H. Busch

发表

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.

Muscle mitochondria from patients with Duchenne muscular dystrophy have a normal beta oxidation, but an impaired oxidative phosphorylation

F. Jennekens, H. Scholte, I. Luyt-Houwen, 1985, Neurology.

Problems with the biochemical diagnosis in mitochondrial (encephalo-)myopathies

R. Sengers, H. Scholte, W. Ruitenbeek, 1993, European Journal of Pediatrics.

Anaerobic threshold as detected from ventilatory and metabolic exercise responses in patients with mitochondrial respiratory chain defect.

J. Bogaard, A. Versprille, H. Scholte, 1986, Advances in cardiology.

Myopathy with abnormal mitochondria, transient low electron transport capacity in the respiratory chain, and absence of energy transduction at sites 1 and 2 in vitro.

J. Berden, K. Toyka, H. Scholte, 1986, Journal of neurology, neurosurgery, and psychiatry.

Oxidative phosphorylation in human muscle in patients with ocular myopathy and after general anaesthesia.

F. Jennekens, B. van Linge, H. Scholte, 1990, Biochimica et biophysica acta.

Early changes of muscle mitochondria in duchenne dystrophy Partition and activity of mitochondrial enzymes in fractionated muscle of unaffected boys and adults and patients

H. Scholte, H. Busch, 1980, Journal of the Neurological Sciences.

Partition and Activity of Mitochondrial Enzymes in Fractionated Muscle of Un- affected Boys and Adults and Patients

H. Scholte, H. Busch, 1980 .

Decreased phosphorylase activity in leucocytes of Duchenne carriers.

H. Scholte, H. Busch, 1980, Clinica chimica acta; international journal of clinical chemistry.

Exercise responses in patients with an enzyme deficiency in the mitochondrial respiratory chain.

J. Bogaard, A. Versprille, H. Scholte, 1988, The European respiratory journal.

Daytime sleep in myotonic dystrophy is not caused by sleep apnoea.

J. Bogaard, F. van der Meché, H. Busch, 1994, Journal of neurology, neurosurgery, and psychiatry.

Inflammatory myopathy in scapulo-ilio-peroneal atrophy with cardiopathy. A study of two families.

N. V. van Hemel, F. Jennekens, H. Busch, 1975, Brain : a journal of neurology.

Ca2+ homeostasis in Brody's disease. A study in skeletal muscle and cultured muscle cells and the effects of dantrolene an verapamil.

P. Jongen, R. Wevers, R. Bindels, 1994, The Journal of clinical investigation.

Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells

H. Busch, H. Scholte, H. Przyrembel, 1987, Journal of Inherited Metabolic Disease.

Increased risk for cardiorespiratory failure associated with the A3302G mutation in the mitochondrial DNA encoded tRNALeu(UUR) gene

H. Smeets, G. Jong, I. D. Coo, 2004, Neuromuscular Disorders.

Riboflavin-responsive complex I deficiency.

J. Bogaard, H. Busch, H. Bakker, 1995, Biochimica et biophysica acta.

Familial AMP deaminase deficiency with skeletal muscle type I atrophy and fatal cardiomyopathy

H. Busch, H. Scholte, I. Luyt-Houwen, 1981, Journal of Inherited Metabolic Disease.