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

Margaret J Jackson

Showing results (1-10 of 8) with videos related to

Pageof 1
Sort By:
Clinical Medicine (London, England)|August 8, 2014
Concise guidance: diagnosis and management of the epilepsies in adultsMargaret J Jackson
Journal of Neurology, Neurosurgery, and Psychiatry|April 15, 2008
Should we accept the status quo? Time for new trials in status epilepticusMargaret J Jackson
The Practitioner|June 26, 2008
Assessing suspected epilepsy in primary careStephan R Jaiser, Margaret J Jackson
Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Spectrum of movement disorders in neuroferritinopathyDouglas E Crompton, Patrick F Chinnery, David Bates, et al.
The FEBS Journal|July 13, 2005
A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeastEmma L Blakely, Anna L Mitchell, Nicholas Fisher, et al.
Neuromuscular Disorders : NMD|June 24, 2004
Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) geneSeyed Bidooki, Margaret J Jackson, Margaret A Johnson, et al.
Brain : a Journal of Neurology|December 5, 2006
Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutationPatrick F Chinnery, Douglas E Crompton, Daniel Birchall, et al.
Blood Cells, Molecules & Diseases|January 28, 2003
Neuroferritinopathy: a window on the role of iron in neurodegenerationDouglas E Crompton, Patrick F Chinnery, Constanze Fey, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Clinical Medicine (London, England)|August 8, 2014
Concise guidance: diagnosis and management of the epilepsies in adultsMargaret J Jackson
Journal of Neurology, Neurosurgery, and Psychiatry|April 15, 2008
Should we accept the status quo? Time for new trials in status epilepticusMargaret J Jackson
The Practitioner|June 26, 2008
Assessing suspected epilepsy in primary careStephan R Jaiser, Margaret J Jackson
Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Spectrum of movement disorders in neuroferritinopathyDouglas E Crompton, Patrick F Chinnery, David Bates, et al.
The FEBS Journal|July 13, 2005
A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeastEmma L Blakely, Anna L Mitchell, Nicholas Fisher, et al.
Neuromuscular Disorders : NMD|June 24, 2004
Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) geneSeyed Bidooki, Margaret J Jackson, Margaret A Johnson, et al.
Brain : a Journal of Neurology|December 5, 2006
Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutationPatrick F Chinnery, Douglas E Crompton, Daniel Birchall, et al.
Blood Cells, Molecules & Diseases|January 28, 2003
Neuroferritinopathy: a window on the role of iron in neurodegenerationDouglas E Crompton, Patrick F Chinnery, Constanze Fey, et al.
Pageof 1