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 *

176 related articles for article (PubMed ID: 19233667)

  • 1. Inherited diseases and syndromes leading to aortic aneurysms and dissections.
    Caglayan AO; Dundar M
    Eur J Cardiothorac Surg; 2009 Jun; 35(6):931-40. PubMed ID: 19233667
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Heritable diseases of the blood vessels.
    Baxter BT
    Cardiovasc Pathol; 2005; 14(4):185-8. PubMed ID: 16009316
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Heritable disorders predisposing to aortic dissection.
    Gleason TG
    Semin Thorac Cardiovasc Surg; 2005; 17(3):274-81. PubMed ID: 16253833
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Familial thoracic aortic aneurysms and dissections (FTAAD)].
    Milanowska B; Michalak E; Janaszek-Sitkowska H; Franaszczyk M; Płoski R; Bilińska ZT
    Kardiol Pol; 2011; 69(12):1291-7. PubMed ID: 22219111
    [No Abstract]   [Full Text] [Related]  

  • 5. Testing patterns for genetically triggered aortic and arterial aneurysms and dissections at an academic center.
    Hicks KL; Byers PH; Quiroga E; Pepin MG; Shalhub S
    J Vasc Surg; 2018 Sep; 68(3):701-711. PubMed ID: 29510914
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Smad2-dependent protease nexin-1 overexpression differentiates chronic aneurysms from acute dissections of human ascending aorta.
    Gomez D; Kessler K; Borges LF; Richard B; Touat Z; Ollivier V; Mansilla S; Bouton MC; Alkoder S; Nataf P; Jandrot-Perrus M; Jondeau G; Vranckx R; Michel JB
    Arterioscler Thromb Vasc Biol; 2013 Sep; 33(9):2222-32. PubMed ID: 23814118
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of fibrillin 1 gene mutations in patients with bicuspid aortic valve (BAV) without Marfan syndrome.
    Pepe G; Nistri S; Giusti B; Sticchi E; Attanasio M; Porciani C; Abbate R; Bonow RO; Yacoub M; Gensini GF
    BMC Med Genet; 2014 Feb; 15():23. PubMed ID: 24564502
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic Scoliosis.
    Haller G; Alvarado DM; Willing MC; Braverman AC; Bridwell KH; Kelly M; Lenke LG; Luhmann SJ; Gurnett CA; Dobbs MB
    J Bone Joint Surg Am; 2015 Sep; 97(17):1411-7. PubMed ID: 26333736
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic testing in patients with aortic aneurysms/dissections: a novel genotype/phenotype correlation?
    Waldmüller S; Müller M; Warnecke H; Rees W; Schöls W; Walterbusch G; Ennker J; Scheffold T
    Eur J Cardiothorac Surg; 2007 Jun; 31(6):970-5. PubMed ID: 17418587
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Aortic dissection: new frontiers in diagnosis and management: Part I: from etiology to diagnostic strategies.
    Nienaber CA; Eagle KA
    Circulation; 2003 Aug; 108(5):628-35. PubMed ID: 12900496
    [No Abstract]   [Full Text] [Related]  

  • 11. New insights into the molecular diagnosis and management of heritable thoracic aortic aneurysms and dissections.
    Campens L; Renard M; Callewaert B; Coucke P; De Backer J; De Paepe A
    Pol Arch Med Wewn; 2013; 123(12):693-700. PubMed ID: 24343123
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Single gene disorders of the aortic wall.
    Halushka MK
    Cardiovasc Pathol; 2012; 21(4):240-4. PubMed ID: 22036072
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Marfan syndrome].
    Schulthess G; Kolyvanos Naumann U; Käser L; Vetter W
    Praxis (Bern 1994); 2006 Mar; 95(10):349-54; quiz 355. PubMed ID: 16550708
    [No Abstract]   [Full Text] [Related]  

  • 14. Cardiovascular manifestations in men and women carrying a FBN1 mutation.
    Détaint D; Faivre L; Collod-Beroud G; Child AH; Loeys BL; Binquet C; Gautier E; Arbustini E; Mayer K; Arslan-Kirchner M; Stheneur C; Halliday D; Beroud C; Bonithon-Kopp C; Claustres M; Plauchu H; Robinson PN; Kiotsekoglou A; De Backer J; Adès L; Francke U; De Paepe A; Boileau C; Jondeau G
    Eur Heart J; 2010 Sep; 31(18):2223-9. PubMed ID: 20709720
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The non-syndromic familial thoracic aortic aneurysms and dissections maps to 15q21 locus.
    Keramati AR; Sadeghpour A; Farahani MM; Chandok G; Mani A
    BMC Med Genet; 2010 Oct; 11():143. PubMed ID: 20937124
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Comparison of clinical presentations and outcomes between patients with TGFBR2 and FBN1 mutations in Marfan syndrome and related disorders.
    Attias D; Stheneur C; Roy C; Collod-Béroud G; Detaint D; Faivre L; Delrue MA; Cohen L; Francannet C; Béroud C; Claustres M; Iserin F; Khau Van Kien P; Lacombe D; Le Merrer M; Lyonnet S; Odent S; Plauchu H; Rio M; Rossi A; Sidi D; Steg PG; Ravaud P; Boileau C; Jondeau G
    Circulation; 2009 Dec; 120(25):2541-9. PubMed ID: 19996017
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Actual management of patients with familial ascending aortic aneurysms and type-A aortic dissections.
    Weigang E; Chang XC; Munk-Schulenburg S; Richter H; von Samson P; Goebel H; Frydrychowicz A; Geibel A; Ammann S; Schwering L; Brunner T; Severin T; Czerny M; Beyersdorf F
    Thorac Cardiovasc Surg; 2007 Feb; 55(1):19-23. PubMed ID: 17285469
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Risk of dissection in thoracic aneurysms associated with mutations of smooth muscle alpha-actin 2 (ACTA2).
    Disabella E; Grasso M; Gambarin FI; Narula N; Dore R; Favalli V; Serio A; Antoniazzi E; Mosconi M; Pasotti M; Odero A; Arbustini E
    Heart; 2011 Feb; 97(4):321-6. PubMed ID: 21212136
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Gly1127Ser mutation in an EGF-like domain of the fibrillin-1 gene is a risk factor for ascending aortic aneurysm and dissection.
    Francke U; Berg MA; Tynan K; Brenn T; Liu W; Aoyama T; Gasner C; Miller DC; Furthmayr H
    Am J Hum Genet; 1995 Jun; 56(6):1287-96. PubMed ID: 7762551
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The genetic basis of aortic disease. Marfan syndrome and beyond.
    Tsipouras P; Silverman DI
    Cardiol Clin; 1999 Nov; 17(4):683-96. PubMed ID: 10589339
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.