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Items: 1 to 50 of 115

1.

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 injury.

Gonzalez PK, Zhuang J, Doctrow SR, Malfroy B, Benson PF, Menconi MJ, Fink MP.

Shock. 1996;6 Suppl 1:S23-6. Review.

PMID:
8828094
2.

EUK-8, a synthetic superoxide dismutase and catalase mimetic, ameliorates acute lung injury in endotoxemic swine.

Gonzalez PK, Zhuang J, Doctrow SR, Malfroy B, Benson PF, Menconi MJ, Fink MP.

J Pharmacol Exp Ther. 1995 Nov;275(2):798-806.

PMID:
7473169
3.

Recent advances in the prenatal diagnosis of the mucopolysaccharidoses.

Fensom AH, Benson PF.

Prenat Diagn. 1994 Jan;14(1):1-12. Review. No abstract available.

PMID:
8183831
4.

The gum-elastic bougie: a life saver.

Benson PF.

Anesth Analg. 1992 Feb;74(2):318. No abstract available.

PMID:
1731566
5.

Progressive mental regression in siblings with Morquio disease type B (mucopolysaccharidosis IV B).

Giugliani R, Jackson M, Skinner SJ, Vimal CM, Fensom AH, Fahmy N, Sjövall A, Benson PF.

Clin Genet. 1987 Nov;32(5):313-25.

PMID:
3121219
6.

Experience with prenatal diagnosis of propionic acidaemia and methylmalonic aciduria.

Fensom AH, Benson PF, Chalmers RA, Tracey BM, Watson D, King GS, Pettit BR, Rodeck CH.

J Inherit Metab Dis. 1984;7 Suppl 2:127-8. No abstract available.

PMID:
6434864
7.

Prenatal tests for Sanfilippo disease type B in four pregnancies.

Mossman J, Young EP, Patrick AD, Fensom AH, Ellis M, Benson PF, Der Kaloustian VM.

Prenat Diagn. 1983 Oct;3(4):347-50.

PMID:
6419220
8.
9.

Prenatal exclusion of homocystinuria (cystathionine beta-synthase deficiency) by assay of phytohaemagglutinin-stimulated fetal lymphocytes.

Fensom AH, Benson PF, Crees MJ, Ellis M, Rodeck CH, Vaughan RW.

Prenat Diagn. 1983 Apr-Jun;3(2):127-30.

PMID:
6622391
10.

Prenatal exclusion of Hurler's disease by leucocyte alpha-L-iduronidase assay.

Rodeck CH, Tansley LR, Benson PF, Fensom AH, Ellis M.

Prenat Diagn. 1983 Jan;3(1):61-3. No abstract available.

PMID:
6405375
11.

Maple syrup urine disease with increased intracranial pressure.

Mikati MA, Dudin GE, Der Kaloustian VM, Benson PF, Fensom AH.

Am J Dis Child. 1982 Jul;136(7):642-3. No abstract available.

PMID:
7091097
12.

Effectiveness of HLA-compatible fibroblasts for enzyme replacement therapy in the mucopolysaccharidoses.

Dean MF, Muir H, Benson PF, Button LR.

Pediatr Res. 1982 Mar;16(3):260-1. No abstract available.

PMID:
6801615
13.

Treatment of the mucopolysaccharidoses by fibroblast or bone marrow transplantation.

Benson PF.

Prog Clin Biol Res. 1982;103 Pt B:597-9. No abstract available.

PMID:
6819573
14.

Reversal of clinical features of Hurler's disease and biochemical improvement after treatment by bone-marrow transplantation.

Hobbs JR, Hugh-Jones K, Barrett AJ, Byrom N, Chambers D, Henry K, James DC, Lucas CF, Rogers TR, Benson PF, Tansley LR, Patrick AD, Mossman J, Young EP.

Lancet. 1981 Oct 3;2(8249):709-12.

PMID:
6116856
15.

Enzyme replacement therapy by transplantation of HLA-compatible fibroblasts in Sanfilippo A syndrome.

Dean MF, Muir H, Benson PF, Button LR.

Pediatr Res. 1981 Jun;15(6):959-63. No abstract available.

