Search Results - "Griese, M"

Pulmonary surfactant in health and human lung diseases: state of the art by Griese, M

“…Pulmonary surfactant is a complex and highly surface active material composed of lipids and proteins which is found in the fluid lining the alveolar surface of…”
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Inhibition of airway proteases in cystic fibrosis lung disease by Griese, M, Kappler, M, Gaggar, A, Hartl, D

“…Progressive lung disease determines the morbidity and mortality of cystic fibrosis (CF) patients. CF lung disease is characterised by endobronchial…”
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Surfactant protein D in human lung diseases by Hartl, D., Griese, M.

“…The lung is continuously exposed to inhaled pollutants, microbes and allergens. Therefore, the pulmonary immune system has to defend against harmful pathogens,…”
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The role of matrix metalloproteinases in cystic fibrosis lung disease by GAGGAR, A, HECTOR, A, BRATCHER, P. E, MALL, M. A, GRIESE, M, HARTL, D

“…Significant airway remodelling is a major component of the increased morbidity and mortality observed in cystic fibrosis (CF) patients. These airways feature…”
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Pulmonary interstitial glycogenosis – A systematic analysis of new cases by Seidl, E., Carlens, J., Reu, S., Wetzke, M., Ley-Zaporozhan, J., Brasch, F., Wesselak, T., Schams, A., Rauch, D., Schuch, L., Kappler, M., Schelstraete, P., Wolf, M., Stehling, F., Haarmann, E., Borensztajn, D., van de Loo, M., Rubak, S., Lex, C., Hinrichs, B., Reiter, K., Schwerk, N., Griese, M.

“…Pulmonary interstitial glycogenosis (PIG) is a rare paediatric interstitial lung disease of unknown cause. The diagnosis can only be made by lung biopsy. Less…”
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Loading capacity of adhesive joints regarding their manufacturing process by Günther, N., Griese, M., Stammen, E., Dilger, K.

“…Adhesive bonding of materials with different thermal expansion coefficients is a major challenge for the manufacturers. Especially the drying process after…”
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Changes of exhaled nitric oxide during steroid treatment of childhood asthma by Beck-Ripp, J, Griese, M, Arenz, S, Koring, C, Pasqualoni, B, Bufler, P

“…Exhaled nitric oxide (eNO) is elevated in several inflammatory airway diseases and is significantly reduced by anti-inflammatory treatment with inhaled…”
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Successful treatment of neonatal respiratory failure caused by a novel surfactant protein C p.Cys121Gly mutation with hydroxychloroquine by Hepping, N, Griese, M, Lohse, P, Garbe, W, Lange, L

“…SFTPC (surfactant protein C) mutations resulting in SP-C deficiency causing ongoing respiratory failure in the neonatal period represent a rare entity. We…”
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Ursodeoxycholic acid therapy in cystic fibrosis liver disease - a retrospective long-term follow-up case-control study by Kappler, M., Espach, C., Schweiger-Kabesch, A., Lang, T., Hartl, D., Hector, A., Glasmacher, C., Griese, M.

“…Summary Background The prevention and treatment of liver disease associated with cystic fibrosis remain a significant unresolved problem. Aim To assess the…”
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Anti-inflammatory cytokines in cystic fibrosis lung disease by Starosta, V, Ratjen, F, Rietschel, E, Paul, K, Griese, M

“…Lung inflammation plays a pivotal role in the pathogenesis of airway disease in cystic fibrosis (CF). An imbalance between pro- and anti-inflammatory mediators…”
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Surfactant protein A--from genes to human lung diseases by Heinrich, S, Hartl, D, Griese, M

“…Surfactant associated protein-A (SP-A) is the most abundant pulmonary surfactant protein and belongs to the family of innate host defense proteins termed…”
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Respiratory disease in Niemann-Pick type C2 is caused by pulmonary alveolar proteinosis by Griese, M, Brasch, F, Aldana, VR, Cabrera, MM, Goelnitz, U, Ikonen, E, Karam, BJ, Liebisch, G, Linder, MD, Lohse, P, Meyer, W, Schmitz, G, Pamir, A, Ripper, J, Rolfs, A, Schams, A, Lezana, FJ

“…Griese M, Brasch F, Aldana VR, Cabrera MM, Goelnitz U, Ikonen E, Karam BJ, Liebisch G, Linder MD, Lohse P, Meyer W, Schmitz G, Pamir A, Ripper J, Rolfs A,…”
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International Experience in Pediatric Extracorporeal Membrane Oxygenation (ECMO) Bridge to Lung Transplantation by Wong, J.Y, Glanville, A.R, Westall, G.P, Goldfarb, S.B, Griese, M, Rottier, B, Budev, M, Balcells-Ramirez, J, Schwerk, N

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Novel method to process cystic fibrosis sputum for determination of oxidative state by Hector, A, Jonas, F, Kappler, M, Feilcke, M, Hartl, D, Griese, M

“…Induced sputum is the most commonly used method to analyze airway inflammation in cystic fibrosis (CF) patients ex vivo. Due to the complex matrix of the…”
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Interstitial lung disease in a baby with a de novo mutation in the SFTPC gene by Brasch, F, Griese, M, Tredano, M, Johnen, G, Ochs, M, Rieger, C, Mulugeta, S, Muller, K.M, Bahuau, M, Beers, M.F

“…Mutations in the surfactant protein C gene (SFTPC) were recently reported in patients with interstitial lung disease. In a 13-month-old infant with severe…”
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Cathepsin H and napsin A are active in the alveoli and increased in alveolar proteinosis by Woischnik, M, Bauer, A, Aboutaam, R, Pamir, A, Stanzel, F, de Blic, J, Griese, M

“…Pulmonary alveolar proteinosis (PAP) is a group of rare diseases with disturbed homeostasis of alveolar surfactant. While 90% of the primary adult forms are…”
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Surfactant protein D in serum from patients with allergic bronchopulmonary aspergillosis by Krane, M, Griese, M

“…Surfactant protein D (SP-D) interacts with Aspergillus fumigatus and is strongly increased in the lavage from animals with acute allergic reactions to the…”
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Protein Oxidation by Chronic Pulmonary Diseases in Children by Starosta, V., Griese, M.

“…The oxidation of proteins may play an important role in the pathogenesis of chronic inflammatory lung diseases, and may contribute to lung damage. However, the…”
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Neonatal respiratory insufficiency caused by an (homozygous) ABCA3-stop mutation: a systematic evaluation of therapeutic options by Winter, J, Essmann, S, Kidszun, A, Aslanidis, C, Griese, M, Poplawska, K, Bartsch, M, Schmitz, G, Mildenberger, E

“…Autosomal recessive ABCA3 (ATP-binding cassette protein A3) gene mutations have been associated with neonatal respiratory distress and pediatric interstitial…”
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Diagnostic and prognostic value of serum antibodies against Pseudomonas aeruginosa in cystic fibrosis by Kappler, M, Kraxner, A, Reinhardt, D, Ganster, B, Griese, M, Lang, T

“…Background: Eradication of Pseudomonas aeruginosa in patients with cystic fibrosis (CF) is possible if initiated early in the course of colonisation. To detect…”
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