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Similar articles for PubMed (Select 2433405)

1.

Clinical and biochemical heterogeneity in conditions with phytanic acid accumulation.

Skjeldal OH, Stokke O, Refsum S, Norseth J, Petit H.

J Neurol Sci. 1987 Jan;77(1):87-96.

PMID:
2433405
2.

Disorders related to the metabolism of phytanic acid.

Stokke O, Skjeldal OH, Høie K.

Scand J Clin Lab Invest Suppl. 1986;184:3-10. Review.

PMID:
2438746
3.

Phytanic acid oxidase activity in cultured skin fibroblasts. Diagnostic usefulness and limitations.

Skjeldal OH, Stokke O, Norseth J, Lie SO.

Scand J Clin Lab Invest. 1986 May;46(3):283-7.

PMID:
2424078
5.

Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders.

Poll-The BT, Skjeldal OH, Stokke O, Poulos A, Demaugre F, Saudubray JM.

Hum Genet. 1989 Jan;81(2):175-81.

PMID:
2463966
6.

The subcellular localization of phytanic acid oxidase in rat liver.

Skjeldal OH, Stokke O.

Biochim Biophys Acta. 1987 Sep 4;921(1):38-42.

PMID:
3620488
7.

Diagnosis of Refsum's disease using [1-14C]phytanic acid as substrate.

Poulos A.

Clin Genet. 1981 Oct;20(4):247-53.

PMID:
6174257
8.
9.

Infantile Refsum's disease (phytanic acid storage disease): a variant of Zellweger's syndrome?

Poulos A, Sharp P, Whiting M.

Clin Genet. 1984 Dec;26(6):579-86.

PMID:
6209040
10.

[Peroxisomal neurologic diseases and Refsum disease: very long chain fatty acids and phytanic acid as diagnostic markers].

Molzer B, Stöckler S, Bernheimer H.

Wien Klin Wochenschr. 1992;104(21):665-70. Review. German.

PMID:
1282286
11.

Patterns of Refsum's disease. Phytanic acid oxidase deficiency.

Poulos A, Pollard AC, Mitchell JD, Wise G, Mortimer G.

Arch Dis Child. 1984 Mar;59(3):222-9.

12.

Neurological disorders and phytanic acid metabolism.

Skjeldal OH, Nyberg-Hansen R, Stokke O.

Acta Neurol Scand. 1988 Oct;78(4):324-8.

PMID:
3223227
13.

Di-, mono- and nonphytanyl triglycerides in the serum: a sensitive parameter of the phytanic acid accumulation in Refsum's disease.

Molzer B, Bernheimer H, Barolin GS, Höfinger E, Lenz H.

Clin Chim Acta. 1979 Jan 15;91(2):133-40.

PMID:
83207
14.

Plasma and skin fibroblast C26 fatty acids in infantile Refsum's disease.

Poulos A, Sharp P.

Neurology. 1984 Dec;34(12):1606-9.

PMID:
6209596
15.
16.

Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's disease.

Wanders RJ, Heymans HS, Schutgens RB, Poll-Thé BT, Saudubray JM, Tager JM, Schrakamp G, van den Bosch H.

J Neurol Sci. 1988 Apr;84(2-3):147-55.

PMID:
2454298
17.

Refsum's disease: a peroxisomal disorder affecting phytanic acid alpha-oxidation.

Wierzbicki AS, Lloyd MD, Schofield CJ, Feher MD, Gibberd FB.

J Neurochem. 2002 Mar;80(5):727-35. Review.

PMID:
11948235
18.

[Zellweger syndrome, neonatal adrenoleukodystrophy or infantile Refsum's disease in a case with generalized peroxisome defect?].

Schmitt K, Molzer B, Stöckler S, Tulzer G, Tulzer W.

Wien Klin Wochenschr. 1993;105(11):320-2. German.

PMID:
7687405
19.

Phytanic acid and very long chain fatty acids in genetic peroxisomal disorders.

Molzer B, Kainz-Korschinsky M, Sundt-Heller R, Bernheimer H.

J Clin Chem Clin Biochem. 1989 May;27(5):309-14.

PMID:
2474624
20.

The significance of plasma phytanic acid levels in adults.

Britton TC, Gibberd FB, Clemens ME, Billimoria JD, Sidey MC.

J Neurol Neurosurg Psychiatry. 1989 Jul;52(7):891-4.

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