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H Lerche

Showing results (81-90 of 92) with videos related to

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ACS Synthetic Biology|March 7, 2020
Mutations in a Single Signaling Pathway Allow Cell Growth in Heavy WaterCaroline Kampmeyer, Jens V Johansen, Christian Holmberg, et al.
Neurology|March 12, 2010
Comparative analysis of brain structure, metabolism, and cognition in myotonic dystrophy 1 and 2Y G Weber, R Roebling, J Kassubek, et al.
Journal of Neurology|December 10, 2015
Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxiaN Schwarz, A Hahn, T Bast, et al.
Nature|May 30, 2008
Magnetic resonance imaging of pH in vivo using hyperpolarized 13C-labelled bicarbonateFerdia A Gallagher, Mikko I Kettunen, Sam E Day, et al.
Cell Transplantation|January 9, 2013
Functionalizable silica-based micron-sized iron oxide particles for cellular magnetic resonance imagingNathanael Raschzok, Carolin M Langer, Christian Schmidt, et al.
Neurology|August 12, 2011
Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defectY G Weber, C Kamm, A Suls, et al.
Nature Biotechnology|October 3, 1999
Identification of a neuritogenic ligand of the neural cell adhesion molecule using a combinatorial library of synthetic peptidesL C Rønn, M Olsen, S Ostergaard, et al.
Brain Stimulation|April 2, 2016
Transcutaneous Vagus Nerve Stimulation (tVNS) for Treatment of Drug-Resistant Epilepsy: A Randomized, Double-Blind Clinical Trial (cMPsE02)S Bauer, H Baier, C Baumgartner, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 12, 2009
Production of hyperpolarized [1,4-13C2]malate from [1,4-13C2]fumarate is a marker of cell necrosis and treatment response in tumorsFerdia A Gallagher, Mikko I Kettunen, De-En Hu, et al.
Neurology|January 28, 2012
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsyP Striano, Y G Weber, M R Toliat, et al.
Pageof 10

Showing results (81-90 of 92) with videos related to

Sort By:
Pageof 10
ACS Synthetic Biology|March 7, 2020
Mutations in a Single Signaling Pathway Allow Cell Growth in Heavy WaterCaroline Kampmeyer, Jens V Johansen, Christian Holmberg, et al.
Neurology|March 12, 2010
Comparative analysis of brain structure, metabolism, and cognition in myotonic dystrophy 1 and 2Y G Weber, R Roebling, J Kassubek, et al.
Journal of Neurology|December 10, 2015
Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxiaN Schwarz, A Hahn, T Bast, et al.
Nature|May 30, 2008
Magnetic resonance imaging of pH in vivo using hyperpolarized 13C-labelled bicarbonateFerdia A Gallagher, Mikko I Kettunen, Sam E Day, et al.
Cell Transplantation|January 9, 2013
Functionalizable silica-based micron-sized iron oxide particles for cellular magnetic resonance imagingNathanael Raschzok, Carolin M Langer, Christian Schmidt, et al.
Neurology|August 12, 2011
Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defectY G Weber, C Kamm, A Suls, et al.
Nature Biotechnology|October 3, 1999
Identification of a neuritogenic ligand of the neural cell adhesion molecule using a combinatorial library of synthetic peptidesL C Rønn, M Olsen, S Ostergaard, et al.
Brain Stimulation|April 2, 2016
Transcutaneous Vagus Nerve Stimulation (tVNS) for Treatment of Drug-Resistant Epilepsy: A Randomized, Double-Blind Clinical Trial (cMPsE02)S Bauer, H Baier, C Baumgartner, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 12, 2009
Production of hyperpolarized [1,4-13C2]malate from [1,4-13C2]fumarate is a marker of cell necrosis and treatment response in tumorsFerdia A Gallagher, Mikko I Kettunen, De-En Hu, et al.
Neurology|January 28, 2012
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsyP Striano, Y G Weber, M R Toliat, et al.
Pageof 10