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Original Article

The Ability of Patients with Heredopathia Atactica Poly-Neukitiformis to ω-Oxidize and Degrade Several Isoprenoid Branch-Chained Fatty Structures

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Pages 141-150 | Received 10 Oct 1965, Published online: 13 May 2010

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Read on this site (4)

K. Try. (1968) The in vitro ω-Oxidation of Phytanic Acid and Other Branched Chain Fatty Acids by Mammalian Liver. Scandinavian Journal of Clinical and Laboratory Investigation 22:3, pages 224-230.
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K. Try & L. Eldjarn. (1967) Normalization of the Tricaprin Test for ω-Oxidation in Refsum's Disease upon Lowering of Serum Phytanic Acid. Scandinavian Journal of Clinical and Laboratory Investigation 20:4, pages 294-296.
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K. Try. (1967) Indications of only a Partial Defect in the a-Oxidation Mechanism in Refsum's Disease. Scandinavian Journal of Clinical and Laboratory Investigation 20:3, pages 255-262.
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L. Eldjarn, O. Stokke & K. Try. (1966) Alpha-Oxidation of Branched Chain Fatty Acids in Man and its Failure in Patients with Refsum's Disease Showing Phytanic Acid Accumulation. Scandinavian Journal of Clinical and Laboratory Investigation 18:6, pages 694-695.
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Articles from other publishers (4)

Rajesh Kumar Sharma, Lic Med Sc & Berndt Ehinger. (1999) Management of Hereditary Retinal Degenerations. Survey of Ophthalmology 43:5, pages 427-444.
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R.G. Ackman & S.N. Hooper. (1968) Examination of isoprenoid fatty acids as distinguishing characteristics of specific marine oils with particular reference to whale oils. Comparative Biochemistry and Physiology 24:2, pages 549-565.
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Daniel Steinberg, James H. HerndonJr.Jr., B. William Uhlendorf, Charles E. Mize, Joel Avigan & G. W. A. Milne. (1967) Refsum's Disease: Nature of the Enzyme Defect. Science 156:3783, pages 1740-1742.
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L. Eldjarn. (1967) Hereditary ataxic polyneuritis: Biochemical anddietary studies. Clinical Biochemistry 1, pages 273-285.
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