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British Journal of Pharmacology|May 24, 2007
Dexrazoxane prevents doxorubicin-induced long-term cardiotoxicity and protects myocardial mitochondria from genetic and functional lesions in ratsD Lebrecht, A Geist, U-P Ketelsen, et al.Helvetica Paediatrica Acta|September 1, 1982
Adrenal insufficiency, myopathic hypotonia, severe psychomotor retardation, failure to thrive, constipation and bladder ectasia in 2 brothers: adrenomyodystrophyW von Petrykowski, R Beckmann, N Böhm, et al.Acta Neuropathologica|January 1, 1995
3.1-kb deletion of mitochondrial DNA in a patient with Kearns-Sayre syndromeT Klopstock, F Bischof, K Gerok, et al.Neuropediatrics|September 3, 2005
Congenital myopathy with arrest of myogenesis prior to formation of myotubesU-P Ketelsen, B Brand-Saberi, B Uhlenberg, et al.Neuromuscular Disorders : NMD|October 12, 2001
Valproic acid triggers acute rhabdomyolysis in a patient with carnitine palmitoyltransferase type II deficiencyM Kottlors, M Jaksch, U P Ketelsen, et al.Neuropediatrics|November 5, 2003
Identification of a novel LAMP2 mutation responsible for X-chromosomal dominant Danon diseaseJ Horváth, U-P Ketelsen, A Geibel-Zehender, et al.European Neurology|January 1, 1991
Histological, enzymatic and mitochondrial DNA studies in patients with Kearns-Sayre syndrome and chronic progressive external ophthalmoplegiaH Reichmann, F Degoul, R Gold, et al.Arzneimittel-Forschung|March 1, 1992
Effect of magnesium pyridoxal 5-phosphate glutamate on the hamster cardiomyopathyH G Olbrich, J F Boeker, S Rachor, et al.Klinische Wochenschrift|July 1, 1988
A double-blind placebo controlled trial of diltiazem in Duchenne dystrophyW Pernice, R Beckmann, U P Ketelsen, et al.Journal of Child Neurology|August 13, 1998
Axonal neuropathy and predominance of type II myofibers in infantile spinal muscular atrophyH Omran, U P Ketelsen, F Heinen, et al.Pageof 4