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

S W Moses

Showing results (21-30 of 71) with videos related to

Pageof 8
Sort By:
Israel Journal of Medical Sciences|January 1, 1988
Attempts to predict the hemolytic potential of drugs in glucose-6-phosphate dehydrogenase deficiency of the Mediterranean type by an in vitro testN Bashan, N Peleg, S W Moses
Blood|December 1, 1972
Glycogen metabolism in the normal red blood cellS W Moses, N Bashan, A Gutman
European Journal of Biochemistry|October 1, 1972
Properties of glycogen synthetase in erythrocytesS W Moses, N Bashan, A Gutman
Advances in Experimental Medicine and Biology|January 1, 1972
Pharmacological modification of glutathione and NADP+ reductionR Gorodischer, S W Moses, N Bashan
Human Genetics|December 24, 1997
Phosphorylase-kinase-deficient liver glycogenosis with an unusual biochemical phenotype in blood cells associated with a missense mutation in the beta subunit gene (PHKB)B Burwinkel, S W Moses, M W Kilimann
Confinia Neurologica|January 1, 1973
The influence of topically applied D-tubocurarine on the taste-induced electrical nerve activity in the frogJ E Steiner, N Gadoth, S W Moses
Biology of the Neonate|January 1, 1977
Caffeine pharmacokinetics in young and adult dogsD Warszawski, R Gorodischer, S W Moses, et al.
Acta Paediatrica Scandinavica|March 1, 1978
Haemorrhagic infarction of the myocardium in a newborn with haemoglobin H disease and erythroblastosisN Gadoth, P Kornmehl, M Gueron, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Impaired glucose transport in polymorphonuclear leukocytes in glycogen storage disease IbN Bashan, R Potashnik, Y Hagay, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Phosphorylase kinase in leukocytes and erythrocytes of a patient with glycogen storage disease type IXN Bashan, R Potashnik, T Ehrlich, et al.
Pageof 8

Showing results (21-30 of 71) with videos related to

Sort By:
Pageof 8
Israel Journal of Medical Sciences|January 1, 1988
Attempts to predict the hemolytic potential of drugs in glucose-6-phosphate dehydrogenase deficiency of the Mediterranean type by an in vitro testN Bashan, N Peleg, S W Moses
Blood|December 1, 1972
Glycogen metabolism in the normal red blood cellS W Moses, N Bashan, A Gutman
European Journal of Biochemistry|October 1, 1972
Properties of glycogen synthetase in erythrocytesS W Moses, N Bashan, A Gutman
Advances in Experimental Medicine and Biology|January 1, 1972
Pharmacological modification of glutathione and NADP+ reductionR Gorodischer, S W Moses, N Bashan
Human Genetics|December 24, 1997
Phosphorylase-kinase-deficient liver glycogenosis with an unusual biochemical phenotype in blood cells associated with a missense mutation in the beta subunit gene (PHKB)B Burwinkel, S W Moses, M W Kilimann
Confinia Neurologica|January 1, 1973
The influence of topically applied D-tubocurarine on the taste-induced electrical nerve activity in the frogJ E Steiner, N Gadoth, S W Moses
Biology of the Neonate|January 1, 1977
Caffeine pharmacokinetics in young and adult dogsD Warszawski, R Gorodischer, S W Moses, et al.
Acta Paediatrica Scandinavica|March 1, 1978
Haemorrhagic infarction of the myocardium in a newborn with haemoglobin H disease and erythroblastosisN Gadoth, P Kornmehl, M Gueron, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Impaired glucose transport in polymorphonuclear leukocytes in glycogen storage disease IbN Bashan, R Potashnik, Y Hagay, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Phosphorylase kinase in leukocytes and erythrocytes of a patient with glycogen storage disease type IXN Bashan, R Potashnik, T Ehrlich, et al.
Pageof 8