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Journal Abstract Search

169 related items for PubMed ID: 21384

  • 1. [Hereditary deficiency in the enzymes of the biosynthesis of collagen. The Ehlers-Danlos syndromes (author's transl)].
    Gajdos A.
    Nouv Presse Med; 1977 Oct 15; 6(34):3101-5. PubMed ID: 21384
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  • 10. The mRNA and the activity of lysyl hydroxylase are up-regulated by the administration of ascorbate and hydralazine to human skin fibroblasts from a patient with Ehlers-Danlos syndrome type VI.
    Yeowell HN, Walker LC, Marshall MK, Murad S, Pinnell SR.
    Arch Biochem Biophys; 1995 Aug 20; 321(2):510-6. PubMed ID: 7646078
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  • 11. Genotyping and prenatal assessment of collagen lysyl hydroxylase deficiency in a family with Ehlers-Danlos syndrome type VI.
    Dembure PP, Priest JH, Snoddy SC, Elsas LJ.
    Am J Hum Genet; 1984 Jul 20; 36(4):783-90. PubMed ID: 6089551
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  • 12. A case of Ehlers Danlos syndrome type VI.
    Salavoura K, Valari M, Kolialexi A, Mavrou A, Kitsiou S.
    Genet Couns; 2006 Jul 20; 17(3):291-4. PubMed ID: 17100196
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  • 14. Abnormal properties of collagen lysyl hydroxylase from skin fibroblasts of siblings with hydroxylysine-deficient collagen.
    Quinn RS, Krane SM.
    J Clin Invest; 1976 Jan 20; 57(1):83-93. PubMed ID: 173744
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  • 19. Hydroxylysine-deficient skin collagen in a patient with a form of the Ehlers-Danlos syndrome.
    Sussman M, Lichtenstein JR, Nigra TP, Martin GR, McKusick VA.
    J Bone Joint Surg Am; 1974 Sep 20; 56(6):1228-34. PubMed ID: 4373475
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