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 *

141 related articles for article (PubMed ID: 23483062)

  • 21. Picture of the month. Infantile Marfan syndrome.
    Fourie DT; Colyn EL; Van der Vyver JD; Tunnessen WW
    Am J Dis Child; 1993 Mar; 147(3):313-4. PubMed ID: 8438817
    [No Abstract]   [Full Text] [Related]  

  • 22. Presenting signs and clinical diagnosis in individuals referred to rule out Marfan syndrome.
    Hamod A; Moodie D; Clark B; Traboulsi EI
    Ophthalmic Genet; 2003 Mar; 24(1):35-9. PubMed ID: 12660864
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prevalence, incidence, and age at diagnosis in Marfan Syndrome.
    Groth KA; Hove H; Kyhl K; Folkestad L; Gaustadnes M; Vejlstrup N; Stochholm K; Østergaard JR; Andersen NH; Gravholt CH
    Orphanet J Rare Dis; 2015 Dec; 10():153. PubMed ID: 26631233
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Neonatal Marfan syndrome: Report of two cases.
    Jurko T; Jurko A; Minarik M; Micieta V; Tonhajzerova I; Kolarovszka H; Zibolen M
    Neuro Endocrinol Lett; 2017 Jul; 38(3):138-140. PubMed ID: 28759179
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Pulmonary emphysema in a neonate with Marfan syndrome.
    Day DL
    Pediatr Radiol; 1988; 18(2):179. PubMed ID: 3353156
    [No Abstract]   [Full Text] [Related]  

  • 26. Recent developments in the diagnosis of Marfan syndrome and related disorders.
    Summers KM; West JA; Hattam A; Stark D; McGill JJ; West MJ
    Med J Aust; 2012 Nov; 197(9):494-7. PubMed ID: 23121584
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Double Trisomy 48,XXY,+21 in a Neonate with Congenital Heart Disease.
    Bijanzadeh M; Rajaei Behbahani S
    Arch Iran Med; 2020 May; 23(5):356-358. PubMed ID: 32383621
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel fibrillin-1 gene missense mutation associated with neonatal Marfan syndrome: a case report and review of the mutation spectrum.
    Peng Q; Deng Y; Yang Y; Liu H
    BMC Pediatr; 2016 Apr; 16():60. PubMed ID: 27138491
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Dilated neonatal cisterna magna and Marfan syndrome.
    Vasu V; Child AH; Modi N; Rutherford M; Cowan F
    BMJ Case Rep; 2011 Jul; 2011():. PubMed ID: 22689843
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The "thumb sign" in children.
    Feingold M
    Clin Pediatr (Phila); 1968 Jul; 7(7):423-4. PubMed ID: 4233066
    [No Abstract]   [Full Text] [Related]  

  • 31. 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]  

  • 32. Haplotype analysis enables the diagnosis of Marfan syndrome.
    Basel D; Kilpatrick MW; Tsipouras P
    Conn Med; 2004; 68(6):363-6. PubMed ID: 15266886
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Osteoporosis in adult with Marfan syndrome: casuality or causality?
    D'Amore M; Minenna G; Scagliusi P; D'Amore S
    Reumatismo; 2005; 57(2):125-7. PubMed ID: 15983637
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Cosegregation of the Marfan syndrome and the long QT syndrome in the same family leads to a severe cardiac phenotype.
    Probst V; Allouis M; Kyndt F; Lande G; Trochu JN; Schott JJ; Le Marec H
    Am J Cardiol; 2003 Mar; 91(5):635-7. PubMed ID: 12615283
    [No Abstract]   [Full Text] [Related]  

  • 35. Novel FBN1 mutation in a family with inherited Marfan Syndrome: p.Cys2672Arg.
    Cetinkaya A; Karaman A; Mutlu MB; Yavuz T
    Congenit Anom (Kyoto); 2018 Jan; 58(1):41-43. PubMed ID: 28321935
    [No Abstract]   [Full Text] [Related]  

  • 36. [Marfan syndrome: prevalence and natural course of cardiovascular manifestations].
    von Kodolitsch Y; Raghunath M; Nienaber CA
    Z Kardiol; 1998 Mar; 87(3):150-60. PubMed ID: 9586150
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The natural history of aortic dilatation in Marfan syndrome.
    Hwa J; Richards JG; Huang H; McKay D; Pressley L; Hughes CF; Jeremy RW
    Med J Aust; 1993 Apr; 158(8):558-62. PubMed ID: 8487722
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Comparison of Evolution of Aortic Root Dilation and Ghent Criteria in Preadolescents and Adolescents with and without Marfan Syndrome.
    Monteil DC; Shikany A; Aljeaid D; Parrott A; Tretter JT; James J; Martin LJ; Weaver KN
    J Pediatr; 2020 Jun; 221():188-195.e1. PubMed ID: 32446479
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Marfan syndrome: pathogenesis, phenotypes and diagnostic value, of various imaging techniques].
    Dieckmann C; Von Kodolitsch Y; Rybczynski M; Adam G
    Rofo; 2003 Nov; 175(11):1482-9. PubMed ID: 14610698
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Marfan's syndrome. Description of a case in a newborn infant].
    Spano B; Olmeo P; Ortu AM
    Pediatr Med Chir; 1992; 14(3):345-7. PubMed ID: 1528807
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.