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Publications by Kotzaeridou, Urania

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Number of items: 3.

Journal article

Demmelmair, Hans; MacDonald, Anita; Kotzaeridou, Urania; Burgard, Peter; Gonzalez-Lamuno, Domingo; Verduci, Elvira; Ersoy, Melike; Gokcay, Gulden; Alyanak, Behiye; Reischl, Eva; Müller-Felber, Wolfgang; Faber, Fabienne Lara; Handel, Uschi; Paci, Sabrina; Koletzko, Berthold (2018): Determinants of Plasma Docosahexaenoic Acid Levels and Their Relationship to Neurological and Cognitive Functions in PKU Patients: A Double Blind Randomized Supplementation Study. In: Nutrients, Vol. 10, No. 12, 1944 [PDF, 2MB]

Dohrn, Maike F.; Glöckle, Nicola; Mulahasanovic, Lejla; Heller, Corina; Mohr, Julia; Bauer, Christine; Riesch, Erik; Becker, Andrea; Battke, Florian; Hörtnagel, Konstanze; Hornemann, Thorsten; Suriyanarayanan, Saranya; Blankenburg, Markus; Schulz, Jörg B.; Claeys, Kristl G.; Gess, Burkhard; Katona, Istvan; Ferbert, Andreas; Vittore, Debora; Grimm, Alexander; Wolking, Stefan; Schöls, Ludger; Lerche, Holger; Korenke, G. Christoph; Fischer, Dirk; Schrank, Bertold; Kotzaeridou, Urania; Kurlemann, Gerhard; Dräger, Bianca; Schirmacher, Anja; Young, Peter; Schlotter-Weigel, Beate; Biskup, Saskia (2017): Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies. In: Journal of Neurochemistry, Vol. 143, No. 5: pp. 507-522

Haack, Tobias B.; Jackson, Christopher B.; Murayama, Kei; Kremer, Laura S.; Schaller, André; Kotzaeridou, Urania; Vries, Maaike C. de; Schottmann, Gudrun; Santra, Saikat; Büchner, Boriana; Wieland, Thomas; Graf, Elisabeth; Freisinger, Peter; Eggimann, Sandra; Ohtake, Akira; Okazaki, Yasushi; Kohda, Masakazu; Kishita, Yoshihito; Tokuzawa, Yoshimi; Sauer, Sascha; Memari, Yasin; Kolb-Kokocinski, Anja; Durbin, Richard; Hasselmann, Oswald; Cremer, Kirsten; Albrecht, Beate; Wieczorek, Dagmar; Engels, Hartmut; Hahn, Dagmar; Zink, Alexander M.; Alston, Charlotte L.; Taylor, Robert W.; Rodenburg, Richard J.; Trollmann, Regina; Sperl, Wolfgang; Strom, Tim M.; Hoffmann, Georg F.; Mayr, Johannes A.; Meitinger, Thomas; Bolognini, Ramona; Schuelke, Markus; Nuoffer, Jean-Marc; Kölker, Stefan; Prokisch, Holger; Klopstock, Thomas (2015): Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement. In: Annals of Clinical and Translational Neurology, Vol. 2, No. 5: pp. 492-509

This list was generated on Thu Aug 13 00:02:58 2020 CEST.