![]() Moulaert AJ, Oppenheimer-Dekker A (1976) Anterolateral muscle bundle of the left ventricle, bulboventricular flange and subaortic stenosis. Van Praagh R, Geva T, Kreutzer J (1989) Ventricular septal defects: how shall we describe, name and classify them? J Am Coll Cardiol 14(5):1298–1299 Kreutzer J, Van Praagh R (2000) Comparison of left ventricular outflow tract obstruction in interruption of the aortic arch and in coarctation of the aorta, with diagnostic, developmental, and surgical implications. Interact Cardiovasc Thorac Surg 15(4):802–804 Uppu SC, Shinkawa T, Imamura M (2012) Single institution experience with a right-sided interrupted aortic arch. Kutsche LM, Van Mierop LH (1984) Cervical origin of the right subclavian artery in aortic arch interruption: pathogenesis and significance. Geva T, Gajarski RJ (1995) Echocardiographic diagnosis of type B interruption of a right aortic arch. A rare condition and a cause of bronchial compression. Pierpont ME, Zollikofer CL, Moller JH, Edwards JE (1982) Interruption of the aortic arch with right descending aorta. Jegatheeswaran A, McCrindle BW, Blackstone EH et al (2010) Persistent risk of subsequent procedures and mortality in patients after interrupted aortic arch repair: a Congenital Heart Surgeons' Society study. Circulation 26:39–59Ĭeloria GC, Patton RB (1959) Congenital absence of the aortic arch. Roberts WC, Morrow AG, Braunwald E (1962) Complete interruption of the aortic arch. Kirby ML, Turnage KL 3rd, Hays BM (1985) Characterization of conotruncal malformations following ablation of "cardiac" neural crest. Am J Cardiol 30(5):514–525īockman DE, Kirby ML (1984) Dependence of thymus development on derivatives of the neural crest. Rudolph AM, Heymann MA, Spitznas U (1972) Hemodynamic considerations in the development of narrowing of the aorta. Van Mierop LH, Kutsche LM (1984) Interruption of the aortic arch and coarctation of the aorta: pathogenetic relations. Van Praagh R, Bernhard WF, Rosenthal A, Parisi LF, Fyler DC (1971) Interrupted aortic arch: surgical treatment. Aortic arch anomalies and the pathogenesis of the DiGeorge syndrome. Eur J Pediatr 161(3):173–174īinder M (1985) The teratogenic effects of a bis(dichloroacetyl)diamine on hamster embryos. ![]() Ito T, Okubo T, Sato H (2002) Familial 22q11.2 deletion: an infant with interrupted aortic arch and DiGeorge syndrome delivered from by a mother with tetralogy of Fallot. Martin DM, Mindell MH, Kwierant CA, Glover TW, Gorski JL (2003) Interrupted aortic arch in a child with trisomy 5q31.1q35.1 due to a maternal (20,5) balanced insertion. Lewin MB, Lindsay EA, Jurecic V, Goytia V, Towbin JA, Baldini A (1997) A genetic etiology for interruption of the aortic arch type B. Goldmuntz E (2005) DiGeorge syndrome: new insights. Van Mierop LH, Kutsche LM (1986) Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor. Am J Cardiol 79(8):1147–1148Ĭonley ME, Beckwith JB, Mancer JF, Tenckhoff L (1979) The spectrum of the DiGeorge syndrome. Powell CB, Stone FM, Atkins DL, Watson DG, Moller JH (1997) Operative mortality and frequency of coexistent anomalies in interruption of the aortic arch. Lancet 1(7899):140–142įyler DC, Buckley LP, Hellenbrand WE, Cohn HE (1980) Report of the New England Regional Infant Cardiac Program. Am J Roentgenol Radium Therapy, Nucl Med 114(2):362–370Įlliott RB, Starling MB, Neutze JM (1975) Medical manipulation of the ductus arteriosus. Gokcebay TM, Batillas J, Pinck RL (1972) Complete interruption of the aorta at the arch. Weisman D, Kesten HD (1948) Absence of transverse aortic arch with defects of cardiac septums report of a case simulating acute abdominal disease in a newborn infant. Steidele RJ (1778) Samml Chir u Med Beob (Vienna) 2:114
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |