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Kirsten Geider | Semantic Scholar
www.semanticscholar.org
Semantic Scholar profile for Kirsten Geider, with 69 highly influential citations and 8 scientific research papers.
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Author Search Results
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Showing of 1 for search: 'Kirsten Geider', query time: 0.01s. Sort. Relevance, Date Descending, Date Ascending, Author, Title, Publication Forum Class ...
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Ausbildung
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic...
kclpure.kcl.ac.uk
Johannes R Lemke ; Dennis Lal ; Eva M Reinthaler ; Isabelle Steiner ; Michael Nothnagel ; Michael Alber ; Kirsten Geider ; Bodo Laube ; Michael Schwake ...
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic...
kclpure.kcl.ac.uk
author = "Lemke, {Johannes R} and Dennis Lal and Reinthaler, {Eva M} and Isabelle Steiner and Michael Nothnagel and Michael Alber and Kirsten Geider and ...
Bücher
heiBIB: Syrbe, Steffen
katalog.ub.uni-heidelberg.de
... Johannes Rudolph: Delineating the GRIN1 phenotypic spectrum / Johannes R. Lemke, Kirsten Geider, Katherine L. Helbig, Henrike O. Heyne, Hannah Schütz ...
DNB, Katalog der Deutschen Nationalbibliothek
portal.dnb.de
Ionotropic glutamate receptor dysfunction in pediatric neurodevelopment / Kirsten Geider. Betreuer: Bodo Laube ; Ralf Galuske Person(en) Geider, Kirsten ...
Ionotropic Glutamate Receptor Dysfunction in Pediatric...
books.google.de
Title, Ionotropic Glutamate Receptor Dysfunction in Pediatric Neurodevelopment. Author, Kirsten Geider. Published, Length, 172 pages. Export Citation, BiBTeX EndNote RefMan ...
Dokumente zum Namen
GRIN2B mutations in west syndrome and intellectual disability with...
www.deepdyve.com
Lemke, Johannes R., Rik Hendrickx, Kirsten Geider, Bodo Laube, Michael Schwake, Robert J. Harvey, Victoria M. James, Alex Pepler, Isabelle ...
Delineating the GRIN1 phenotypic spectrum | Neurology
n.neurology.org
Kirsten Geider, PhD,. More articles by Kirsten Geider · Kirsten Geider on Google Scholar · Kirsten Geider on PubMed. Katherine L. Helbig, MS,.
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA...
www.scienceopen.com
... Lionel Van Maldergem, H Hilger Ropers, Ute Moog, Kirsten Geider, Dagmar Wieczorek, Sarah von Riedemann, Sabine Endele, Bodo Laube, ...
Wissenschaftliche Veröffentlichungen
Kirsten Geider – ScienceOpen
www.scienceopen.com
... ScienceOpen on Twitter · ScienceOpen on YouTube · ScienceOpen on LinkedIn · ScienceOpen on Google+ · ScienceOpen on Facebook ... Kirsten Geider.
Delineating the GRIN1 phenotypic spectrum / Johannes R. Lemke, …
suche.thulb.uni-jena.de
Delineating the GRIN1 phenotypic spectrum / Johannes R. Lemke, Kirsten Geider, Katherine L. Helbig, Henrike O. Heyne, Hannah Schütz, Julia Hentschel, Carolina ...
Ionotropic glutamate receptor dysfunction in pediatric...
tuprints.ulb.tu-darmstadt.de
2015 Ionotropic glutamate receptor dysfunction in pediatric neurodevelopment Technische Universität Geider Kirsten Kirsten Geider ...
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic...
www.ikmb.uni-kiel.de
Johannes R Lemke, Dennis Lal, Eva M Reinthaler, Isabelle Steiner, Michael Nothnagel, Michael Alber, Kirsten Geider, Bodo Laube, Michael Schwake, Katrin Finsterwalder ...
Veröffentlichungen allgemein
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA...
core.ac.uk
By Sabine Endele, Georg Rosenberger, Kirsten Geider, Bernt Popp, Ceyhun Tamer, Irina Stefanova, Mathieu Milh, Fanny Kortum, Angela Fritsch, Friederike K ...
GRIN2B Mutations in West Syndrome and Intellectual Disability with...
core.ac.uk
By Johannes R. Lemke, Rik Hendrickx, Kirsten Geider, Bodo Laube, Michael Schwake, Robert J. Harvey, Victoria M. James, Alex Pepler, Isabelle Steiner, ...
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic...
core.ac.uk
By Johannes R Lemke, Dennis Lal, Eva M Reinthaler, Isabelle Steiner, Michael Nothnagel, Michael Alber, Kirsten Geider, Bodo Laube, Michael Schwake, Katrin ...
Artikel & Meinungen
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic...
www.nature.com
Sarah von Spiczak, Holger Lerche and colleagues identify mutations in GRIN2A that cause idiopathic focal epilepsy with rolandic spikes.
