthias
(2022):
Healthcare resource utilisation and medical costs for children with interstitial lung diseases (chILD) in Europe.
In: Thorax, Bd. 77, Nr. 8: S. 781-789
[PDF, 997kB]
Seidl, Elias ORCID: https://orcid.org/0000-0001-6610-3756; Schwerk, Nicolaus ORCID: https://orcid.org/0000-0002-5496-7749; Carlens, Julia ORCID: https://orcid.org/0000-0001-8578-864X; Wetzke, Martin ORCID: https://orcid.org/0000-0002-1462-9569; Emiralioğlu, Nagehan ORCID: https://orcid.org/0000-0002-1405-8401; Kiper, Nural ORCID: https://orcid.org/0000-0003-1261-7393; Lange, Joanna ORCID: https://orcid.org/0000-0003-4165-6455; Krenke, Katarzyna ORCID: https://orcid.org/0000-0002-8370-784X; Szepfalusi, Zsolt ORCID: https://orcid.org/0000-0003-4852-3102; Stehling, Florian ORCID: https://orcid.org/0000-0002-2417-2048; Baden, Winfried; Hämmerling, Susanne; Jerkic, Silvija-Pera ORCID: https://orcid.org/0000-0003-2972-649X; Proesmans, Marijke ORCID: https://orcid.org/0000-0002-5576-9517; Ullmann, Nicola ORCID: https://orcid.org/0000-0003-1111-5690; Buchvald, Frederik ORCID: https://orcid.org/0000-0003-4196-3893; Knoflach, Katrin; Kappler, Matthias ORCID: https://orcid.org/0000-0003-3889-9552 und Griese, Matthias ORCID: https://orcid.org/0000-0003-0113-912X
(2022):
Acute exacerbations in children’s interstitial lung disease.
In: Thorax, Bd. 77, Nr. 8: S. 799-804
[PDF, 1MB]
Torrent-Vernetta, Alba; Gaboli, Mirella; Castillo-Corullon, Silvia; Mondejar-Lopez, Pedro; Sanz Santiago, Veronica; Costa-Colomer, Jordi; Osona, Borja; Torres-Borrego, Javier; De la Serna-Blazquez, Olga; Bellon Alonso, Sara; Caro Aguilera, Pilar; Gimeno-Diaz De Atauri, Alvaro; Valenzuela Soria, Alfredo; Ayats, Roser; Martin de Vicente, Carlos; Velasco Gonzalez, Valle; Moure Gonzalez, Jose Domingo; Canino Calderin, Elisa Maria; Dolores Pastor-Vivero, Maria; Villar Alvarez, Maria Angeles; Rovira-Amigo, Sandra; Iglesias Serrano, Ignacio; Diez Izquierdo, Ana; de Mir Messa, Ines; Gartner, Silvia; Navarro, Alexandra; Baz-Redon, Noelia; Carmona, Rosario; Camats-Tarruella, Nuria; Fernandez-Cancio, Monica; Rapp, Christina; Dopazo, Joaquin; Griese, Matthias und Moreno-Galdo, Antonio
(2022):
Incidence and Prevalence of Children's Diffuse Lung Disease in Spain.
In: Archivos De Bronconeumologia, Bd. 58, Nr. 1: S. 22-29
Schuetz, Katharina; Happel, Christoph M.; Keil, Oliver; Dingemann, Jens; Carlens, Julia; Wetzke, Martin; Mueller, Carsten; Koeditz, Harald; Griese, Matthias; Reiter, Karl; Schweiger-Kabesch, Andrea; Backendorf, Alexander; Scharff, AnnaZychlinsky; Bertram, Harald und Schwerk, Nicolaus
(2022):
Interventional Bronchus Occlusion Using Amplatzer Devices - A Promising Treatment Option for Children with Persistent Air Leak.
In: Klinische Padiatrie, Bd. 234, Nr. 5: S. 293-300
Terwiel, Michelle; Borie, Raphael; Crestani, Bruno; Galvin, Liam; Bonella, Francesco; Fabre, Aurelie; Froidure, Antoine; Griese, Matthias; Grutters, Jan C.; Johannson, Kerri; Kannengiesser, Caroline; Kawano-Dourado, Leticia; Molina-Molina, Maria; Prasse, Antje; Renzoni, Elisabetta A.; Smagt, Jasper van der; Poletti, Venerino; Antoniou, Katerina und Moorsel, Coline H. M. van
(2022):
Genetic testing in interstitial lung disease: An international survey.
In: Respirology, Bd. 27, Nr. 9: S. 747-757
Forstner, Maria; Lin, Sean; Yang, Xiaohua; Kinting, Susanna; Rothenaigner, Ina; Schorpp, Kenji; Li, Yang; Hadian, Kamyar und Griese, Matthias
(2022):
High-Content Screening Identifies Cyclosporin A as a Novel ABCA3-Specific Molecular Corrector.
In: American Journal of Respiratory Cell and Molecular Biology, Bd. 66, Nr. 4: S. 382-390
Länger, Florian Peter; Schwerk, Nicolaus; Dingemann, Jens; Welte, Tobias; Auber, Bernd; Verleden, Stijn; Ackermann, Maximilian; Mentzer, Steven J.; Griese, Matthias und Jonigk, Danny
(2022):
Interstitial lung disease in infancy and early childhood: a clinicopathological primer.
In: European Respiratory Review, Bd. 31, Nr. 163, 210251
Chang, Anne B.; Boyd, Jeanette; Bush, Andrew; Hill, Adam T.; Powell, Zena; Zacharasiewicz, Angela; Alexopoulou, Efthymia; Chalmers, James D.; Collaro, Andrew J.; Constant, Carolina; Douros, Konstantinos; Fortescue, Rebecca; Griese, Matthias; Grigg, Jonathan; Hector, Andreas; Karadag, Bulent; Mazulov, Oleksandr; Midulla, Fabio; Moeller, Alexander; Proesmans, Marijke; Wilson, Christine; Yerkovich, Stephanie T.; Kantar, Ahmad und Grimwood, Keith
(2022):
Quality standards for managing children and adolescents with bronchiectasis: an international consensus.
