A trial of therapy by nucleosides and nucleotides in muscular dystrophy

Abstract
Six patients with Duchenne-type muscular dystrophy and 1 patient with the limb-girdle form were treated by intravenous infusions in Ringer''s solution of a nucleotide-nucleoside preparation (Laevadosin). Progress was evaluated by muscle strength measurements and assays of the serum enzymes aldolase, GOT and GPT. Results suggest some amelioration of the dystrophic process related to the therapy. Significant data pertaining to the Duchenne-type dystrophy can be obtained from SGOT and SGPT assays but serum aldolase assays seem to be necessary in the limb-girdle type dystrophy.

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