Herman Bentlage

Relationship of Genotype to Phenotype in Fibroblast-derived Transmitochondrial Cell Lines Carrying the 3243 Mutation Associated with the Melas Encephalomyopathy: Shift towards Mutant Genotype and Role of mtDNA Copy Number

Herman Bentlage, Giuseppe Attardi · Human Molecular Genetics · 1996 · 82 citations

Lethal infantile mitochondrial disease with isolated complex I deficiency in fibroblasts but with combined complex I and IV deficiencies in muscle

Herman Bentlage, U. Wendel, Hermann Schägger et al. · Neurology · 1996 · 74 citations

Genetics, Pathology, Molecular Genetics +17

Clinical heterogeneity in respiratory chain complex III deficiency in childhood

J. Mourmans, U. Wendel, Herman Bentlage et al. · Journal of the Neurological Sciences · 1997 · 62 citations

Asthma, Pediatric Epidemiology, Respiratory Diseases +9

Extreme variability of clinical symptoms among sibs in a MELAS family correlated with heteroplasmy for the mitochondrial A3243G mutation

Daniëlle de Vries, Ilse de Wijs, W. Ruitenbeek et al. · Journal of the Neurological Sciences · 1994 · 49 citations

Clinical Symptoms, Mendelian Disorder, Melas Family +10

Human Diseases with Defects in Oxidative Phosphorylation

Herman Bentlage, I.F.M. de Coo, H. ter Laak et al. · European Journal of Biochemistry · 1995 · 48 citations

Mitochondrial Trna Leu, Cell Death, Pathology +20