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Journal Abstract Search
92 related items for PubMed ID: 14959451
1. Tricuspid atresia associated with common arterial trunk and 22q11 chromosome deletion. Alva C, David F, Hernández M, Argüero R, Ortegón J, Martínez A, López D, Jiménez S, Sánchez A. Arch Cardiol Mex; 2003; 73(4):271-4. PubMed ID: 14959451 [Abstract] [Full Text] [Related]
2. Truncus arteriosus communis associated with chromosome 22q11 deletion. Momma K, Ando M, Matsuoka R. J Am Coll Cardiol; 1997 Oct; 30(4):1067-71. PubMed ID: 9316541 [Abstract] [Full Text] [Related]
3. Tricuspid atresia associated with truncus arteriosus versus aortopulmonary window: combining fetal and postnatal echocardiography to make the diagnosis. Hauck A, da Cruz EM, Jaggers J, Jone PN. Echocardiography; 2013 Nov; 30(10):E336-9. PubMed ID: 24033694 [Abstract] [Full Text] [Related]
4. Tricuspid atresia and 22q11 deletion. Marino B, Digilio MC, Novelli G, Giannotti A, Dallapiccola B. Am J Med Genet; 1997 Oct 03; 72(1):40-2. PubMed ID: 9295072 [Abstract] [Full Text] [Related]
5. Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion. Momma K, Kondo C, Matsuoka R. J Am Coll Cardiol; 1996 Jan 03; 27(1):198-202. PubMed ID: 8522695 [Abstract] [Full Text] [Related]
6. Chromosome 22q11 deletion in patients with truncus arteriosus. McElhinney DB, Driscoll DA, Emanuel BS, Goldmuntz E. Pediatr Cardiol; 2003 Jan 03; 24(6):569-73. PubMed ID: 12947506 [Abstract] [Full Text] [Related]
7. Prenatal diagnosis of an unexpected interstitial 22q11.2 deletion causing truncus arteriosus and thymic hypoplasia in a ring 22 chromosome derived from a maternally inherited paracentric inversion. McClarren J, Donnenfeld AE, Ravnan JB. Prenat Diagn; 2006 Dec 03; 26(13):1212-5. PubMed ID: 17099929 [Abstract] [Full Text] [Related]
8. [22q11 deletion in conotruncal anomalies]. Kádár K. Orv Hetil; 2005 Feb 20; 146(8):363-6. PubMed ID: 15803887 [Abstract] [Full Text] [Related]
9. Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies. Beauchesne LM, Warnes CA, Connolly HM, Ammash NM, Grogan M, Jalal SM, Michels VV. J Am Coll Cardiol; 2005 Feb 15; 45(4):595-8. PubMed ID: 15708709 [Abstract] [Full Text] [Related]
10. [Tricuspid atresia associated with common trunk. A case report]. Ramírez Ramírez L, Lázaro Castillo JL, Gayosso Dominguez A, Manrique Valle M, Carpio Hernández JC, Munayer Calderón J, Aguilar Arteaga L, Arellano Ostoa D. Arch Cardiol Mex; 2008 Feb 15; 78(4):413-6. PubMed ID: 19205550 [Abstract] [Full Text] [Related]
11. Tricuspid atresia with truncus arteriosus: successful surgical treatment. Roldan S, Pieles G, Caputo M, Morgan G, Stoica S, Parry A. Ann Thorac Surg; 2014 Aug 15; 98(2):721-3. PubMed ID: 25087803 [Abstract] [Full Text] [Related]
12. Prenatal diagnosis of tricuspid atresia: intrauterine course and outcome. Berg C, Lachmann R, Kaiser C, Kozlowski P, Stressig R, Schneider M, Asfour B, Herberg U, Breuer J, Gembruch U, Geipel A. Ultrasound Obstet Gynecol; 2010 Feb 15; 35(2):183-90. PubMed ID: 20101636 [Abstract] [Full Text] [Related]
13. DiGeorge syndrome with truncus arteriosus: report of one case. Liang PH, Chen MR, Shyur SD, Lee YJ, Lin SP, Yu MT, Chiu IS, Chen SJ. Acta Paediatr Taiwan; 2004 Feb 15; 45(3):174-7. PubMed ID: 15493739 [Abstract] [Full Text] [Related]
14. Double trouble: A hitherto undescribed association of tricuspid atresia and common arterial trunk! Deshpande AA, Nandi D, Malhi AS, Kumar S, Sachdeva S, Ramakrishnan S. J Card Surg; 2021 Aug 15; 36(8):2941-2943. PubMed ID: 34053105 [No Abstract] [Full Text] [Related]
15. Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction. Chen CP, Chern SR, Chang TY, Lee CC, Chen LF, Tzen CY, Wang W, Lin CJ, Yang BP, Yang LS. Prenat Diagn; 2003 Jan 15; 23(1):40-3. PubMed ID: 12533811 [Abstract] [Full Text] [Related]
16. Tricuspid atresia with persistent truncus arteriosus. Wang JN, Wu MH, Wang JK, Lue HC. J Formos Med Assoc; 1999 Apr 15; 98(4):290-1. PubMed ID: 10389376 [Abstract] [Full Text] [Related]
17. Brief clinical report: deletion of the long arm of chromosome 11, [del(11)(q23)]. Monteleone PL, Chen SC, Nouri-Moghaddam S, Blair JD, Tietjens M. Am J Med Genet; 1982 Nov 15; 13(3):299-304. PubMed ID: 6891182 [Abstract] [Full Text] [Related]