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

A E Harding

Showing results (111-120 of 241) with videos related to

Pageof 25
Sort By:
Annals of Neurology|March 1, 1991
A genetic study of idiopathic focal dystoniasH M Waddy, N A Fletcher, A E Harding, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1990
Pontine myelinolysis presenting with acute parkinsonism as a sequel of corrected hyponatraemiaR Tinker, M G Anderson, P Anand, et al.
Archives of Disease in Childhood|November 1, 1994
Mitochondrial DNA 8993 (NARP) mutation presenting with a heterogeneous phenotype including 'cerebral palsy'A Fryer, R Appleton, M G Sweeney, et al.
Lancet (London, England)|June 25, 1988
Deletions of muscle mitochondrial DNAI J Holt, J M Cooper, J A Morgan-Hughes, et al.
Journal of the Neurological Sciences|September 15, 1996
The GTP-cyclohydrolase I gene in atypical parkinsonian patients: a clinico-genetic studyO Bandmann, S Daniel, C D Marsden, et al.
Journal of the Neurological Sciences|June 1, 1995
Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A-->G (MERRF) mutation: relationship to proportion of mutant mitochondrial DNAM G Hanna, I P Nelson, J A Morgan-Hughes, et al.
Annals of Neurology|March 1, 1992
A follow-up study of isolated cases of suspected Huntington's diseaseD Bateman, A M Boughey, F Scaravilli, et al.
Journal of Neurology|July 1, 1991
Discordance for late-onset degenerative ataxia in monozygous tripletsA E Harding, T Sura, P Tippett, et al.
Annals of Neurology|May 1, 1992
Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1)P J Hallam, A E Harding, J Berciano, et al.
American Journal of Human Genetics|March 1, 1990
A new mitochondrial disease associated with mitochondrial DNA heteroplasmyI J Holt, A E Harding, R K Petty, et al.
Pageof 25

Showing results (111-120 of 241) with videos related to

Sort By:
Pageof 25
Annals of Neurology|March 1, 1991
A genetic study of idiopathic focal dystoniasH M Waddy, N A Fletcher, A E Harding, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1990
Pontine myelinolysis presenting with acute parkinsonism as a sequel of corrected hyponatraemiaR Tinker, M G Anderson, P Anand, et al.
Archives of Disease in Childhood|November 1, 1994
Mitochondrial DNA 8993 (NARP) mutation presenting with a heterogeneous phenotype including 'cerebral palsy'A Fryer, R Appleton, M G Sweeney, et al.
Lancet (London, England)|June 25, 1988
Deletions of muscle mitochondrial DNAI J Holt, J M Cooper, J A Morgan-Hughes, et al.
Journal of the Neurological Sciences|September 15, 1996
The GTP-cyclohydrolase I gene in atypical parkinsonian patients: a clinico-genetic studyO Bandmann, S Daniel, C D Marsden, et al.
Journal of the Neurological Sciences|June 1, 1995
Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A-->G (MERRF) mutation: relationship to proportion of mutant mitochondrial DNAM G Hanna, I P Nelson, J A Morgan-Hughes, et al.
Annals of Neurology|March 1, 1992
A follow-up study of isolated cases of suspected Huntington's diseaseD Bateman, A M Boughey, F Scaravilli, et al.
Journal of Neurology|July 1, 1991
Discordance for late-onset degenerative ataxia in monozygous tripletsA E Harding, T Sura, P Tippett, et al.
Annals of Neurology|May 1, 1992
Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1)P J Hallam, A E Harding, J Berciano, et al.
American Journal of Human Genetics|March 1, 1990
A new mitochondrial disease associated with mitochondrial DNA heteroplasmyI J Holt, A E Harding, R K Petty, et al.
Pageof 25