PMID:
6787549
16.

Correct prenatal diagnosis of a Hurler fetus where amniotic fluid cell cultures were of maternal origin.

Mossman J, Patrick AD, Fensom AH, Tansley LR, Benson PF, Der Kaloustian VM, Dudin G.

Prenat Diagn. 1981 Apr;1(2):121-4.

PMID:
6810332
17.

Prenatal diagnosis of argininosuccinic aciduria: effect of mycoplasma contamination on the indirect assay for argininosuccinate lyase.

Fensom AH, Benson PF, Baker JE, Mutton DE.

Am J Hum Genet. 1980 Sep;32(5):761-3. No abstract available.

18.

Fibroblast alpha-galactosidase A activity for identification of Fabry's disease heterozygotes.

Fensom AH, Benson PF, Grant AR, Jacobs L.

J Inherit Metab Dis. 1980;2(1):9-12.

PMID:
6273649
19.

Detection of cystic fibrosis with plasma hydrolases.

Harris A, Benson PF, Fensom AH.

Lancet. 1979 Dec 22-29;2(8156-8157):1371. No abstract available.

PMID:
92712
20.

Prenatal diagnosis of Farber's disease.

Fensom AH, Benson PF, Neville BR, Moser HW, Moser AE, Dulaney JT.

Lancet. 1979 Nov 10;2(8150):990-2.

PMID:
91777
21.
22.

Lumbar kyphosis in Hunter's disease (MPS ii).

Benson PF, Button LR, Fensom AH, Dean MF.

Clin Genet. 1979 Nov;16(5):317-22.

PMID:
117962
23.

Gestational age at termination of pregnancy on medical indications.

Polani PE, Benson PF, Blunt S, Seller MJ, Coltart T.

Lancet. 1979 Aug 25;2(8139):410.

PMID:
89461
24.

Prenatal diagnosis for metabolic disorder.

Benson PF, Fensom AH, Polani PE.

Lancet. 1979 Jul 21;2(8134):153. No abstract available.

PMID:
88591
25.

Prenatal diagnosis of two Hurler fetuses using an improved assay for methylumbelliferyl-alpha-L-iduronidase.

Stirling JL, Robinson D, Fensom AH, Benson PF, Baker JE, Button LR.

Lancet. 1979 Jul 7;2(8132):37. No abstract available.

PMID:
87908
26.

Sixteen years' experience of counselling, diagnosis, and prenatal detection in one genetic centre: progress, results, and problems.

Polani PE, Alberman E, Alexander BJ, Benson PF, Berry AC, Blunt S, Daker MG, Fensom AH, Garrett DM, McGuire VM, Roberts JA, Seller MJ, Singer JD.

J Med Genet. 1979 Jun;16(3):166-75.

27.

Clinical, genetic and DNA repair studies on a consecutive series of patients with xeroderma pigmentosum.

Pawsey SA, Magnus IA, Ramsay CA, Benson PF, Giannelli F.

Q J Med. 1979 Apr;48(190):179-210.

PMID:
504548
28.

Prenatal diagnosis of metabolic errors.

Benson PF, Fensom AH, Polani PE.

Lancet. 1979 Jan 20;1(8108):161. No abstract available.

PMID:
84185
29.

Prenatal diagnosis of a galactosaemia heterozygote by fetal blood enzyme assay.

Fensom AH, Benson PF, Rodeck CH, Campbell S, Gould JD.

Br Med J. 1979 Jan 6;1(6155):21-2. No abstract available.

30.

Enzyme replacement therapy by fibroblast transplantation: long-term biochemical study in three cases of Hunter's syndrome.

Dean MF, Stevens RL, Muir H, Benson PF, Button LR, Anderson RL, Boylston A, Mowbray J.

J Clin Invest. 1979 Jan;63(1):138-46.

32.

Fluorimetric assay for prenatal detection of Hurler and Scheie homozygotes or heterozygotes.

Stirling JL, Robinson D, Fensom AH, Benson PF, Baker JE.

Lancet. 1978 Jan 21;1(8056):147. No abstract available.

PMID:
87574
33.

Fibroblast phosphodiesterase deficiency in Niemann-Pick disease.

