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Thomas Klopstock
Thomas Klopstock
Dept. of Neurology, University of Munich
Verified email at med.lmu.de
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Cited by
Cited by
Year
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
106692021
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
17712006
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
7962000
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
6792009
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
5472011
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
5282014
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 biology 8 (9), e1000479, 2010
4972010
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
4522006
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
3952013
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
3932012
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
3912009
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), 1285-1292, 2009
3422009
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
2912009
The Spastic Paraplegia Rating Scale (SPRS) a reliable and valid measure of disease severity
R Schule, T Holland-Letz, S Klimpe, J Kassubek, T Klopstock, V Mall, ...
Neurology 67 (3), 430-434, 2006
2832006
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
2662011
Hereditary spastic paraplegia: clinicogenetic lessons from 608 patients
R Schüle, S Wiethoff, P Martus, KN Karle, S Otto, S Klebe, S Klimpe, ...
Annals of neurology 79 (4), 646-658, 2016
2632016
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), 214-219, 2013
2592013
Prevalence of sexual dimorphism in mammalian phenotypic traits
NA Karp, J Mason, AL Beaudet, Y Benjamini, L Bower, RE Braun, ...
Nature communications 8 (1), 15475, 2017
2342017
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
2342006
Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing
TB Haack, B Haberberger, EM Frisch, T Wieland, A Iuso, M Gorza, ...
Journal of medical genetics 49 (4), 277-283, 2012
2192012
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