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

H Sakuraba

Showing results (121-130 of 128) with videos related to

Pageof 13
Sort By:
You have reached the last page of results.This site can display upto 128 results.
Journal of the Neurological Sciences|April 30, 1998
Adult Sandhoff's disease: R505Q and I207V substitutions in the HEXB gene of the first Japanese caseA Hara, E Uyama, M Uchino, et al.
Journal of Human Genetics|August 17, 2000
Molecular and structural studies of Japanese patients with sialidosis type 1Y Naganawa, K Itoh, M Shimmoto, et al.
Human Genetics|July 1, 1996
Two novel gene mutations (Glu174-->Lys, Phe383-->Tyr) causing the "hepatic" form of carnitine palmitoyltransferase II deficiencyS Yamamoto, H Abe, T Kohgo, et al.
Journal of Natural Toxins|December 31, 2002
Fishing for bioactive substances from scorpionfish and some sea urchinsF Satoh, H Nakagawa, H Yamada, et al.
Acta Neurologica Scandinavica|May 25, 2002
Western blotting analysis of the beta-hexosaminidase alpha- and beta-subunits in cultured fibroblasts from cases of various forms of GM2 gangliosidosisK Utsumi, A Tsuji, R Kase, et al.
Neurology|February 5, 1999
GM2 gangliosidosis AB variant: clinical and biochemical studies of a Japanese patientH Sakuraba, K Itoh, M Shimmoto, et al.
Journal of Inherited Metabolic Disease|May 20, 2005
Enzyme replacement therapy in Japanese Fabry disease patients: the results of a phase 2 bridging studyY Eto, T Ohashi, Y Utsunomiya, et al.
Journal of Medical Genetics|June 1, 1996
Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotypeJ L Keulemans, A J Reuser, M A Kroos, et al.
Pageof 13

Showing results (121-130 of 128) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 128 results.
Journal of the Neurological Sciences|April 30, 1998
Adult Sandhoff's disease: R505Q and I207V substitutions in the HEXB gene of the first Japanese caseA Hara, E Uyama, M Uchino, et al.
Journal of Human Genetics|August 17, 2000
Molecular and structural studies of Japanese patients with sialidosis type 1Y Naganawa, K Itoh, M Shimmoto, et al.
Human Genetics|July 1, 1996
Two novel gene mutations (Glu174-->Lys, Phe383-->Tyr) causing the "hepatic" form of carnitine palmitoyltransferase II deficiencyS Yamamoto, H Abe, T Kohgo, et al.
Journal of Natural Toxins|December 31, 2002
Fishing for bioactive substances from scorpionfish and some sea urchinsF Satoh, H Nakagawa, H Yamada, et al.
Acta Neurologica Scandinavica|May 25, 2002
Western blotting analysis of the beta-hexosaminidase alpha- and beta-subunits in cultured fibroblasts from cases of various forms of GM2 gangliosidosisK Utsumi, A Tsuji, R Kase, et al.
Neurology|February 5, 1999
GM2 gangliosidosis AB variant: clinical and biochemical studies of a Japanese patientH Sakuraba, K Itoh, M Shimmoto, et al.
Journal of Inherited Metabolic Disease|May 20, 2005
Enzyme replacement therapy in Japanese Fabry disease patients: the results of a phase 2 bridging studyY Eto, T Ohashi, Y Utsunomiya, et al.
Journal of Medical Genetics|June 1, 1996
Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotypeJ L Keulemans, A J Reuser, M A Kroos, et al.
Pageof 13