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P F Benson

Showing results (51-60 of 71) with videos related to

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Birth Defects Original Article Series|January 1, 1976
Phenotypic expression of galactokinase deficiency in heterozygous and homozygous subjects: in vivo and in vitro studiesP F Benson, S P Brown, J Cree, et al.
The Quarterly Journal of Medicine|April 1, 1979
Clinical, genetic and DNA repair studies on a consecutive series of patients with xeroderma pigmentosumS A Pawsey, I A Magnus, C A Ramsay, et al.
British Medical Journal|January 6, 1979
Prenatal diagnosis of a galactosaemia heterozygote by fetal blood enzyme assayA H Fensom, P F Benson, C H Rodeck, et al.
Prenatal Diagnosis|January 1, 1983
Prenatal exclusion of Hurler's disease by leucocyte alpha-L-iduronidase assayC H Rodeck, L R Tansley, P F Benson, et al.
Lancet (London, England)|September 20, 1975
Letter: Prenatal diagnosis of metabolic disordersP F Benson, S Blunt, A H Fensom, et al.
Biochemical and Biophysical Research Communications|February 7, 1977
Fibroblast phosphodiesterase deficiency in Niemann-Pick diseaseA H Fensom, P F Benson, A W Babarik, et al.
Nature|May 27, 1976
Enzyme replacement therapy by fibroblast transplantation in a case of Hunter syndromeM F Dean, H Muir, P F Benson, et al.
American Journal of Diseases of Children (1960)|July 1, 1982
Maple syrup urine disease with increased intracranial pressureM A Mikati, G E Dudin, V M Der Kaloustian, et al.
Nature|October 16, 1975
Increased breakdown of glycosaminoglycans and appearance of corrective enzyme after skin transplants in Hunter syndromeM F Dean, H Muir, P F Benson, et al.
Lancet (London, England)|July 7, 1979
Prenatal diagnosis of two Hurler fetuses using an improved assay for methylumbelliferyl-alpha-L-iduronidaseJ L Stirling, D Robinson, A H Fensom, et al.
Pageof 8

Showing results (51-60 of 71) with videos related to

Sort By:
Pageof 8
Birth Defects Original Article Series|January 1, 1976
Phenotypic expression of galactokinase deficiency in heterozygous and homozygous subjects: in vivo and in vitro studiesP F Benson, S P Brown, J Cree, et al.
The Quarterly Journal of Medicine|April 1, 1979
Clinical, genetic and DNA repair studies on a consecutive series of patients with xeroderma pigmentosumS A Pawsey, I A Magnus, C A Ramsay, et al.
British Medical Journal|January 6, 1979
Prenatal diagnosis of a galactosaemia heterozygote by fetal blood enzyme assayA H Fensom, P F Benson, C H Rodeck, et al.
Prenatal Diagnosis|January 1, 1983
Prenatal exclusion of Hurler's disease by leucocyte alpha-L-iduronidase assayC H Rodeck, L R Tansley, P F Benson, et al.
Lancet (London, England)|September 20, 1975
Letter: Prenatal diagnosis of metabolic disordersP F Benson, S Blunt, A H Fensom, et al.
Biochemical and Biophysical Research Communications|February 7, 1977
Fibroblast phosphodiesterase deficiency in Niemann-Pick diseaseA H Fensom, P F Benson, A W Babarik, et al.
Nature|May 27, 1976
Enzyme replacement therapy by fibroblast transplantation in a case of Hunter syndromeM F Dean, H Muir, P F Benson, et al.
American Journal of Diseases of Children (1960)|July 1, 1982
Maple syrup urine disease with increased intracranial pressureM A Mikati, G E Dudin, V M Der Kaloustian, et al.
Nature|October 16, 1975
Increased breakdown of glycosaminoglycans and appearance of corrective enzyme after skin transplants in Hunter syndromeM F Dean, H Muir, P F Benson, et al.
Lancet (London, England)|July 7, 1979
Prenatal diagnosis of two Hurler fetuses using an improved assay for methylumbelliferyl-alpha-L-iduronidaseJ L Stirling, D Robinson, A H Fensom, et al.
Pageof 8