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

H Houlden

Showing results (1-10 of 80) with videos related to

Pageof 8
Sort By:
Journal of Neurology, Neurosurgery, and Psychiatry|June 24, 2006
Apolipoprotein E4 and traumatic brain injuryH Houlden, R Greenwood
British Journal of Hospital Medicine|April 4, 1993
Alzheimer's disease aetiology: amyloid and chromosome 14H Houlden, M Mullan
Eye (London, England)|July 19, 2008
Pupil abnormalities in 131 cases of genetically defined inherited peripheral neuropathyH Houlden, M M Reilly, S Smith
The British Journal of Ophthalmology|March 20, 2004
Genotypic and phenotypic heterogeneity in familial microcoriaF D Bremner, H Houlden, S E Smith
Neuroscience Letters|May 14, 1993
Screening for the APP codon 670/671 mutations in Alzheimer's diseaseH Houlden, F Crawford, M Rossor, et al.
Neuroscience Letters|September 12, 2006
PANK2 gene analysis confirms genetic heterogeneity in neurodegeneration with brain iron accumulation (NBIA) but mutations are rare in other types of adult neurodegenerative diseaseM M Matarin, A B Singleton, H Houlden
Neuropathology and Applied Neurobiology|April 15, 2015
Review: Insights into molecular mechanisms of disease in neurodegeneration with brain iron accumulation: unifying theoriesC E Arber, A Li, H Houlden, et al.
Journal of Neurology|August 16, 2012
Clinical variability and L-Dopa responsive Parkinsonism in hereditary spastic paraplegia 11C M Everett, E Kara, K E Maresh, et al.
Neuropathology and Applied Neurobiology|August 18, 2012
Review: genetics and neuropathology of primary pure dystoniaR Paudel, J Hardy, T Revesz, et al.
Neurology|March 14, 2008
SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegiaC Paisan-Ruiz, O Dogu, A Yilmaz, et al.
Pageof 8

Showing results (1-10 of 80) with videos related to

Sort By:
Pageof 8
Journal of Neurology, Neurosurgery, and Psychiatry|June 24, 2006
Apolipoprotein E4 and traumatic brain injuryH Houlden, R Greenwood
British Journal of Hospital Medicine|April 4, 1993
Alzheimer's disease aetiology: amyloid and chromosome 14H Houlden, M Mullan
Eye (London, England)|July 19, 2008
Pupil abnormalities in 131 cases of genetically defined inherited peripheral neuropathyH Houlden, M M Reilly, S Smith
The British Journal of Ophthalmology|March 20, 2004
Genotypic and phenotypic heterogeneity in familial microcoriaF D Bremner, H Houlden, S E Smith
Neuroscience Letters|May 14, 1993
Screening for the APP codon 670/671 mutations in Alzheimer's diseaseH Houlden, F Crawford, M Rossor, et al.
Neuroscience Letters|September 12, 2006
PANK2 gene analysis confirms genetic heterogeneity in neurodegeneration with brain iron accumulation (NBIA) but mutations are rare in other types of adult neurodegenerative diseaseM M Matarin, A B Singleton, H Houlden
Neuropathology and Applied Neurobiology|April 15, 2015
Review: Insights into molecular mechanisms of disease in neurodegeneration with brain iron accumulation: unifying theoriesC E Arber, A Li, H Houlden, et al.
Journal of Neurology|August 16, 2012
Clinical variability and L-Dopa responsive Parkinsonism in hereditary spastic paraplegia 11C M Everett, E Kara, K E Maresh, et al.
Neuropathology and Applied Neurobiology|August 18, 2012
Review: genetics and neuropathology of primary pure dystoniaR Paudel, J Hardy, T Revesz, et al.
Neurology|March 14, 2008
SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegiaC Paisan-Ruiz, O Dogu, A Yilmaz, et al.
Pageof 8