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

B N Harding

Showing results (1-10 of 39) with videos related to

Pageof 4
Sort By:
Journal of Child Neurology|October 1, 1990
Progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher syndrome): a personal reviewB N Harding
Journal of the Neurological Sciences|August 1, 1991
Intractable seizures from infancy can be associated with dentato-olivary dysplasiaB N Harding, S G Boyd
Brain : a Journal of Neurology|December 1, 1994
Pathogenic factors underlying the lesions in Leigh's disease. Tissue responses to cellular energy deprivation and their clinico-pathological consequencesJ B Cavanagh, B N Harding
Epilepsy Research|October 9, 1999
Neuronal migration disorders in humans and in mouse models--an overviewA J Copp, B N Harding
Neuropathology and Applied Neurobiology|February 1, 1995
The familial syndrome of proliferative vasculopathy and hydranencephaly-hydrocephaly: immunocytochemical and ultrastructural evidence for endothelial proliferationB N Harding, P Ramani, P Thurley
European Journal of Pediatrics|February 1, 1984
Ornithine carbamoyl transferase deficiency: a neuropathological studyB N Harding, J V Leonard, M Erdohazi
Neuropathology and Applied Neurobiology|April 1, 1991
Propionic acidaemia: a neuropathological study of two patients presenting in infancyB N Harding, J V Leonard, M Erdohazi
American Journal of Medical Genetics|July 1, 1985
Osteodysplastic primordial dwarfism: report of a further patient with manifestations similar to those seen in patients with types I and IIIR M Winter, J Wigglesworth, B N Harding
Brain & Development|January 1, 1985
Neuropathological studies in a child showing some features of the Rett syndromeB N Harding, A J Tudway, J Wilson
Journal of Medical Genetics|December 1, 1989
Unknown syndrome: pachygyria, joint contractures, and facial abnormalitiesR M Winter, B N Harding, J Hyde
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Journal of Child Neurology|October 1, 1990
Progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher syndrome): a personal reviewB N Harding
Journal of the Neurological Sciences|August 1, 1991
Intractable seizures from infancy can be associated with dentato-olivary dysplasiaB N Harding, S G Boyd
Brain : a Journal of Neurology|December 1, 1994
Pathogenic factors underlying the lesions in Leigh's disease. Tissue responses to cellular energy deprivation and their clinico-pathological consequencesJ B Cavanagh, B N Harding
Epilepsy Research|October 9, 1999
Neuronal migration disorders in humans and in mouse models--an overviewA J Copp, B N Harding
Neuropathology and Applied Neurobiology|February 1, 1995
The familial syndrome of proliferative vasculopathy and hydranencephaly-hydrocephaly: immunocytochemical and ultrastructural evidence for endothelial proliferationB N Harding, P Ramani, P Thurley
European Journal of Pediatrics|February 1, 1984
Ornithine carbamoyl transferase deficiency: a neuropathological studyB N Harding, J V Leonard, M Erdohazi
Neuropathology and Applied Neurobiology|April 1, 1991
Propionic acidaemia: a neuropathological study of two patients presenting in infancyB N Harding, J V Leonard, M Erdohazi
American Journal of Medical Genetics|July 1, 1985
Osteodysplastic primordial dwarfism: report of a further patient with manifestations similar to those seen in patients with types I and IIIR M Winter, J Wigglesworth, B N Harding
Brain & Development|January 1, 1985
Neuropathological studies in a child showing some features of the Rett syndromeB N Harding, A J Tudway, J Wilson
Journal of Medical Genetics|December 1, 1989
Unknown syndrome: pachygyria, joint contractures, and facial abnormalitiesR M Winter, B N Harding, J Hyde
Pageof 4