Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Korenke, Christoph G."'
The phenotype and long-term follow-up in 11 patients with juvenile selenoprotein N1-related myopathy
Autor:
Schara, Ulrike, Kress, Wolfram, Bönnemann, Carsten G., Breitbach-Faller, Nico, Korenke, Christoph G., Schreiber, Gudrun, Stoetter, Mechthild, Ferreiro, Ana, von der Hagen, Maja
Publikováno v:
In European Journal of Paediatric Neurology 2008 12(3):224-230
Haematopoietic stem cell transplantation in 12 patients with cerebral X-linked adrenoleukodystrophy.
Autor:
Baumann, Matthias, Korenke, Christoph G., Weddige-Diedrichs, Almuth, Wilichowski, Ekkehard, Hunneman, Donald H., Wilken, Bernd, Brockmann, Knut, Klingebiel, Thomas, Niethammer, Dietrich, Kühl, Jörn, Ebell, Wolfram, Hanefeld, Folker
Publikováno v:
European Journal of Pediatrics. 2003, Vol. 162 Issue 1, p6. 9p.
Autor:
von Moers, Arpad, Brockmann, Knut, Wang, Dong, Korenke, Christoph G., Huppke, Peter, De Vivo, Darryl C., Hanefeld, Folker
Publikováno v:
Epilepsia (Series 4); Aug2002, Vol. 43 Issue 8, p941-945, 5p
Autor:
Brockmann, Knut, Bjornstad, Alf, Dechent, Peter, Korenke, Christoph G., Smeitink, Jan, Trijbels, J. M. Frans, Athanassopoulos, Sabine, Villagran, Rafael, Skjeldal, Ola H., Wilichowski, Ekkehard, Frahm, Jens, Hanefeld, Folker
Publikováno v:
Annals of Neurology; 2002, Vol. 52 Issue 1, p38-46, 9p
Autor:
Brockmann, Knut, Wang, Dong, Korenke, Christoph G., Von Moers, Arpad, Ho, Yuan-Yuan, Pascual, Juan M., Kuang, Kunyan, Yang, Hong, Ma, Li, Kranz-Eble, Pamela, Fischbarg, Jorge, Hanefeld, Folker, De Vivo, Darryl C., Brockmann, K, Wang, D, Korenke, C G, von Moers, A, Ho, Y Y, Pascual, J M, Kuang, K
Publikováno v:
Annals of Neurology; 2001, Vol. 50 Issue 4, p476-485, 10p
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Schene IF; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, The Netherlands., Korenke CG; Department of Neuropediatrics, Children's Hospital Klinikum Oldenburg, Oldenburg, Germany., Huidekoper HH; Department of Pediatrics, Center for Lysosomal and Metabolic Diseases, Erasmus Medical Center, Rotterdam, The Netherlands., van der Pol L; Department of Neurology, University Medical Centre Utrecht, Utrecht, The Netherlands., Dooijes D; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands., Breur JMPJ; Department of Pediatric Cardiology, Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, The Netherlands., Biskup S; CeGaT GmbH and Praxis für Humangenetik Tübingen, Tübingen, Germany., Fuchs SA; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, The Netherlands., Visser G; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, The Netherlands. G.Visser-4@umcutrecht.nl.
Publikováno v:
JIMD reports [JIMD Rep] 2019; Vol. 45, pp. 99-104. Date of Electronic Publication: 2018 Dec 20.