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ERJ Open Research|November 29, 2023
Lung transplantation outcome in adult surfactant-related interstitial lung disease: first evidence to move onEffrosyni D Manali, Matthias Griese, Spyros A PapirisPaediatric Anaesthesia|January 5, 2011
Whole-lung lavage in infants and children with pulmonary alveolar proteinosisKarl Reiter, Carola Schoen, Matthias Griese, et al.Pediatric Pulmonology|December 11, 2014
Hydroxychloroquine in children with interstitial (diffuse parenchymal) lung diseasesSarah Braun, Marion Ferner, Kai Kronfeld, et al.BMJ Case Reports|March 21, 2014
Successful weaning from mechanical ventilation in a patient with surfactant protein C deficiency presenting with severe neonatal respiratory distressJeroen van Hoorn, Arno Brouwers, Matthias Griese, et al.Proteomics|July 12, 2002
Bronchoalveolar lavage protein patterns in children with malignancies, immunosuppression, fever and pulmonary infiltratesManfred Neumann, Christina von Bredow, Felix Ratjen, et al.Orphanet Journal of Rare Diseases|September 27, 2015
Categorizing diffuse parenchymal lung disease in childrenMatthias Griese, Armin Irnstetter, Meike Hengst, et al.American Journal of Respiratory and Critical Care Medicine|October 17, 2015
Persistent Tachypnea of Infancy. Usual and AberrantDaniela Rauch, Martin Wetzke, Simone Reu, et al.Klinische Padiatrie|December 18, 2023
[Kids Lung Registry and Child-EU Project - Progress in Rare and Interstitial Lung Diseases in Childhood Through Collaboration]Matthias Griese, Angelika Gold, Florian Gothe, et al.Orphanet Journal of Rare Diseases|July 23, 2022
Randomized controlled phase 2 trial of hydroxychloroquine in childhood interstitial lung diseaseMatthias Griese, Matthias Kappler, Florian Stehling, et al.The European Respiratory Journal|November 18, 2011
CXCR1 and CXCR2 haplotypes synergistically modulate cystic fibrosis lung diseaseMichael S D Kormann, Andreas Hector, Veronica Marcos, et al.Pageof 34