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Clinical Oral Investigations|March 10, 2016
Normoxic accumulation of HIF1α is associated with glutaminolysisMatthias Kappler, Ulrike Pabst, Swetlana Rot, et al.
Pediatric Pulmonology|October 23, 2020
Comorbidity and long-term clinical outcome of laryngotracheal clefts types III and IV: Systematic analysis of new casesElias Seidl, Johanna Kramer, Florian Hoffmann, et al.
ERJ Open Research|March 6, 2024
Single-centre prospective evaluation of the first 5 years of cystic fibrosis newborn screening in GermanyFlorian Gesenhues, Katarzyna Michel, Tobias Greve, et al.
American Journal of Human Genetics|November 24, 2001
Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiencyAndreas Holzinger, Esther M Maier, Cornelius Bück, et al.
Journal of the Pediatric Infectious Diseases Society|November 14, 2020
SARS-CoV-2 Triggering Severe Acute Respiratory Distress Syndrome and Secondary Hemophagocytic Lymphohistiocytosis in a 3-Year-Old Child With Down SyndromeSarah Kim-Hellmuth, Matthias Hermann, Julia Eilenberger, et al.
Frontiers in Pharmacology|August 19, 2021
Insights Into Patient Variability During Ivacaftor-Lumacaftor Therapy in Cystic FibrosisPatrick O Hanafin, Isabelle Sermet-Gaudelus, Matthias Griese, et al.
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