Literature DB >> 3520308

A trial of flunarizine in the treatment of Duchenne muscular dystrophy.

D J Dick, D Gardner-Medwin, P G Gates, M Gibson, J M Simpson, T J Walls.   

Abstract

Twenty-seven boys with Duchenne muscular dystrophy (DMD) entered a double-blind controlled trial of treatment with the calcium antagonist flunarizine. They were matched for age and disability. At monthly intervals, muscle power, functional ability, locomotor score, contractures, and forced vital capacity were measured by a team not involved in clinical care. Over a period of 1 year, flunarizine in a dose of up to 0.25 mg/kg/day had no effect on the clinical course of the disease.

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Year:  1986        PMID: 3520308     DOI: 10.1002/mus.880090412

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  7 in total

1.  A double-blind placebo controlled trial of diltiazem in Duchenne dystrophy.

Authors:  W Pernice; R Beckmann; U P Ketelsen; M Frey; B Schmidt-Redemann; K P Haap; R Roehren; M Sauer
Journal:  Klin Wochenschr       Date:  1988-07-01

Review 2.  Current understanding and management of dilated cardiomyopathy in Duchenne and Becker muscular dystrophy.

Authors:  Rita Wen Kaspar; Hugh D Allen; Federica Montanaro
Journal:  J Am Acad Nurse Pract       Date:  2009-05

3.  Duchenne Muscular Dystrophy.

Authors:  Susan T. Iannaccone; Zohair Nanjiani
Journal:  Curr Treat Options Neurol       Date:  2001-03       Impact factor: 3.972

4.  Experimental models of duchenne muscular dystrophy: relationship with cardiovascular disease.

Authors:  Venus Ameen; Lesley G Robson
Journal:  Open Cardiovasc Med J       Date:  2010-11-26

Review 5.  Genetic evidence in the mouse solidifies the calcium hypothesis of myofiber death in muscular dystrophy.

Authors:  A R Burr; J D Molkentin
Journal:  Cell Death Differ       Date:  2015-06-19       Impact factor: 15.828

Review 6.  Discovery of Novel Therapeutics for Muscular Dystrophies using Zebrafish Phenotypic Screens.

Authors:  Jeffrey J Widrick; Genri Kawahara; Matthew S Alexander; Alan H Beggs; Louis M Kunkel
Journal:  J Neuromuscul Dis       Date:  2019

7.  Pharmacological therapeutics targeting the secondary defects and downstream pathology of Duchenne muscular dystrophy.

Authors:  Janelle M Spinazzola; Louis M Kunkel
Journal:  Expert Opin Orphan Drugs       Date:  2016-10-18       Impact factor: 0.694

  7 in total

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