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Journal of the Neurological Sciences|January 1, 1979
Carnitine palmitoyltransferase II deficiency with normal carnitine palmitoyltransferase I in skeletal muscle and leucocytesH R Scholte, F G Jennekens, J J BouvyEuropean Journal of Pediatrics|August 1, 1984
Systemic carnitine deficiency: benefit of oral carnitine supplements vs. persisting biochemical abnormalitiesM Duran, J B de Klerk, S K Wadman, et al.Wiener Klinische Wochenschrift|January 6, 1989
Carnitine deficiency, mitochondrial dysfunction and the heart. Identical defect of oxidative phosphorylation in muscle mitochondria in cardiomyopathy due to carnitine loss and in Duchenne muscular dystrophyH R Scholte, R Rodrigues Pereira, H F Busch, et al.Clinical Neurology and Neurosurgery|January 1, 1992
Medical therapy in spinal muscular atrophy: a realistic expectation?F G JennekensClinical Neurology and Neurosurgery|January 1, 1993
Peripheral nerve lesions: the neuropharmacological outlookH Kerkhoff, F G JennekensLeprosy Review|September 1, 1992
Neurological examination of patients suffering from leprosy: is it worthwhile?F G Jennekens, A Jennekens-SchinkelJournal of Neurology, Neurosurgery, and Psychiatry|October 1, 1987
Proximal weakness of the extremities as main feature of amyloid myopathyF G Jennekens, J H WokkeNederlands Tijdschrift Voor Geneeskunde|March 29, 1997
[Peer review in requests for subsidy]F G Jennekens, H F BuschJournal of Bioenergetics and Biomembranes|April 1, 1988
The biochemical basis of mitochondrial diseasesH R ScholteJournal of the Neurological Sciences|September 1, 1977
Immunofluorescence studies in a case of rheumatoid neuropathyJ M Van Lis, F G JennekensPageof 17