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Journal Abstract Search

167 related items for PubMed ID: 16775108

  • 1. Variability of aortic stiffness is not associated with the fibrillin 1 genotype in patients with Marfan's syndrome.
    De Backer J, Nollen GJ, Devos D, Pals G, Coucke P, Verstraete K, van der Wall EE, De Paepe A, Mulder BJ.
    Heart; 2006 Jul; 92(7):977-8. PubMed ID: 16775108
    [No Abstract] [Full Text] [Related]

  • 2. A molecular approach to the stratification of cardiovascular risk in families with Marfan's syndrome.
    Pereira L, Levran O, Ramirez F, Lynch JR, Sykes B, Pyeritz RE, Dietz HC.
    N Engl J Med; 1994 Jul 21; 331(3):148-53. PubMed ID: 8008028
    [Abstract] [Full Text] [Related]

  • 3. A novel mutation in the fibrillin gene (FBN1) in familial arachnodactyly.
    Hayward C, Porteous ME, Brock DJ.
    Mol Cell Probes; 1994 Aug 21; 8(4):325-7. PubMed ID: 7870075
    [Abstract] [Full Text] [Related]

  • 4. Fibrillin-1 mutations in Marfan syndrome and other type-1 fibrillinopathies.
    Hayward C, Brock DJ.
    Hum Mutat; 1997 Aug 21; 10(6):415-23. PubMed ID: 9401003
    [Abstract] [Full Text] [Related]

  • 5. [Contribution of genetics to pathogenicity and diagnosis of Marfan syndrome].
    Boileau C, Collod G, Bonnet D.
    Arch Mal Coeur Vaiss; 1997 Dec 21; 90(12 Suppl):1707-12. PubMed ID: 9587455
    [Abstract] [Full Text] [Related]

  • 6. A novel mutation of the fibrillin-1 gene in a newborn with severe Marfan syndrome.
    Kochilas L, Gundogan F, Atalay M, Bliss JM, Vatta M, Pena LS, Abuelo D.
    J Perinatol; 2008 Apr 21; 28(4):303-5. PubMed ID: 18379569
    [Abstract] [Full Text] [Related]

  • 7. Fibrillin-1 genetic deficiency leads to pathological ageing of arteries in mice.
    Mariko B, Pezet M, Escoubet B, Bouillot S, Andrieu JP, Starcher B, Quaglino D, Jacob MP, Huber P, Ramirez F, Faury G.
    J Pathol; 2011 May 21; 224(1):33-44. PubMed ID: 21432852
    [Abstract] [Full Text] [Related]

  • 8. Marfan's syndrome.
    Judge DP, Dietz HC.
    Lancet; 2005 Dec 03; 366(9501):1965-76. PubMed ID: 16325700
    [Abstract] [Full Text] [Related]

  • 9. Coexistent Marfan's syndrome and ankylosing spondylitis.
    Kiss C, Jónap I, Gergely P, Poór G.
    J Rheumatol; 2006 Jun 03; 33(6):1199-200. PubMed ID: 16755670
    [Abstract] [Full Text] [Related]

  • 10. Gene symbol: FBN1.
    Tinkle B.
    Hum Genet; 2007 Apr 03; 121(2):294. PubMed ID: 17598213
    [No Abstract] [Full Text] [Related]

  • 11. Fibrillin (FBN1) mutations in Marfan syndrome.
    Hayward C, Keston M, Brock DJ, Dietz HC.
    Hum Mutat; 1992 Apr 03; 1(1):79. PubMed ID: 1301195
    [No Abstract] [Full Text] [Related]

  • 12. The FBN1 (R2726W) mutation is not fully penetrant.
    Buoni S, Zannolli R, Macucci F, Ansaldi S, Grasso M, Arbustini E, Fois A.
    Ann Hum Genet; 2004 Nov 03; 68(Pt 6):633-8. PubMed ID: 15598221
    [Abstract] [Full Text] [Related]

  • 13. [Marfan's syndrome].
    Shinawi S, Mandel H.
    Harefuah; 2000 Apr 02; 138(7):598-603. PubMed ID: 10883194
    [No Abstract] [Full Text] [Related]

  • 14. [Acute lymphoblastic leukemia in a pediatric patient with Marfan's syndrome].
    Miyajima Y, Kitase Y, Mizuno S, Sakai H, Matsumoto N, Ogawa A.
    Rinsho Ketsueki; 2011 Jan 02; 52(1):28-31. PubMed ID: 21378479
    [Abstract] [Full Text] [Related]

  • 15. Muscle fibrillin deficiency in Marfan's syndrome myopathy.
    Behan WM, Longman C, Petty RK, Comeglio P, Child AH, Boxer M, Foskett P, Harriman DG.
    J Neurol Neurosurg Psychiatry; 2003 May 02; 74(5):633-8. PubMed ID: 12700307
    [Abstract] [Full Text] [Related]

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  • 17. Genetic fibrillinopathies: new insights in molecular diagnosis and clinical management.
    Loeys BL, Matthys DM, de Paepe AM.
    Acta Clin Belg; 2003 May 02; 58(1):3-11. PubMed ID: 12723256
    [Abstract] [Full Text] [Related]

  • 18. [Molecular mechanisms for the improvement of wound healing ability of periodontal ligament in Marfan's syndrome].
    Saito M, Tsuji T.
    Clin Calcium; 2012 Jan 02; 22(1):35-42. PubMed ID: 22201097
    [Abstract] [Full Text] [Related]

  • 19. Neonatal Marfan syndrome caused by an exon 25 mutation of the fibrillin-1 gene.
    Elçioglu NH, Akalin F, Elçioglu M, Comeglio P, Child AH.
    Genet Couns; 2004 Jan 02; 15(2):219-25. PubMed ID: 15287423
    [Abstract] [Full Text] [Related]

  • 20. Dermal fibroblast culture as a model system for studies of fibrillin assembly and pathogenetic mechanisms: defects in distinct groups of individuals with Marfan's syndrome.
    Brenn T, Aoyama T, Francke U, Furthmayr H.
    Lab Invest; 1996 Sep 02; 75(3):389-402. PubMed ID: 8804362
    [Abstract] [Full Text] [Related]

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