In: Breathe, Bd. 18, Nr. 3, 220144
del Alamo, Marta; Buhrer, Christoph; Fisher, Dirk; Griese, Matthias; Lingor, Paul; Palladini, Giovanni; Sireau, Nicolas; Hivert, Virginie; Sangiorgi, Luca; Guillot, Florence; Halftermeyer, Juliane; Souckova, Lenka; Noskova, Kristyna und Demlova, Regina
(2022):
Identifying obstacles hindering the conduct of academic-sponsored trials for drug repurposing on rare-diseases: an analysis of six use cases.
In: Trials, Bd. 23, Nr. 1, 783
Papiris, Spyros A. A.; Kannengiesser, Caroline; Borie, Raphael; Kolilekas, Lykourgos; Kallieri, Maria; Apollonatou, Vasiliki; Ba, Ibrahima; Nathan, Nadia; Bush, Andrew; Griese, Matthias; Dieude, Philippe; Crestani, Bruno und Manali, Effrosyni D. D.
(2022):
Genetics in Idiopathic Pulmonary Fibrosis: A Clinical Perspective.
In: Diagnostics, Bd. 12, Nr. 12, 2928
Wan, Rensheng; Faender, Johannes; Zakaraia, Ia; Lee-Kirsch, Min Ae; Wolf, Christine; Lucas, Nadja; Olfe, Lisa Isabel; Hendrich, Corinna; Jonigk, Danny; Holzinger, Dirk; Steindor, Mathis; Schmidt, Gunnar; Davenport, Claudia; Klemann, Christian; Schwerk, Nicolaus; Griese, Matthias; Schlegelberger, Brigitte; Stehling, Florian; Happle, Christine; Auber, Bernd; Steinemann, Doris; Wetzke, Martin und Hardenberg, Sandra von
(2022):
Phenotypic spectrum in recessive STING-associated vasculopathy with onset in infancy: Four novel cases and analysis of previously reported cases.
In: Frontiers in Immunology, Bd. 13, 1029423
Knoflach, Katrin; Holzapfel, Eva; Roser, Timo; Rudolph, Lieselotte; Paolini, Marco; Münchhoff, Maximilian; Osterman, Andreas; Griese, Matthias; Kappler, Matthias und von Both, Ulrich
(17. Dezember 2021):
Case Report: Unilateral Sixth Cranial Nerve Palsy Associated With COVID-19 in a 2-year-old Child.
In: Frontiers in Pediatrics, Bd. 9, 756014
[PDF, 558kB]
Hanafin, Patrick O.; Sermet-Gaudelus, Isabelle; Griese, Matthias; Kappler, Matthias; Ellemunter, Helmut; Schwarz, Carsten; Wilson, John; Tan, Marsha; Velkov, Tony; Rao, Gauri G. und Schneider-Futschik, Elena K.
(2. August 2021):
Insights Into Patient Variability During Ivacaftor-Lumacaftor Therapy in Cystic Fibrosis.
In: Frontiers in Pharmacology, Bd. 12, 577263
[PDF, 1MB]
Seidl, Elias; Kramer, Johanna; Hoffmann, Florian; Schön, Carola; Griese, Matthias; Kappler, Matthias; Lisec, Kristina; Hubertus, Jochen; Schweinitz, Dietrich von; Dio, Diana di; Sittel, Christian und Reiter, Karl
(2021):
Comorbidity and long‐term clinical outcome of laryngotracheal clefts types III and IV: Systematic analysis of new cases.
In: Pediatric Pulmonology, Bd. 56, Nr. 1: S. 138-144
[PDF, 537kB]
Deterding, Robin; Griese, Matthias; Deutsch, Gail; Warburton, David; DeBoer, Emily M.; Cunningham, Steven; Clement, Annick; Schwerk, Nicolaus; Flaherty, Kevin R.; Brown, Kevin K.; Voss, Florian; Schmid, Ulrike; Schlenker-Herceg, Rozsa; Verri, Daniela; Dumistracel, Mihaela; Schiwek, Marilisa; Stowasser, Susanne; Tetzlaff, Kay; Clerisme-Beaty, Emmanuelle und Young, Lisa R.
(2021):
Study design of a randomised, placebo-controlled trial of nintedanib in children and adolescents with fibrosing interstitial lung disease.
In: Erj Open Research, Bd. 7, Nr. 2, 00805-2020
Gothe, Florian; Gehrig, Jonathan; Rapp, Christina K.; Knoflach, Katrin; Reu-Hofer, Simone; Langer, Florian; Schramm, Dirk; Ley-Zaporozhan, Julia; Ehl, Stephan; Schwerk, Nicolaus; Faletti, Laura und Griese, Matthias
(2021):
Early-onset, fatal interstitial lung disease in STAT3 gain-of-function patients.
In: Pediatric Pulmonology, Bd. 56, Nr. 12: S. 3934-3941
Griese, Matthias; Stehling, Florian; Schwerk, Nicolaus; Rosewich, Martin; Jerkic, Pera-Silvija; Rock, Hans; Ruckes, Christian; Kronfeld, Kai; Sebah, Daniela; Wetzke, Martin und Seidl, Elias
(2021):
Hypersensitivity pneumonitis: Lessons from a randomized controlled trial in children.
