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David Beeson

Showing results (11-20 of 139) with videos related to

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BMC Neurology|October 9, 2016
A rare c.183_187dupCTCAC mutation of the acetylcholine receptor CHRNE gene in a South Asian female with congenital myasthenic syndrome: a case reportThashi Chang, Judith Cossins, David Beeson
Annals of the New York Academy of Sciences|January 31, 2018
Therapeutic strategies for congenital myasthenic syndromesManon Lee, David Beeson, Jacqueline Palace
Current Opinion in Neurology|July 25, 2024
Congenital myasthenic syndromes: increasingly complexSithara Ramdas, David Beeson, Yin Yao Dong
Muscle & Nerve|December 26, 2001
The agrin/muscle-specific kinase pathway: new targets for autoimmune and genetic disorders at the neuromuscular junctionYohan Liyanage, Werner Hoch, David Beeson, et al.
Journal of Neuroimmunology|April 19, 2005
Inhibition of acetylcholine receptor function by seronegative myasthenia gravis non-IgG factor correlates with desensitisationIan Spreadbury, Uday Kishore, David Beeson, et al.
International Journal of Molecular Sciences|June 8, 2018
The Neuromuscular Junction and Wide Heterogeneity of Congenital Myasthenic SyndromesPedro M Rodríguez Cruz, Jacqueline Palace, David Beeson
Frontiers in Molecular Neuroscience|October 5, 2020
The Structure, Function, and Physiology of the Fetal and Adult Acetylcholine Receptor in MuscleHakan Cetin, David Beeson, Angela Vincent, et al.
Journal of Neurology|October 12, 2014
Inherited disorders of the neuromuscular junction: an updatePedro M Rodríguez Cruz, Jacqueline Palace, David Beeson
Current Opinion in Neurology|August 28, 2014
Congenital myasthenic syndromes and the neuromuscular junctionPedro M Rodríguez Cruz, Jacqueline Palace, David Beeson
Journal of Rnai and Gene Silencing : an International Journal of RNA and Gene Targeting Research|September 23, 2009
Selective cleavage of AChR cRNAs harbouring mutations underlying the slow channel myasthenic syndrome by hammerhead ribozymesAmr Abdelgany, John Ealing, Matthew Wood, et al.
Pageof 14

Showing results (11-20 of 139) with videos related to

Sort By:
Pageof 14
BMC Neurology|October 9, 2016
A rare c.183_187dupCTCAC mutation of the acetylcholine receptor CHRNE gene in a South Asian female with congenital myasthenic syndrome: a case reportThashi Chang, Judith Cossins, David Beeson
Annals of the New York Academy of Sciences|January 31, 2018
Therapeutic strategies for congenital myasthenic syndromesManon Lee, David Beeson, Jacqueline Palace
Current Opinion in Neurology|July 25, 2024
Congenital myasthenic syndromes: increasingly complexSithara Ramdas, David Beeson, Yin Yao Dong
Muscle & Nerve|December 26, 2001
The agrin/muscle-specific kinase pathway: new targets for autoimmune and genetic disorders at the neuromuscular junctionYohan Liyanage, Werner Hoch, David Beeson, et al.
Journal of Neuroimmunology|April 19, 2005
Inhibition of acetylcholine receptor function by seronegative myasthenia gravis non-IgG factor correlates with desensitisationIan Spreadbury, Uday Kishore, David Beeson, et al.
International Journal of Molecular Sciences|June 8, 2018
The Neuromuscular Junction and Wide Heterogeneity of Congenital Myasthenic SyndromesPedro M Rodríguez Cruz, Jacqueline Palace, David Beeson
Frontiers in Molecular Neuroscience|October 5, 2020
The Structure, Function, and Physiology of the Fetal and Adult Acetylcholine Receptor in MuscleHakan Cetin, David Beeson, Angela Vincent, et al.
Journal of Neurology|October 12, 2014
Inherited disorders of the neuromuscular junction: an updatePedro M Rodríguez Cruz, Jacqueline Palace, David Beeson
Current Opinion in Neurology|August 28, 2014
Congenital myasthenic syndromes and the neuromuscular junctionPedro M Rodríguez Cruz, Jacqueline Palace, David Beeson
Journal of Rnai and Gene Silencing : an International Journal of RNA and Gene Targeting Research|September 23, 2009
Selective cleavage of AChR cRNAs harbouring mutations underlying the slow channel myasthenic syndrome by hammerhead ribozymesAmr Abdelgany, John Ealing, Matthew Wood, et al.
Pageof 14