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INDUCTION OF NUCLEAR DECONDENSATION OF MAMMALIAN SPERMATOZOA IN VITRO

2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM Guidelines for the Diagnosis and Management of Patients With Thoracic Aortic Disease

Revised diagnostic criteria for the Marfan syndrome

Surgical management of children and young adults with marfan syndrome and pectus excavatum

Pectus excavatum repair: Experience with standard and minimal invasive techniques

Recommendations for Quantification Methods During the Performance of a Pediatric Echocardiogram: A Report From the Pediatric Measurements Writing Group of the American Society of Echocardiography Pediatric and Congenital Heart Disease Council

Five Years of GWAS Discovery

Minimally invasive repair of pectus excavatum in patients with Marfan syndrome and marfanoid features

Marfan's syndrome

Outcome of pectus excavatum in patients with Marfan syndrome and in the general population

FGF-21 as a novel metabolic regulator

Twenty-One Years of Experience With Minimally Invasive Repair of Pectus Excavatum by the Nuss Procedure in 1215 Patients

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

Mapping a gene for Noonan syndrome to the long arm of chromosome 12

Chronic β-blocker therapy improves outcome and reduces treatment costs in chronic type B aortic dissection

Phenotypic features and impact of Beta blocker or calcium antagonist therapy on Aortic lumen size in the Marfan syndrome

Hypertrophic Scarring and Keloids: Pathomechanisms and Current and Emerging Treatment Strategies

The hormone resistin links obesity to diabetes

Expert Consensus Document on the Treatment of Descending Thoracic Aortic Disease Using Endovascular Stent-Grafts

Deconstructing Type 2 Diabetes

On the Nature of Hypertrophic Scars and Keloids: A Review

International Clinical Recommendations on Scar Management

Genetics of keloid scarring

Wound repair and regeneration: Mechanisms, signaling, and translation

Noonan syndrome: A review

Formes frustes of Marfan's syndrome presenting with severe aortic regurgitation. Clinicogenetic study of 18 families.

2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM Guidelines for the Diagnosis and Management of Patients With Thoracic Aortic Disease

ACC/AHA 2008 Guidelines for the Management of Adults With Congenital Heart Disease

ACC/AHA 2008 Guidelines for the Management of Adults With Congenital Heart Disease: Executive Summary

Keloids and hypertrophic scars

Decondensation of sperm nuclei in vitro

Stability of Y Chromosome Fluorescence During Freeze-Thawing and Frozen Storage of Human Spermatozoa

Ehlers-Danlos syndrome.

Endocrine-metabolic relationships in patients with leprechaunism.

A prospectus on the prevention of aortic rupture in the Marfan syndrome with data on survivorship without treatment.

Chromosome 13 long arm interstitial deletion associated with features of Noonan phenotype.

Delineation of multiple cardiac anomalies associated with the Noonan syndrome in an adult and review of the literature.

Possible etiologic mechanisms of the short stature in the Noonan syndrome.

Children With Marfanʼs Syndrome and Pectus Excavatum