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

William B Rizzo

Showing results (1-10 of 50) with videos related to

Pageof 5
Sort By:
Dermato-Endocrinology|June 23, 2011
The role of fatty aldehyde dehydrogenase in epidermal structure and functionWilliam B Rizzo
Molecular Genetics and Metabolism|September 26, 2006
Sjögren-Larsson syndrome: molecular genetics and biochemical pathogenesis of fatty aldehyde dehydrogenase deficiencyWilliam B Rizzo
Biochimica Et Biophysica Acta|September 17, 2013
Fatty aldehyde and fatty alcohol metabolism: review and importance for epidermal structure and functionWilliam B Rizzo
Expert Opinion on Orphan Drugs|August 23, 2016
Genetics and prospective therapeutic targets for Sjögren-Larsson SyndromeWilliam B Rizzo
Human Mutation|June 3, 2005
Sjögren-Larsson syndrome: diversity of mutations and polymorphisms in the fatty aldehyde dehydrogenase gene (ALDH3A2)William B Rizzo, Gael Carney
Seminars in Pediatric Neurology|August 19, 2008
Mitochondrial fatty-acid oxidation disordersMichelle Kompare, William B Rizzo
Journal of Child Neurology|July 28, 2021
A Neurodegenerative Phenotype Associated With Sjögren-Larsson SyndromeSimone Warrack, Terri Love, William B Rizzo
Human Mutation|July 9, 2004
Sjögren-Larsson syndrome: seven novel mutations in the fatty aldehyde dehydrogenase gene ALDH3A2Gael Carney, Shu Wei, William B Rizzo
Seminars in Neurology|March 17, 2012
Recognition and diagnosis of neuro-ichthyotic syndromesWilliam B Rizzo, Sabrina Malone Jenkens, Philip Boucher
Ophthalmic Genetics|September 13, 2019
Sjögren-Larsson syndrome: a complex metabolic disease with a distinctive ocular phenotypeSamiksha Fouzdar-Jain, Donny W Suh, William B Rizzo
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Dermato-Endocrinology|June 23, 2011
The role of fatty aldehyde dehydrogenase in epidermal structure and functionWilliam B Rizzo
Molecular Genetics and Metabolism|September 26, 2006
Sjögren-Larsson syndrome: molecular genetics and biochemical pathogenesis of fatty aldehyde dehydrogenase deficiencyWilliam B Rizzo
Biochimica Et Biophysica Acta|September 17, 2013
Fatty aldehyde and fatty alcohol metabolism: review and importance for epidermal structure and functionWilliam B Rizzo
Expert Opinion on Orphan Drugs|August 23, 2016
Genetics and prospective therapeutic targets for Sjögren-Larsson SyndromeWilliam B Rizzo
Human Mutation|June 3, 2005
Sjögren-Larsson syndrome: diversity of mutations and polymorphisms in the fatty aldehyde dehydrogenase gene (ALDH3A2)William B Rizzo, Gael Carney
Seminars in Pediatric Neurology|August 19, 2008
Mitochondrial fatty-acid oxidation disordersMichelle Kompare, William B Rizzo
Journal of Child Neurology|July 28, 2021
A Neurodegenerative Phenotype Associated With Sjögren-Larsson SyndromeSimone Warrack, Terri Love, William B Rizzo
Human Mutation|July 9, 2004
Sjögren-Larsson syndrome: seven novel mutations in the fatty aldehyde dehydrogenase gene ALDH3A2Gael Carney, Shu Wei, William B Rizzo
Seminars in Neurology|March 17, 2012
Recognition and diagnosis of neuro-ichthyotic syndromesWilliam B Rizzo, Sabrina Malone Jenkens, Philip Boucher
Ophthalmic Genetics|September 13, 2019
Sjögren-Larsson syndrome: a complex metabolic disease with a distinctive ocular phenotypeSamiksha Fouzdar-Jain, Donny W Suh, William B Rizzo
Pageof 5