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Susan Maxwell

Showing results (31-40 of 46) with videos related to

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Brain : a Journal of Neurology|October 22, 2019
β2-Adrenergic receptor agonists ameliorate the adverse effect of long-term pyridostigmine on neuromuscular junction structureAn E Vanhaesebrouck, Richard Webster, Susan Maxwell, et al.
Brain : a Journal of Neurology|June 1, 2010
N-methyl-D-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexesSarosh R Irani, Katarzyna Bera, Patrick Waters, et al.
Neurology|February 1, 2015
Antibodies to GABAA receptor α1 and γ2 subunits: clinical and serologic characterizationPhilippa Pettingill, Holger B Kramer, Jan Adriaan Coebergh, et al.
Cellular and Molecular Life Sciences : CMLS|March 13, 2024
Unraveling the molecular interactions between α7 nicotinic receptor and a RIC3 variant associated with backward speechAditi Pradhan, Hayley Mounford, Jessica Peixinho, et al.
Science (New York, N.Y.)|August 19, 2006
Dok-7 mutations underlie a neuromuscular junction synaptopathyDavid Beeson, Osamu Higuchi, Jackie Palace, et al.
Fertility and Sterility|June 6, 2017
Detailed investigation into the cytogenetic constitution and pregnancy outcome of replacing mosaic blastocysts detected with the use of high-resolution next-generation sequencingSantiago Munné, Joshua Blazek, Michael Large, et al.
American Journal of Human Genetics|June 30, 2012
Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregatesKatsiaryna Belaya, Sarah Finlayson, Clarke R Slater, et al.
Brain : a Journal of Neurology|February 14, 2013
Congenital myasthenic syndromes due to mutations in ALG2 and ALG14Judith Cossins, Katsiaryna Belaya, Debbie Hicks, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 6, 2016
Clinical features of the myasthenic syndrome arising from mutations in GMPPBPedro M Rodríguez Cruz, Katsiaryna Belaya, Keivan Basiri, et al.
American Journal of Human Genetics|December 3, 2015
Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 ChainClare V Logan, Judith Cossins, Pedro M Rodríguez Cruz, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Brain : a Journal of Neurology|October 22, 2019
β2-Adrenergic receptor agonists ameliorate the adverse effect of long-term pyridostigmine on neuromuscular junction structureAn E Vanhaesebrouck, Richard Webster, Susan Maxwell, et al.
Brain : a Journal of Neurology|June 1, 2010
N-methyl-D-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexesSarosh R Irani, Katarzyna Bera, Patrick Waters, et al.
Neurology|February 1, 2015
Antibodies to GABAA receptor α1 and γ2 subunits: clinical and serologic characterizationPhilippa Pettingill, Holger B Kramer, Jan Adriaan Coebergh, et al.
Cellular and Molecular Life Sciences : CMLS|March 13, 2024
Unraveling the molecular interactions between α7 nicotinic receptor and a RIC3 variant associated with backward speechAditi Pradhan, Hayley Mounford, Jessica Peixinho, et al.
Science (New York, N.Y.)|August 19, 2006
Dok-7 mutations underlie a neuromuscular junction synaptopathyDavid Beeson, Osamu Higuchi, Jackie Palace, et al.
Fertility and Sterility|June 6, 2017
Detailed investigation into the cytogenetic constitution and pregnancy outcome of replacing mosaic blastocysts detected with the use of high-resolution next-generation sequencingSantiago Munné, Joshua Blazek, Michael Large, et al.
American Journal of Human Genetics|June 30, 2012
Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregatesKatsiaryna Belaya, Sarah Finlayson, Clarke R Slater, et al.
Brain : a Journal of Neurology|February 14, 2013
Congenital myasthenic syndromes due to mutations in ALG2 and ALG14Judith Cossins, Katsiaryna Belaya, Debbie Hicks, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 6, 2016
Clinical features of the myasthenic syndrome arising from mutations in GMPPBPedro M Rodríguez Cruz, Katsiaryna Belaya, Keivan Basiri, et al.
American Journal of Human Genetics|December 3, 2015
Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 ChainClare V Logan, Judith Cossins, Pedro M Rodríguez Cruz, et al.
Pageof 5