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Heart (British Cardiac Society)|July 16, 2004
Multiple pathogenetic mechanisms in X linked dilated cardiomyopathyN Cohen, F MuntoniHuman Genetics|April 1, 1996
Alternative splicing of dystrophin exon 4 in normal human muscleS Torelli, F MuntoniActa Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 25, 2006
The modulation of skeletal muscle glycosylation as a potential therapeutic intervention in muscular dystrophiesM Brockington, F MuntoniBiochemical and Biophysical Research Communications|February 3, 1998
The 5' region of intron 11 of the dystrophin gene contains target sequences for mobile elements and three overlapping ORFsA Ferlini, F MuntoniFEBS Letters|July 31, 1989
Transcription of the dystrophin gene in Duchenne muscular dystrophy muscleF Muntoni, P N StrongJournal of Neurology, Neurosurgery, and Psychiatry|June 18, 2009
Diagnosis and new treatments in muscular dystrophiesA Y Manzur, F MuntoniCurrent Opinion in Neurology|December 11, 1999
Inherited disorders of the extracellular matrixC A Sewry, F MuntoniPostgraduate Medical Journal|November 7, 2009
Diagnosis and new treatments in muscular dystrophiesA Y Manzur, F MuntoniEuropean Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 1, 1997
Epilepsy in Duchenne and Becker muscular dystrophiesF Goodwin, F Muntoni, V DubowitzNeuromuscular Disorders : NMD|January 1, 1991
Passive avoidance behaviour deficit in the mdx mouseF Muntoni, A Mateddu, G SerraPageof 166