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1. The Human Phenotype Ontology in 2024: phenotypes around the world

3. Impact of COVID-19 infection on lung function and nutritional status amongst individuals with cystic fibrosis: A global cohort study

6. A core outcome set for bronchiectasis in children and adolescents for use in clinical research: an international consensus study

8. A multi-platform approach to identify a blood-based host protein signature for distinguishing between bacterial and viral infections in febrile children (PERFORM): a multi-cohort machine learning study

9. Impact of elexacaftor/tezacaftor/ivacaftor on lung function, nutritional status, pulmonary exacerbation frequency and sweat chloride in people with cystic fibrosis: real-world evidence from the German CF Registry

10. Relationship between molecular pathogen detection and clinical disease in febrile children across Europe: a multicentre, prospective observational study

11. The Human Phenotype Ontology in 2021

12. Impact of infection on proteome-wide glycosylation revealed by distinct signatures for bacterial and viral pathogens

14. Biallelic variants in the calpain regulatory subunit CAPNS1 cause pulmonary arterial hypertension

15. Multilamellated Basement Membranes in the Capillary Network of Alveolar Capillary Dysplasia

18. Incidence and Prevalence of Children's Diffuse Lung Disease in Spain

20. Genetics and Genomics of Pulmonary Fibrosis: Charting the Molecular Landscape and Shaping Precision Medicine.

23. Multivalent, calcium-independent binding of surfactant protein A and D to sulfated glycosaminoglycans of the alveolar epithelial glycocalyx

24. Single-center prospective evaluation of the first five years of cystic fibrosis newborn screening in Germany

25. A core outcome set for bronchiectasis in children and adolescents for use in clinical research: an international consensus study

35. Inhaled recombinant GM-CSF reduces the need for whole lung lavage and improves gas exchange in autoimmune pulmonary alveolar proteinosis patients

36. The Human Phenotype Ontology in 2024: phenotypes around the world

38. Long-Term Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in People With Cystic Fibrosis and at Least OneF508delAllele: 144-Week Interim Results From a 192-Week Open-label Extension Study

42. Autoimmune Pulmonary Alveolar Proteinosis (aPAP) in Greece: 20 years in progress

44. International consensus statement on core outcomes for clinical trials in children and adolescents with bronchiectasis – Child-BEAR-net ERS CRC

45. The effect of nutritional parameters on the prognosis of childhood interstitial lung diseases

47. Variants in FGF10 cause early onset of severe childhood interstitial lung disease: A detailed description of four affected children

48. Impact of infection on proteome-wide glycosylation revealed by distinct signatures for bacterial and viral pathogens

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