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 *

205 related articles for article (PubMed ID: 28555287)

  • 41. 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]  

  • 42. Antagonism of GxxPG fragments ameliorates manifestations of aortic disease in Marfan syndrome mice.
    Guo G; Muñoz-García B; Ott CE; Grünhagen J; Mousa SA; Pletschacher A; von Kodolitsch Y; Knaus P; Robinson PN
    Hum Mol Genet; 2013 Feb; 22(3):433-43. PubMed ID: 23100322
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Marfan syndrome: literature review of mortality studies.
    Krause KJ
    J Insur Med; 2000; 32(2):79-88. PubMed ID: 15912906
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Genetic testing of the FBN1 gene in Chinese patients with Marfan/Marfan-like syndrome.
    Yang H; Luo M; Chen Q; Fu Y; Zhang J; Qian X; Sun X; Fan Y; Zhou Z; Chang Q
    Clin Chim Acta; 2016 Aug; 459():30-35. PubMed ID: 27234404
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys-Dietz syndromes.
    Baetens M; Van Laer L; De Leeneer K; Hellemans J; De Schrijver J; Van De Voorde H; Renard M; Dietz H; Lacro RV; Menten B; Van Criekinge W; De Backer J; De Paepe A; Loeys B; Coucke PJ
    Hum Mutat; 2011 Sep; 32(9):1053-62. PubMed ID: 21542060
    [TBL] [Abstract][Full Text] [Related]  

  • 46. 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]  

  • 47. Identification of a novel TGFBR2 gene mutation in a Korean patient with Loeys-Dietz aortic aneurysm syndrome; no mutation in TGFBR2 gene in 30 patients with classic Marfan's syndrome.
    Ki CS; Jin DK; Chang SH; Kim JE; Kim JW; Park BK; Choi JH; Park IS; Yoo HW
    Clin Genet; 2005 Dec; 68(6):561-3. PubMed ID: 16283890
    [No Abstract]   [Full Text] [Related]  

  • 48. [Diagnosis and treatment of aortic diseases : new guidelines of the European Society of Cardiology 2014].
    Eggebrecht H;
    Herz; 2014 Dec; 39(8):931-40. PubMed ID: 25406331
    [TBL] [Abstract][Full Text] [Related]  

  • 49. CT angiographic evaluation of genetic vascular disease: role in detection, staging, and management of complex vascular pathologic conditions.
    Chu LC; Johnson PT; Dietz HC; Fishman EK
    AJR Am J Roentgenol; 2014 May; 202(5):1120-9. PubMed ID: 24758669
    [TBL] [Abstract][Full Text] [Related]  

  • 50. TGF-β signalopathies as a paradigm for translational medicine.
    Cannaerts E; van de Beek G; Verstraeten A; Van Laer L; Loeys B
    Eur J Med Genet; 2015 Dec; 58(12):695-703. PubMed ID: 26598797
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Pathophysiology of aortic aneurysm: insights from human genetics and mouse models.
    Wilson NK; Gould RA; Gallo MacFarlane E; Consortium ML
    Pharmacogenomics; 2016 Dec; 17(18):2071-2080. PubMed ID: 27922338
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Diagnostic Accuracy of Aortic Root Cross-sectional Area/Height Ratio in Children and Young Adults with Marfan and Loeys-Dietz Syndrome.
    Mariucci E; Donti A; Guidarini M; Oppido G; Angeli E; Lovato L; Wischmeijer A; Finlay M; Gargiulo GD; Picchio FM; Bonvicini M
    Congenit Heart Dis; 2016 May; 11(3):276-82. PubMed ID: 26555028
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Management of aortic aneurysms in patients with connective tissue disease.
    Schoenhoff F; Schmidli J; Czerny M; Carrel TP
    J Cardiovasc Surg (Torino); 2013 Feb; 54(1 Suppl 1):125-34. PubMed ID: 23443597
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Loeys-Dietz syndrome in pregnancy: a case description and report of a novel mutation.
    Gutman G; Baris HN; Hirsch R; Mandel D; Yaron Y; Lessing JB; Kuperminc MJ
    Fetal Diagn Ther; 2009; 26(1):35-7. PubMed ID: 19816028
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Genetically Triggered Aortic Disease Outcomes: On the Long Road to Personalized Medicine.
    Evangelista A; Teixido-Tura G
    J Am Coll Cardiol; 2022 May; 79(21):2082-2084. PubMed ID: 35618344
    [No Abstract]   [Full Text] [Related]  

  • 56. Genetics and Precision Medicine: Heritable Thoracic Aortic Disease.
    Demo E; Rigelsky C; Rideout AL; Graf M; Pariani M; Regalado E; MacCarrick G
    Med Clin North Am; 2019 Nov; 103(6):1005-1019. PubMed ID: 31582001
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Definition and delivery of an aortopathy bundle of care (ABC): a tool for improving diagnosis and management of Marfan syndrome and related conditions.
    Wright EB; Henriques S; Houghton C; Clarke B; Keavney B; Venetucci L
    Clin Med (Lond); 2016 Jun; 16 Suppl 3(Suppl 3):s30. PubMed ID: 27252334
    [No Abstract]   [Full Text] [Related]  

  • 58. Aortic dilation, genetic testing, and associated diagnoses.
    Zarate YA; Sellars E; Lepard T; Tang X; Collins RT
    Genet Med; 2016 Apr; 18(4):356-63. PubMed ID: 26133393
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Pitfalls in Genetic Diagnostics: Why Phenotyping is Essential.
    Gburek-Augustat J; Schoene-Bake JC; Bültmann E; Haack T; Buchert R; Synofzik M; Biskup S; Feuerhake F; Sorge I; Hartmann H
    Neuropediatrics; 2021 Aug; 52(4):274-283. PubMed ID: 33791999
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Laser diagnostics for gas dynamics: introduction to the feature issue.
    Allen MG; Linne MA; Varghese PL
    Appl Opt; 2005 Nov; 44(31):6525. PubMed ID: 16270540
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.