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

Andrew G Engel

Showing results (51-60 of 129) with videos related to

Pageof 13
Sort By:
Neurology|November 9, 2014
Mutant SNAP25B causes myasthenia, cortical hyperexcitability, ataxia, and intellectual disabilityXin-Ming Shen, Duygu Selcen, Joan Brengman, et al.
Medwave|June 22, 2019
Congenital myasthenic syndrome due to rapsyn deficiency: A case report with a new mutation and compound heterozygosityIvan O Espinoza, Carolina Reynoso, Giulliana Chávez, et al.
The Journal of Biological Chemistry|January 2, 2004
C-terminal and heparin-binding domains of collagenic tail subunit are both essential for anchoring acetylcholinesterase at the synapseLewis M Kimbell, Kinji Ohno, Andrew G Engel, et al.
Chemico-Biological Interactions|September 18, 2012
Specific binding of collagen Q to the neuromuscular junction is exploited to cure congenital myasthenia and to explore bases of myasthenia gravisKinji Ohno, Mikako Ito, Yu Kawakami, et al.
The Lancet. Neurology|March 21, 2015
Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatmentAndrew G Engel, Xin-Ming Shen, Duygu Selcen, et al.
Neuromuscular Disorders : NMD|September 7, 2010
Sporadic centronuclear myopathy with muscle pseudohypertrophy, neutropenia, and necklace fibers due to a DNM2 mutationTeerin Liewluck, Tracy L Lovell, Anna V Bite, et al.
Journal of Molecular Neuroscience : MN|August 19, 2009
What have we learned from the congenital myasthenic syndromesAndrew G Engel, Xin-Ming Shen, Duygu Selcen, et al.
Annals of the New York Academy of Sciences|November 1, 2003
Congenital myasthenic syndromes: multiple molecular targets at the neuromuscular junctionAndrew G Engel, Kinji Ohno, Xin-Ming Shen, et al.
Pediatric Neurology|July 5, 2012
Neuromuscular junction acetylcholinesterase deficiency responsive to albuterolSophelia H S Chan, Virginia C N Wong, Andrew G Engel
Neuromuscular Disorders : NMD|November 13, 2012
Scapuloperoneal muscular dystrophy phenotype due to TRIM32-sarcotubular myopathy in South Dakota HutteriteTeerin Liewluck, Jennifer A Tracy, Eric J Sorenson, et al.
Pageof 13

Showing results (51-60 of 129) with videos related to

Sort By:
Pageof 13
Neurology|November 9, 2014
Mutant SNAP25B causes myasthenia, cortical hyperexcitability, ataxia, and intellectual disabilityXin-Ming Shen, Duygu Selcen, Joan Brengman, et al.
Medwave|June 22, 2019
Congenital myasthenic syndrome due to rapsyn deficiency: A case report with a new mutation and compound heterozygosityIvan O Espinoza, Carolina Reynoso, Giulliana Chávez, et al.
The Journal of Biological Chemistry|January 2, 2004
C-terminal and heparin-binding domains of collagenic tail subunit are both essential for anchoring acetylcholinesterase at the synapseLewis M Kimbell, Kinji Ohno, Andrew G Engel, et al.
Chemico-Biological Interactions|September 18, 2012
Specific binding of collagen Q to the neuromuscular junction is exploited to cure congenital myasthenia and to explore bases of myasthenia gravisKinji Ohno, Mikako Ito, Yu Kawakami, et al.
The Lancet. Neurology|March 21, 2015
Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatmentAndrew G Engel, Xin-Ming Shen, Duygu Selcen, et al.
Neuromuscular Disorders : NMD|September 7, 2010
Sporadic centronuclear myopathy with muscle pseudohypertrophy, neutropenia, and necklace fibers due to a DNM2 mutationTeerin Liewluck, Tracy L Lovell, Anna V Bite, et al.
Journal of Molecular Neuroscience : MN|August 19, 2009
What have we learned from the congenital myasthenic syndromesAndrew G Engel, Xin-Ming Shen, Duygu Selcen, et al.
Annals of the New York Academy of Sciences|November 1, 2003
Congenital myasthenic syndromes: multiple molecular targets at the neuromuscular junctionAndrew G Engel, Kinji Ohno, Xin-Ming Shen, et al.
Pediatric Neurology|July 5, 2012
Neuromuscular junction acetylcholinesterase deficiency responsive to albuterolSophelia H S Chan, Virginia C N Wong, Andrew G Engel
Neuromuscular Disorders : NMD|November 13, 2012
Scapuloperoneal muscular dystrophy phenotype due to TRIM32-sarcotubular myopathy in South Dakota HutteriteTeerin Liewluck, Jennifer A Tracy, Eric J Sorenson, et al.
Pageof 13