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International Journal of Molecular Sciences|July 9, 2022
Peripheral Ion Channel Gene Screening in Painful- and Painless-Diabetic NeuropathyMilena Ślęczkowska, Rowida Almomani, Margherita Marchi, et al.
European Journal of Human Genetics : EJHG|August 24, 2021
Pathogenic SLIRP variants as a novel cause of autosomal recessive mitochondrial encephalomyopathy with complex I and IV deficiencyLe Guo, Bob P H Engelen, Irene M G M Hemel, et al.
The Journal of Clinical Endocrinology and Metabolism|July 18, 2012
Physical activity is the key determinant of skeletal muscle mitochondrial function in type 2 diabetesF H J van Tienen, S F E Praet, H M de Feyter, et al.
Andrology|August 24, 2024
Innovative all-in-one exome sequencing strategy for diagnostic genetic testing in male infertility: Validation and 10-month experienceManon S Oud, Nicole de Leeuw, Dominique F C M Smeets, et al.
Cell Reports|July 5, 2016
Differences in Strength and Timing of the mtDNA Bottleneck between Zebrafish Germline and Non-germline CellsAuke B C Otten, Tom E J Theunissen, Josien G Derhaag, et al.
Frontiers in Molecular Neuroscience|November 3, 2017
Selection and Characterization of Palmitic Acid Responsive Patients with an OXPHOS Complex I DefectTom E J Theunissen, Mike Gerards, Debby M E I Hellebrekers, et al.
Human Molecular Genetics|January 8, 2016
Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneckIan J Wilson, Phillipa J Carling, Charlotte L Alston, et al.
Orphanet Journal of Rare Diseases|June 25, 2021
Healthcare needs, expectations, utilization, and experienced treatment effects in patients with hereditary spastic paraplegia: a web-based survey in the NetherlandsHans C J W Kerstens, Bas J H Van Lith, Maarten J Nijkrake, et al.
Psychosomatic Medicine|October 15, 2019
Placebo Effects in the Neuroendocrine System: Conditioning of the Oxytocin ResponsesAleksandrina Skvortsova, Dieuwke S Veldhuijzen, Gustavo Pacheco-Lopez, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 19, 2025
Intra-arterial transplantation of autologous mesoangioblasts in m.3243A>G mutation carriers is safe: First phase 1/2 human clinical studyFlorence H J van Tienen, Janneke G J Hoeijmakers, Christiaan van der Leij, et al.
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