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 D Cederbaum

Showing results (11-20 of 93) with videos related to

Pageof 10
Sort By:
Journal of Inherited Metabolic Disease|January 1, 1981
Urinary pyrimidine excretion in arginase deficiencyE W Naylor, S D Cederbaum
The Journal of Pediatrics|January 10, 2001
Laboratory evaluation of urea cycle disordersR D Steiner, S D Cederbaum
The New England Journal of Medicine|May 24, 1984
Four-year treatment of systemic carnitine deficiencyS D Cederbaum, N Auestad, J Bernar
The Journal of Pediatrics|April 1, 1977
HyperargininemiaS D Cederbaum, K N Shaw, M Valente
Pediatrics|September 1, 1984
Symposium on genetic engineering and phenylketonuriaS D Cederbaum, R Koch, G N Donnell
Journal of Inherited Metabolic Disease|May 11, 1999
Successful pregnancy outcome in a woman with argininosuccinate lyase deficiencyM R Mardach, K Roe, S D Cederbaum
Biochemical Medicine|February 1, 1982
Hollow-fiber reactors containing mammalian arginase: an approach to enzyme replacement therapyJ J Kanalas, E B Spector, S D Cederbaum
Clinical Genetics|January 1, 1974
Pedigree analysis to determine the mode of inheritance in a family with retinitis pigmentosaM A Spence, R C Elston, S D Cederbaum
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1977
Rapid diagnosis of pyruvate and ketoglutarate dehydrogenase deficiencies in platelet-enriched preparations from bloodJ P Blass, S D Cederbaum, R A Kark
Lancet (London, England)|August 21, 1971
"Spontaneous" abortion and haemorrhage following attempted amniocentesis in a carrier of haemophilia AS D Cederbaum, G B Holzman, R S Sparkes
Pageof 10

Showing results (11-20 of 93) with videos related to

Sort By:
Pageof 10
Journal of Inherited Metabolic Disease|January 1, 1981
Urinary pyrimidine excretion in arginase deficiencyE W Naylor, S D Cederbaum
The Journal of Pediatrics|January 10, 2001
Laboratory evaluation of urea cycle disordersR D Steiner, S D Cederbaum
The New England Journal of Medicine|May 24, 1984
Four-year treatment of systemic carnitine deficiencyS D Cederbaum, N Auestad, J Bernar
The Journal of Pediatrics|April 1, 1977
HyperargininemiaS D Cederbaum, K N Shaw, M Valente
Pediatrics|September 1, 1984
Symposium on genetic engineering and phenylketonuriaS D Cederbaum, R Koch, G N Donnell
Journal of Inherited Metabolic Disease|May 11, 1999
Successful pregnancy outcome in a woman with argininosuccinate lyase deficiencyM R Mardach, K Roe, S D Cederbaum
Biochemical Medicine|February 1, 1982
Hollow-fiber reactors containing mammalian arginase: an approach to enzyme replacement therapyJ J Kanalas, E B Spector, S D Cederbaum
Clinical Genetics|January 1, 1974
Pedigree analysis to determine the mode of inheritance in a family with retinitis pigmentosaM A Spence, R C Elston, S D Cederbaum
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1977
Rapid diagnosis of pyruvate and ketoglutarate dehydrogenase deficiencies in platelet-enriched preparations from bloodJ P Blass, S D Cederbaum, R A Kark
Lancet (London, England)|August 21, 1971
"Spontaneous" abortion and haemorrhage following attempted amniocentesis in a carrier of haemophilia AS D Cederbaum, G B Holzman, R S Sparkes
Pageof 10