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

P F Benson

Showing results (61-70 of 71) with videos related to

Pageof 8
Sort By:
Prenatal Diagnosis|April 1, 1983
Prenatal exclusion of homocystinuria (cystathionine beta-synthase deficiency) by assay of phytohaemagglutinin-stimulated fetal lymphocytesA H Fensom, P F Benson, M J Crees, et al.
Lancet (London, England)|November 10, 1979
Prenatal diagnosis of Farber's diseaseA H Fensom, P F Benson, B R Neville, et al.
The Journal of Pharmacology and Experimental Therapeutics|November 1, 1995
EUK-8, a synthetic superoxide dismutase and catalase mimetic, ameliorates acute lung injury in endotoxemic swineP K Gonzalez, J Zhuang, S R Doctrow, et al.
Shock (Augusta, Ga.)|January 1, 1996
Role of oxidant stress in the adult respiratory distress syndrome: evaluation of a novel antioxidant strategy in a porcine model of endotoxin-induced acute lung injuryP K Gonzalez, J Zhuang, S R Doctrow, et al.
Prenatal Diagnosis|April 1, 1981
Correct prenatal diagnosis of a Hurler fetus where amniotic fluid cell cultures were of maternal originJ Mossman, A D Patrick, A H Fensom, et al.
Prenatal Diagnosis|October 1, 1983
Prenatal tests for Sanfilippo disease type B in four pregnanciesJ Mossman, E P Young, A D Patrick, et al.
Clinical Genetics|November 1, 1987
Progressive mental regression in siblings with Morquio disease type B (mucopolysaccharidosis IV B)R Giugliani, M Jackson, S J Skinner, et al.
The Journal of Clinical Investigation|January 1, 1979
Enzyme replacement therapy by fibroblast transplantation: long-term biochemical study in three cases of Hunter's syndromeM F Dean, R L Stevens, H Muir, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Experience with prenatal diagnosis of propionic acidaemia and methylmalonic aciduriaA H Fensom, P F Benson, R A Chalmers, et al.
Journal of Medical Genetics|June 1, 1979
Sixteen years' experience of counselling, diagnosis, and prenatal detection in one genetic centre: progress, results, and problemsP E Polani, E Alberman, B J Alexander, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
Prenatal Diagnosis|April 1, 1983
Prenatal exclusion of homocystinuria (cystathionine beta-synthase deficiency) by assay of phytohaemagglutinin-stimulated fetal lymphocytesA H Fensom, P F Benson, M J Crees, et al.
Lancet (London, England)|November 10, 1979
Prenatal diagnosis of Farber's diseaseA H Fensom, P F Benson, B R Neville, et al.
The Journal of Pharmacology and Experimental Therapeutics|November 1, 1995
EUK-8, a synthetic superoxide dismutase and catalase mimetic, ameliorates acute lung injury in endotoxemic swineP K Gonzalez, J Zhuang, S R Doctrow, et al.
Shock (Augusta, Ga.)|January 1, 1996
Role of oxidant stress in the adult respiratory distress syndrome: evaluation of a novel antioxidant strategy in a porcine model of endotoxin-induced acute lung injuryP K Gonzalez, J Zhuang, S R Doctrow, et al.
Prenatal Diagnosis|April 1, 1981
Correct prenatal diagnosis of a Hurler fetus where amniotic fluid cell cultures were of maternal originJ Mossman, A D Patrick, A H Fensom, et al.
Prenatal Diagnosis|October 1, 1983
Prenatal tests for Sanfilippo disease type B in four pregnanciesJ Mossman, E P Young, A D Patrick, et al.
Clinical Genetics|November 1, 1987
Progressive mental regression in siblings with Morquio disease type B (mucopolysaccharidosis IV B)R Giugliani, M Jackson, S J Skinner, et al.
The Journal of Clinical Investigation|January 1, 1979
Enzyme replacement therapy by fibroblast transplantation: long-term biochemical study in three cases of Hunter's syndromeM F Dean, R L Stevens, H Muir, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Experience with prenatal diagnosis of propionic acidaemia and methylmalonic aciduriaA H Fensom, P F Benson, R A Chalmers, et al.
Journal of Medical Genetics|June 1, 1979
Sixteen years' experience of counselling, diagnosis, and prenatal detection in one genetic centre: progress, results, and problemsP E Polani, E Alberman, B J Alexander, et al.
Pageof 8