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

L S Wolfe

Showing results (101-110 of 106) with videos related to

Pageof 11
Sort By:
You have reached the last page of results.This site can display upto 106 results.
Annals of Neurology|March 1, 1986
Urinary sediment dolichols in the diagnosis of neuronal ceroid-lipofuscinosisL S Wolfe, J Palo, P Santavuori, et al.
The American Journal of Medicine|March 1, 1987
Elevated urinary dolichol excretion in the Hermansky-Pudlak syndrome. Indicator of lysosomal dysfunctionC J Witkop, L S Wolfe, S X Cal, et al.
American Journal of Human Genetics|November 1, 1979
Infantile sialidosis: a phenocopy of type 1 GM1 gangliosidosis distinguished by genetic complementation and urinary oligosaccharidesR A Gravel, J A Lowden, J W Callahan, et al.
Advances in Prostaglandin, Thromboxane, and Leukotriene Research|January 1, 1989
Brain hepoxilins: formation and actionC R Pace-Asciak, S Asotra, L Pellerin, et al.
American Journal of Medical Genetics|February 15, 1992
Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)D N Palmer, I M Fearnley, J E Walker, et al.
Advances in Experimental Medicine and Biology|January 1, 1989
Lysosomal storage of the DCCD reactive proteolipid subunit of mitochondrial ATP synthase in human and ovine ceroid lipofuscinosesD N Palmer, I M Fearnley, S M Medd, et al.
Pageof 11

Showing results (101-110 of 106) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 106 results.
Annals of Neurology|March 1, 1986
Urinary sediment dolichols in the diagnosis of neuronal ceroid-lipofuscinosisL S Wolfe, J Palo, P Santavuori, et al.
The American Journal of Medicine|March 1, 1987
Elevated urinary dolichol excretion in the Hermansky-Pudlak syndrome. Indicator of lysosomal dysfunctionC J Witkop, L S Wolfe, S X Cal, et al.
American Journal of Human Genetics|November 1, 1979
Infantile sialidosis: a phenocopy of type 1 GM1 gangliosidosis distinguished by genetic complementation and urinary oligosaccharidesR A Gravel, J A Lowden, J W Callahan, et al.
Advances in Prostaglandin, Thromboxane, and Leukotriene Research|January 1, 1989
Brain hepoxilins: formation and actionC R Pace-Asciak, S Asotra, L Pellerin, et al.
American Journal of Medical Genetics|February 15, 1992
Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)D N Palmer, I M Fearnley, J E Walker, et al.
Advances in Experimental Medicine and Biology|January 1, 1989
Lysosomal storage of the DCCD reactive proteolipid subunit of mitochondrial ATP synthase in human and ovine ceroid lipofuscinosesD N Palmer, I M Fearnley, S M Medd, et al.
Pageof 11