ANOMALIA DE EBSTEIN FISIOPATOLOGIA PDF

JavaScript is disabled for your browser. Some features of this site may not work without it. Congenital Heart Disease: emerging themes linking genetics and development. When lithium hurts: A look at ebstein anomaly.

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JavaScript is disabled for your browser. Some features of this site may not work without it. Congenital Heart Disease: emerging themes linking genetics and development. When lithium hurts: A look at ebstein anomaly. Cardiol Rev. H, Toews WH. Ebstein anomaly associated with left ventricular noncompaction: An autosomal dominant condition that can be caused by mutations in MYH7.

Familial ebstein anomaly, left ventricular hypertrabeculation, and ventricular septal defect associated with a MYH7 mutation. Mutations in the sarcomere gene MYH7 in Ebstein anomaly. Circ Cardiovasc Genet. J Thorac Cardiovasc Surg [Internet]. Rev Gastrohnup. Insights into the genetic basis of congenital heart disease. Cell Mol Life Sci. De novo mutations in histone modifying genes in congenital heart disease.

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Med J Aust. The genetics of congenital heart disease.. Curr Opin Pediatr. Libr la salud Cardiovasc [Internet]. Enfermedad Valvular Cardiaca. Complicaciones y Conducta a seguir. Estenosis pulmonar valvular. Rev Esp Cardiol. Ebstein Anomaly of the Tricuspid Valve. Pediatr Cardiovasc Med Second Ed. Swiss Med Wkly. Rev Mex Cardiol. Circulation [Internet]. Mutations in the cardiac transcription factor NKX2.

J Clin Invest. Identification of clinically relevant phenotypes in patients with Ebstein anomaly. Clin Cardiol. Update on Kleefstra syndrome. Mol Syndromol. Am J Hum Genet [Internet]. Mol Syndromol [Internet]. J Am Coll Cardiol [Internet]. J Med Genet. Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications.

Brain Dev [Internet]. Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy. Appl Clin Genet [Internet]. Identification of critical regions and candidate genes for Cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p PLoS One.

Ebstein anomaly: Genetic heterogeneity and association with microdeletions 1p36 and 8p HHS Public Access. Gene [Internet]. In-frame mutations in exon 1 of SKI cause dominant shprintzen-goldberg syndrome. Am J Hum Genet. Eur J Hum Genet. Mol Cell Biol. Para el correcto ejercicio de mi derecho de habeas data cuento con la cuenta de correo habeasdata urosario. Nombre : 2. Buscar en EdocUR. Acceder Registro. Restrepo, Carlos M. Silva, Claudia T. Quero Angarita, Rossi Isabel. Nora JJ, Nora a.

Postma A V. Madrid A, Restrepo JP. Garg V. Abigail Simmons M, Brueckner M. Shah PM. Paranon S, Acar P. Firth H V.

ANDREA PIRLO AUTOBIOGRAPHY PDF

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Skip to search form Skip to main content You are currently offline. Some features of the site may not work correctly. Compared to other congenital heart diseases, the anomaly described has a slower clinical course, with possible repercussions occurring only later in life. Save to Library.

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Ebstein's anomaly: a case report

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