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 *

370 related articles for article (PubMed ID: 26124674)

  • 1. Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome.
    von Kodolitsch Y; De Backer J; Schüler H; Bannas P; Behzadi C; Bernhardt AM; Hillebrand M; Fuisting B; Sheikhzadeh S; Rybczynski M; Kölbel T; Püschel K; Blankenberg S; Robinson PN
    Appl Clin Genet; 2015; 8():137-55. PubMed ID: 26124674
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Revised Ghent Criteria is Comparable to Original Diagnostic Criteria for Marfan Syndrome with Increased Ability to Clinically Diagnose Related Disorders.
    Penpattharakul W; Pithukpakorn M
    J Med Assoc Thai; 2016 Jan; 99(1):34-9. PubMed ID: 27455822
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A comparison of the Ghent and revised Ghent nosologies for the diagnosis of Marfan syndrome in an adult Korean population.
    Yang JH; Han H; Jang SY; Moon JR; Sung K; Chung TY; Lee HJ; Ki CS; Kim DK
    Am J Med Genet A; 2012 May; 158A(5):989-95. PubMed ID: 22162372
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Diagnostic yield in adults screened at the Marfan outpatient clinic using the 1996 and 2010 Ghent nosologies.
    Aalberts JJ; Thio CH; Schuurman AG; van Langen IM; van der Pol BA; van Tintelen JP; van den Berg MP
    Am J Med Genet A; 2012 May; 158A(5):982-8. PubMed ID: 22461464
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The new Ghent criteria for Marfan syndrome: what do they change?
    Faivre L; Collod-Beroud G; Adès L; Arbustini E; Child A; Callewaert BL; Loeys B; Binquet C; Gautier E; Mayer K; Arslan-Kirchner M; Grasso M; Beroud C; Hamroun D; Bonithon-Kopp C; Plauchu H; Robinson PN; De Backer J; Coucke P; Francke U; Bouchot O; Wolf JE; Stheneur C; Hanna N; Detaint D; De Paepe A; Boileau C; Jondeau G
    Clin Genet; 2012 May; 81(5):433-42. PubMed ID: 21564093
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The revised Ghent nosology for the Marfan syndrome.
    Loeys BL; Dietz HC; Braverman AC; Callewaert BL; De Backer J; Devereux RB; Hilhorst-Hofstee Y; Jondeau G; Faivre L; Milewicz DM; Pyeritz RE; Sponseller PD; Wordsworth P; De Paepe AM
    J Med Genet; 2010 Jul; 47(7):476-85. PubMed ID: 20591885
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Decreased frequency of FBN1 missense variants in Ghent criteria-positive Marfan syndrome and characterization of novel FBN1 variants.
    Baudhuin LM; Kotzer KE; Lagerstedt SA
    J Hum Genet; 2015 May; 60(5):241-52. PubMed ID: 25652356
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The revised ghent nosology; reclassifying isolated ectopia lentis.
    Chandra A; Patel D; Aragon-Martin JA; Pinard A; Collod-Béroud G; Comeglio P; Boileau C; Faivre L; Charteris D; Child AH; Arno G
    Clin Genet; 2015 Mar; 87(3):284-7. PubMed ID: 24635535
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of phenotype and genotype information for the diagnosis of Marfan syndrome.
    Sheikhzadeh S; Kade C; Keyser B; Stuhrmann M; Arslan-Kirchner M; Rybczynski M; Bernhardt AM; Habermann CR; Hillebrand M; Mir T; Robinson PN; Berger J; Detter C; Blankenberg S; Schmidtke J; von Kodolitsch Y
    Clin Genet; 2012 Sep; 82(3):240-7. PubMed ID: 21883168
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genotype and phenotype analysis of 171 patients referred for molecular study of the fibrillin-1 gene FBN1 because of suspected Marfan syndrome.
    Loeys B; Nuytinck L; Delvaux I; De Bie S; De Paepe A
    Arch Intern Med; 2001 Nov; 161(20):2447-54. PubMed ID: 11700157
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience.
    Mannucci L; Luciano S; Salehi LB; Gigante L; Conte C; Longo G; Ferradini V; Piumelli N; Brancati F; Ruvolo G; Novelli G; Sangiuolo F
    Clin Chim Acta; 2020 Feb; 501():154-164. PubMed ID: 31730815
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Joint Hypermobility as a Potential Indicator of Marfan Syndrome and Ehlers-Danlos Syndrome.
    Zou H; Waalkes P
    Cureus; 2022 Aug; 14(8):e27574. PubMed ID: 36059296
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Kid-Short Marfan Score (Kid-SMS) Is a Useful Diagnostic Tool for Stratifying the Pre-Test Probability of Marfan Syndrome in Childhood.
    Stark VC; Arndt F; Harring G; von Kodolitsch Y; Kozlik-Feldmann R; Mueller GC; Steiner KJ; Mir TS
    Diseases; 2015 Mar; 3(1):24-33. PubMed ID: 28943606
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Marfan syndrome and related connective tissue disorders in the current era in Switzerland in 103 patients: medical and surgical management and impact of genetic testing.
    Bombardieri E; Rohrbach M; Greutmann M; Matyas G; Weber R; Radulovic J; Fasnacht Boillat M; Linka A; De Pasquale G; Bonassin F; Attenhofer Jost CH
    Swiss Med Wkly; 2020 Mar; 150():w20189. PubMed ID: 32242911
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of Protrusio Acetabuli Using a CT-based Diagnostic Method in Korean Patients with Marfan Syndrome: Prevalence and Association with Other Manifestations.
    Chun KJ; Yang JH; Jang SY; Lee SH; Gwag HB; Chung TY; Huh J; Ki CS; Sung K; Choi SH; Kim SM; Choe YH; Kim DK
    J Korean Med Sci; 2015 Sep; 30(9):1260-5. PubMed ID: 26339165
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Critical appraisal of the revised Ghent criteria for diagnosis of Marfan syndrome.
    Radonic T; de Witte P; Groenink M; de Bruin-Bon RA; Timmermans J; Scholte AJ; van den Berg MP; Baars MJ; van Tintelen JP; Kempers M; Zwinderman AH; Mulder BJ
    Clin Genet; 2011 Oct; 80(4):346-53. PubMed ID: 21332468
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of a novel pathogenic variant in FBN1 associated with Marfan Syndrome.
    Pereira JP; Ferreira JR; Botelho APA; Melo MM; Dias GM
    Cold Spring Harb Mol Case Stud; 2022 May; 8(4):. PubMed ID: 35589387
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Marfan syndrome: An eyesight of syndrome.
    Kumar A; Agarwal S
    Meta Gene; 2014 Dec; 2():96-105. PubMed ID: 25606393
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A comparison of the Berlin and Ghent nosologies and the influence of dural ectasia in the diagnosis of Marfan syndrome.
    Rose PS; Levy HP; Ahn NU; Sponseller PD; Magyari T; Davis J; Francomano CA
    Genet Med; 2000; 2(5):278-82. PubMed ID: 11399208
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.