Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Elias Seidl"'
Publikováno v:
ERJ Open Research, Vol 10, Iss 4 (2024)
Background Primary ciliary dyskinesia (PCD) is a rare multisystem genetic disease caused by dysfunctional motile cilia. Despite PCD being the second most common inherited airway disease after cystic fibrosis, PCD continues to be under-recognised glob
Externí odkaz:
https://doaj.org/article/525d74c50a6f4bbdbd5af755d6d3bb11
Publikováno v:
ERJ Open Research, Vol 10, Iss 1 (2024)
Background Reversible airway obstruction is common in children with primary ciliary dyskinesia. However, the diagnostic value of adding bronchodilator (BD) response testing to routine spirometry is unclear. Methods This is a retrospective analysis of
Externí odkaz:
https://doaj.org/article/21cbd2b21aed431aa1de159357fd5545
Publikováno v:
Biomedicines, Vol 12, Iss 2, p 431 (2024)
Background: Electronic nose (eNose) technology can be used to characterize volatile organic compound (VOC) mixes in breath. While previous reports have shown that eNose can detect lung infections with pathogens such as Staphylococcus aureus (SA) in p
Externí odkaz:
https://doaj.org/article/b53ba30a390546c1af7565c0f8248a87
Autor:
Matthias Griese, Matthias Kappler, Florian Stehling, Johannes Schulze, Winfried Baden, Cordula Koerner-Rettberg, Julia Carlens, Freerk Prenzel, Lutz Nährlich, Andreas Thalmeier, Daniela Sebah, Kai Kronfeld, Hans Rock, Christian Ruckes, the HCQ-study group, Martin Wetzke, Elias Seidl, Nicolaus Schwerk
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-11 (2022)
Abstract Background No results of controlled trials are available for any of the few treatments offered to children with interstitial lung diseases (chILD). We evaluated hydroxychloroquine (HCQ) in a phase 2, prospective, multicentre, 1:1-randomized,
Externí odkaz:
https://doaj.org/article/e1d315d7f4aa42e2ab8a8f6ece846959
Autor:
Matthias Griese, Meike Köhler, Sabine Witt, Daniela Sebah, Matthias Kappler, Martin Wetzke, Nicolaus Schwerk, Nagehan Emiralioglu, Nural Kiper, Kai Kronfeld, Christian Ruckes, Hans Rock, Gisela Anthony, Elias Seidl
Publikováno v:
Trials, Vol 21, Iss 1, Pp 1-9 (2020)
Abstract Background Interstitial lung diseases in children (chILD) are rare and consist of many different entities that affect the parenchyma of the lungs, leading to a chronic lung disease. The natural course of many of these diseases is connected w
Externí odkaz:
https://doaj.org/article/7f0f68745bd744c9a1f5e7cee447adcd
Autor:
Yang Li, Elias Seidl, Katrin Knoflach, Florian Gothe, Maria Elisabeth Forstner, Katarzyna Michel, Ingo Pawlita, Florian Gesenhues, Franziska Sattler, Xiaohua Yang, Carolin Kroener, Simone Reu-Hofer, Julia Ley-Zaporozhan, Birgit Kammer, Ingrid Krüger-Stollfuß, Julien Dinkel, Julia Carlens, Martin Wetzke, Antonio Moreno-Galdó, Alba Torrent-Vernetta, Joanna Lange, Katarzyna Krenke, Nisreen Rumman, Sarah Mayell, Tugba Sismanlar, Ayse Aslan, Nicolas Regamey, Marijke Proesmans, Florian Stehling, Lutz Naehrlich, Kilinc Ayse, Sebastian Becker, Cordula Koerner-Rettberg, Erika Plattner, Effrosyni D Manali, Spyridon A Papiris, Ilaria Campo, Matthias Kappler, Nicolaus Schwerk, Matthias Griese
BackgroundThe majority of patients with childhood interstitial lung disease (chILD) caused by pathogenic variants in ATP binding cassette subfamily A member 3 (ABCA3) develop severe respiratory insufficiency within their first year of life and succum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::345af061d5d8a30e301c537e2228edc6
https://opus4.kobv.de/opus4-fau/frontdoor/index/index/docId/23188
https://opus4.kobv.de/opus4-fau/frontdoor/index/index/docId/23188
Autor:
Mitsuaki Kawashima, Elias Seidl, Hartmut Grasemann, Seyed Alireza Rabi, Terunaga Inage, Kazuhiro Yasufuku, Shaf Keshavjee, Jordan J. Feld, Marcelo Cypel
Publikováno v:
JTCVS Techniques. 14:212-214
Autor:
Dirk Schramm, Carola Schön, Michael H. Albert, Matthias Kappler, Matthias Griese, Simone Reu-Hofer, Elias Seidl, Fabian Hauck, Karl Reiter, Ingo Pawlita
Publikováno v:
Pediatric Pulmonology. 57:273-277
Introduction Pulmonary alveolar proteinosis (PAP) is defined by increased accumulation of surfactant in the alveolar space. PAP has been reported to be associated with a large number of clinical conditions and diseases. Whole lung lavages can be help
Publikováno v:
Psychoanalytic Psychotherapy. 36:64-80
Tinnitus aurium is the conscious perception of an acoustic sensation in the absence of a corresponding external stimulus. Besides other psychological factors, psychodynamic factors play an importan...
Autor:
Joanna Lange, Stanislaw Boguslawski, Honorata Marczak, Matthias Griese, Tomasz Urbankowski, Elias Seidl, Katarzyna Krenke, Joanna Peradzyńska
Publikováno v:
Pediatric Pulmonology. 56:3952-3959
BACKGROUND Persistent tachypnea of infancy (PTI) is the most common interstitial lung disease in young children. As no standardized therapeutic guidelines exist, different pharmaceuticals are used to treat PTI; inhaled corticosteroids (ICS) and bronc