J. Jeneson

Magnetic resonance reveals mitochondrial dysfunction and muscle remodelling in spinal muscular atrophy

B. Bartels, A. Nederveen, W. L. van der Pol, 2021, Brain : a journal of neurology.

Mitochondrial affinity for ADP is twofold lower in creatine kinase knock‐out muscles

K. Nicolay, F. ter Veld, J. Jeneson, 2005, The FEBS journal.

Vitamin-responsive complex I deficiency in a myopathic patient with increased activity of the terminal respiratory chain and lactic acidosis

N. Abeling, H. Bakker, A. H. Gennip, 1994, Journal of Inherited Metabolic Disease.

Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotype

B. Andresen, B. Poorthuis, H. Scholte, 1999, Neuromuscular Disorders.

Deficiency of the Adenine Nucleotide Translocator in Muscle of a Patient with Myopathy and Lactic Acidosis: A New Mitochondrial Defect

R. Wanders, R. Sengers, N. Abeling, 1993, Pediatric Research.

Adenine nucleotide translocator deficiency in muscle: Potential therapeutic value of vitamin E

R. Wanders, N. Abeling, H. Bakker, 1993, Journal of Inherited Metabolic Disease.

Vitamin E in a mitochondrial myopathy with proliferating mitochondria

H. Scholte, J. Jeneson, H. Bakker, 1993, The Lancet.

1H MR imaging of anatomical compartments within the finger flexor muscles of the human forearm

D. Vigneron, June S. Taylor, L. Carvajal, 1990, Magnetic resonance in medicine.