In: Pediatric Pulmonology, Bd. 56, Nr. 8: S. 2627-2633
Koehler, Sebastian; Gargano, Michael; Matentzoglu, Nicolas; Carmody, Leigh C.; Lewis-Smith, David; Vasilevsky, Nicole A.; Danis, Daniel; Balagura, Ganna; Baynam, Gareth; Brower, Amy M.; Callahan, Tiffany J.; Chute, Christopher G.; Est, Johanna L.; Galer, Peter D.; Ganesan, Shiva; Griese, Matthias; Haimel, Matthias; Pazmandi, Julia; Hanauer, Marc; Harris, Nomi L.; Hartnett, Michael J.; Hastreiter, Maximilian; Hauck, Fabian; He, Yongqun; Jeske, Tim; Kearney, Hugh; Kindle, Gerhard; Klein, Christoph; Knoflach, Katrin; Krause, Roland; Lagorce, David; McMurry, Julie A.; Miller, Jillian A.; Munoz-Torres, Monica C.; Peters, Rebecca L.; Rapp, Christina K.; Rath, Ana M.; Rind, Shahmir A.; Rosenberg, Avi Z.; Segal, Michael M.; Seidel, Markus G.; Smedley, Damian; Talmy, Tomer; Thomas, Yarlalu; Wiafe, Samuel A.; Xian, Julie; Yueksel, Zafer; Helbig, Ingo; Mungall, Christopher J.; Haendel, Melissa A. und Robinson, Peter N.
(2021):
The Human Phenotype Ontology in 2021.
In: Nucleic Acids Research, Bd. 49, Nr. D1:
D1207-D1217
Magg, Thomas; Okano, Tsubasa; Koenig, Lars M.; Boehmer, Daniel F. R.; Schwartz, Samantha L.; Inoue, Kento; Heimall, Jennifer; Licciardi, Francesco; Ley-Zaporozhan, Julia; Ferdman, Ronald M.; Caballero-Oteyza, Andres; Park, Esther N.; Calderon, Brenda M.; Dey, Debayan; Kanegane, Hirokazu; Cho, Kazutoshi; Montin, Davide; Reiter, Karl; Griese, Matthias; Albert, Michael H.; Rohlfs, Meino; Gray, Paul; Walz, Christoph; Conn, Graeme L.; Sullivan, Kathleen E.; Klein, Christoph; Morio, Tomohiro und Hauck, Fabian
(2021):
Heterozygous OAS1 gain-of-function variants cause an autoinflammatory immunodeficiency.
In: Science Immunology, Bd. 6, Nr. 60, eabf9564
Marczak, Honorata; Peradzynska, Joanna; Seidl, Elias; Griese, Matthias; Urbankowski, Tomasz; Lange, Joanna; Boguslawski, Stanislaw und Krenke, Katarzyna
(2021):
The improved clinical course of persistent tachypnea of infancy with inhaled bronchodilators and corticosteroids.
In: Pediatric Pulmonology, Bd. 56, Nr. 12: S. 3952-3959
Piaggi, Simona; Marchi, Elisabetta; Carnicelli, Vittoria; Zucchi, Riccardo; Griese, Matthias; Hector, Andreas; Sorio, Claudio; Pompella, Alfonso und Corti, Alessandro
(2021):
Airways glutathione S-transferase omega-1 and its A140D polymorphism are associated with severity of inflammation and respiratory dysfunction in cystic fibrosis.
In: Journal of Cystic Fibrosis, Bd. 20, Nr. 6: S. 1053-1061
Rapp, Christina K.; Dijck, Ine van; Laugwitz, Lucia; Boon, Mieke; Briassoulis, George; Ilia, Stavroula; Kammer, Birgit; Reu, Simone; Hornung, Stefanie; Buchert, Rebecca; Sofan, Linda; Froukh, Tawfiq; Witters, Peter; Rymen, Daisy; Haack, Tobias B.; Proesmans, Marijke und Griese, Matthias
(2021):
Expanding the phenotypic spectrum of FINCA (fibrosis, neurodegeneration, and cerebral angiomatosis) syndrome beyond infancy.
In: Clinical Genetics, Bd. 100, Nr. 4: S. 453-461
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
Seidl, Elias; Schramm, Dirk; Schoen, Carola; Reiter, Karl; Pawlita, Ingo; Kappler, Matthias; Reu-Hofer, Simone; Hauck, Fabian; Albert, Michael und Griese, Matthias
(2021):
Pulmonary alveolar proteinosis due to heterozygous mutation in OAS1: Whole lung lavages for long-term bridging to hematopoietic stem cell transplantation.
In: Pediatric Pulmonology, Bd. 57, Nr. 1: S. 273-277
Vavassori, Stefano; Chou, Janet; Faletti, Laura Eva; Haunerdinger, Veronika; Opitz, Lennart; Joset, Pascal; Fraser, Christopher J.; Prader, Seraina; Gao, Xianfei; Schuch, Luise A.; Wagner, Matias; Hoefele, Julia; Maccari, Maria Elena; Zhu, Ying; Elakis, George; Gabbett, Michael T.; Forstner, Maria; Omran, Heymut; Kaiser, Thomas; Kessler, Christina; Olbrich, Heike; Frosk, Patrick; Almutairi, Abduarahman; Platt, Craig D.; Elkins, Megan; Weeks, Sabrina; Rubin, Tamar; Planas, Raquel; Marchetti, Tommaso; Koovely, Danil; Klambt, Verena; Soliman, Neveen A.; Hardenberg, Sandra von; Klemann, Christian; Baumann, Ulrich; Lenz, Dominic; Klein-Franke, Andreas; Schwemmle, Martin; Huber, Michael; Sturm, Ekkehard; Hartleif, Steffen; Haffner, Karsten; Gimpel, Charlotte; Brotschi, Barbara; Laube, Guido; Gungor, Tayfun; Buckley, Michael F.; Kottke, Raimund; Staufner, Christian; Hildebrandt, Friedhelm; Reu-Hofer, Simone; Moll, Solange; Weber, Achim; Kaur, Hundeep; Ehl, Stephan; Hiller, Sebastian; Geha, Raif; Roscioli, Tony; Griese, Matthias und Schmid, Jana Pachlopnik
(2021):
Multisystem inflammation and susceptibility to viral infections in human ZNFX1 deficiency.
