These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

230 related articles for article (PubMed ID: 15708907)

  • 1. Tenascin-X: a candidate gene for benign joint hypermobility syndrome and hypermobility type Ehlers-Danlos syndrome?
    Zweers MC; Kucharekova M; Schalkwijk J
    Ann Rheum Dis; 2005 Mar; 64(3):504-5. PubMed ID: 15708907
    [No Abstract]   [Full Text] [Related]  

  • 2. 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; 345(16):1167-75. PubMed ID: 11642233
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 67(4):330-4. PubMed ID: 15733269
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Recognizing the tenascin-X deficient type of Ehlers-Danlos syndrome: a cross-sectional study in 17 patients.
    Demirdas S; Dulfer E; Robert L; Kempers M; van Beek D; Micha D; van Engelen BG; Hamel B; Schalkwijk J; Loeys B; Maugeri A; Voermans NC
    Clin Genet; 2017 Mar; 91(3):411-425. PubMed ID: 27582382
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Measurement of Serum Tenascin-X in Joint Hypermobility Syndrome Patients.
    Yamada K; Watanabe A; Takeshita H; Fujita A; Miyake N; Matsumoto N; Matsumoto KI
    Biol Pharm Bull; 2019; 42(9):1596-1599. PubMed ID: 31474720
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Joint hypermobility syndromes: the pathophysiologic role of tenascin-X gene defects.
    Zweers MC; Hakim AJ; Grahame R; Schalkwijk J
    Arthritis Rheum; 2004 Sep; 50(9):2742-9. PubMed ID: 15457441
    [No Abstract]   [Full Text] [Related]  

  • 7. The genetic basis of the joint hypermobility syndromes.
    Malfait F; Hakim AJ; De Paepe A; Grahame R
    Rheumatology (Oxford); 2006 May; 45(5):502-7. PubMed ID: 16418200
    [No Abstract]   [Full Text] [Related]  

  • 8. Measurement of serum tenascin-X in patients with congenital adrenal hyperplasia at risk for Ehlers-Danlos contiguous gene deletion syndrome CAH-X.
    Kolli V; Kim H; Rao H; Lao Q; Gaynor A; Milner JD; Merke DP
    BMC Res Notes; 2019 Oct; 12(1):711. PubMed ID: 31666125
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Tenascin-X deficiency mimics Ehlers-Danlos syndrome in mice through alteration of collagen deposition.
    Mao JR; Taylor G; Dean WB; Wagner DR; Afzal V; Lotz JC; Rubin EM; Bristow J
    Nat Genet; 2002 Apr; 30(4):421-5. PubMed ID: 11925569
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Ehlers-Danlos syndrome--diagnosis and subclassification].
    Rand-Hendriksen S; Wekre LL; Paus B
    Tidsskr Nor Laegeforen; 2006 Aug; 126(15):1903-7. PubMed ID: 16915311
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 163(6):1340-5. PubMed ID: 20649799
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Low tendon stiffness and abnormal ultrastructure distinguish classic Ehlers-Danlos syndrome from benign joint hypermobility syndrome in patients.
    Nielsen RH; Couppé C; Jensen JK; Olsen MR; Heinemeier KM; Malfait F; Symoens S; De Paepe A; Schjerling P; Magnusson SP; Remvig L; Kjaer M
    FASEB J; 2014 Nov; 28(11):4668-76. PubMed ID: 25122555
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 139C(1):24-30. PubMed ID: 16278880
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical study of hereditary disorders of connective tissues in a Chilean population: joint hypermobility syndrome and vascular Ehlers-Danlos syndrome.
    Bravo JF; Wolff C
    Arthritis Rheum; 2006 Feb; 54(2):515-23. PubMed ID: 16447226
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Tenascin-X, collagen, and Ehlers-Danlos syndrome: tenascin-X gene defects can protect against adverse cardiovascular events.
    Petersen JW; Douglas JY
    Med Hypotheses; 2013 Sep; 81(3):443-7. PubMed ID: 23830591
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Tenascin-X deficiency is associated with Ehlers-Danlos syndrome.
    Burch GH; Gong Y; Liu W; Dettman RW; Curry CJ; Smith L; Miller WL; Bristow J
    Nat Genet; 1997 Sep; 17(1):104-8. PubMed ID: 9288108
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Marfanoid hypermobility syndrome associated with Duane's retraction syndrome.
    Rozen S; Rozenman Y; Arnon N; Zylberman R; Berson D
    Ann Ophthalmol; 1983 Sep; 15(9):862-4. PubMed ID: 6660731
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Need for a consensus on the methods by which to measure joint mobility and the definition of norms for hypermobility that reflect age, gender and ethnic-dependent variation: is revision of criteria for joint hypermobility syndrome and Ehlers-Danlos syndrome hypermobility type indicated?
    Remvig L; Engelbert RH; Berglund B; Bulbena A; Byers PH; Grahame R; Juul-Kristensen B; Lindgren KA; Uitto J; Wekre LL
    Rheumatology (Oxford); 2011 Jun; 50(6):1169-71. PubMed ID: 21482540
    [No Abstract]   [Full Text] [Related]  

  • 19. [Changes in the hand in Ehlers-Danlos syndrome type IV].
    Meinel A; Scharizer E
    Handchir Mikrochir Plast Chir; 1989 Mar; 21(2):103-6. PubMed ID: 2707649
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Tenascin-X haploinsufficiency associated with Ehlers-Danlos syndrome in patients with congenital adrenal hyperplasia.
    Merke DP; Chen W; Morissette R; Xu Z; Van Ryzin C; Sachdev V; Hannoush H; Shanbhag SM; Acevedo AT; Nishitani M; Arai AE; McDonnell NB
    J Clin Endocrinol Metab; 2013 Feb; 98(2):E379-87. PubMed ID: 23284009
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.