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 S Holmes

Showing results (21-30 of 25) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 25 results.
Annals of Neurology|December 1, 1995
Early copper therapy in classic Menkes disease patients with a novel splicing mutationS G Kaler, N R Buist, C S Holmes, et al.
Neurology|October 16, 1999
Clinical and therapeutic observations in aromatic L-amino acid decarboxylase deficiencyK J Swoboda, K Hyland, D S Goldstein, et al.
Biochemical and Molecular Medicine|February 1, 1996
Successful early copper therapy in Menkes disease associated with a mutant transcript containing a small In-frame deletionS G Kaler, S Das, B Levinson, et al.
Nature Genetics|October 1, 1994
Occipital horn syndrome and a mild Menkes phenotype associated with splice site mutations at the MNK locusS G Kaler, L K Gallo, V K Proud, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 5, 1998
Monoaminergic effects of high-dose corticotropin in corticotropin-responsive pediatric opsoclonus-myoclonusM R Pranzatelli, Y Y Huang, E Tate, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Annals of Neurology|December 1, 1995
Early copper therapy in classic Menkes disease patients with a novel splicing mutationS G Kaler, N R Buist, C S Holmes, et al.
Neurology|October 16, 1999
Clinical and therapeutic observations in aromatic L-amino acid decarboxylase deficiencyK J Swoboda, K Hyland, D S Goldstein, et al.
Biochemical and Molecular Medicine|February 1, 1996
Successful early copper therapy in Menkes disease associated with a mutant transcript containing a small In-frame deletionS G Kaler, S Das, B Levinson, et al.
Nature Genetics|October 1, 1994
Occipital horn syndrome and a mild Menkes phenotype associated with splice site mutations at the MNK locusS G Kaler, L K Gallo, V K Proud, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 5, 1998
Monoaminergic effects of high-dose corticotropin in corticotropin-responsive pediatric opsoclonus-myoclonusM R Pranzatelli, Y Y Huang, E Tate, et al.
Pageof 3