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Journal Abstract Search

4211 related items for PubMed ID: 20232788

  • 21. [Cardiovascular manifestations of hereditary dysplasias of connective tissue].
    Bennis A, Mehadji BA, Soulami S, Tahiri A, Chraibi N.
    Ann Cardiol Angeiol (Paris); 1993 Apr; 42(4):173-81. PubMed ID: 8517593
    [Abstract] [Full Text] [Related]

  • 22. [Modern therapy of cardiac insufficiency].
    Stojsić D, Jelkić N.
    Med Pregl; 1999 Apr; 52(3-5):113-24. PubMed ID: 10518395
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  • 23. Marfan syndrome: what internists and pediatric or adult cardiologists need to know.
    Kaemmerer H, Oechslin E, Seidel H, Neuhann T, Neuhann IM, Mayer HM, Hess J.
    Expert Rev Cardiovasc Ther; 2005 Sep; 3(5):891-909. PubMed ID: 16181034
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  • 24. Clinical measurement of arterial stiffness obtained from noninvasive pressure waveforms.
    Nichols WW.
    Am J Hypertens; 2005 Jan; 18(1 Pt 2):3S-10S. PubMed ID: 15683725
    [Abstract] [Full Text] [Related]

  • 25. 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
    [Abstract] [Full Text] [Related]

  • 26. Ectopia lentis as the presenting and primary feature in Marfan syndrome.
    Zadeh N, Bernstein JA, Niemi AK, Dugan S, Kwan A, Liang D, Hyland JC, Hoyme HE, Hudgins L, Manning MA.
    Am J Med Genet A; 2011 Nov; 155A(11):2661-8. PubMed ID: 21932315
    [Abstract] [Full Text] [Related]

  • 27. Differences in Cardiovascular Manifestation of Marfan Syndrome Between Children and Adults.
    Wozniak-Mielczarek L, Sabiniewicz R, Drezek-Nojowicz M, Nowak R, Gilis-Malinowska N, Mielczarek M, Łabuc A, Waldoch A, Wierzba J.
    Pediatr Cardiol; 2019 Feb; 40(2):393-403. PubMed ID: 30417312
    [Abstract] [Full Text] [Related]

  • 28. Relation between genotype and left-ventricular dilatation in patients with Marfan syndrome.
    Aalberts JJ, van Tintelen JP, Meijboom LJ, Polko A, Jongbloed JD, van der Wal H, Pals G, Osinga J, Timmermans J, de Backer J, Bakker MK, van Veldhuisen DJ, Hofstra RM, Mulder BJ, van den Berg MP.
    Gene; 2014 Jan 15; 534(1):40-3. PubMed ID: 24161884
    [Abstract] [Full Text] [Related]

  • 29. [Clinical aspects of Marfan syndrome].
    Belsing TZ, Lund AM, Søndergaard L, Friis-Hansen L, Abildstrøm SZ.
    Ugeskr Laeger; 2011 Jan 31; 173(5):337-42. PubMed ID: 21276396
    [Abstract] [Full Text] [Related]

  • 30. The Marfan syndrome - features, natural history and treatment options - our experiences.
    Kwiatkowska J, Wierzba J, Pawlaczyk R, Waldoch A, Aleszewicz-Baranowska J.
    Georgian Med News; 2011 Apr 31; (193):41-5. PubMed ID: 21617273
    [Abstract] [Full Text] [Related]

  • 31. Marfan syndrome--a diagnostic challenge caused by phenotypic and genetic heterogeneity.
    Baumgartner C, Mátyás G, Steinmann B, Baumgartner D.
    Methods Inf Med; 2005 Apr 31; 44(4):487-97. PubMed ID: 16342915
    [Abstract] [Full Text] [Related]

  • 32. Utility of molecular analyses in the exploration of extreme intrafamilial variability in the Marfan syndrome.
    De Backer J, Loeys B, Leroy B, Coucke P, Dietz H, De Paepe A.
    Clin Genet; 2007 Sep 31; 72(3):188-98. PubMed ID: 17718856
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  • 33. Genotype and clinical phenotype of children with Marfan syndrome in Southeastern Anatolia.
    Karaoglan M, Nacarkahya G, Aytac EH, Keskin M.
    Eur J Pediatr; 2024 Aug 31; 183(8):3219-3232. PubMed ID: 38700693
    [Abstract] [Full Text] [Related]

  • 34. Missense mutations in FBN1 exons 41 and 42 cause Weill-Marchesani syndrome with thoracic aortic disease and Marfan syndrome.
    Cecchi A, Ogawa N, Martinez HR, Carlson A, Fan Y, Penny DJ, Guo DC, Eisenberg S, Safi H, Estrera A, Lewis RA, Meyers D, Milewicz DM.
    Am J Med Genet A; 2013 Sep 31; 161A(9):2305-10. PubMed ID: 23897642
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  • 35. Relationship between fibrillin-1 genotype and severity of cardiovascular involvement in Marfan syndrome.
    Franken R, Teixido-Tura G, Brion M, Forteza A, Rodriguez-Palomares J, Gutierrez L, Garcia Dorado D, Pals G, Mulder BJ, Evangelista A.
    Heart; 2017 Nov 31; 103(22):1795-1799. PubMed ID: 28468757
    [Abstract] [Full Text] [Related]

  • 36. The Marfan syndrome.
    Pyeritz RE.
    Annu Rev Med; 2000 Nov 31; 51():481-510. PubMed ID: 10774478
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  • 37. 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 31; 81(5):433-42. PubMed ID: 21564093
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  • 38. 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 31; 99(1):34-9. PubMed ID: 27455822
    [Abstract] [Full Text] [Related]

  • 39. Diagnosis and management of Marfan syndrome.
    Iams HD.
    Curr Sports Med Rep; 2010 Jan 31; 9(2):93-8. PubMed ID: 20220350
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  • 40. 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 31; 47(7):476-85. PubMed ID: 20591885
    [Abstract] [Full Text] [Related]

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