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Archives of Neurology|November 1, 1993
Duchenne-Becker muscular dystrophy and the nondystrophic myotonias. Paradigms for loss of function and change of function of gene productsE P Hoffman, J WangThe Journal of Biological Chemistry|July 15, 1994
Pathophysiology of sodium channelopathies. Studies of sodium channel expression by quantitative multiplex fluorescence polymerase chain reactionJ Zhou, E P HoffmanCurrent Opinion in Neurology|June 27, 1998
Current status of genetic discoveries in migraine: familial hemiplegic migraine and beyondK Gardner, E P HoffmanNeuromuscular Disorders : NMD|December 1, 1996
Autosomal recessive muscular dystrophy and mutations of the sarcoglycan complexD J Duggan, E P HoffmanNeurologic Clinics|November 1, 1994
Molecular diagnosis and modern management of Duchenne muscular dystrophyR G Miller, E P HoffmanMolecular and Cellular Biology|December 1, 1984
Correct temperature induction and developmental regulation of a cloned heat shock gene transformed into the Drosophila germ lineE P Hoffman, V G CorcesThe American Journal of Sports Medicine|September 1, 1983
Roentgenographic skeletal injury patterns in parachute jumpingA F Petras, E P HoffmanJournal of Bacteriology|July 1, 1970
Genetic mapping and dominance of the amber suppressor, Su1 (supD), in Escherichia coli K-12E P Hoffman, R C WilhelmCurrent Opinion in Neurology|September 20, 2001
The ABC's of limb-girdle muscular dystrophy: alpha-sarcoglycanopathy, Bethlem myopathy, calpainopathy and moreE S Gordon, E P HoffmanPageof 19