In: Journal of Allergy and Clinical Immunology, Bd. 148, Nr. 2: S. 381-393
Griese, Matthias; Köhler, Meike; Witt, Sabine; Sebah, Daniela; Kappler, Matthias; Wetzke, Martin; Schwerk, Nicolaus; Emiralioglu, Nagehan; Kiper, Nural; Kronfeld, Kai; Ruckes, Christian; Rock, Hans; Anthony, Gisela und Seidl, Elias
(2020):
Prospective evaluation of hydroxychloroquine in pediatric interstitial lung diseases. Study protocol for an investigator-initiated, randomized controlled, parallel-group clinical trial.
In: Trials
21:307
[PDF, 760kB]
Urbankowska, Emilia; Urbankowski, Tomasz; Drobczynski, Lukasz; Griese, Matthias; Lange, Joanna; Brzewski, Michal; Kulus, Marek und Krenke, Katarzyna
(2020):
Lung ultrasound-a new diagnostic modality in persistent tachypnea of infancy.
In: Pediatric Pulmonology, Bd. 55, Nr. 4: S. 1028-1036
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
Emiralioglu, Nagehan; Orhan, Diclehan; Cinel, Guzin; Tugcu, Gokcen Dilsa; Yalcin, Ebru; Dogru, Deniz; Ozcelik, Ugur; Griese, Matthias und Kiper, Nural
(2020):
Variation in the bombesin staining of pulmonary neuroendocrine cells in pediatric pulmonary disorders-A useful marker for airway maturity.
In: Pediatric Pulmonology, Bd. 55, Nr. 9: S. 2383-2388
Seidl, Elias; Carlens, Julia; Schwerk, Nicolaus; Wetzke, Martin; Marczak, Honorata; Lange, Joanna; Krenke, Katarzyna; Mayell, Sarah J.; Escribano, Amparo; Seidenberg, Jurgen; Ahrens, Frank; Hebestreit, Helge; Naehrlich, Lutz; Sismanlar, Tugba; Aslan, Ayse T.; Snijders, Deborah; Ullmann, Nicola; Kappler, Matthias und Griese, Matthias
(2020):
Persistent tachypnea of infancy: Follow up at school age.
In: Pediatric Pulmonology, Bd. 55, Nr. 11: S. 3119-3125
[PDF, 809kB]
Lenz, Dominic; Stahl, Mirjam; Seidl, Elias; Schoendorf, Dominik; Brennenstuhl, Heiko; Gesenhues, Florian; Heinzmann, Tina; Longerich, Thomas; Mendes, Marisa I.; Prokisch, Holger; Salomons, Gajja S.; Schoen, Carola; Smith, Desiree E. C.; Sommerburg, Olaf; Wagner, Matias; Westhoff, Jens H.; Reiter, Karl; Staufner, Christian und Griese, Matthias
(2020):
Rescue of respiratory failure in pulmonary alveolar proteinosis due to pathogenic MARS1 variants.
In: Pediatric Pulmonology, Bd. 55, Nr. 11: S. 3057-3066
Cunningham, Steve; Graham, Catriona; MacLean, Morag; Aurora, Paul; Ashworth, Michael; Barbato, Angelo; Calder, Alistair; Carlens, Julia; Clement, Annick; Hengst, Meike; Kammer, Birgit; Kiper, Nural; Krenke, Katarzyna; Kronfeld, Kai; Lange, Joanna; Ley-Zaporozhan, Julia; Nicholson, Andrew G.; Reu, Simone; Wesselak, Traudl; Wetzke, Martin; Bush, Andrew; Schwerk, Nicolaus und Griese, Matthias
(2020):
One-year outcomes in a multicentre cohort study of incident rare diffuse parenchymal lung disease in children (ChILD).
In: Thorax, Bd. 75, Nr. 2: S. 172-175
[PDF, 472kB]
Jerkic, Silvija-Pera; Brinkmann, Folke; Calder, Alistair; Casey, Alicia; Dishop, Megan; Griese, Matthias; Kurland, Geoffrey; Niemitz, Mandy; Nyilas, Sylvia; Schramm, Dirk; Schubert, Ralf; Tamm, Michael; Zielen, Stefan und Rosewich, Martin
(2020):
Postinfectious Bronchiolitis Obliterans in Children: Diagnostic Workup and Therapeutic Options: A Workshop Report.
In: Canadian Respiratory Journal, Bd. 2020, 5852827
[PDF, 4MB]
Ring, Astrid Madsen; Carlens, Julia; Bush, Andy; Castillo-Corullon, Silvia; Fasola, Salvatore; Gaboli, Mirella Piera; Griese, Matthias; Koucky, Vaclav; La Grutta, Stefania; Lombardi, Enrico; Proesmans, Marijke; Schwerk, Nicolaus; Snijders, Deborah; Nielsen, Kim Gjerum und Buchvald, Frederik
(2020):
Pulmonary function testing in children's interstitial lung disease.
In: European Respiratory Review, Bd. 29, Nr. 157, 200019
Li, Yang; Kinting, Susanna; Hoeppner, Stefanie; Forstner, Maria Elisabeth; Uhl, Olaf; Koletzko, Berthold und Griese, Matthias
(2019):
Metabolic labelling of choline phospholipids probes ABCA3 transport in lamellar bodies.
In: Biochimica et Biophysica Acta-Molecular and Cell Biology of Lipids, Bd. 1864, Nr. 12, UNSP 158516
Seidl, Elias; Kiermeier, Hannah; Liebisch, Gerhard; Ballmann, Manfred; Hesse, Sebastian; Paul-Buck, Karl; Ratjen, Felix; Rietscherl, Ernst und Griese, Matthias
(2019):
Lavage lipidomics signatures in children with cystic fibrosis and protracted bacterial bronchitis.
