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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.Neuroreport|July 17, 1998
Quinidine normalizes the open duration of slow-channel mutants of the acetylcholine receptorT Fukudome, K Ohno, J M Brengman, et al.Physical Review. E|February 17, 2024
Spin-orbit-coupled fractional oscillators and trapped Bose-Einstein condensatesV A Stephanovich, E V Kirichenko, G Engel, et al.British Journal of Clinical Pharmacology|February 12, 1998
The involvement of CYP1A2 and CYP3A4 in the metabolism of clozapineB Eiermann, G Engel, I Johansson, et al.Journal of Neuropathology and Experimental Neurology|March 1, 1980
Ultrastructural localization of the terminal and lytic ninth complement component (C9) at the motor end-plate in myasthenia gravisK Sahashi, A G Engel, E H Lambert, et al.The Journal of Urology|February 1, 1980
The role of excretory urography and cystoscopy in the evaluation and management of women with recurrent urinary tract infectionG Engel, A J Schaeffer, J T Grayhack, 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.Blood|June 1, 1994
Isolation and characterization of the human interleukin-9 receptor geneM S Chang, G Engel, C Benedict, 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.Pageof 61