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 (101-110 of 242) with videos related to

Pageof 25
Sort By:
Journal of Neuropathology and Experimental Neurology|September 1, 1993
Experimental lovastatin myopathyA J Waclawik, S Lindal, A G Engel
Der Nervenarzt|February 11, 2004
[Differential congenital myasthenia syndrome diagnosis]S Spuler, T-N Lehmann, A G Engel
Neurology|December 1, 1973
Study of long-term anticholinesterase therapy. Effects on neuromuscular transmission and on motor end-plate fine structureA G Engel, E H Lambert, T Santa
Neurology|September 1, 1974
Motor end-plate fine structure in acrylamide dying-back neuropathy: a sequential morphometric studyM Tsujihata, A G Engel, E H Lambert
Neurology|January 1, 1972
Histometric study of neuromuscular junction ultrastructure. I. Myasthenia gravisT Santa, A G Engel, E H Lambert
Neurology|September 1, 1973
Sarcotubular myopathy. A newly recognized, benign, congenital, familial muscle diseaseF Jerusalem, A G Engel, M R Gomez
Advances in Neurology|January 1, 1988
Assay of acyl-CoA dehydrogenases in muscle and liver and identification of four new cases of medium-chain acyl-CoA dehydrogenase deficiency associated with systemic carnitine deficiencyS Zierz, A G Engel, C A Romshe
Journal of Neuroimmunology|December 1, 1995
Analysis of cytokine expression in muscle in inflammatory myopathies, Duchenne dystrophy, and non-weak controlsI Lundberg, J M Brengman, A G Engel
Neurology|February 1, 1975
Human muscle fiber fine structure: morphometric data on controlsF Jerusalem, A G Engel, H A Peterson
Journal of Physiology, Paris|October 23, 1998
Congenital myasthenic syndromes: experiments of natureA G Engel, K Ohno, S M Sine
Pageof 25

Showing results (101-110 of 242) with videos related to

Sort By:
Pageof 25
Journal of Neuropathology and Experimental Neurology|September 1, 1993
Experimental lovastatin myopathyA J Waclawik, S Lindal, A G Engel
Der Nervenarzt|February 11, 2004
[Differential congenital myasthenia syndrome diagnosis]S Spuler, T-N Lehmann, A G Engel
Neurology|December 1, 1973
Study of long-term anticholinesterase therapy. Effects on neuromuscular transmission and on motor end-plate fine structureA G Engel, E H Lambert, T Santa
Neurology|September 1, 1974
Motor end-plate fine structure in acrylamide dying-back neuropathy: a sequential morphometric studyM Tsujihata, A G Engel, E H Lambert
Neurology|January 1, 1972
Histometric study of neuromuscular junction ultrastructure. I. Myasthenia gravisT Santa, A G Engel, E H Lambert
Neurology|September 1, 1973
Sarcotubular myopathy. A newly recognized, benign, congenital, familial muscle diseaseF Jerusalem, A G Engel, M R Gomez
Advances in Neurology|January 1, 1988
Assay of acyl-CoA dehydrogenases in muscle and liver and identification of four new cases of medium-chain acyl-CoA dehydrogenase deficiency associated with systemic carnitine deficiencyS Zierz, A G Engel, C A Romshe
Journal of Neuroimmunology|December 1, 1995
Analysis of cytokine expression in muscle in inflammatory myopathies, Duchenne dystrophy, and non-weak controlsI Lundberg, J M Brengman, A G Engel
Neurology|February 1, 1975
Human muscle fiber fine structure: morphometric data on controlsF Jerusalem, A G Engel, H A Peterson
Journal of Physiology, Paris|October 23, 1998
Congenital myasthenic syndromes: experiments of natureA G Engel, K Ohno, S M Sine
Pageof 25