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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.International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|July 1, 1994
Oxyphilic Sertoli cell tumor of the ovary: a report of three cases, two in patients with the Peutz-Jeghers syndromeJ A Ferry, R H Young, G Engel, 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 EngelNeuromuscular 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.Applied Optics|March 12, 2009
Modeling the absorption behavior of solar thermal collector coatings utilizing graded alpha-C:H/TiC layersD P Gruber, G Engel, H Sormann, et al.The Journal of Physiology|March 11, 2006
The human adult subtype ACh receptor channel has high Ca2+ permeability and predisposes to endplate Ca2+ overloadingSergio Fucile, Antonietta Sucapane, Francesca Grassi, et al.Pageof 63