Sonstiges
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of …
www.bionity.com
Authors: Sabine Endele, Georg Rosenberger, Kirsten Geider, Bernt Popp, Ceyhun Tamer, Irina Stefanova, Mathieu Milh, Fanny Kortüm, Angela Fritsch, Friederike K Pientka, Yorck Hellenbroich, Vera M Kalscheuer, Jürgen Kohlhase, Ute Moog, Gudrun Rappold, Anita Rauch, Hans-Hilger Ropers, Sarah von Spiczak, Holger Tönnies, Nathalie Villeneuve, Laurent Villard, Bernhard Zabel, …
Magnetenzephalographie-Studien zu antizipatorischen Aktivitäten im...
docplayer.org
4 II Großer Dank gilt auch meinen beiden Ex-Diplomarbeitskolleginnen und unverzichtbaren Freundinnen Kirsten Geider und Katharina Schmitz, ...
Actualización del Síndrome de West - PDF Descargar libre
docplayer.es
Johannes R. Lemke, MD,1,2 Rik Hendrickx, to-moderate Dose Intramuscular Corticotropin BSc,3,4 Kirsten Geider, MSc,5, Bodo Laube, for Improvement of ...
Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA...
hal.archives-ouvertes.fr
Johannes R. Lemke Kirsten Geider Katherine L. Helbig 1 Henrike O. Heyne Hannah Schutz Julia Hentschel Carolina Courage Christel Depienne 2, 3 Caroline ...
Delineating the GRIN1 phenotypic spectrum | Neurology
n.neurology.org
Johannes R. Lemke, Kirsten Geider, Katherine L. Helbig, Henrike O. Heyne, Hannah Schütz, Julia Hentschel, Carolina Courage, Christel ...
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic...
researchportal.helsinki.fi
Johannes R. Lemke, Dennis Lal, Eva M. Reinthaler, Isabelle Steiner, Michael Nothnagel, Michael Alber, Kirsten Geider, Bodo Laube, Michael Schwake, Katrin ...
[PDF] Delineating the GRIN1 phenotypic spectrum | Semantic Scholar
www.semanticscholar.org
Johannes R Lemke, Kirsten Geider, +55 authors Steffen Syrbe; Published in Neurology; DOI: WNL OBJECTIVE To ...
Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA...
researchportal.vub.be
author = "Lemke, {Johannes R} and Kirsten Geider and Helbig, {Katherine L} and Heyne, {Henrike O} and Hannah Sch{\"u}tz and Julia Hentschel and Carolina ...
Sarah E Buerki - Publications List
publicationslist.org
Nothnagel, Michael Alber, Kirsten Geider, Bodo Laube, Michael Schwake, Katrin
...
GRIN2B mutations in west syndrome and Wiley Online Library -...
moam.info
Bodo Laube, PhD,5 Michael Schwake, PhD,6 Robert J. Harvey, PhD,7. Victoria M. James, PhD,7 Alex Pepler, MBiol,7,8 Isabel...
SpringerCitations - Details Page
citations.springernature.com
Johannes R. Lemke, Rik Hendrickx, Kirsten Geider, Bodo Laube, Michael Schwake, Robert J. Harvey, Victoria M. James, Alex Pepler, Isabelle Steiner, ...
GRIN2A mutations in acquired epileptic aphasia and related ...read.qxmd.com › read
read.qxmd.com
... Michael Nothnagel, Michael Alber, Kirsten Geider, Bodo Laube, Michael Schwake, Katrin Finsterwalder, Andre Franke, Markus Schilhabel, Johanna A Jähn, ...
Katia Hardies | Research Portal
researchportal.be
Authors: Johannes R. Lemke, Kirsten Geider, Katherine L. Helbig, Isabelle Schrauwen, Sarah Weckhuysen, Katia Hardies, Peter De Jonghe, ...
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA...
go.gale.com
includes Mutations in GRIN2A and GRIN2B encoding regulatory subu by Sabine Endele, Georg Rosenberger, Kirst. Click to explore.
GRIN2B mutations in west syndrome and intellectual disability with...
www.infona.pl
Kirsten Geider. Department of Neurophysiology and Neurosensory Systems, Technical University Darmstadt. Bodo Laube. Department of Neurophysiology and ...
REVISTA CHILENA DE EPILEPSIA - PDF Free Download
docplayer.es
Brain & Development 2013; 35: Johannes R. Lemke, MD,1,2 Rik Hendrickx, BSc,3,4 Kirsten Geider, MSc,5, Bodo Laube, PhD,5 Michael Schwake, PhD,6 Robert ...
Supplementary Information - PDF Free Download
businessdocbox.com
... NMDA receptors cause different neurodevelopmental phenotypes Supplementary Information Sabine Endele 1,19, Georg Rosenberger 2,19, Kirsten Geider 3, ...
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA...
www.bionity.com
Authors: Sabine Endele, Georg Rosenberger, Kirsten Geider, Bernt Popp, Ceyhun Tamer, Irina Stefanova, Mathieu Milh, Fanny Kortüm, Angela Fritsch, ...
The N-terminal domain of the GluN3A subunit determines the efficacy...
pubmed.ncbi.nlm.nih.gov
Authors. Ivana Mesic , Christian Madry , Kirsten Geider , Max Bernhard , Heinrich Betz , Bodo Laube. Affiliations. 1 Department of Neurochemistry, ...
Verwandte Suchanfragen zu Kirsten Geider
Michael Nothnagel Michael Alber Hannah Schütz | Georg Rosenberger Sabine Endele Kristin Gaida |
Person "Geider" (2) Vorname "Kirsten" (15299) Name "Geider" (146) |
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