In: Journal of Cystic Fibrosis, Bd. 18, Nr. 6: S. 790-795
Noethe-Menchen, Tabea; Wallmeier, Julia; Pennekamp, Petra; Hoeben, Inga M.; Olbrich, Heike; Loges, Niki T.; Raidt, Johanna; Dougherty, Gerard W.; Hjeij, Rim; Dworniczak, Bernd; Omran, Heymut; Amirav, Israel; Biebach, Luisa; Fabricius, Dorit; Griese, Matthias; Grosse-Onnebrink, Jörg; Haeffner, Karsten; Hector, Andreas; Jung, Andreas; Kaiser-Labusch, Petra; Kaiser, Thomas; Kessler, Christina; Kitz, Richard; Knowles, Michael R.; Koerner-Rettberg, Cordula; Kristoffersson, Ulf; Leigh, Margaret W.; Mertsch, Pontus; Mischo, Bernhard; Nielsen, Kim G.; Poeta, Marco; Rietschel, Ernst; Roth, Samra; Santamaria, Francesca; Schmalstieg, Christian; Schmidts, Miriam; Schwarz, Carsten; Schwerk, Nicolaus; Seithe, Horst; Tebbe, Johannes; Werner, Claudius und Zariwala, Maimoona A.
(2019):
Randomization of Left-Right Asymmetry and Congenital Heart Defects The Role of DNAH5 in Humans and Mice.
In: Circulation-Genomic and Precision Medicine, Bd. 12, Nr. 11, e002686
Kroener, Carolin; Neumann, Jens; Ley-Zaporozhan, Julia; Hagl, Beate; Meixner, Iris; Spielberger, Benedikt D.; Dueckers, Gregor; Belohradsky, Bernd H.; Niehues, Tim; Borte, Michael; Rosenecker, Joseph; Kappler, Matthias; Naehrig, Susanne; Reu, Simone; Griese, Matthias und Renner, Ellen D.
(2019):
Lung disease in STAT3 hyper-IgE syndrome requires intense therapy.
In: Allergy, Bd. 74, Nr. 9: S. 1691-1702
Galambos, Csaba; Mullen, Mary P.; Shieh, Joseph T.; Schwerk, Nicolaus; Kielt, Matthew J.; Ullmann, Nicola; Boldrini, Renata; Stucin-Gantar, Irena; Haass, Cristina; Bansal, Manish; Agrawal, Pankaj B.; Johnson, Joyce; Peca, Donatella; Surace, Cecilia; Cutrera, Renato; Pauciulo, Michael W.; Nichols, William C.; Griese, Matthias; Ivy, Dunbar; Abman, Steven H.; Austin, Eric D. und Danhaive, Olivier
(2019):
Phenotype characterisation of TBX4 mutation and deletion carriers with neonatal and paediatric pulmonary hypertension.
In: European Respiratory Journal, Bd. 54, Nr. 2, 1801965
Niemitz, Mandy; Schrader, Miriam; Carlens, Julia; Hengst, Meike; Eismann, Claudia; Goldbeck, Lutz; Griese, Matthias und Schwerk, Nicolaus
(2019):
Patient education for children with interstitial lung diseases and their caregivers: A pilot study.
In: Patient Education and Counseling, Bd. 102, Nr. 6: S. 1131-1139
Diets, Illja J.; van der Donk, Roos; Baltrunaite, Kristina; Waanders, Esme; Reijnders, Margot R. F.; Dingemans, Alexander J. M.; Pfundt, Rolph; Vulto-van Silfhout, Anneke T.; Wiel, Laurens; Gilissen, Christian; Thevenon, Julien; Perrin, Laurence; Afenjar, Alexandra; Nava, Caroline; Keren, Boris; Bartz, Sarah; Peri, Bethany; Beunders, Gea; Verbeek, Nienke; van Gassen, Koen; Thiffault, Isabelle; Cadieux-Dion, Maxime; Huerta-Saenz, Lina; Wagner, Matias; Konstantopoulou, Vassiliki; Vodopiutz, Julia; Griese, Matthias; Boel, Annekatrien; Callewaert, Bert; Brunner, Han G.; Kleefstra, Tjitske; Hoogerbrugge, Nicoline; de Vries, Bert B. A.; Hwa, Vivian; Dauber, Andrew; Hehir-Kwa, Jayne Y.; Kuiper, Roland P. und Jongmans, Marjolijn C. J.
(2019):
De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial Dysmorphism.
In: American Journal of Human Genetics, Bd. 104, Nr. 4: S. 758-766
Trapnell, Bruce C.; Nakata, Koh; Bonella, Francesco; Campo, Ilaria; Griese, Matthias; Hamilton, John; Wang, Tisha; Morgan, Cliff; Cottin, Vincent und McCarthy, Cormac
(2019):
Pulmonary alveolar proteinosis.
In: Nature Reviews Disease Primers, Bd. 5, 16
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]
Griese, Matthias; Seidl, Elias; Hengst, Meike; Reu, Simone; Rock, Hans; Anthony, Gisela; Kiper, Nural; Emiralioglu, Nagehan; Snijders, Deborah; Goldbeck, Lutz; Leidl, Reiner; Ley-Zaporozhan, Julia; Krüger-Stollfuss, Ingrid; Kammer, Birgit; Wesselak, Traudl; Eismann, Claudia; Schams, Andrea; Neuner, Doerthe; MacLean, Morag; Nicholson, Andrew G.; Lauren, McCann; Clement, Annick; Epaud, Ralph; Blic, Jacques de; Ashworth, Michael; Aurora, Paul; Calder, Alistair; Wetzke, Martin; Kappler, Matthias; Cunningham, Steve; Schwerk, Nicolaus und Bush, Andy
(2018):
International management platform for children’s interstitial lung disease (chILD-EU).
In: Thorax, Bd. 73, Nr. 3: S. 231-239
[PDF, 803kB]
Donaldson, Scott H.; Pilewski, Joseph M.; Griese, Matthias; Cooke, Jon; Viswanathan, Lakshmi; Tullis, Elizabeth; Davies, Jane C.; Lekstrom-Himes, Julie A. und Wang, Linda T.
