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

Brian Harding

Showing results (21-30 of 51) with videos related to

Pageof 6
Sort By:
Pediatric Neurology|September 8, 2004
Acute fulminant subacute sclerosing panencephalitis with absent measles and PCR studies in cerebrospinal fluidBrian H Y Chung, Patrick P K Ip, Virginia C N Wong, et al.
The Journal of Clinical Endocrinology and Metabolism|June 30, 2005
A novel EXT1 splice site mutation in a kindred with hereditary multiple exostosis and osteoporosisManuel C Lemos, Peter Kotanko, Paul T Christie, et al.
Endocrinology|October 2, 2012
Proliferation rates of multiple endocrine neoplasia type 1 (MEN1)-associated tumorsGerard V Walls, Anita A C Reed, Jeshmi Jeyabalan, et al.
Nature Communications|April 28, 2022
Molecular and functional heterogeneity in dorsal and ventral oligodendrocyte progenitor cells of the mouse forebrain in response to DNA damageEnrica Boda, Martina Lorenzati, Roberta Parolisi, et al.
Journal of Neurosurgery. Pediatrics|July 4, 2020
The utility of brain biopsy in pediatric cryptogenic neurological diseaseHugo Layard Horsfall, Sebastian M Toescu, Patrick J Grover, et al.
Brain : a Journal of Neurology|October 23, 2003
Encephalitis lethargica syndrome: 20 new cases and evidence of basal ganglia autoimmunityRussell C Dale, Andrew J Church, Robert A H Surtees, et al.
The Journal of Clinical Endocrinology and Metabolism|April 9, 2004
Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 geneBranca M Cavaco, Laura Guerra, Karin J Bradley, et al.
The Journal of Clinical Endocrinology and Metabolism|January 10, 2003
Genetic mapping studies of familial juvenile hyperuricemic nephropathy on chromosome 16p11-p13Joanna M Stacey, Jeremy J O Turner, Brian Harding, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|February 20, 2016
Degos disease mimicking primary vasculitis of the CNSSabrina Gmuca, Markus D Boos, Amanda Treece, et al.
The Journal of Clinical Investigation|September 17, 2005
An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidismMichael R Bowl, M Andrew Nesbit, Brian Harding, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
Pediatric Neurology|September 8, 2004
Acute fulminant subacute sclerosing panencephalitis with absent measles and PCR studies in cerebrospinal fluidBrian H Y Chung, Patrick P K Ip, Virginia C N Wong, et al.
The Journal of Clinical Endocrinology and Metabolism|June 30, 2005
A novel EXT1 splice site mutation in a kindred with hereditary multiple exostosis and osteoporosisManuel C Lemos, Peter Kotanko, Paul T Christie, et al.
Endocrinology|October 2, 2012
Proliferation rates of multiple endocrine neoplasia type 1 (MEN1)-associated tumorsGerard V Walls, Anita A C Reed, Jeshmi Jeyabalan, et al.
Nature Communications|April 28, 2022
Molecular and functional heterogeneity in dorsal and ventral oligodendrocyte progenitor cells of the mouse forebrain in response to DNA damageEnrica Boda, Martina Lorenzati, Roberta Parolisi, et al.
Journal of Neurosurgery. Pediatrics|July 4, 2020
The utility of brain biopsy in pediatric cryptogenic neurological diseaseHugo Layard Horsfall, Sebastian M Toescu, Patrick J Grover, et al.
Brain : a Journal of Neurology|October 23, 2003
Encephalitis lethargica syndrome: 20 new cases and evidence of basal ganglia autoimmunityRussell C Dale, Andrew J Church, Robert A H Surtees, et al.
The Journal of Clinical Endocrinology and Metabolism|April 9, 2004
Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 geneBranca M Cavaco, Laura Guerra, Karin J Bradley, et al.
The Journal of Clinical Endocrinology and Metabolism|January 10, 2003
Genetic mapping studies of familial juvenile hyperuricemic nephropathy on chromosome 16p11-p13Joanna M Stacey, Jeremy J O Turner, Brian Harding, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|February 20, 2016
Degos disease mimicking primary vasculitis of the CNSSabrina Gmuca, Markus D Boos, Amanda Treece, et al.
The Journal of Clinical Investigation|September 17, 2005
An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidismMichael R Bowl, M Andrew Nesbit, Brian Harding, et al.
Pageof 6