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Author/Creator Herkenrath, Peter

1. A heritable microduplication encompassing TBL1XR1 causes a genomic sister‐disorder for the 3q26.32 microdeletion syndrome. Issue 8 (2nd June 2017)

Authors:
Riehmer, Vera; Erger, Florian; Herkenrath, Peter; Seland, Saskia; Jackels, Miriam; Wiater, Alfred; Heller, Raoul; Beck, Bodo B.; Netzer, Christian
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 8(2017)
Page Start:
2132
Record Type:
Journal Article
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3. Oligoclonal bands predict multiple sclerosis in children with optic neuritis. Issue 6 (11th May 2015)

Authors:
Heussinger, Nicole; Kontopantelis, Evangelos; Gburek‐Augustat, Janina; Jenke, Andreas; Vollrath, Gesa; Korinthenberg, Rudolf; Hofstetter, Peter; Meyer, Sascha; Brecht, Isabel; Kornek, Barbara; Herkenrath, Peter; Schimmel, Mareike; Wenner, Kirsten; Häusler, Martin; Lutz, Soeren; Karenfort, Michael...
Journal:
Annals of neurology
Issue:
Volume 77:Issue 6(2015:Jun.)
Page Start:
1076
Record Type:
Journal Article
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4. Rasmussen encephalitis: Incidence and course under randomized therapy with tacrolimus or intravenous immunoglobulins. Issue 3 (6th December 2012)

Authors:
Bien, Christian G.; Tiemeier, Henning; Sassen, Robert; Kuczaty, Stefan; Urbach, Horst; von Lehe, Marec; Becker, Albert J.; Bast, Thomas; Herkenrath, Peter; Karenfort, Michael; Kruse, Bernd; Kurlemann, Gerhard; Rona, Sabine; Schubert‐Bast, Susanne; Vieker, Silvia; Vlaho, Stefan; Wilken, Bernd; Elg...
Journal:
Epilepsia
Issue:
Volume 54:Issue 3(2013:Mar.)
Page Start:
543
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