(2018):
Tezacaftor/Ivacaftor in Subjects with Cystic Fibrosis and F508del/F508del-CFTR or F508del/G551D-CFTR.
In: American Journal of Respiratory and Critical Care Medicine, Bd. 197, Nr. 2: S. 214-224
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
Höppner, Stefanie; Kinting, Susanna; Torrano, Adriano A.; Schindlbeck, Ulrike; Bräuchle, Christoph; Zarbock, Ralf; Wittmann, Thomas und Griese, Matthias
(2017):
Quantification of volume and lipid filling of intracellular vesicles carrying the ABCA3 transporter.
In: Biochimica et Biophysica Acta-Molecular Cell Research, Bd. 1864, Nr. 12: S. 2330-2335
Long, Xiaoping; He, Xuan; Ohshimo, Shinichiro; Griese, Matthias; Sarria, Rafael; Guzman, Josune; Costabel, Ulrich und Bonella, Francesco
(2017):
Serum YKL-40 as predictor of outcome in hypersensitivity pneumonitis.
In: European Respiratory Journal, Bd. 49, Nr. 2, 1501924
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]
Campo, Ilaria; Luisetti, Maurizio; Griese, Matthias; Trapnell, Bruce C.; Bonella, Francesco; Grutters, Jan; Nakata, Koh; Van Moorsel, Coline H. M.; Costabel, Ulrich; Cottin, Vincent; Ichiwata, Toshio; Inoue, Yoshikazu; Braschi, Antonio; Bonizzoni, Giacomo; Iotti, Giorgio A.; Tinelli, Carmine und Rodi, Giuseppe
(2016):
Whole lung lavage therapy for pulmonary alveolar proteinosis: a global survey of current practices and procedures.
In: Orphanet Journal of Rare Diseases
11:115
[PDF, 1MB]
Papaioannou, Andriana I.; Kostikas, Konstantinos; Manali, Effrosyni D.; Papadaki, Georgia; Roussou, Aneza; Spathis, Aris; Mazioti, Argyro; Tomos, Ioannis; Papanikolaou, Ilias; Loukides, Stelios; Chainis, Kyriakos; Karakitsos, Petros; Griese, Matthias und Papiris, Spyros
(2016):
Serum Levels of Surfactant Proteins in Patients with Combined Pulmonary Fibrosis and Emphysema (CPFE).
In: PLOS ONE
11(6), e0157789
[PDF, 1MB]
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]
Campo, Ilaria; Luisetti, Maurizio; Griese, Matthias; Trapnell, Bruce C.; Bonella, Francesco; Grutters, Jan C.; Nakata, Koh; Moorsel, Coline H. M. Van; Costabel, Ulrich; Cottin, Vincent; Ichiwata, Toshio; Inoue, Yoshikazu; Braschi, Antonio; Bonizzoni, Giacomo; Iotti, Giorgio A.; Tinelli, Carmine und Rodi, Giuseppe
(2016):
A Global Survey on Whole Lung Lavage in Pulmonary Alveolar Proteinosis.
In: Chest, Bd. 150, Nr. 1: S. 251-253
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
Wallmeier, Julia; Shiratori, Hidetaka; Dougherty, Gerard W.; Edelbusch, Christine; Hjeij, Rim; Loges, Niki T.; Menchen, Tabea; Olbrich, Heike; Pennekamp, Petra; Raidt, Johanna; Werner, Claudius; Minegishi, Katsura; Shinohara, Kyosuke; Asai, Yasuko; Takaoka, Katsuyoshi; Lee, Chanjae; Griese, Matthias; Memari, Yasin; Durbin, Richard; Kolb-Kokocinski, Anja; Sauer, Sascha; Wallingford, John B.; Hamada, Hiroshi und Omran, Heymut
(2016):
TTC25 Deficiency Results in Defects of the Outer Dynein Arm Docking Machinery and Primary Ciliary Dyskinesia with Left-Right Body Asymmetry Randomization.
In: American Journal of Human Genetics, Bd. 99, Nr. 2: S. 460-469
Hector, Andreas; Kirn, Tobias; Ralhan, Anjali; Graepler-Mainka, Ute; Berenbrinker, Sina; Riethmueller, Joachim; Hogardt, Michael; Wagner, Marlies; Pfleger, Andreas; Autenrieth, Ingo; Kappler, Matthias; Griese, Matthias; Eber, Ernst; Martus, Peter und Hartl, Dominik
(2016):
Microbial colonization and lung function in adolescents with cystic fibrosis.
In: Journal of Cystic Fibrosis, Bd. 15, Nr. 3: S. 340-349
Szentes, B.; Witt, S.; Bush, A.; Cunningham, S.; Emiraliouglu, N.; Goldbeck, L.; Griese, Matthias; Hengst, M.; Kiper, N.; Krenke, K.; Lange, J.; Leidl, Reiner ORCID: https://orcid.org/0000-0002-7115-7510; Schwerk, N. und Schwarzkopf, L.
(2016):
Current Practice of Drug Treatment In Children with ILD: First Insights From The Child-Eu Registry.
In: Value in Health, Bd. 19, Nr. 7:
A558-A558
Bush, Andrew; Barbato, Angelo; Clement, Annick; Cunningham, Steve; Blic, Jacques de; Gilbert, Carlee; Goldbeck, Lutz; Kiper, Nural; Schwerk, Nicolaus und Griese, Matthias
(2016):
European idiopathic pulmonary fibrosis Patient Charter: a missed opportunity.
In: European Respiratory Journal, Bd. 48, Nr. 1: S. 282-283
Clement, Annick; Blic, Jacques de; Epaud, Ralph; Galeron, Laurie; Nathan, Nadia; Hadchouel, Alice; Barbato, Angelo; Snijders, Deborah; Kiper, Nural; Cunningham, Steve; Griese, Matthias; Bush, Andrew und Schwerk, Nicolaus
(2016):
Management of children with interstitial lung diseases: the difficult issue of acute exacerbations.
