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 *

77 related articles for article (PubMed ID: 26391944)

  • 1. Chest Pain in Children With Suspected Type I Fibrillinopathy: A Case Report.
    Rodríguez-González M; Matamala-Morillo MÁ; Segado-Arenas A; Marín-Iglesias Mdel R; Lechuga-Sancho AM
    Pediatrics; 2015 Oct; 136(4):e1035-8. PubMed ID: 26391944
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ascending aortic aneurysm with or without features of Marfan syndrome and other fibrillinopathies: new insights.
    Furthmayr H; Francke U
    Semin Thorac Cardiovasc Surg; 1997 Jul; 9(3):191-205. PubMed ID: 9263339
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations.
    Faivre L; Masurel-Paulet A; Collod-Béroud G; Callewaert BL; Child AH; Stheneur C; Binquet C; Gautier E; Chevallier B; Huet F; Loeys BL; Arbustini E; Mayer K; Arslan-Kirchner M; Kiotsekoglou A; Comeglio P; Grasso M; Halliday DJ; Béroud C; Bonithon-Kopp C; Claustres M; Robinson PN; Adès L; De Backer J; Coucke P; Francke U; De Paepe A; Boileau C; Jondeau G
    Pediatrics; 2009 Jan; 123(1):391-8. PubMed ID: 19117906
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cardiovascular characteristics in Marfan syndrome and their relation to the genotype.
    De Backer J
    Verh K Acad Geneeskd Belg; 2009; 71(6):335-71. PubMed ID: 20232788
    [TBL] [Abstract][Full Text] [Related]  

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

  • 6. 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; 15(2):219-25. PubMed ID: 15287423
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Marfan syndrome type II: there is more to Marfan syndrome than fibrillin 1.
    Zangwill SD; Brown MD; Bryke CR; Cava JR; Segura AD
    Congenit Heart Dis; 2006 Sep; 1(5):229-32. PubMed ID: 18377530
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dural ectasia in individuals with Marfan-like features but exclusion of mutations in the genes FBN1, TGFBR1 and TGFBR2.
    Sheikhzadeh S; Rybczynski M; Habermann CR; Bernhardt AM; Arslan-Kirchner M; Keyser B; Kaemmerer H; Mir TS; Staebler A; Oezdal N; Robinson PN; Berger J; Meinertz T; von Kodolitsch Y
    Clin Genet; 2011 Jun; 79(6):568-74. PubMed ID: 20662850
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations of FBN1 and genotype-phenotype correlations in Marfan syndrome and related fibrillinopathies.
    Robinson PN; Booms P; Katzke S; Ladewig M; Neumann L; Palz M; Pregla R; Tiecke F; Rosenberg T
    Hum Mutat; 2002 Sep; 20(3):153-61. PubMed ID: 12203987
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dural ectasia and FBN1 mutation screening of 40 patients with Marfan syndrome and related disorders: role of dural ectasia for the diagnosis.
    Attanasio M; Pratelli E; Porciani MC; Evangelisti L; Torricelli E; Pellicanò G; Abbate R; Gensini GF; Pepe G
    Eur J Med Genet; 2013 Jul; 56(7):356-60. PubMed ID: 23684891
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands.
    Faivre L; Collod-Beroud G; Child A; Callewaert B; Loeys BL; Binquet C; Gautier E; Arbustini E; Mayer K; Arslan-Kirchner M; Stheneur C; Kiotsekoglou A; Comeglio P; Marziliano N; Halliday D; Beroud C; Bonithon-Kopp C; Claustres M; Plauchu H; Robinson PN; Adès L; De Backer J; Coucke P; Francke U; De Paepe A; Boileau C; Jondeau G
    J Med Genet; 2008 Jun; 45(6):384-90. PubMed ID: 18310266
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of sixty-two novel and twelve known FBN1 mutations in eighty-one unrelated probands with Marfan syndrome and other fibrillinopathies.
    Arbustini E; Grasso M; Ansaldi S; Malattia C; Pilotto A; Porcu E; Disabella E; Marziliano N; Pisani A; Lanzarini L; Mannarino S; Larizza D; Mosconi M; Antoniazzi E; Zoia MC; Meloni G; Magrassi L; Brega A; Bedeschi MF; Torrente I; Mari F; Tavazzi L
    Hum Mutat; 2005 Nov; 26(5):494. PubMed ID: 16222657
    [TBL] [Abstract][Full Text] [Related]  

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

  • 14. Neonatal progeroid variant of Marfan syndrome with congenital lipodystrophy results from mutations at the 3' end of FBN1 gene.
    Jacquinet A; Verloes A; Callewaert B; Coremans C; Coucke P; de Paepe A; Kornak U; Lebrun F; Lombet J; Piérard GE; Robinson PN; Symoens S; Van Maldergem L; Debray FG
    Eur J Med Genet; 2014 Apr; 57(5):230-4. PubMed ID: 24613577
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Marfan syndrome: genetic basis and clinical manifestations.
    Tsipouras P; Devereux RB
    Semin Dermatol; 1993 Sep; 12(3):219-28. PubMed ID: 8217560
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel fibrillin 1 mutation in a case of neonatal Marfan syndrome: the increasing importance of early recognition.
    Sutherell J; Zarate Y; Tinkle BT; Markham LW; Cripe LH; Hyland JC; Witte D; Hopkin RJ; Hinton RB
    Congenit Heart Dis; 2007; 2(5):342-6. PubMed ID: 18377451
    [TBL] [Abstract][Full Text] [Related]  

  • 17. FBN1 mutation screening of patients with Marfan syndrome and related disorders: detection of 46 novel FBN1 mutations.
    Attanasio M; Lapini I; Evangelisti L; Lucarini L; Giusti B; Porciani M; Fattori R; Anichini C; Abbate R; Gensini G; Pepe G
    Clin Genet; 2008 Jul; 74(1):39-46. PubMed ID: 18435798
    [TBL] [Abstract][Full Text] [Related]  

  • 18. TGGE screening of the entire FBN1 coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies.
    Katzke S; Booms P; Tiecke F; Palz M; Pletschacher A; Türkmen S; Neumann LM; Pregla R; Leitner C; Schramm C; Lorenz P; Hagemeier C; Fuchs J; Skovby F; Rosenberg T; Robinson PN
    Hum Mutat; 2002 Sep; 20(3):197-208. PubMed ID: 12203992
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular analysis for diagnosis of Marfan syndrome and Marfan-associated disorders.
    Gao LG; Yao XP; Zhang L; Hui RT; Zhou XL
    Chin Med J (Engl); 2011 Mar; 124(6):930-4. PubMed ID: 21518605
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation screening of the fibrillin-1 (FBN1) gene in 76 unrelated patients with Marfan syndrome or Marfanoid features leads to the identification of 11 novel and three previously reported mutations.
    Rommel K; Karck M; Haverich A; Schmidtke J; Arslan-Kirchner M
    Hum Mutat; 2002 Nov; 20(5):406-7. PubMed ID: 12402346
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.