Thomas Klopstock
0000-0003-2805-4652
Publication & Citation Trends
Publications
715 total
rAAV2/2-ND4 for the Treatment of Leber Hereditary Optic Neuropathy (LHON): Final Results from the RESCUE and REVERSE Phase III Clinical Trials and Experimental Data in Nonhuman Primates to Support a Bilateral Effect (2339)
Cited by 5
Semantic Scholar
O.24 Loss of function of MGME1, a novel player in mitochondrial DNA replication, causes a distinct autosomal recessive mitochondrial disorder
Cited by 1
Semantic Scholar
Twenty-third Meeting of the European Neurological Society, 8–11 June, 2013 Barcelona, Spain OA
Cited by 5
Semantic Scholar
Spinocerebellar ataxia type 36 (SCA36): Expanding the Genotype and Phenotype
Cited by 0
Semantic Scholar
P5.50 Clinical Lipidomics – An approach towards clinical readout in orphan an common neuromuscular diseases
Cited by 0
Semantic Scholar
P4.44 mitoNET – German network for mitochondrial disorders
Cited by 0
Semantic Scholar
Autosomal dominant Progressive External Ophthalmoplegia (adPEO) due to mutations in the PEO1 gene: A clinical, histochemical and molecular survey of 33 patients
Cited by 0
Semantic Scholar
Dopaminergic midbrain neurons are the prime target for mitochondrial DNA deletions
Cited by 88
Semantic Scholar
Research Topics
Mitochondrial Function and Pathology
(231)
Metabolism and Genetic Disorders
(138)
Genetic Neurodegenerative Diseases
(88)
Neurological diseases and metabolism
(62)
ATP Synthase and ATPases Research
(50)
Affiliations
Centre National de la Recherche Scientifique
United Negro College Fund
University of Nottingham
Innsbruck Medical University
Radboud University Nijmegen