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 (131-140 of 241) with videos related to

Pageof 25
Sort By:
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1991
An adult onset hexosaminidase A deficiency syndrome with sensory neuropathy and internuclear ophthalmoplegiaD Barnes, V P Misra, E P Young, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1984
Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness: a clinicopathological reportM Baraitser, W Gooddy, A M Halliday, et al.
Neurology|September 1, 1994
Nigral degeneration in neuroacanthocytosisJ O Rinne, S E Daniel, F Scaravilli, et al.
American Journal of Human Genetics|March 1, 1992
Prenatal diagnosis of mitochondrial DNA8993 T----G diseaseA E Harding, I J Holt, M G Sweeney, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1990
Diaphragmatic weakness in hereditary motor and sensory neuropathyR Hardie, A E Harding, N Hirsch, et al.
Acta Neuropathologica|January 1, 1991
Peripheral neuropathy in the Chediak-Higashi syndromeV P Misra, R H King, A E Harding, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1997
Spinal and cutaneous schwannomatosis is a variant form of type 2 neurofibromatosis: a clinical and molecular studyD G Evans, S Mason, S M Huson, et al.
Nature Genetics|May 1, 1993
A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathiesM Brockington, M G Sweeney, S R Hammans, et al.
American Journal of Human Genetics|October 1, 1992
Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathyM G Sweeney, M B Davis, A Lashwood, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1994
Debrisoquine hydroxylase gene polymorphism in familial Parkinson's diseaseV Planté-Bordeneuve, M B Davis, D M Maraganore, et al.
Pageof 25

Showing results (131-140 of 241) with videos related to

Sort By:
Pageof 25
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1991
An adult onset hexosaminidase A deficiency syndrome with sensory neuropathy and internuclear ophthalmoplegiaD Barnes, V P Misra, E P Young, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1984
Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness: a clinicopathological reportM Baraitser, W Gooddy, A M Halliday, et al.
Neurology|September 1, 1994
Nigral degeneration in neuroacanthocytosisJ O Rinne, S E Daniel, F Scaravilli, et al.
American Journal of Human Genetics|March 1, 1992
Prenatal diagnosis of mitochondrial DNA8993 T----G diseaseA E Harding, I J Holt, M G Sweeney, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1990
Diaphragmatic weakness in hereditary motor and sensory neuropathyR Hardie, A E Harding, N Hirsch, et al.
Acta Neuropathologica|January 1, 1991
Peripheral neuropathy in the Chediak-Higashi syndromeV P Misra, R H King, A E Harding, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1997
Spinal and cutaneous schwannomatosis is a variant form of type 2 neurofibromatosis: a clinical and molecular studyD G Evans, S Mason, S M Huson, et al.
Nature Genetics|May 1, 1993
A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathiesM Brockington, M G Sweeney, S R Hammans, et al.
American Journal of Human Genetics|October 1, 1992
Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathyM G Sweeney, M B Davis, A Lashwood, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1994
Debrisoquine hydroxylase gene polymorphism in familial Parkinson's diseaseV Planté-Bordeneuve, M B Davis, D M Maraganore, et al.
Pageof 25