Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Robin Kennett

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
Journal of Neurology|February 9, 2012
Modern electroencephalographyRobin Kennett
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|June 7, 2005
Reversible optic neuropathy associated with low-dose methotrexate therapyGerry Clare, Stephen Colley, Robin Kennett, et al.
Seizure|June 7, 2017
LGI1-antibody encephalitis is characterised by frequent, multifocal clinical and subclinical seizuresSidra Aurangzeb, Mkael Symmonds, Ravi K Knight, et al.
Brain : a Journal of Neurology|April 25, 2007
Clinical features of the DOK7 neuromuscular junction synaptopathyJacqueline Palace, Daniel Lashley, John Newsom-Davis, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 21, 2013
Isolated paediatric neurosarcoidosis presenting as epilepsia partialis continua: a case report and review of literatureGeetha Anand, Fang En Sin, Elizabeth Soilleux, et al.
Archives of Neurology|June 13, 2012
Presence and pathogenic relevance of antibodies to clustered acetylcholine receptor in ocular and generalized myasthenia gravisSaiju Jacob, Stuart Viegas, Maria Isabel Leite, et al.
Brain : a Journal of Neurology|May 5, 2006
MRI and clinical studies of facial and bulbar muscle involvement in MuSK antibody-associated myasthenia gravisMaria Elena Farrugia, Matthew D Robson, Linda Clover, 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.
Brain : a Journal of Neurology|July 3, 2015
Mutations in GMPPB cause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathiesKatsiaryna Belaya, Pedro M Rodríguez Cruz, Wei Wei Liu, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Journal of Neurology|February 9, 2012
Modern electroencephalographyRobin Kennett
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|June 7, 2005
Reversible optic neuropathy associated with low-dose methotrexate therapyGerry Clare, Stephen Colley, Robin Kennett, et al.
Seizure|June 7, 2017
LGI1-antibody encephalitis is characterised by frequent, multifocal clinical and subclinical seizuresSidra Aurangzeb, Mkael Symmonds, Ravi K Knight, et al.
Brain : a Journal of Neurology|April 25, 2007
Clinical features of the DOK7 neuromuscular junction synaptopathyJacqueline Palace, Daniel Lashley, John Newsom-Davis, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 21, 2013
Isolated paediatric neurosarcoidosis presenting as epilepsia partialis continua: a case report and review of literatureGeetha Anand, Fang En Sin, Elizabeth Soilleux, et al.
Archives of Neurology|June 13, 2012
Presence and pathogenic relevance of antibodies to clustered acetylcholine receptor in ocular and generalized myasthenia gravisSaiju Jacob, Stuart Viegas, Maria Isabel Leite, et al.
Brain : a Journal of Neurology|May 5, 2006
MRI and clinical studies of facial and bulbar muscle involvement in MuSK antibody-associated myasthenia gravisMaria Elena Farrugia, Matthew D Robson, Linda Clover, 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.
Brain : a Journal of Neurology|July 3, 2015
Mutations in GMPPB cause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathiesKatsiaryna Belaya, Pedro M Rodríguez Cruz, Wei Wei Liu, et al.
Pageof 1