The new Ghent criteria for Marfan syndrome: what do they change?
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Marfan syndrome: current perspectivesEducational paper. Connective tissue disorders with vascular involvement: from gene to therapyPerspectives on the revised Ghent criteria for the diagnosis of Marfan syndromeWhen flexibility is not necessarily a virtue: a review of hypermobility syndromes and chronic or recurrent musculoskeletal pain in childrenNovel mutation in FBN1 causes ectopia lentis and varicose great saphenous vein in one Chinese autosomal dominant family.Analysis of oxidative stress enzymes and structural and functional proteins on human aortic tissue from different aortopathies.A novel fibrillin 1 gene mutation leading to marfan syndrome with minimal cardiac features.Prevalence, incidence, and age at diagnosis in Marfan Syndrome.Genetic dissection of marfan syndrome and related connective tissue disorders: an update 2012.Musculo-skeletal abnormalities in patients with Marfan syndrome.Infusion of Hibiscus sabdariffa L. Modulates Oxidative Stress in Patients with Marfan Syndrome.Marfan Syndrome: Clinical, Surgical, and Anesthetic Considerations.The revised ghent nosology; reclassifying isolated ectopia lentis.Cardiovascular manifestations in Marfan syndrome and related diseases; multiple genes causing similar phenotypes.[Aneurysms of the ascending aorta and aortic arch].Kid-Short Marfan Score (Kid-SMS) Is a Useful Diagnostic Tool for Stratifying the Pre-Test Probability of Marfan Syndrome in ChildhoodStudy of phenotype evolution during childhood in Marfan syndrome to improve clinical recognition.The Kid-Short Marfan Score (Kid-SMS) - an easy executable risk score for suspected paediatric patients with Marfan syndrome.Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disability.Marfan Sartan: a randomized, double-blind, placebo-controlled trial.Novel FBN1 mutation in a family with inherited Marfan Syndrome: p.Cys2672Arg.WES/WGS Reporting of Mutations from Cardiovascular "Actionable" Genes in Clinical Practice: A Key Role for UMD Knowledgebases in the Era of Big Databases.Targeted genetic analysis in a large cohort of familial and sporadic cases of aneurysm or dissection of the thoracic aorta.The phenotypic heterogeneity of patients with Marfan-related disorders and their variant spectrums.Marfan Syndrome: oral implication and management.The 8th international research symposium on the Marfan Syndrome and related conditions
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P2860
The new Ghent criteria for Marfan syndrome: what do they change?
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2011年の論文
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The new Ghent criteria for Marfan syndrome: what do they change?
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The new Ghent criteria for Marfan syndrome: what do they change?
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The new Ghent criteria for Marfan syndrome: what do they change?
@en
The new Ghent criteria for Marfan syndrome: what do they change?
@nl
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The new Ghent criteria for Marfan syndrome: what do they change?
@en
The new Ghent criteria for Marfan syndrome: what do they change?
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P2093
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The new Ghent criteria for Marfan syndrome: what do they change?
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P2093
A De Paepe
C Bonithon-Kopp
C Stheneur
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P304
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10.1111/J.1399-0004.2011.01703.X
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P577
2011-06-02T00:00:00Z