Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A G Engel

Showing results (71-80 of 242) with videos related to

Pageof 25
Sort By:
Electroencephalography and Clinical Neurophysiology. Supplement|January 1, 1987
Congenital myasthenic syndromesA G Engel, E H Lambert
Archives of Neurology|August 1, 1972
Lipid storage myopathy responsive to prednisoneA G Engel, R G Siekert
Brain Research|September 24, 1993
Ephedrine: effects on neuromuscular transmissionJ P Sieb, A G Engel
Neurology|August 1, 1970
Emetine myopathyD D Duane, A G Engel
Neurology|July 1, 1981
Primary systemic carnitine deficiency: I. Carnitine biosynthesisC J Rebouche, A G Engel
Annals of Neurology|April 18, 1998
Quinidine sulfate therapy for the slow-channel congenital myasthenic syndromeC M Harper, A G Engel
In Vitro|May 1, 1982
Carnitine transport in cultured muscle cells and skin fibroblasts from patients with primary systemic carnitine deficiencyC J Rebouche, A G Engel
Journal of the Neurological Sciences|January 1, 1978
Experimental lipid storage myopathy. A quantitative ultrastructural and biochemical studyA K Brownell, A G Engel
Neurology|July 1, 1973
Normal and denervated muscle. A morphometric study of fine structureH H Stonnington, A G Engel
Neurology|September 1, 1987
Are hypercontracted muscle fibers artifacts and do they cause rupture of the plasma membrane?B P Lotz, A G Engel
Pageof 25

Showing results (71-80 of 242) with videos related to

Sort By:
Pageof 25
Electroencephalography and Clinical Neurophysiology. Supplement|January 1, 1987
Congenital myasthenic syndromesA G Engel, E H Lambert
Archives of Neurology|August 1, 1972
Lipid storage myopathy responsive to prednisoneA G Engel, R G Siekert
Brain Research|September 24, 1993
Ephedrine: effects on neuromuscular transmissionJ P Sieb, A G Engel
Neurology|August 1, 1970
Emetine myopathyD D Duane, A G Engel
Neurology|July 1, 1981
Primary systemic carnitine deficiency: I. Carnitine biosynthesisC J Rebouche, A G Engel
Annals of Neurology|April 18, 1998
Quinidine sulfate therapy for the slow-channel congenital myasthenic syndromeC M Harper, A G Engel
In Vitro|May 1, 1982
Carnitine transport in cultured muscle cells and skin fibroblasts from patients with primary systemic carnitine deficiencyC J Rebouche, A G Engel
Journal of the Neurological Sciences|January 1, 1978
Experimental lipid storage myopathy. A quantitative ultrastructural and biochemical studyA K Brownell, A G Engel
Neurology|July 1, 1973
Normal and denervated muscle. A morphometric study of fine structureH H Stonnington, A G Engel
Neurology|September 1, 1987
Are hypercontracted muscle fibers artifacts and do they cause rupture of the plasma membrane?B P Lotz, A G Engel
Pageof 25