P. F. Benson

Oregon State University — United States

Medicine · Health Sciences

24h-index2.1kcitations112works1.72yr avg
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Research Topics

Lysosomal Storage Disorders Research(21), Metabolism and Genetic Disorders(18), Neonatal Health and Biochemistry(10), Prenatal Screening and Diagnostics(7), Pancreatic function and diabetes(6)

Publications112 total

Transforming acid whey retentate into effective fat replacer in fat-free cream cheese
Food Hydrocolloids·2025· 2 cited
Exploring the role of immunotherapy in the management of follicular cell-derived thyroid cancer
Immunotherapy·2025· 3 citedOpen Access
Letters From Our Readers
The Angle Orthodontist·2024Open Access
EUK-8, a synthetic superoxide dismutase and catalase mimetic, ameliorates acute lung injury in endotoxemic swine.
Journal of Pharmacology and Experimental Therapeutics·1995· 135 cited
Recent advances in the prenatal diagnosis of the mucopolysaccharidoses
Prenatal Diagnosis·1994· 30 cited
A mild form of mucolipidosis type III in four Baluch siblings
Clinical Genetics·1993· 9 cited
Hereditary Xanthinuria in 2 Pakistani Sisters: Asymptomatic in One with β-Thalassemia but Causing Xanthine Stone, Obstructive Uropathy and Hypertension in the Other
The Journal of Urology·1988· 10 cited
Progressive mental regression in siblings with Morquio disease Type B (mucopolysaccharidosis IV B)
Clinical Genetics·1987· 36 cited
Screening and management of potentially treatable genetic metabolic disorders : proceedings of the workshop held in London, March 17-18, 1983
Medical Entomology and Zoology·1984
Experience with Prenatal Diagnosis of Propionic Acidaemia and Methylmalonic Aciduria
1984· 8 cited
Treatment of Lysosomal Storage Diseases by Bone Marrow Transplantation
1984· 1 cited
Prenatal exclusion of late infantile metachromatic leucodystrophy in a late‐presenting pregnancy by assay of fetal leucocytes
Prenatal Diagnosis·1983· 2 cited
Prenatal exclusion of homocystinuria (cystathionine β‐synthase deficiency) by assay of phytohaemagglutinin‐stimulated fetal lymphocytes
Prenatal Diagnosis·1983· 7 cited
Prenatal exclusion of Hurler's disease by leucocyte α‐<scp>L</scp>‐iduronidase assay
Prenatal Diagnosis·1983· 10 cited
LABORATORIES IN REGIONAL GENETIC SERVICES
The Lancet·1982
Reversal of clinical features of hurler's disease and biochemical improvement after treatment by bone marrow transplantation
Journal of Inherited Metabolic Disease·1982· 139 cited
Letter to the Editor: Effectiveness of HLA-Compatible Fibroblasts for Enzyme Replacement Therapy in the Mucopolysaccharidoses
Pediatric Research·1982· 6 citedOpen Access
Enzyme substitution by fibroblast transplantation
1982
Inborn Errors of Metabolism
Journal of Medical Genetics·1981Open Access
Inborn Errors of Metabolism
Biochemical Society Transactions·1981· 1 cited
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Frequent Co-authors

A. H. Fensom(7), Mark Dean(6), Anthony H. Fensom(6), F. Giannelli(4), L R Button(4), Helen Muir(4), P. E. Polani(3), S. Blunt(3), N. R. Butler(3), S. A. Pawsey(2), Linda R. Tansley(2), H Muir(2), A W Boylston(2), J.F. Mowbray(2), G. Rankin(2), Jennifer Southgate(2), A. Babarik(2), A. R. Grant(2), L. Jacobs(2), Charles H. Rodeck(2)