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D Beeson

Showing results (71-80 of 102) with videos related to

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The Journal of Clinical Investigation|November 15, 1996
Association of arthrogryposis multiplex congenita with maternal antibodies inhibiting fetal acetylcholine receptor functionS Riemersma, A Vincent, D Beeson, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Congenital myasthenic syndromes. Studies of the AChR and other candidate genesD Beeson, C Newland, R Croxen, et al.
The Journal of Clinical Investigation|July 4, 2001
Acetylcholine receptor delta subunit mutations underlie a fast-channel myasthenic syndrome and arthrogryposis multiplex congenitaS Brownlow, R Webster, R Croxen, et al.
Proceedings. Biological Sciences|October 22, 1993
Detection of alpha-subunit isoforms in human muscle acetylcholine receptor by specific T cells from a myasthenia gravis patientG Harcourt, A P Batocchi, S Hawke, et al.
International Journal of Molecular Medicine|February 17, 2001
Dominantly inherited familial myasthenia gravis as a separate genetic entity without involvement of defined candidate gene lociF Li, A Szobor, R Croxen, et al.
Annals of the New York Academy of Sciences|June 21, 1993
Clinical and experimental observations in patients with congenital myasthenic syndromesA Vincent, J Newsom-Davis, D Wray, et al.
Neurology|July 27, 2002
Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromesR Croxen, C Hatton, C Shelley, et al.
Biochemical Society Transactions|May 1, 1994
Involvement of cation channels in autoimmune diseaseA Vincent, R Barrett-Jolley, P Shillito, et al.
Neurology|January 21, 2009
Voluntary partial retraction of: Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromesR Croxen, C Hatton, C Shelley, et al.
The Journal of Clinical Investigation|May 29, 1998
A pathogenetic role for the thymoma in myasthenia gravis. Autosensitization of IL-4- producing T cell clones recognizing extracellular acetylcholine receptor epitopes presented by minority class II isotypesN Nagvekar, A M Moody, P Moss, et al.
Pageof 11

Showing results (71-80 of 102) with videos related to

Sort By:
Pageof 11
The Journal of Clinical Investigation|November 15, 1996
Association of arthrogryposis multiplex congenita with maternal antibodies inhibiting fetal acetylcholine receptor functionS Riemersma, A Vincent, D Beeson, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Congenital myasthenic syndromes. Studies of the AChR and other candidate genesD Beeson, C Newland, R Croxen, et al.
The Journal of Clinical Investigation|July 4, 2001
Acetylcholine receptor delta subunit mutations underlie a fast-channel myasthenic syndrome and arthrogryposis multiplex congenitaS Brownlow, R Webster, R Croxen, et al.
Proceedings. Biological Sciences|October 22, 1993
Detection of alpha-subunit isoforms in human muscle acetylcholine receptor by specific T cells from a myasthenia gravis patientG Harcourt, A P Batocchi, S Hawke, et al.
International Journal of Molecular Medicine|February 17, 2001
Dominantly inherited familial myasthenia gravis as a separate genetic entity without involvement of defined candidate gene lociF Li, A Szobor, R Croxen, et al.
Annals of the New York Academy of Sciences|June 21, 1993
Clinical and experimental observations in patients with congenital myasthenic syndromesA Vincent, J Newsom-Davis, D Wray, et al.
Neurology|July 27, 2002
Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromesR Croxen, C Hatton, C Shelley, et al.
Biochemical Society Transactions|May 1, 1994
Involvement of cation channels in autoimmune diseaseA Vincent, R Barrett-Jolley, P Shillito, et al.
Neurology|January 21, 2009
Voluntary partial retraction of: Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromesR Croxen, C Hatton, C Shelley, et al.
The Journal of Clinical Investigation|May 29, 1998
A pathogenetic role for the thymoma in myasthenia gravis. Autosensitization of IL-4- producing T cell clones recognizing extracellular acetylcholine receptor epitopes presented by minority class II isotypesN Nagvekar, A M Moody, P Moss, et al.
Pageof 11