Search Results - Lichter‐Konecki, Uta

Consensus guidelines for management of hyperammonaemia in paediatric patients receiving continuous kidney replacement therapy by Raina, Rupesh (Author) , Bedoyan, Jirair K. (Author) , Lichter-Konecki, Uta (Author) , Jouvet, Philippe (Author) , Picca, Stefano (Author) , Mew, Nicholas Ah (Author) , Machado, Marcel C. (Author) , Chakraborty, Ronith (Author) , Vemuganti, Meghana (Author) , Grewal, Manpreet K. (Author) , Bunchman, Timothy (Author) , Sethi, Sidharth Kumar (Author) , Krishnappa, Vinod (Author) , McCulloch, Mignon (Author) , Alhasan, Khalid (Author) , Bagga, Arvind (Author) , Basu, Rajit K. (Author) , Schaefer, Franz (Author) , Filler, Guido (Author) , Warady, Bradley A. (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): the ClinGen IEM Working Group and the phenylalanine hydroxylase gene by Zastrow, Diane B. (Author) , Baudet, Heather (Author) , Shen, Wei (Author) , Thomas, Amanda (Author) , Si, Yue (Author) , Weaver, Meredith A. (Author) , Lager, Angela M. (Author) , Liu, Jixia (Author) , Mangels, Rachel (Author) , Dwight, Selina S. (Author) , Wright, Matt W. (Author) , Dobrowolski, Steven F. (Author) , Eilbeck, Karen (Author) , Enns, Gregory M. (Author) , Feigenbaum, Annette (Author) , Lichter‐Konecki, Uta (Author) , Lyon, Elaine (Author) , Pasquali, Marzia (Author) , Watson, Michael (Author) , Blau, Nenad (Author) , Steiner, Robert D. (Author) , Craigen, William J. (Author) , Mao, Rong (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Feasibility of adjunct therapeutic hypothermia treatment for hyperammonemia and encephalopathy due to urea cycle disorders and organic acidemias by Lichter-Konecki, Uta (Author) , Nadkarni, Vinay (Author) , Moudgil, Asha (Author) , Cook, Noah (Author) , Pöschl, Johannes (Author) , Meyer, Michael T. (Author) , Dimmock, David (Author) , Baumgart, Stephen (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Aufklärung der molekularen Basis für die phänotypische Heterogenität angeborener Stoffwechselerkrankungen am Beispiel der Hyperphenylalaninämien by Lichter-Konecki, Uta (Author)

Zentralnervöse Komplikationen bei Kindern unter Cytostatikatherapie by Lichter-Konecki, Uta (Author)