Thomas Klopstock
Thomas Klopstock
Dept. of Neurology, University of Munich
Verified email at
Cited by
Cited by
Guidelines for the use and interpretation of assays for monitoring autophagy
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy, 1-382, 2021
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease
A Bender, KJ Krishnan, CM Morris, GA Taylor, AK Reeve, RH Perry, ...
Nature genetics 38 (5), 515-517, 2006
Genome-wide, large-scale production of mutant mice by ENU mutagenesis
MH de Angelis, H Flaswinkel, H Fuchs, B Rathkolb, D Soewarto, ...
Nature genetics 25 (4), 444-447, 2000
A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice
W Enard, S Gehre, K Hammerschmidt, SM Hölter, T Blass, M Somel, ...
Cell 137 (5), 961-971, 2009
Phenotypic spectrum associated with mutations of the mitochondrial polymerase γ gene
R Horvath, G Hudson, G Ferrari, N Fütterer, S Ahola, E Lamantea, ...
Brain 129 (7), 1674-1684, 2006
Post-stroke inhibition of induced NADPH oxidase type 4 prevents oxidative stress and neurodegeneration
C Kleinschnitz, H Grund, K Wingler, ME Armitage, E Jones, M Mittal, ...
PLoS Biol 8 (9), e1000479, 2010
A randomized placebo-controlled trial of idebenone in Leber’s hereditary optic neuropathy
T Klopstock, P Yu-Wai-Man, K Dimitriadis, J Rouleau, S Heck, M Bailie, ...
Brain 134 (9), 2677-2686, 2011
Targeted next generation sequencing as a diagnostic tool in epileptic disorders
JR Lemke, E Riesch, T Scheurenbrand, M Schubach, C Wilhelm, I Steiner, ...
Epilepsia 53 (8), 1387-1398, 2012
Rapamycin extends murine lifespan but has limited effects on aging
F Neff, D Flores-Dominguez, DP Ryan, M Horsch, S Schröder, T Adler, ...
The Journal of clinical investigation 123 (8), 3272-3291, 2013
Gene–environment interactions in Leber hereditary optic neuropathy
MA Kirkman, P Yu-Wai-Man, A Korsten, M Leonhardt, K Dimitriadis, ...
Brain 132 (9), 2317-2326, 2009
Aberrant methylation of t RNA s links cellular stress to neuro‐developmental disorders
S Blanco, S Dietmann, JV Flores, S Hussain, C Kutter, P Humphreys, ...
The EMBO journal 33 (18), 2020-2039, 2014
Neuron-glia communication via EphA4/ephrin-A3 modulates LTP through glial glutamate transport
A Filosa, S Paixão, SD Honsek, MA Carmona, L Becker, B Feddersen, ...
Nature neuroscience 12 (10), 1285, 2009
SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathy
D Ghezzi, P Goffrini, G Uziel, R Horvath, T Klopstock, H Lochmüller, ...
Nature genetics 41 (6), 654-656, 2009
Creatine supplementation in Parkinson disease: a placebo-controlled randomized pilot trial
A Bender, W Koch, M Elstner, Y Schombacher, J Bender, M Moeschl, ...
Neurology 67 (7), 1262-1264, 2006
Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study
MC Walter, H Lochmüller, P Reilich, T Klopstock, R Huber, M Hartard, ...
Neurology 54 (9), 1848-1850, 2000
Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation
MB Hartig, A Iuso, T Haack, T Kmiec, E Jurkiewicz, K Heim, S Roeber, ...
The American Journal of Human Genetics 89 (4), 543-550, 2011
Introducing the German Mouse Clinic: open access platform for standardized phenotyping
V Gailus-Durner, H Fuchs, L Becker, I Bolle, M Brielmeier, ...
Nature methods 2 (6), 403-404, 2005
Transfection of mitochondria: strategy towards a gene therapy of mitochondrial DNA diseases
P Seibel, J Trappe, G Villani, T Klopstock, S Papa, H Reichmann
Nucleic acids research 23 (1), 10-17, 1995
The Spastic Paraplegia Rating Scale (SPRS): a reliable and valid measure of disease severity
R Schüle, T Holland-Letz, S Klimpe, J Kassubek, T Klopstock, V Mall, ...
Neurology 67 (3), 430-434, 2006
Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease
C Kornblum, TJ Nicholls, TB Haack, S Schöler, V Peeva, K Danhauser, ...
Nature genetics 45 (2), 214, 2013
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