P. Smits

Distinct Clinical Phenotypes Associated with a Mutation in the Mitochondrial Translation Elongation Factor EFTs

Orly Elpeleg, Hana Antonická, Heleen Diepstra et al. · The American Journal of Human Genetics · 2006 · 190 citations · Full text

Mitochondrial Biogenesis, Mitochondrial Function, Genetic Disorder +8

Reconstructing the evolution of the mitochondrial ribosomal proteome

P. Smits, Jan A. M. Smeitink, Lambert P. van den Heuvel et al. · Nucleic Acids Research · 2007 · 183 citations · Full text

Genetics, Molecular Biology, Genomics +16

Mutation in mitochondrial ribosomal protein MRPS22 leads to Cornelia de Lange-like phenotype, brain abnormalities and hypertrophic cardiomyopathy

P. Smits, Ann Saada, Saskia B. Wortmann et al. · European Journal of Human Genetics · 2010 · 96 citations · Full text

Mitochondrial Myopathy, Lange-like Phenotype, Cardiomyopathy +9

Mutation in subdomain G' of mitochondrial elongation factor G1 is associated with combined OXPHOS deficiency in fibroblasts but not in muscle

P. Smits, Hana Antonická, Peter M. van Hasselt et al. · European Journal of Human Genetics · 2010 · 51 citations · Full text

Molecular Physiology, Mitochondrial Biogenesis, Mitochondrial Function +11

A new flexible DBD device for treating infected wounds:<i>in vitro</i>and<i>ex vivo</i>evaluation and comparison with a RF argon plasma jet

Bouke K. H. L. Boekema, Marcel Vlig, D Guijt et al. · Journal of Physics D Applied Physics · 2015 · 45 citations · Full text