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ACS Synthetic Biology
|
March 7, 2020
Mutations in a Single Signaling Pathway Allow Cell Growth in Heavy Water
Caroline 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 2
Y 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 ataxia
N Schwarz, A Hahn, T Bast, et al.
Nature
|
May 30, 2008
Magnetic resonance imaging of pH in vivo using hyperpolarized 13C-labelled bicarbonate
Ferdia 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 imaging
Nathanael Raschzok, Carolin M Langer, Christian Schmidt, et al.
Neurology
|
August 12, 2011
Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect
Y 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 peptides
L 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 tumors
Ferdia A Gallagher, Mikko I Kettunen, De-En Hu, et al.
Neurology
|
January 28, 2012
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy
P Striano, Y G Weber, M R Toliat, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 92) with videos related to
Sort By:
Page
of 10
ACS Synthetic Biology
|
March 7, 2020
Mutations in a Single Signaling Pathway Allow Cell Growth in Heavy Water
Caroline 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 2
Y 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 ataxia
N Schwarz, A Hahn, T Bast, et al.
Nature
|
May 30, 2008
Magnetic resonance imaging of pH in vivo using hyperpolarized 13C-labelled bicarbonate
Ferdia 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 imaging
Nathanael Raschzok, Carolin M Langer, Christian Schmidt, et al.
Neurology
|
August 12, 2011
Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect
Y 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 peptides
L 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 tumors
Ferdia A Gallagher, Mikko I Kettunen, De-En Hu, et al.
Neurology
|
January 28, 2012
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy
P Striano, Y G Weber, M R Toliat, et al.
Page
of 10