Baby Lion Study Ultra-rapid whole genome sequencing in critically ill children 05/2022 - 04/2024 Rare genetic diseases are a major cause of critical illness and mortality in children (Wright, 2018). S
Schmelzle M, Pratschke J, Chopra S. The influence of the COVID-19 pandemic on surgical therapy and care: a cross-sectional study. BMC Surg. 2022 Jul 5;22(1):259. doi: 10.1186/s12893-022-01708-7. PMID: 35791027;
pluripotent stem cells repairs the cellular phenotype in pulmonary alveolar proteinosis. Am J Respir Crit Care Med 189, no. 2:167. * #Authors contributed equally. Martens, A., Rojas, S.V., Baraki, H., Rathert
likation Tsikas,Dimitrios ; Homoarginine in health and disease, England,Curr.Opin.Clin.Nutr.Metab.Care,2023;26(1):42-49, 10.1097/MCO.0000000000000889 Berichtsjahr:2022 | ID: RefID:24609-tsikas2023homoarginine