W. Ruitenbeek

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

J. M. W. van den Ouweland, H.H.P.J. Lemkes, W. Ruitenbeek et al. · Nature Genetics · 1992 · 1.1K citations

Genetic Determinant, Mendelian Disorder, Genetic Disorder +9

Differential investigation of the capacity of succinate oxidation in human skeletal muscle

Johan Fischer, W. Ruitenbeek, J.A. Berden et al. · Clinica Chimica Acta · 1985 · 466 citations

Muscle Function, Differential Investigation, Muscle Injury +10

Demonstration of a New Pathogenic Mutation in Human Complex I Deficiency: A 5-bp Duplication in the Nuclear Gene Encoding the 18-kD (AQDQ) Subunit

Lambert van den Heuvel, W. Ruitenbeek, Roel Smeets et al. · The American Journal of Human Genetics · 1998 · 264 citations · Full text

Human Complex, Genetic Disorder, Genetics +9

A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome

D. Daniëlle de Vries, Baziel G.M. van Engelen, F.J.M. Gabreëls et al. · Annals of Neurology · 1993 · 262 citations

Altered Ca2+ Responses in Muscles with Combined Mitochondrial and Cytosolic Creatine Kinase Deficiencies

Karen Steeghs, Ad A.G.M. Benders, Frank Oerlemans et al. · Cell · 1997 · 254 citations · Full text

Combined Mitochondrial, Muscle Function, Signal Transduction +11