Fensom AH, Benson PF, Babarik AW, Grant AR, Jacobs L.

Biochem Biophys Res Commun. 1977 Feb 7;74(3):877-83. No abstract available.

PMID:
191016
34.

Ultraviolet light sensitivity and delayed DNA-chain maturation in Bloom's syndrome fibroblasts.

Gianneli F, Benson PF, Pawsey SA, Polani PE.

Nature. 1977 Feb 3;265(5593):466-9. No abstract available.

PMID:
834301
35.

Corneal clouding in GM1-generalized gangliosidosis.

Babarik A, Benson PF, Fensom AH.

Br J Ophthalmol. 1976 Aug;60(8):565-7.

36.

Enzyme replacement therapy by fibroblast transplantation in a case of Hunter syndrome.

Dean MF, Muir H, Benson PF, Button LR, Boylston A, Mowbray J.

Nature. 1976 May 27;261(5558):323-5. No abstract available.

PMID:
818571
37.

Amniotic cell 4-methylumbelliferyl-alpha-glucosidase activity for prenatal diagnosis of Pompe's disease.

Fensom AH, Benson PF, Blunt S, Brown SP, Coltart TM.

J Med Genet. 1976 Apr;13(2):148-9.

38.

Letter: Schilder's disease: cholesterol metabolism in cultured fibroblasts.

Benson PF, Fensom AH, Wilson J.

Arch Dis Child. 1976 Mar;51(3):242-3. No abstract available.

39.

GM1-generalized gangliosidosis variant with cardiomegaly.

Benson PF, Barbarik A, Brown SP, Mann TP.

Postgrad Med J. 1976 Mar;52(605):159-65. No abstract available.

40.

Phenotypic expression of galactokinase deficiency in heterozygous and homozygous subjects: in vivo and in vitro studies.

Benson PF, Brown SP, Cree J, Fensom AH, Grant AR.

Birth Defects Orig Artic Ser. 1976;12(3):305-12.

PMID:
182297
41.

Increased breakdown of glycosaminoglycans and appearance of corrective enzyme after skin transplants in Hunter syndrome.

Dean MF, Muir H, Benson PF, Button LR, Batchelor JR, Bewick M.

Nature. 1975 Oct 16;257(5527):609-12. No abstract available.

PMID:
126383
42.

Letter: Prenatal diagnosis of metabolic disorders.

Benson PF, Blunt S, Fensom AH, Polani PE, Coltart TM.

Lancet. 1975 Sep 20;2(7934):552-3. No abstract available.

PMID:
51372
43.
44.

Proceedings: Alpha-L-iduronidase deficiency associated with chondroitin sulphate mucopolysaccharidosis.

Babarik A, Benson PF, Dean MF, Muir H.

Arch Dis Child. 1975 Apr;50(4):329-30. No abstract available.

45.

Letter: Gene dosage effect in trisomy 21.

Benson PF.

Lancet. 1975 Mar 8;1(7906):584. No abstract available.

PMID:
47069
46.

The effect of dextran infusions on glycosaminoglycan excretion in the Sanfilippo syndrome.

Dean MF, Benson PF, Muir H.

Dev Med Child Neurol. 1975 Feb;17(1):47-51.

PMID:
123516
47.

Prenatal diagnosis of galactosaemia.

Fensom AH, Benson PF, Blunt S.

Br Med J. 1974 Nov 16;4(5941):386-7.

48.

Letter: Chondroitinsulphaturia with alpha-L-iduronidase deficiency.

Babarik A, Benson PF, Dean MF, Muir H.

Lancet. 1974 Aug 24;2(7878):464-5. No abstract available.

PMID:
4136880
49.

Enzyme defects of glycosaminoglycan degradation in the mucopolysaccharidoses.

Benson PF.

Dev Med Child Neurol. 1974 Aug;16(4):534-9. No abstract available.

PMID:
4277471
50.

In vivo effect of adenosine 3', 5'-monophosphate on Ehrlich ascites tumour cells.

Seller MJ, Benson PF.

Eur J Cancer. 1973 Jul;9(7):525-6. No abstract available.

PMID:
4372053

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