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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.
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.
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