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

C J Ellaway

Showing results (1-10 of 13) with videos related to

Pageof 2
Sort By:
Journal of Paediatrics and Child Health|October 2, 2002
Clinical approach to inborn errors of metabolism presenting in the newborn periodC J Ellaway, B Wilcken, J Christodoulou
Journal of Paediatrics and Child Health|April 1, 1997
Progressive myoclonic epilepsies: recent genetic advancesC J Ellaway, E J Elliott, J Christodoulou
Journal of Inherited Metabolic Disease|January 5, 2002
Successful pregnancy outcome in atypical hyperglycinaemiaC J Ellaway, H Mundy, P J Lee
Journal of Inherited Metabolic Disease|December 22, 1999
Novel mitochondrial 16S rRNA polymorphism in a girl with Rett syndromeC J Ellaway, L R McQuade, J Christodoulou
Archives of Disease in Childhood|April 20, 1999
Prolonged QT interval in Rett syndromeC J Ellaway, G Sholler, H Leonard, et al.
Lancet (London, England)|May 5, 1999
Clumsiness, confusion, coma, and valproateC J Ellaway, B Bennetts, R R Tuck, et al.
Journal of Medical Genetics|January 7, 2005
Rett syndrome: clinical review and genetic updateL S Weaving, C J Ellaway, J Gécz, et al.
Brain & Development|December 12, 2001
Medium-term open label trial of L-carnitine in Rett syndromeC J Ellaway, J Peat, K Williams, et al.
Clinical Dysmorphology|July 12, 2001
A case of multiple congenital anomalies in association with Rett syndrome confirmed by MECP2 mutation screeningC J Ellaway, N Badawi, L Raffaele, et al.
Journal of Inherited Metabolic Disease|August 7, 2008
Glutaric aciduria type I: outcome following detection by newborn screeningS Bijarnia, V Wiley, K Carpenter, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Journal of Paediatrics and Child Health|October 2, 2002
Clinical approach to inborn errors of metabolism presenting in the newborn periodC J Ellaway, B Wilcken, J Christodoulou
Journal of Paediatrics and Child Health|April 1, 1997
Progressive myoclonic epilepsies: recent genetic advancesC J Ellaway, E J Elliott, J Christodoulou
Journal of Inherited Metabolic Disease|January 5, 2002
Successful pregnancy outcome in atypical hyperglycinaemiaC J Ellaway, H Mundy, P J Lee
Journal of Inherited Metabolic Disease|December 22, 1999
Novel mitochondrial 16S rRNA polymorphism in a girl with Rett syndromeC J Ellaway, L R McQuade, J Christodoulou
Archives of Disease in Childhood|April 20, 1999
Prolonged QT interval in Rett syndromeC J Ellaway, G Sholler, H Leonard, et al.
Lancet (London, England)|May 5, 1999
Clumsiness, confusion, coma, and valproateC J Ellaway, B Bennetts, R R Tuck, et al.
Journal of Medical Genetics|January 7, 2005
Rett syndrome: clinical review and genetic updateL S Weaving, C J Ellaway, J Gécz, et al.
Brain & Development|December 12, 2001
Medium-term open label trial of L-carnitine in Rett syndromeC J Ellaway, J Peat, K Williams, et al.
Clinical Dysmorphology|July 12, 2001
A case of multiple congenital anomalies in association with Rett syndrome confirmed by MECP2 mutation screeningC J Ellaway, N Badawi, L Raffaele, et al.
Journal of Inherited Metabolic Disease|August 7, 2008
Glutaric aciduria type I: outcome following detection by newborn screeningS Bijarnia, V Wiley, K Carpenter, et al.
Pageof 2