In: European Respiratory Journal, Bd. 48, Nr. 6: S. 1559-1563
Hector, Andreas; Chotirmall, Sanjay H.; Lavelle, Gillian M.; Mirković, Bojana; Horan, Deirdre; Eichler, Laura; Mezger, Markus; Singh, Anurag; Ralhan, Anjai; Berenbrinker, Sina; Mack, Ines; Ensenauer, Regina; Riethmüller, Joachim; Graepler-Mainka, Ute; Murray, Michelle A.; Griese, Matthias; McElvaney, N. Gerry und Hartl, Dominik
(2016):
Chitinase activation in patients with fungus-associated cystic fibrosis lung disease.
In: Journal of Allergy and Clinical Immunology, Bd. 138, Nr. 4: S. 1183-1189
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
Fuchs, Susanne I.; Schwerk, Nicolaus; Pittschieler, Klaus; Ahrens, Frank; Baden, Winfried; Bals, Robert; Fähndrich, Sebastian; Gleiber, Wolfgang; Griese, Matthias; Hülskamp, Georg; Köhnlein, Thomas; Reckling, Ludmilla; Rietschel, Ernst; Staab, Doris und Gappa, Monika
(2016):
Lung clearance index for monitoring early lung disease in alpha-1-antitrypsin deficiency.
In: Respiratory Medicine, Bd. 116: S. 93-99
Manali, Effrosyni D.; Papadaki, Georgia; Konstantonis, Dimitrios; Tsangaris, Iraklis; Papaioannou, Andriana I.; Kolilekas, Likurgos; Schams, Andrea; Kagouridis, Konstantinos; Karakatsani, Anna; Orfanos, Stylianos; Griese, Matthias und Papiris, Spyros A.
(2016):
Cardiovascular risk in pulmonary alveolar proteinosis.
In: Expert Review of Respiratory Medicine, Bd. 10, Nr. 2: S. 235-240
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
Kappler, Matthias; Nagel, Felicitas; Feilcke, Maria; Kröner, Carolin; Pawlita, Ingo; Naehrig, Susanne; Ripper, Jan; Hengst, Meike; Both, Ulrich von; Forstner, Maria; Hector, Andreas und Griese, Matthias
(2016):
Eradication of methicillin resistant Staphylococcus aureus detected for the first time in cystic fibrosis: A single center observational study.
In: Pediatric Pulmonology, Bd. 51, Nr. 10: S. 1010-1019
Frixel, Sabrina; Lotz-Havla, Amelie S.; Kern, Sunčana; Kaltenborn, Eva; Wittmann, Thomas; Gersting, Søren W.; Muntau, Ania C.; Zarbock, Ralf und Griese, Matthias
(2016):
Homooligomerization of ABCA3 and its functional significance.
In: International Journal of Molecular Medicine, Bd. 38, Nr. 2: S. 558-566
Griese, Matthias; Zarbock, Ralf; Costabel, Ulrich; Hildebrandt, Jenna; Theegarten, Dirk; Albert, Michael; Thiel, Antonia; Schams, Andrea; Lange, Joanna; Krenke, Katazyrna; Wesselak, Traudl; Schön, Carola; Kappler, Matthias; Blum, Helmut; Krebs, Stefan; Jung, Andreas; Kröner, Carolin; Klein, Christoph; Campo, Ilaria; Luisetti, Maurizio und Bonella, Francesco
(2015):
GATA2 deficiency in children and adults with severe pulmonary alveolar proteinosis and hematologic disorders.
In: BMC Pulmonary Medicine
15:87
[PDF, 1MB]
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]
Szatmari, Viktor; Teske, Erik; Nikkels, Peter G. J.; Griese, Matthias; de Jong, Pim A.; Grinwis, Guy; Theegarten, Dirk; Veraa, Stefanie; Steenbeek, Frank G. van; Drent, Marjolein und Bonella, Francesco
(2015):
Pulmonary alveolar proteinosis in a cat.
In: BMC Veterinary Research
11:302
[PDF, 3MB]
Marcos, Veronica; Zhou-Suckow, Zhe; Yildirim, Ali Önder; Bohla, Alexander; Hector, Andreas; Vitkov, Ljubomir; Krautgartner, Wolf Dietrich; Stoiber, Walter; Griese, Matthias; Eickelberg, Oliver; Mall, Marcus A. und Hartl, Dominik
(2015):
Free DNA in Cystic Fibrosis Airway Fluids Correlates with Airflow Obstruction.
In: Mediators of inflammation, 408935
[PDF, 4MB]
Bush, Andrew; Cunningham, Steve; Blic, Jacques de; Barbato, Angelo; Clement, Annick; Epaud, Ralph; Hengst, Meike; Kiper, Nural; Nicholson, Andrew G.; Wetzke, Martin; Snijders, Deborah; Schwerk, Nicolaus und Griese, Matthias
(2015):
European protocols for the diagnosis and initial treatment of interstitial lung disease in children.
In: Thorax, Bd. 70, Nr. 11: S. 1078-1084
[PDF, 601kB]
Hildebrandt, Jenna; Yalcin, Ebru; Bresser, Hans-Georg; Cinel, Guzin; Gappa, Monika; Haghighi, Alireza; Kiper, Nural; Khalilzadeh, Soheila; Reiter, Karl; Sayer, John; Schwerk, Nicolaus; Sibbersen, Anke; Daele, Sabine van; Nübling, Georg; Lohse, Peter und Griese, Matthias
(26. November 2014):
Characterization of CSF2RA mutation related juvenile pulmonary alveolar proteinosis.
