Single gene disorders of the aortic wall

Cardiovascular Pathology

Volumn 21, Issue 4, 2012, Pages 240-244

  Halushka, Marc K ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Aortic root; Ascending aorta; Genetic diseases

Indexed keywords

FIBRILLIN 1; MATRIX METALLOPROTEINASE; MITOGEN ACTIVATED PROTEIN KINASE; MONOCYTE CHEMOTACTIC PROTEIN 1; MYOSIN HEAVY CHAIN; PROCOLLAGEN TYPE 3 AMINOPROPEPTIDE; SMAD2 PROTEIN; SMAD3 PROTEIN; SMAD4 PROTEIN; TRANSFORMING GROWTH FACTOR BETA; TRANSFORMING GROWTH FACTOR BETA RECEPTOR 1; TRANSFORMING GROWTH FACTOR BETA RECEPTOR 2;

AORTA ANEURYSM; AORTA ANOMALY; AORTA DISSECTION; AORTA ROOT; CARDIOVASCULAR DISEASE; CARDIOVASCULAR MAGNETIC RESONANCE; CLINICAL FEATURE; CONGENITAL HEART DISEASE; DEATH; DISEASE SEVERITY; EHLERS DANLOS SYNDROME; ENZYME ACTIVITY; ENZYME PHOSPHORYLATION; FAMILIAL THORACIC AORTIC ANEURYSM AND DISSECTION; GENE MUTATION; GENETIC DISORDER; HISTOPATHOLOGY; HUMAN; LOEYS DIETZ SYNDROME; MARFAN SYNDROME; MONOSOMY; MORTALITY; PRIORITY JOURNAL; REVIEW; SURVIVAL; TURNER SYNDROME; X CHROMOSOME;

ADOLESCENT; ANEURYSM, DISSECTING; AORTA; AORTIC ANEURYSM, THORACIC; AORTIC DISEASES; CHILD; EHLERS-DANLOS SYNDROME; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LOEYS-DIETZ SYNDROME; MARFAN SYNDROME; MUTATION; TURNER SYNDROME;

EID: 84861195289     PISSN: 10548807     EISSN: 18791336     Source Type: Journal    
DOI: 10.1016/j.carpath.2011.09.004     Document Type: Review

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