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The Clinical Investigator|May 1, 1993
Inclusion body myositis: clinical and histopathological features of 36 patientsS Beyenburg, S Zierz, F JerusalemJournal of Neurology|February 1, 1989
Coenzyme Q in serum and muscle of 5 patients with Kearns-Sayre syndrome and 12 patients with ophthalmoplegia plusS Zierz, G Jahns, F JerusalemThe Clinical Investigator|October 1, 1993
Inhibition of carnitine palmitoyltransferase in normal human skeletal muscle and in muscle of patients with carnitine palmitoyltransferase deficiency by long- and short-chain acylcarnitine and acyl-coenzyme AS Zierz, S Neumann-Schmidt, F JerusalemThe Clinical Investigator|December 1, 1993
Biochemical evidence for heterozygosity in muscular carnitine palmitoyltransferase deficiencyS Zierz, R R Mundegar, F JerusalemJournal of the Neurological Sciences|March 1, 1990
Exogenous coenzyme Q (coq) fails to increase coq in skeletal muscle of two patients with mitochondrial myopathiesS Zierz, O von Wersebe, J Bleistein, et al.Journal of Neurology|February 1, 1994
Abnormal dystrophin expression in patients with limb girdle syndromesS Beyenburg, S Zierz, K Arahata, et al.Zeitschrift Fur Kardiologie|January 1, 1990
[Indications for pacemaker therapy in ophthalmoplegia plus and Kearns-Sayre syndrome]J Nitsch, S Zierz, K P Janssen, et al.Journal of Neurology|January 1, 1976
Hypotheses and recent findings concerning aetiology and pathogenesis of the muscular dystrophiesF JerusalemSchweizerische Medizinische Wochenschrift|January 22, 1977
[Myasthenia gravis. New results on etiology, diagnosis and therapy]F JerusalemThe Clinical Investigator|December 1, 1994
Limited trypsin proteolysis renders carnitine palmitoyltransferase insensitive to inhibition by malonyl-CoA in patients with muscle carnitine palmitoyltransferase deficiencyS ZierzPageof 19