Benson PF - Search Results

1

Fibroblast phosphodiesterase deficiency in Niemann-Pick disease.

Fensom AH, Benson PF, Babarik AW, Grant AR, Jacobs L. Fensom AH, et al. Among authors: benson pf. Biochem Biophys Res Commun. 1977 Feb 7;74(3):877-83. doi: 10.1016/0006-291x(77)91600-x. Biochem Biophys Res Commun. 1977. PMID: 191016 No abstract available.

2

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

Fensom AH, Benson PF, Grant AR, Jacobs L. Fensom AH, et al. Among authors: benson pf. J Inherit Metab Dis. 1980;2(1):9-12. doi: 10.1007/BF01805555. J Inherit Metab Dis. 1980. PMID: 6273649

3

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. Benson PF, et al. Birth Defects Orig Artic Ser. 1976;12(3):305-12. Birth Defects Orig Artic Ser. 1976. PMID: 182297

4

Corneal clouding in GM1-generalized gangliosidosis.

Babarik A, Benson PF, Fensom AH. Babarik A, et al. Among authors: benson pf. Br J Ophthalmol. 1976 Aug;60(8):565-7. doi: 10.1136/bjo.60.8.565. Br J Ophthalmol. 1976. PMID: 823960 Free PMC article.

5

Prenatal diagnosis of Farber's disease.

Fensom AH, Benson PF, Neville BR, Moser HW, Moser AE, Dulaney JT. Fensom AH, et al. Among authors: benson pf. Lancet. 1979 Nov 10;2(8150):990-2. doi: 10.1016/s0140-6736(79)92562-5. Lancet. 1979. PMID: 91777

6

A rapid method for assay of branched-chain keto acid decarboxylation in cultured cells and its application to prenatal diagnosis of maple syrup urine disease.

Fensom AH, Benson PF, Baker JE. Fensom AH, et al. Among authors: benson pf. Clin Chim Acta. 1978 Jul 1;87(1):169-74. doi: 10.1016/0009-8981(78)90072-4. Clin Chim Acta. 1978. PMID: 668138

7

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

Babarik A, Benson PF, Dean MF, Muir H. Babarik A, et al. Among authors: benson pf. Arch Dis Child. 1975 Apr;50(4):329-30. doi: 10.1136/adc.50.4.329-b. Arch Dis Child. 1975. PMID: 807169 Free PMC article. No abstract available.

8

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

Benson PF, Fensom AH, Wilson J. Benson PF, et al. Arch Dis Child. 1976 Mar;51(3):242-3. doi: 10.1136/adc.51.3.242. Arch Dis Child. 1976. PMID: 952560 Free PMC article. No abstract available.

9

Assay of galactose-1-phosphate uridyl transferase in cultured amniotic cells for prenatal diagnosis of galactosaemia.

Fensom AH, Benson PF. Fensom AH, et al. Among authors: benson pf. Clin Chim Acta. 1975 Jul 23;62(2):189-94. doi: 10.1016/0009-8981(75)90227-2. Clin Chim Acta. 1975. PMID: 1149286

10

Letter: Chondroitinsulphaturia with alpha-L-iduronidase deficiency.

Babarik A, Benson PF, Dean MF, Muir H. Babarik A, et al. Among authors: benson pf. Lancet. 1974 Aug 24;2(7878):464-5. doi: 10.1016/s0140-6736(74)91846-7. Lancet. 1974. PMID: 4136880 No abstract available.

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