In: Orphanet Journal of Rare Diseases
9:171
[PDF, 961kB]
Enaud, Laurent; Hadchouel, Alice; Coulomb, Aurore; Berteloot, Laureline; Lacaille, Florence; Boccon-Gibod, Liliane; Boulay, Vincent; Darcel, Francoise; Griese, Matthias; Linard, Mélinée; Louha, Malek; Renouil, Michel; Riviere, Jean-Pierre; Toupance, Bruno; Verkarre, Virginie; Delacourt, Christophe und de Blic, Jacques
(2014):
Pulmonary alveolar proteinosis in children on La Reunion Island: a new inherited disorder?
In: Orphanet Journal of Rare Diseases
9:85
[PDF, 2MB]
Campo, Ilaria; Zorzetto, Michele; Mariani, Francesca; Kadija, Zamir; Morbini, Patrizia; Dore, Roberto; Kaltenborn, Eva; Frixel, Sabrina; Zarbock, Ralf; Liebisch, Gerhard; Hegermann, Jan; Wrede, Christoph; Griese, Matthias und Luisetti, Maurizio
(2014):
A large kindred of pulmonary fibrosis associated with a novel ABCA3 gene variant.
In: Respiratory Research
15:43
[PDF, 2MB]
Thorwarth, Anne; Schnittert-Hübener, Sarah; Ullmann, Reinhard; Krude, Heiko; Schrumpf, Pamela; Müller, Ines; Jyrch, Sabine; Dame, Christof; Biebermann, Heike; Kleinau, Gunnar; Katchanov, Juri; Schülke, Markus; Ebert, Grit; Steininger, Anne; Bönnemann, Carsten; Brockmann, Knut; Christen, Hans-Jürgen; Crock, Patricia; Zegher, Francis de; Griese, Matthias; Hewitt, Jacqueline; Ivarsson, Sten; Hübner, Christoph; Kapelari, Klaus; Plecko, Barbara; Rating, Dietz; Stoeva, Iva; Ropers, Hans-Hilger und Grüters, Annette
(2014):
Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum.
In: Journal of Medical Genetics, Bd. 51, Nr. 6: S. 375-387
[PDF, 2MB]
Bush, Andrew; Anthony, Gisela; Barbato, Angelo; Cunningham, Steve; Clement, Annick; Epaud, R.; Gilbert, Carlee; Goldbeck, Lutz; Kronfeld, Kai; Nicholson, Andrew G.; Schwerk, Nicolaus; Griese, Matthias und Collaborators, Ch-ILD
(Oktober 2013):
Research in progress: put the orphanage out of business.
In: Thorax, Bd. 68, Nr. 10: S. 971-973
[PDF, 91kB]
Griese, Matthias; Heinrich, Stephanie; Ratjen, Felix; Kabesch, Michael; Paul, Karl; Ballmann, Manfred; Rietschel, Ernst und Kappler, Matthias
(2012):
Surfactant protein a in cystic fibrosis: supratrimeric structure and pulmonary outcome.
In: PLOS ONE
7(12), e51050
[PDF, 305kB]
Zarbock, Ralf; Woischnik, Markus; Sparr, Christiane; Thurm, Tobias; Kern, Suncana; Kaltenborn, Eva; Hector, Andreas; Hartl, Dominik; Liebisch, Gerhard; Schmitz, Gerd und Griese, Matthias
(2012):
The surfactant protein C mutation A116D alters cellular processing, stress tolerance, surfactant lipid composition, and immune cell activation.
In: BMC Pulmonary Medicine
12:15
[PDF, 3MB]
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]
Hector, Andreas; Kormann, Michael S. D.; Mack, Ines; Latzin, Philipp; Casaulta, Carmen; Kieninger, Elisabeth; Zhou, Zhe; Yildirim, Ali Ö.; Bohla, Alexander; Rieber, Nikolaus; Kappler, Matthias; Koller, Barbara; Eber, Ernst; Eickmeier, Olaf; Zielen, Stefan; Eickelberg, Oliver; Griese, Matthias; Mall, Marcus A. und Hartl, Dominik
(2011):
The chitinase-like protein YKL-40 modulates cystic fibrosis lung disease.
In: PLOS ONE
6(9), e24399
[PDF, 246kB]
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]
Woischnik, Markus; Sparr, Christiane; Kern, Suncana; Thurm, Tobias; Hector, Andreas; Hartl, Dominik; Liebisch, Gerhard; Mulugeta, Surafel; Beers, Michael F.; Schmitz, Gerd und Griese, Matthias
(2010):
A non-BRICHOS surfactant protein c mutation disrupts epithelial cell function and intercellular signaling.
In: BMC Cell Biology
11:88
[PDF, 1MB]
Marcos, Veronica; Latzin, Phillip; Hector, Andreas; Sonanini, Sebastian; Hoffmann, Florian; Lacher, Martin; Koller, Barbara; Bufler, Philip; Nicolai, Thomas; Hartl, Dominik und Griese, Matthias
(2010):
Expression, regulation and clinical significance of soluble and membrane CD14 receptors in pediatric inflammatory lung diseases.
In: Respiratory Research
11:32
[PDF, 1MB]
Stanke, F.; Ballmann, M.; Bronsveld, I.; Dörk, T.; Gallati, S.; Laabs, U.; Derichs, N.; Ritzka, M.; Posselt, H.-G.; Harms, H. K.; Griese, Matthias; Blau, H.; Mastella, G.; Bijman, J.; Veeze, V. und Tümmler, B.
(2008):
Diversity of the basic defect of homozygous CFTR mutation genotypes in humans.
In: Journal of Medical Genetics, Bd. 45, Nr. 1: S. 47-54
[PDF, 248kB]
Mueller, Hanna; End, Caroline; Renner, Marcus; Helmke, Burkhard M.; Gassler, Nikolaus; Weiss, Christel; Hartl, Dominik; Griese, Matthias; Hafner, Mathias; Poustka, Annemarie; Mollenhauer, Jan und Poeschl, Johannes
(2007):
Deleted in Malignant Brain Tumors 1 (DMBT1) is present in hyaline membranes and modulates surface tension of surfactant.
In: Respiratory Research
8:69
[PDF, 769kB]
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