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Medizinische Klinik, Intensivmedizin Und Notfallmedizin|June 22, 2021
[Childhood emergencies-worsening healthcare bottlenecks for children in a systematic long-term analysis of the EMS system in a German metropolis]F Hoffmann, M Landeg, W Rittberg, et al.Der Unfallchirurg|October 13, 2020
[Development of a new module for the TraumaRegister DGU® : Better collation of the sequelae of severe injuries during pregnancy]H Trentzsch, A Weißleder, T Annecke, et al.European Journal of Pediatrics|October 26, 2020
Implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis-implications for process quality and patient careGwendolyn Gramer, Inken Brockow, Christiane Labitzke, et al.Plos Neglected Tropical Diseases|February 18, 2021
Identifying and validating the presence of Guanine-Quadruplexes (G4) within the blood fluke parasite Schistosoma mansoniHolly M Craven, Riccardo Bonsignore, Vasilis Lenis, et al.European Journal of Human Genetics : EJHG|January 1, 1997
Association of extracolonic manifestations of familial adenomatous polyposis with acetylation phenotype in a large FAP kindredR J Scott, W Taeschner, K Heinimann, et al.Pediatric Research|March 22, 2006
Phenylalanine reduces synaptic density in mixed cortical cultures from miceFriederike Hörster, Marina A Schwab, Sven W Sauer, et al.Orphanet Journal of Rare Diseases|June 17, 2017
Incidence, disease onset and short-term outcome in urea cycle disorders -cross-border surveillance in Germany, Austria and SwitzerlandSusanne Nettesheim, Stefan Kölker, Daniela Karall, et al.Journal of Inherited Metabolic Disease|October 27, 2004
Excitotoxicity and bioenergetics in glutaryl-CoA dehydrogenase deficiencyS Kölker, D M Koeller, S Sauer, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|February 1, 2007
Qualitative and quantitative analysis of antibody response against IFNbeta in patients with multiple sclerosisF Gilli, F Hoffmann, A Sala, et al.International Journal of Neonatal Screening|March 27, 2024
New Cases of Maleylacetoacetate Isomerase Deficiency with Detection by Newborn Screening and Natural History over 32 Years: Experience from a German Newborn Screening CenterGwendolyn Gramer, Saskia B Wortmann, Junmin Fang-Hoffmann, et al.Pageof 108