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Publications by Zschocke, Johannes

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Number of items: 5.

Journal article

Toth, Bettina; Wuerfel, Wolfgang; Bohlmann, Michael; Zschocke, Johannes; Rudnik-Schöneborn, Sabine; Nawroth, Frank; Schleussner, Ekkehard; Rogenhofer, Nina; Wischmann, Tewes; Wolff, Michael von; Hancke, Katharina; Otte, Sören von; Kuon, Ruben; Feil, Katharina; Tempfer, Clemens (2018): Recurrent Miscarriage: Diagnostic and Therapeutic Procedures. Guideline of the DGGG, OEGGG and SGGG (S2k-Level, AWMF Registry Number 015/050). In: Geburtshilfe und Frauenheilkunde, Vol. 78, No. 4: pp. 364-380

Alhaddad, Bader; Schossig, Anna; Haack, Tobias B.; Kovacs-Nagy, Reka; Braunisch, Matthias C.; Makowski, Christine; Senderek, Jan; Vill, Katharina; Müller-Felber, Wolfgang; Strom, Tim M.; Krabichler, Birgit; Freisinger, Peter; Deshpande, Charu; Polster, Tilman; Wolf, Nicole; Desguerre, Isabelle; Wörmann, Friedrich; Rotig, Agnes; Ahting, Uwe; Kopajtich, Robert; Prokisch, Holger; Meitinger, Thomas; Feichtinger, Rene G.; Mayr, Johannes A.; Jungbluth, Heinz; Hubmann, Michael; Zschocke, Johannes; Distelmaier, Felix; Koch, Johannes (2018): PRUNE1 Deficiency: Expanding the Clinical and Genetic Spectrum. In: Neuropediatrics, Vol. 49, No. 5: pp. 330-338

Boy, Nikolas; Mühlhausen, Chris; Maier, Esther M.; Heringer, Jana; Assmann, Birgit; Burgard, Peter; Dixon, Marjorie; Fleissner, Sandra; Greenberg, Cheryl R.; Harting, Inga; Hoffmann, Georg F.; Karall, Daniela; Koeller, David M.; Krawinkel, Michael; Okun, Jürgen G.; Opladen, Thomas; Posset, Roland; Sahm, Katja; Zschocke, Johannes; Kolker, Stefan (2017): Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision. In: Journal of inherited metabolic disease, Vol. 40, No. 1: pp. 75-101

Burgard, Peter; Ullrich, Kurt; Ballhausen, Diana; Hennermann, Julia B.; Hollak, Carla E. M.; Langeveld, Mirjam; Karall, Daniela; Konstantopoulou, Vassiliki; Maier, Esther M.; Lang, Frauke; Lachmann, Robin; Murphy, Elaine; Garbade, Sven; Hoffmann, Georg F.; Kölker, Stefan; Lindner, Martin; Zschocke, Johannes (2017): Issues with European guidelines for phenylketonuria. In: Lancet Diabetes & Endocrinology, Vol. 5, No. 9: pp. 681-683

Danecka, Marta K.; Woidy, Mathias; Zschocke, Johannes; Feillet, Francois; Muntau, Ania C.; Gersting, Søren W. (2015): Mapping the functional landscape of frequent phenylalanine hydroxylase (PAH) genotypes promotes personalised medicine in phenylketonuria. In: Journal of Medical Genetics, Vol. 52, No. 3: pp. 175-185 [PDF, 5MB]

This list was generated on Fri Jan 22 01:26:48 2021 CET.