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Journal Abstract Search

283 related items for PubMed ID: 24443025

  • 1.
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  • 2. The Ehlers-Danlos syndrome, a disorder with many faces.
    De Paepe A, Malfait F.
    Clin Genet; 2012 Jul; 82(1):1-11. PubMed ID: 22353005
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  • 6. A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency.
    Schalkwijk J, Zweers MC, Steijlen PM, Dean WB, Taylor G, van Vlijmen IM, van Haren B, Miller WL, Bristow J.
    N Engl J Med; 2001 Oct 18; 345(16):1167-75. PubMed ID: 11642233
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  • 7. Bleeding in the heritable connective tissue disorders: mechanisms, diagnosis and treatment.
    Malfait F, De Paepe A.
    Blood Rev; 2009 Sep 18; 23(5):191-7. PubMed ID: 19592142
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  • 8. The Ehlers-Danlos syndromes.
    Yeowell HN, Pinnell SR.
    Semin Dermatol; 1993 Sep 18; 12(3):229-40. PubMed ID: 8217561
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  • 9. Tenascin-X, collagen, elastin, and the Ehlers-Danlos syndrome.
    Bristow J, Carey W, Egging D, Schalkwijk J.
    Am J Med Genet C Semin Med Genet; 2005 Nov 15; 139C(1):24-30. PubMed ID: 16278880
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  • 10. Understanding the basis of Ehlers-Danlos syndrome in the era of the next-generation sequencing.
    Cortini F, Villa C, Marinelli B, Combi R, Pesatori AC, Bassotti A.
    Arch Dermatol Res; 2019 May 15; 311(4):265-275. PubMed ID: 30826961
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  • 11. The Ehlers-Danlos syndromes, rare types.
    Brady AF, Demirdas S, Fournel-Gigleux S, Ghali N, Giunta C, Kapferer-Seebacher I, Kosho T, Mendoza-Londono R, Pope MF, Rohrbach M, Van Damme T, Vandersteen A, van Mourik C, Voermans N, Zschocke J, Malfait F.
    Am J Med Genet C Semin Med Genet; 2017 Mar 15; 175(1):70-115. PubMed ID: 28306225
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  • 12. The 2017 international classification of the Ehlers-Danlos syndromes.
    Malfait F, Francomano C, Byers P, Belmont J, Berglund B, Black J, Bloom L, Bowen JM, Brady AF, Burrows NP, Castori M, Cohen H, Colombi M, Demirdas S, De Backer J, De Paepe A, Fournel-Gigleux S, Frank M, Ghali N, Giunta C, Grahame R, Hakim A, Jeunemaitre X, Johnson D, Juul-Kristensen B, Kapferer-Seebacher I, Kazkaz H, Kosho T, Lavallee ME, Levy H, Mendoza-Londono R, Pepin M, Pope FM, Reinstein E, Robert L, Rohrbach M, Sanders L, Sobey GJ, Van Damme T, Vandersteen A, van Mourik C, Voermans N, Wheeldon N, Zschocke J, Tinkle B.
    Am J Med Genet C Semin Med Genet; 2017 Mar 15; 175(1):8-26. PubMed ID: 28306229
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  • 14. Bleeding and bruising in patients with Ehlers-Danlos syndrome and other collagen vascular disorders.
    De Paepe A, Malfait F.
    Br J Haematol; 2004 Dec 15; 127(5):491-500. PubMed ID: 15566352
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  • 15. Elastic fiber abnormalities in hypermobility type Ehlers-Danlos syndrome patients with tenascin-X mutations.
    Zweers MC, Dean WB, van Kuppevelt TH, Bristow J, Schalkwijk J.
    Clin Genet; 2005 Apr 15; 67(4):330-4. PubMed ID: 15733269
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  • 17. [Vascular Ehlers-Danlos syndromes--biochemical and molecular-genetic investigations].
    Lund AM.
    Ugeskr Laeger; 2006 Feb 27; 168(9):915-20. PubMed ID: 16513057
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  • 19. Tenascin-X deficiency and Ehlers-Danlos syndrome: a case report and review of the literature.
    O'Connell M, Burrows NP, van Vlijmen-Willems MJ, Clark SM, Schalkwijk J.
    Br J Dermatol; 2010 Dec 27; 163(6):1340-5. PubMed ID: 20649799
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