Showing results (1-10 of 108) with videos related to
Sort By:
Pageof 11
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 2, 1978
The fatty acid composition of various lipid fractions isolated from erythrocytes and blood plasma of patients with Duchenne and congenital myotonic muscular dystrophyW RuitenbeekHistochemistry|January 1, 1976
Polyacrylamide gel technique for the histochemical demonstration of soluble enzymesW Ruitenbeek, H R ScholteJournal of the Neurological Sciences|April 1, 1979
Fatty acid activation and transfer in blood cells of patients with muscular dystrophyW Ruitenbeek, H R ScholteClinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1979
Osmotic stability of erythrocytes in human muscular dystrophy before and after phospholipase treatmentW Ruitenbeek, M J Edixhoven, H R ScholteMuscle & Nerve|January 1, 1987
Prevention of recurrent exertional rhabdomyolysis by dantrolene sodiumP J Haverkort-Poels, E M Joosten, W RuitenbeekJournal of Inherited Metabolic Disease|January 1, 1996
Genetic counselling and prenatal diagnosis in disorders of the mitochondrial energy metabolismW Ruitenbeek, U Wendel, B C Hamel, et al.Pediatric Neurology|January 1, 1992
Assessment and therapy monitoring of Leigh disease by MRI and proton spectroscopyI Krägeloh-Mann, W Grodd, G Niemann, et al.Tijdschrift Voor Kindergeneeskunde|August 1, 1984
[Mitochondrial myopathy associated with cytochrome oxidase deficiency]R C Sengers, J M Trijbels, W Ruitenbeek, et al.Journal of the Neurological Sciences|September 1, 1993
Treatment of complex I deficiency with riboflavinP L Bernsen, F J Gabreëls, W Ruitenbeek, et al.Developmental Medicine and Child Neurology|June 1, 1990
A mitochondrial myopathy in an infant with lactic acidosisV Griebel, I Krägeloh-Mann, W Ruitenbeek, et al.Pageof 11